5421 NP_705833 N830H not found in SNVbox database
286 NP_001070868 A717V not found in SNVbox database
764 NP_001070868 V193L not found in SNVbox database
2022 NP_001070868 N31H not found in SNVbox database
2144 NP_001070868 V442L not found in SNVbox database
2197 NP_705833 N1006Y not found in SNVbox database
2201 NP_001070868 K213N not found in SNVbox database
2671 NP_705833 G213A not found in SNVbox database
3784 NP_705833 S725T not found in SNVbox database
4462 NP_705833 P451Q not found in SNVbox database
4893 NP_001070868 A732D not found in SNVbox database
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:58858920 G>T maps to NM_130786.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:58864327 G>T maps to NM_130786.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58862862 C>A maps to NM_130786.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:52566514 G>T maps to NM_138932.2 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:52603770 C>A maps to NM_138932.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:52566489 C>T maps to NM_138932.2 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:52575817 G>T maps to NM_138932.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr10:52619637 G>A maps to NM_138932.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr10:52566524 T>A maps to NM_138932.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:52601736 C>A maps to NM_138932.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr10:52575817 G>C maps to NM_138932.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:52619631 C>G maps to NM_138932.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:7703844 C>A maps to NM_145891.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:7759056 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:7703883 C>T maps to NM_145891.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr16:7645643 G>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr16:7645644 T>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:7743370 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:7726786 T>C maps to NM_145891.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr16:7383026 C>T maps to NM_145891.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr16:7721576 T>A maps to NM_145891.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:7759064 C>A maps to NM_145891.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr16:7568186 T>A maps to NM_145891.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:7568324 C>A maps to NM_145891.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:7645588 G>T maps to NM_145891.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:7703919 G>T maps to NM_145891.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:9265988 C>T maps to NM_000014.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:9251202 C>T maps to NM_000014.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:9248290 G>A maps to NM_000014.4 Y619Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:9231859 G>T maps to NM_000014.4 G1033G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:9264759 C>A maps to NM_000014.4 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:9242574 C>A maps to NM_000014.4 E881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:9010578 C>T maps to NM_144670.3 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:8990975 C>A maps to NM_144670.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:8976458 C>G maps to NM_144670.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:8998703 C>T maps to NM_144670.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:9004397 G>A maps to NM_144670.3 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:9004532 C>A maps to NM_144670.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:9001431 C>A maps to NM_144670.3 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:137850008 G>T maps to NM_016161.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:137850092 C>T maps to NM_016161.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:137843387 G>C maps to NM_016161.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:53709520 T>C maps to NM_015665.5 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:125618603 C>T maps to NM_023928.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:125618591 C>T maps to NM_023928.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:125626688 G>T maps to NM_023928.3 G645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:125613887 G>T maps to NM_023928.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:125619372 C>T maps to NM_023928.3 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr12:125613929 C>T maps to NM_023928.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:125576000 G>T maps to NM_023928.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:151535366 G>T maps to NM_001086.2 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151474961 G>A maps to NM_207365.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:151474790 T>C maps to NM_207365.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:151461908 A>G maps to NM_207365.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:12785390 C>T maps to NM_001103170.1 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:12785398 G>T maps to NM_001103170.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:12785377 C>A maps to NM_001103170.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:12785266 C>A maps to NM_001103170.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:12779533 C>T maps to NM_001103170.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:12726346 A>G maps to NM_001013630.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr1:12726493 A>G maps to NM_001013630.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:12726520 C>T maps to NM_001013630.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:12711242 C>A maps to NM_001013630.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:171010793 A>C maps to ENST00000509167 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:171010811 C>G maps to ENST00000509167 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:69784099 A>T maps to NM_014911.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:219132259 G>A maps to ENST00000444053 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:219129809 G>T maps to ENST00000444053 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:74466033 C>A maps to NM_001166579.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr16:70292120 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:70301625 G>C maps to ENST00000418685 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:70302227 G>A maps to ENST00000418685 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:44270226 C>A maps to NM_020745.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:44270196 C>A maps to NM_020745.2 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr6:44278180 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:41106914 C>A maps to NM_001136042.2 G485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:57220928 A>T maps to NM_181806.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr4:57220213 A>G maps to NM_181806.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:57221478 T>C maps to NM_181806.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:57220955 C>A maps to NM_181806.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:57217623 C>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr4:57220267 C>T maps to NM_181806.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr4:57204687 A>G maps to NM_181806.2 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr4:57219585 T>C maps to NM_181806.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:105948472 A>G maps to NM_015423.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:105948529 C>G maps to NM_015423.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:121717922 G>C maps to NM_005763.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr7:121717988 C>T maps to NM_005763.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:121738538 C>T maps to NM_005763.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:121756791 C>T maps to NM_005763.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121733184 A>C maps to NM_005763.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:121757011 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:35344012 A>G maps to NM_012138.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:79094915 G>A maps to NM_001080395.2 D940D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8844284 G>T maps to NM_001127448.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:8870280 G>T maps to NM_001127448.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:8868782 G>T maps to NM_001127448.1 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr16:8868745 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:8870253 G>T maps to NM_001127448.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:107578465 C>G maps to NM_005502.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:107568677 C>T maps to NM_005502.3 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:107560863 C>A maps to NM_005502.3 V1653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr9:107550272 G>A maps to NM_005502.3 N2044N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr9:107562811 C>T maps to NM_005502.3 L1584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr9:107558438 C>G maps to NM_005502.3 V1759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:107591241 G>A maps to NM_005502.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr9:107562254 G>A maps to NM_005502.3 N1596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr9:107602758 C>G maps to NM_005502.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr9:107566947 C>A maps to NM_005502.3 S1506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:67189377 T>C maps to NM_080282.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67170782 C>A maps to NM_080282.3 G1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:67170783 C>A maps to NM_080282.3 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:67151276 C>A maps to NM_080282.3 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:67215831 C>T maps to NM_080282.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:67171588 G>T maps to NM_080282.3 C945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:67152029 C>A maps to NM_080282.3 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:67170882 G>A maps to NM_080282.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:67152974 G>A maps to NM_080282.3 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:67153031 G>A maps to NM_080282.3 V1132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:67188716 C>A maps to NM_080282.3 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:215884139 A>T maps to NM_173076.2 L526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:215843638 T>C maps to NM_173076.2 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:215848371 T>G maps to NM_173076.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:215819925 C>A maps to NM_173076.2 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:215846999 G>C maps to NM_173076.2 S1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:215821446 A>T maps to NM_173076.2 L2058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:215855533 G>T maps to NM_173076.2 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:215882823 C>A maps to NM_173076.2 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr2:215838675 G>C maps to NM_173076.2 V1853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:215815683 A>G maps to NM_173076.2 Y2257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:215862466 A>T maps to NM_173076.2 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:215848573 C>A maps to NM_173076.2 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:215865682 G>C maps to NM_173076.2 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr2:215880342 G>A maps to NM_173076.2 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:48411994 G>T maps to NM_152701.3 A3678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:48311758 C>A maps to NM_152701.3 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48431670 G>A maps to NM_152701.3 L3936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:48520640 A>T maps to NM_152701.3 P4328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:48311972 G>T maps to NM_152701.3 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48313591 T>C maps to NM_152701.3 N1443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:48311677 G>A maps to NM_152701.3 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:48550738 A>T maps to NM_152701.3 T4528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:48411988 T>C maps to NM_152701.3 N3676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:48320967 C>T maps to NM_152701.3 Q2919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:48337961 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:48311620 T>C maps to NM_152701.3 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:48311667 G>A maps to NM_152701.3 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:48285187 G>T maps to NM_152701.3 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:48431673 G>T maps to NM_152701.3 L3937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:48335364 C>T maps to NM_152701.3 S3008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr7:48634391 G>C maps to NM_152701.3 A4909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:48390324 C>A maps to NM_152701.3 C3430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:48315430 A>G maps to NM_152701.3 E2056E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:48318327 A>T maps to NM_152701.3 R2513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:48314883 C>G maps to NM_152701.3 S1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:48319267 G>A maps to NM_152701.3 W2826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:48312458 A>T maps to NM_152701.3 K1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr7:48313690 A>T maps to NM_152701.3 T1476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:48520718 G>A maps to NM_152701.3 E4354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:48318230 T>A maps to NM_152701.3 G2480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:139913230 C>A maps to ENST00000355090 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr9:139913462 C>T maps to ENST00000355090 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr9:139903001 G>A maps to ENST00000355090 Q2411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr9:139905665 C>T maps to ENST00000355090 E1995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:2347903 G>A maps to NM_001089.2 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:2333252 G>A maps to NM_001089.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:2338147 G>A maps to NM_001089.2 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2331081 G>C maps to NM_001089.2 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr16:2349402 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:2336747 G>A maps to NM_001089.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr16:2354053 C>T maps to NM_001089.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr16:2335496 G>A maps to NM_001089.2 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:2376170 G>A maps to NM_001089.2 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:2347835 C>G maps to NM_001089.2 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr16:2333333 A>T maps to NM_001089.2 Y1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94512563 C>T maps to NM_000350.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:94502754 C>A maps to NM_000350.2 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:94476462 C>G maps to NM_000350.2 P1869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:94508893 G>C maps to NM_000350.2 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:94471098 G>T maps to NM_000350.2 G2015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:94522204 C>T maps to NM_000350.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:94544949 C>A maps to NM_000350.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:94526107 C>A maps to NM_000350.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:94546250 C>T maps to NM_000350.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:67309239 T>C maps to ENST00000392677 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:67305459 C>A maps to ENST00000392677 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:67270187 G>A maps to ENST00000392677 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:67103889 G>C maps to NM_080284.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:67082842 C>A maps to NM_080284.2 E1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67081857 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:67098977 T>A maps to NM_080284.2 K958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:67119513 G>A maps to NM_080284.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:67081324 T>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:67079362 C>A maps to NM_080284.2 G1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:67129975 C>T maps to NM_080284.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr17:67109502 T>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:67114098 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:1057025 G>A maps to NM_019112.3 Q1569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:1063562 G>A maps to NM_019112.3 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:1056363 G>T maps to NM_019112.3 V1484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:1053824 A>C maps to NM_019112.3 T1154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:1052100 C>A maps to NM_019112.3 R1041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:1055120 G>T maps to NM_019112.3 E1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:1042749 C>G maps to NM_019112.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:1055904 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:1061872 G>T maps to NM_019112.3 V1852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:1061792 C>T maps to NM_019112.3 L1826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:66928444 G>T maps to NM_007168.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:66873754 G>A maps to NM_007168.2 N1328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:66928613 A>T maps to NM_007168.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:66883271 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:66878831 G>A maps to NM_007168.2 Q1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr17:66902183 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:66928586 G>T maps to NM_007168.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:66881434 C>A maps to NM_007168.2 G1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:66925833 C>T maps to NM_007168.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:66887653 G>A maps to NM_007168.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:66938151 C>A maps to NM_007168.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:66980198 C>A maps to NM_080283.3 L1499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:66982324 G>A maps to NM_080283.3 D1396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr17:67039721 T>A maps to NM_080283.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:67013931 T>C did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr17:66985996 C>T maps to NM_080283.3 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:67022603 C>T maps to NM_080283.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:67016572 A>T maps to NM_080283.3 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:66982456 C>T maps to NM_080283.3 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:66985242 C>A maps to NM_080283.3 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr17:67045514 A>G maps to NM_080283.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr17:66978701 C>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:67031404 G>A maps to NM_080283.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:67031799 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:87190634 G>T maps to NM_000927.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:87179871 G>T maps to NM_000927.3 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:87173486 G>T maps to NM_000927.3 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87148757 G>A maps to NM_000927.3 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:87179274 G>T maps to NM_000927.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:87144690 G>T maps to NM_000927.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:87160717 C>T maps to NM_000927.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:87183172 A>G maps to NM_000927.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:87174222 G>T maps to NM_000927.3 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:87168582 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:87199500 C>A maps to NM_000927.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:87214951 T>A maps to NM_000927.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:87160608 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:229661862 C>A maps to NM_012089.2 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:229661863 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:169791860 A>C maps to NM_003742.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:169850326 G>T maps to NM_003742.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:169787279 C>A maps to NM_003742.2 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:169824974 C>T maps to NM_003742.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:169780290 G>T maps to NM_003742.2 T1269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr2:169853213 G>A maps to NM_003742.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:169792772 A>T maps to NM_003742.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:169781253 G>T maps to NM_003742.2 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:169792754 C>A maps to NM_003742.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr2:169780332 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:87082320 G>A maps to NM_018849.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:87081013 G>T maps to NM_018849.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:87076409 G>T maps to NM_018849.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:87082308 C>A maps to NM_018849.2 G163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:87104727 C>T maps to NM_018849.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr7:87083864 T>C maps to NM_018849.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:87104739 G>T maps to NM_018849.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr7:87079360 T>A maps to NM_018849.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:20784904 C>A maps to NM_001163941.1 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20691246 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:20721144 T>C maps to NM_001163941.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:20739715 G>T maps to NM_001163941.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:20698687 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:20691041 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:20767982 C>T maps to NM_001163941.1 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20721219 G>A maps to NM_001163941.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:20685434 G>T maps to NM_001163941.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:20782585 C>A maps to NM_001163941.1 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:20687652 G>T maps to NM_001163941.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:20762763 C>T maps to NM_001163941.1 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:20795082 G>T maps to NM_001163941.1 G1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:20668360 G>T maps to NM_001163941.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:20698190 C>A maps to NM_001163941.1 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:20685482 C>A maps to NM_001163941.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr7:20721240 T>A maps to NM_001163941.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:20685745 C>T maps to NM_001163941.1 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:20762706 C>T maps to NM_001163941.1 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:20782522 G>A maps to NM_001163941.1 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:20784878 G>T maps to NM_001163941.1 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:20721223 G>T maps to NM_001163941.1 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:20698212 C>T maps to NM_001163941.1 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:20685728 G>T maps to NM_001163941.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:20782624 G>A maps to NM_001163941.1 G1050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr7:20738103 G>A maps to NM_001163941.1 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:20721219 G>T maps to NM_001163941.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:74291486 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:74273348 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:74295223 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:74290241 C>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr23:74288883 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:74375974 G>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:74295408 C>G did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:74280086 C>G did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:74291422 C>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:74293741 C>T did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:74332725 C>G did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:74318788 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:74332751 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:74273221 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:150732735 G>C maps to ENST00000297504 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:150730964 T>C maps to ENST00000297504 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:150742327 C>G maps to ENST00000297504 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:150738264 G>T maps to ENST00000297504 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150739142 G>T maps to ENST00000297504 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr7:150733015 G>C maps to ENST00000297504 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:123424726 C>T maps to NM_203444.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:123419911 G>A maps to NM_203444.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:16130397 G>A maps to ENST00000399408 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:16219687 C>T maps to ENST00000399408 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:16215881 C>T maps to ENST00000399408 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr16:16215936 C>T maps to ENST00000399408 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr16:16225668 A>T maps to ENST00000399408 T1291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:16225761 C>T maps to ENST00000399408 H1322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:16146666 G>T maps to ENST00000399408 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr16:16173331 C>T maps to ENST00000399408 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:43415471 G>A maps to NM_033450.2 V1224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:43411979 G>T maps to NM_033450.2 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr6:43400263 C>G maps to NM_033450.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr6:43400665 G>C maps to NM_033450.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:43417224 C>T maps to NM_033450.2 T1395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:48248818 G>T maps to NM_032583.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr16:48244897 C>T maps to NM_032583.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48204060 C>T maps to NM_032583.3 E1282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:48201238 C>T maps to NM_032583.3 K1365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:48226494 G>T maps to NM_032583.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr16:48232096 C>T maps to NM_032583.3 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:48226556 G>T maps to NM_032583.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:48256676 C>T maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr16:48204878 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:48249114 G>A maps to NM_032583.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr16:48227810 G>A maps to NM_032583.3 Y829Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:48218374 G>T maps to NM_032583.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:48256676 C>A maps to NM_032583.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:48234195 G>A maps to NM_032583.3 H691H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:48261805 C>T maps to NM_032583.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr16:48249176 C>A maps to NM_032583.3 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:48162468 G>T maps to NM_033226.2 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:48117855 G>T maps to NM_033226.2 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:48174703 C>T maps to NM_033226.2 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:48167678 C>T maps to NM_033226.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr16:48149519 G>T maps to NM_033226.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:48162528 G>A maps to NM_033226.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:48121985 C>T maps to NM_033226.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:48117861 T>A maps to NM_033226.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:48134856 G>A maps to NM_033226.2 F988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:48174657 G>T maps to NM_033226.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr16:48174750 G>A maps to NM_033226.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr16:48142349 C>T did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr16:48138270 C>T maps to NM_033226.2 K894K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:101605388 G>C maps to NM_000392.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:101606845 G>T maps to NM_000392.3 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:101560181 G>A maps to NM_000392.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr10:101578647 G>C maps to NM_000392.3 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:101603569 G>T maps to NM_000392.3 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:101595909 C>A maps to NM_000392.3 I1159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:101610457 A>G maps to NM_000392.3 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:101544462 C>A maps to NM_000392.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:101591888 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr10:101590191 T>C did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr17:48742524 C>T maps to NM_003786.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:48762200 G>A maps to NM_003786.3 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr17:48750366 C>G maps to NM_003786.3 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:48734067 G>T maps to NM_003786.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:48741077 C>A maps to NM_003786.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:95840796 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:95818481 G>C maps to NM_005845.3 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr13:95723951 C>T maps to NM_005845.3 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr13:95858784 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:95858878 C>G maps to NM_005845.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:95818410 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:95862947 G>A maps to NM_005845.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:95705393 G>A maps to NM_005845.3 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr13:95840727 G>A maps to NM_005845.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:183669352 C>T maps to NM_005688.2 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:183682980 G>A maps to NM_005688.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:183645219 T>A maps to NM_005688.2 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:183667662 C>A maps to NM_005688.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:183639186 C>T maps to NM_005688.2 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr3:183700741 C>A maps to NM_005688.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr3:183667833 T>A maps to NM_005688.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:16297268 G>A maps to NM_001171.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:16284194 C>A maps to NM_001171.5 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:16267178 C>A maps to NM_001171.5 G917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:16297292 G>A maps to NM_001171.5 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:16256970 C>A maps to NM_001171.5 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr16:16248519 C>T maps to NM_001171.5 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:17483339 C>T maps to ENST00000302539 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:17432167 C>G maps to ENST00000302539 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:17464265 C>T did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:17414644 G>A maps to ENST00000302539 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr11:17464291 G>C maps to ENST00000302539 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:17434942 G>T maps to ENST00000302539 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:17418593 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:17428909 C>A maps to ENST00000302539 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:17498185 G>A maps to ENST00000302539 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:17428533 G>C maps to ENST00000302539 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:21971083 C>A maps to NM_005691.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:22012542 G>A maps to NM_005691.2 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:21960372 T>C maps to NM_005691.2 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:22012521 A>G maps to NM_005691.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:22063912 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:22078927 C>A maps to NM_005691.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:22028651 A>G maps to NM_005691.2 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22086857 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:22063858 T>A maps to NM_005691.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr12:22025638 T>C maps to NM_005691.2 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:22068750 G>A maps to NM_005691.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:22005367 C>A maps to NM_005691.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:22025599 G>A maps to NM_005691.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:152994852 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:152991455 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:153008743 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:153001803 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:153005659 C>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr12:40013042 A>T maps to NM_005164.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:40012997 A>T maps to NM_005164.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:39947746 C>G maps to NM_005164.3 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:40012754 C>A maps to NM_005164.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:40013090 C>A maps to NM_005164.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:94933551 A>T maps to ENST00000454898 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:74759023 C>A maps to NM_005050.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30553990 C>T maps to NM_001025091.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:30545195 G>A maps to NM_001025091.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr6:30550877 A>T maps to NM_001025091.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:30553955 C>T maps to NM_001025091.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:30552238 C>A maps to NM_001025091.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:150916205 C>A maps to NM_005692.3 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:150919702 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183911182 A>T maps to NM_018358.2 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:183909003 C>T maps to NM_018358.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:183910684 G>T did not map to a codon.
Sequencing variant TCGA-78-8648-01A-11D-2393-08 chr3:183908908 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:183906917 G>T maps to NM_018358.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:43708162 C>T maps to NM_004915.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:43705991 T>C maps to NM_004915.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:43645890 A>T maps to NM_004915.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr21:43711289 C>T maps to NM_004915.3 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89052257 G>A maps to NM_004827.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:89034565 G>T maps to NM_004827.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr4:89018622 G>A maps to NM_004827.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:89052317 G>A maps to NM_004827.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr4:89016683 T>A maps to NM_004827.2 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr4:89020601 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:89034606 C>A maps to NM_004827.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr4:89042902 T>C maps to NM_004827.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:119025541 C>T maps to NM_001142505.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:119027326 G>T maps to NM_001142505.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:119029412 C>A maps to NM_001142505.1 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:119024757 C>T maps to NM_001142505.1 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:119029014 G>A maps to NM_001142505.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:119029567 G>T maps to NM_001142505.1 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:44051103 G>T maps to NM_022436.2 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:44047093 G>A maps to NM_022436.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44053559 C>A maps to NM_022436.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:44065078 G>T maps to NM_022436.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:44051073 G>T maps to NM_022436.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:44064971 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:44050015 C>T maps to NM_022436.2 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:44047178 G>T maps to NM_022436.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:44050062 G>A maps to NM_022436.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:44049934 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:44071701 C>G maps to NM_022437.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:44079548 C>A maps to NM_022437.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:44079960 C>A maps to NM_022437.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:44100964 C>A maps to NM_022437.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:44078813 C>G maps to NM_022437.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr2:44104922 T>C maps to NM_022437.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:44099211 T>A maps to NM_022437.2 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:44073349 C>A maps to NM_022437.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:27346890 T>A maps to NM_032604.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:73150995 G>T maps to NM_148912.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr7:73153055 G>A maps to NM_148912.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:73152655 A>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:25319883 T>A maps to NM_015600.3 K99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:51352563 A>T maps to ENST00000337334 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:51352377 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:108881887 G>T maps to NM_032859.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr13:108881820 A>G maps to NM_032859.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:52005521 G>A maps to NM_032750.2 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:27893423 G>T maps to NM_198147.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr15:89738464 A>T maps to NM_152924.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr15:89698595 A>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr18:19239162 A>G maps to NM_138340.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:23072499 G>C maps to NM_022060.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:23070660 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:23078734 C>A maps to NM_022060.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:43743968 G>A maps to NM_016006.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:43744034 A>G maps to NM_016006.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:43743797 G>A maps to NM_016006.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:17405098 C>A maps to NM_024527.4 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:27048009 T>A maps to NM_005470.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr10:27060002 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:27112234 C>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:204267335 C>G maps to ENST00000295851 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:204259425 G>A maps to ENST00000295851 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:204259512 C>G maps to ENST00000295851 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:47295249 C>T maps to NM_016428.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:47297530 C>T maps to NM_016428.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:47299959 C>A maps to NM_016428.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:47295216 G>T maps to NM_016428.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:47297632 C>A maps to NM_016428.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:100511564 G>T maps to ENST00000471714 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:100621463 G>T maps to ENST00000471714 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:133738223 G>T maps to NM_007313.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:133759422 C>A maps to NM_007313.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:133753853 G>A maps to NM_007313.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr9:133760829 C>T maps to NM_007313.2 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:133760559 G>T maps to NM_007313.2 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:133738211 G>C maps to NM_007313.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr9:133747589 G>A maps to NM_007313.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179076924 C>A maps to NM_007314.3 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:179095583 C>A maps to NM_007314.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:179078349 T>C maps to NM_007314.3 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:179077434 C>G maps to NM_007314.3 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:179087821 C>A maps to NM_007314.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:179078091 G>A maps to NM_007314.3 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:116203884 T>A maps to ENST00000277895 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr10:116307425 G>A maps to ENST00000277895 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr4:8046911 C>A maps to NM_001130083.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr4:8089920 G>A maps to NM_001130083.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:8034408 T>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:8108359 C>A maps to NM_001130083.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr4:8021390 G>T maps to NM_001130083.1 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148630008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:148586661 C>A maps to NM_014945.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:148617108 T>A maps to NM_014945.2 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:148563036 C>A maps to NM_014945.2 Y12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:148626045 G>T maps to NM_014945.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr9:136131528 C>A maps to NM_020469.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:150554718 C>G maps to ENST00000416793 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:150553578 C>G maps to ENST00000416793 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr7:150554514 C>G maps to ENST00000416793 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:150555072 G>A maps to ENST00000416793 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr17:995057 G>C maps to NM_021962.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr8:107782192 G>A maps to NM_139166.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr8:107773357 G>C maps to NM_139166.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:107773441 G>A maps to NM_139166.4 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:26597219 G>T maps to NM_013375.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:26597231 A>T maps to NM_013375.2 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:127395386 C>T maps to NM_172027.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:34218873 T>C maps to NM_145804.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:34173996 C>T maps to NM_145804.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:34181801 G>T maps to NM_145804.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr18:47317870 T>A maps to NM_006111.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:35687288 A>G maps to NM_198834.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:35608974 C>T maps to NM_198834.1 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:35445975 C>A maps to NM_198834.1 E2309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:35627713 G>A maps to NM_198834.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:35614760 G>A maps to NM_198834.1 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:35578664 C>A maps to NM_198834.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:35609867 G>A maps to NM_198834.1 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr17:35640263 G>T maps to NM_198834.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:35487102 C>A maps to NM_198834.1 G1907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:109577746 T>C maps to NM_001093.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:109690857 G>C maps to NM_001093.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:109637269 G>T maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:109637269 G>A maps to NM_001093.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:109654628 C>T maps to NM_001093.3 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:109613742 A>T maps to NM_001093.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr12:109617029 G>T maps to NM_001093.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:109577644 C>A maps to NM_001093.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109609685 G>T maps to NM_001093.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680289 C>T maps to NM_001093.3 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:109680381 G>T maps to NM_001093.3 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:109670471 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:109678884 C>T maps to NM_001093.3 I1607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:109698351 C>A maps to NM_001093.3 P2188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:109683477 C>T maps to NM_001093.3 I1742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:109674995 C>T maps to NM_001093.3 H1491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:109678896 G>A maps to NM_001093.3 V1611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:109577485 A>C maps to NM_001093.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:112184049 C>T maps to NM_001136538.1 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:112147406 G>T maps to NM_001136538.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:112130647 G>C maps to NM_001136538.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:112182570 G>T maps to NM_001136538.1 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:132378550 C>A maps to NM_032169.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:132295847 C>A maps to NM_032169.4 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:134131718 G>T maps to NM_014384.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:128622926 C>T maps to NM_014049.4 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:211059989 G>A maps to NM_001608.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:211085420 C>G maps to NM_001608.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:76216216 A>T maps to ENST00000370834 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:76199313 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:76211577 A>T maps to ENST00000370834 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121177208 G>T maps to NM_000017.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:121175682 C>T maps to NM_000017.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:124793960 A>T maps to NM_001609.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr10:124802686 G>A maps to NM_001609.3 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:7125567 G>A maps to ENST00000356839 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:89382101 C>A maps to NM_013227.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:89400399 C>T maps to NM_013227.3 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:89392930 A>G maps to NM_013227.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89385033 G>A maps to NM_013227.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr15:89386859 C>T maps to NM_013227.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:89400831 C>A maps to NM_013227.3 A1672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:89382143 C>T maps to NM_013227.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr15:89382236 C>A maps to NM_013227.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr15:89398155 G>A maps to NM_013227.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:89401395 C>A maps to NM_013227.3 S1860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:89398272 C>T maps to NM_013227.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:89403615 G>T maps to NM_013227.3 G2298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:89415264 G>T maps to NM_013227.3 L2379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:89386625 C>T maps to NM_013227.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:89395199 C>A maps to NM_013227.3 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr15:89386757 C>T maps to NM_013227.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr15:89382206 T>A maps to NM_013227.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:195063240 T>A maps to NM_012287.5 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1237393 C>A maps to NM_030649.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:1231131 C>A maps to NM_030649.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:1235382 C>A maps to NM_030649.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr11:108010911 G>T maps to NM_000019.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr11:108004608 G>A maps to NM_000019.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:108016990 T>C maps to NM_000019.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:160199278 A>G maps to NM_005891.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:43213882 C>T maps to NM_001135706.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:43214492 G>C maps to NM_001135706.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr10:27507107 C>T maps to ENST00000375888 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr10:27497290 T>A maps to ENST00000375888 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:27506907 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr10:27497246 C>G maps to ENST00000375888 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:180257515 G>A maps to NM_032360.3 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:180257593 G>T maps to NM_032360.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:32483251 G>T maps to NM_001094.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:31438992 C>A maps to NM_183377.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:31618845 G>T maps to NM_183377.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:31618818 C>T maps to NM_183377.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:31344624 C>A maps to NM_183377.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:32483002 G>A maps to NM_001094.4 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:31352946 G>A maps to NM_183377.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:50472280 C>T maps to NM_020039.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:50452897 C>T maps to NM_020039.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr12:50452665 G>C maps to NM_020039.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:150748968 T>C maps to NM_020321.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:150748965 C>A maps to NM_020321.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:150748968 T>C maps to NM_020321.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:150748262 C>A maps to NM_020321.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:150748965 C>A maps to NM_020321.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:150748968 T>C maps to NM_020321.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:220379742 G>A maps to NM_018674.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:220379437 C>A maps to NM_018674.4 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:220396523 G>T maps to NM_018674.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr2:220396514 C>T maps to NM_018674.4 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:156751141 C>A maps to NM_017419.2 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:156787351 T>C maps to NM_017419.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:156751015 C>A maps to NM_017419.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:156763422 G>T maps to NM_017419.2 C315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr4:156763446 A>G maps to NM_017419.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:44105127 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44092855 G>C maps to NM_032592.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:44105100 C>G maps to NM_032592.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:44074272 A>G maps to NM_001031854.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:44080220 T>C maps to NM_001031854.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:67691945 C>T maps to NM_001082486.1 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr16:67691687 G>A maps to NM_001082486.1 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:67694281 G>A maps to NM_001082486.1 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:61568577 G>T maps to NM_000789.3 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:61557854 C>A maps to NM_000789.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:61564381 C>T maps to NM_000789.3 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:61574335 G>T maps to NM_000789.3 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61555353 G>T maps to NM_000789.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:61574531 C>T maps to NM_000789.3 R1242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr17:61561747 C>T maps to NM_000789.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:61562711 C>T maps to NM_000789.3 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:61562272 C>T maps to NM_152830.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:61562273 C>T maps to NM_152830.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:61564031 C>T maps to NM_000789.3 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:61566416 C>A maps to NM_000789.3 Y855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:15607531 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:15603663 C>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:15591572 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:15580053 T>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:15584481 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:15613017 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:15599455 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:15584412 C>T did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:15605909 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:15584407 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:15618934 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:6307195 C>T maps to NM_133492.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:6306757 G>T maps to NM_133492.2 Y254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19424710 C>A maps to NM_001010887.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:19423858 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:100490352 G>A maps to NM_000665.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:100491142 G>T maps to NM_000665.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:100491460 G>A maps to NM_000665.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:100490920 G>C maps to NM_000665.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:23532767 G>A maps to NM_014977.3 Q930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr14:23532786 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr14:23531433 G>A maps to NM_014977.3 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr14:23549649 C>T maps to NM_014977.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:40063718 G>A maps to ENST00000401700 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:40065830 C>A maps to ENST00000401700 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:135628550 C>G maps to NM_138326.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:135621050 G>A maps to NM_138326.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:96810321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:32436253 T>C maps to NM_002197.2 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:32407427 G>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:32421014 G>A maps to NM_002197.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:41923335 C>A maps to ENST00000396512 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr22:41921282 C>A maps to ENST00000396512 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr22:41911487 C>T maps to ENST00000396512 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr22:41865167 A>G maps to ENST00000396512 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr22:41913579 C>T maps to ENST00000396512 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr22:41919917 G>A maps to ENST00000396512 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr22:41895791 G>T maps to ENST00000396512 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:55060275 G>A maps to NM_015547.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:80655812 C>A maps to NM_130767.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:80655734 A>G maps to NM_130767.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:80626662 G>A maps to NM_130767.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:80631600 C>T maps to NM_130767.2 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:80643711 T>C maps to NM_130767.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74061970 G>C maps to NM_152331.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:74086095 T>A maps to NM_001037162.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:74083896 G>C did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:6387460 C>A maps to NM_007274.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:6324698 C>T maps to NM_007274.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:6324737 C>T maps to NM_007274.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:44470569 C>T maps to NM_005469.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:44477210 G>A maps to NM_005469.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:23723692 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:23749029 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:23740785 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:23740786 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:23722068 T>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:8407758 C>A maps to NM_003501.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:8418140 C>T maps to NM_003501.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:8418164 C>T maps to NM_003501.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:8417513 G>T maps to NM_003501.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:8417720 G>A maps to NM_003501.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:111789244 G>T maps to NM_001142807.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:111542307 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:111850515 C>A maps to NM_001142807.1 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:111691149 G>T maps to NM_001142807.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:111850527 G>T maps to NM_001142807.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:277225 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:277078 C>G maps to NM_004300.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:264963 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:47261719 G>A maps to NM_001610.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr19:11687315 T>A maps to NM_001111036.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:147120176 G>A maps to NM_016361.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr3:141006209 C>T maps to NM_001037172.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:141011152 C>T maps to NM_001037172.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:132063769 G>C did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:132047112 G>A maps to NM_001134194.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:51298091 C>T maps to NM_033068.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:51182597 C>T maps to NM_001097.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:51182633 G>A maps to NM_001097.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:6749348 G>A maps to NM_032489.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:6756074 C>G maps to NM_032489.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:70832326 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:70811980 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:70824042 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:70824129 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:70824183 G>C did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:70823586 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:70824336 G>C did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:70823922 G>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:70823952 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:70823694 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:70823471 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:70832807 G>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:70823899 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:70824259 A>G did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:70823511 G>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:125546296 G>T maps to NM_001612.5 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:78487042 G>T maps to NM_015162.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr15:78474873 G>A maps to NM_015162.4 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:78474870 A>T maps to NM_015162.4 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:78465983 C>T maps to NM_015162.4 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr15:78526711 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6185605 T>G maps to NM_030924.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:6183091 C>G maps to NM_030924.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:6185605 T>A maps to NM_030924.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:48551067 G>A maps to ENST00000427954 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr17:48549835 G>T maps to ENST00000427954 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr16:89178531 G>T maps to NM_174917.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr16:89180749 G>A maps to NM_174917.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:89169020 C>T maps to NM_174917.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:89169121 G>A maps to NM_174917.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr16:89220528 G>T maps to NM_174917.2 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:185697769 G>C maps to NM_001995.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:185705146 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:185709867 T>C maps to NM_001995.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:185687868 C>T maps to NM_001995.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:185681539 G>A maps to NM_001995.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:185694264 G>A maps to NM_001995.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr2:223786027 C>G maps to NM_203372.1 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:108911375 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:108926641 A>G did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:108902738 C>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:108902653 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:108904810 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:108926434 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:108924286 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:114136114 G>T maps to NM_016234.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr10:114181794 T>A did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr10:114154796 G>C maps to NM_016234.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:131310520 C>T maps to NM_015256.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:131312362 G>C maps to NM_001009185.1 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:131309042 G>A maps to NM_001009185.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr5:131302123 G>A maps to NM_001009185.1 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr5:131303680 G>A maps to NM_001009185.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:131321139 A>T maps to NM_001009185.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:20648731 C>A maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:20696551 A>G maps to NM_052956.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:20638524 G>A maps to NM_052956.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:20702412 G>C maps to NM_052956.2 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20636756 C>A maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:20648731 C>T maps to NM_052956.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:20635537 C>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:20696589 G>A maps to NM_052956.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr16:20648081 C>T maps to NM_052956.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:20696581 G>A maps to NM_052956.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:20702396 T>C maps to NM_052956.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:20693590 G>T maps to NM_052956.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:20482504 C>A maps to NM_001010845.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr16:20494499 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:20497894 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr16:20497955 C>T maps to NM_001010845.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:20492236 A>T maps to NM_001010845.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr16:20477002 C>A maps to NM_001010845.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:20487037 G>A maps to NM_001010845.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20491953 G>A maps to NM_001010845.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:20486998 C>A maps to NM_001010845.2 C334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:20494387 G>A maps to NM_001010845.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:20548588 A>T maps to NM_182617.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:20576095 G>A maps to NM_182617.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr16:20554584 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr16:20554244 G>T maps to NM_182617.3 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:20554524 C>T maps to NM_182617.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr16:20565131 G>T maps to NM_182617.3 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr16:20566664 A>G maps to NM_182617.3 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr16:20565242 C>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20788794 A>G maps to NM_005622.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7476107 C>A maps to NM_001080454.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:7476110 C>A maps to NM_001080454.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:7480966 T>C maps to NM_001080454.1 *581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:20448430 C>A maps to NM_017888.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:20429418 C>G maps to NM_017888.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20432711 G>T maps to NM_017888.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:20435267 C>T maps to NM_017888.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:20439153 C>T maps to NM_017888.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:20451222 A>G maps to NM_017888.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20429493 G>C maps to NM_017888.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:20448426 G>C maps to NM_017888.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:20422946 G>A maps to NM_017888.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:20435255 C>T maps to NM_017888.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:20432666 C>A maps to NM_017888.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:20441104 C>G maps to NM_017888.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr16:20422952 G>T maps to NM_017888.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr16:20451725 C>A maps to NM_017888.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:20432578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:25038480 G>C maps to NM_032501.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:25003718 T>A maps to NM_032501.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr20:24995867 T>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:33509650 T>A maps to NM_001076552.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr20:33500967 C>T maps to NM_001076552.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:33509665 T>C maps to NM_001076552.2 Y528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:81593167 G>C maps to NM_024560.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:81503374 C>T maps to NM_024560.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:81472165 C>T maps to NM_024560.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr12:81647171 T>C maps to NM_024560.2 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:81472084 C>T maps to NM_024560.2 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:81545703 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:81593201 T>C maps to NM_024560.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:81503419 C>T maps to NM_024560.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:81610761 C>A maps to NM_024560.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:81648697 A>T maps to NM_024560.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:81648673 C>T maps to NM_024560.2 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:229568534 C>T maps to NM_001100.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:229568585 G>T maps to NM_001100.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:229568736 G>A maps to NM_001100.3 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:229568342 G>T maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:229567266 G>T maps to NM_001100.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:229568612 A>G maps to NM_001100.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:5569007 C>T maps to NM_001101.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:5569225 G>A maps to NM_001101.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr7:5567817 T>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr5:56778405 G>A maps to NM_001017992.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:56777819 G>T maps to NM_001017992.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:35083386 A>T maps to NM_005159.4 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:35086985 G>A maps to NM_005159.4 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:35085665 G>A maps to NM_005159.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:79478069 G>T maps to NM_001614.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:74128467 G>T maps to NM_001615.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:74143789 T>A maps to NM_001615.3 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:74129497 G>T maps to NM_001615.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:74129498 G>T maps to NM_001615.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr3:179287925 C>T maps to NM_004301.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:179294441 T>C maps to NM_004301.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr7:100243922 G>A maps to NM_016188.4 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:100252639 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:100246285 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:100240934 C>T maps to NM_016188.4 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:111617730 C>T maps to NM_006686.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:111617358 C>A maps to NM_006686.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:18149613 G>T maps to NM_030812.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:18152749 C>T maps to NM_030812.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:18152599 G>A maps to NM_030812.2 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:8808679 G>T maps to NM_178525.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:8807929 G>T maps to NM_178525.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:8808745 G>T maps to NM_178525.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr19:8808685 C>T maps to NM_178525.3 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:8808109 G>C maps to NM_178525.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:69347640 C>T maps to NM_001130004.1 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:69349270 C>A maps to NM_001130004.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:69347565 C>A maps to NM_001130004.1 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:69345240 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236912563 G>A maps to NM_001103.2 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:236906332 T>A maps to NM_001103.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236898980 C>A maps to NM_001103.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:236908061 C>A maps to NM_001103.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:236914774 G>T maps to NM_001103.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:236924412 G>T maps to NM_001103.2 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:236881159 C>A maps to NM_001103.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:236917278 C>G maps to NM_001103.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:236918377 G>A maps to NM_001103.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:236918344 C>T maps to NM_001103.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:236924323 G>T maps to NM_001103.2 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:236924457 C>A maps to NM_001103.2 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:236894570 C>T maps to NM_001103.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:236891014 C>A maps to NM_001103.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:236911068 C>A maps to NM_001103.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr1:236917317 T>G maps to NM_001103.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:66322788 T>C maps to NM_001104.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:66328218 G>A maps to NM_001104.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66328120 C>T maps to NM_001104.1 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39214591 C>T maps to NM_004924.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr19:39200909 G>T maps to NM_004924.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr19:39212307 C>T maps to NM_004924.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr14:58701085 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:58681921 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:104245438 G>A maps to NM_005736.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:104244123 T>A maps to NM_005736.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:104247995 C>A maps to NM_005736.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:98277102 C>A maps to NM_005735.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:65473743 G>A maps to NM_001005386.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:114709123 T>A maps to NM_005721.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:114699824 G>T maps to NM_005721.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:152549329 G>A maps to NM_020445.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:152549305 C>T maps to NM_020445.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:37384543 G>A maps to NM_024855.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:100606230 G>A maps to NM_022496.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:53911339 T>A maps to NM_022899.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:53910668 T>A maps to NM_022899.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:127185555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:127185704 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:127185300 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:127186047 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:127186092 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:127185640 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:127185206 G>C did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:127185967 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:127185487 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:127185253 T>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr23:127185953 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:127185977 A>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:127185084 C>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:127186008 T>A did not map to a codon.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr23:127185635 C>A did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:127185759 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:127185519 G>C did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:127185830 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:127185846 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:127185829 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:127185796 A>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:127185588 G>C did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:127185588 G>T did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr23:127186088 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:127185245 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:127185865 A>C did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:127186072 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:127185518 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:127185277 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:127185278 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:127185198 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:127185217 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:2938327 T>A maps to NM_080431.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:2939236 C>A maps to NM_080431.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:2939020 C>T maps to NM_080431.4 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:2938888 G>A maps to NM_080431.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:2939245 G>T maps to NM_080431.4 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:2938382 C>T maps to NM_080431.4 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:2938970 G>T maps to NM_080431.4 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:158622627 A>G maps to NM_001111067.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:52377795 G>A maps to NM_020328.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:52370312 G>A maps to NM_020328.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:158406902 A>G maps to NM_145259.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:158399246 T>A maps to NM_145259.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:158390462 A>G maps to NM_145259.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr2:158390504 T>A maps to NM_145259.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:148683667 C>T maps to NM_001616.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:148684647 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:38524627 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:38524705 G>T maps to NM_001106.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:52314646 C>T maps to NM_001077401.1 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:52314549 C>G maps to NM_001077401.1 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:52314607 C>A maps to NM_001077401.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr12:52309020 C>G maps to NM_001077401.1 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:52308317 C>A maps to NM_001077401.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr12:52314572 G>T maps to NM_001077401.1 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:52307400 C>T maps to NM_001077401.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:52021459 G>T maps to ENST00000463937 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:54365807 G>T maps to NM_138448.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:43249763 G>A maps to NM_000022.2 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:43248976 G>T maps to NM_000022.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr4:123336762 C>A maps to NM_139243.3 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr4:123314763 G>T maps to NM_139243.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:84229856 G>T maps to NM_139174.3 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr15:43638097 G>T maps to ENST00000422466 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr15:43641178 C>T maps to ENST00000422466 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:58957350 G>C maps to NM_001110.2 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:58933071 C>A maps to NM_001110.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:42854946 C>T maps to NM_002390.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:42854955 G>T maps to NM_002390.4 E630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:42854900 G>T maps to NM_002390.4 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:42849174 G>T maps to NM_002390.4 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:42851876 G>A maps to NM_002390.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:127755306 C>A maps to NM_003474.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:127724786 G>T maps to NM_003474.4 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:127731627 G>A maps to NM_003474.4 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr10:127806654 G>A maps to NM_003474.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:127967523 G>T maps to NM_003474.4 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:127760147 C>G maps to NM_003474.4 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr10:127705849 A>T maps to NM_003474.4 *910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr10:127843828 G>A maps to NM_003474.4 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:127708340 G>T maps to NM_003474.4 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr10:127798372 C>A maps to NM_003474.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:128019078 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:155029446 C>T maps to NM_207197.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:155028312 G>T maps to NM_207197.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:155030751 G>A maps to NM_207197.1 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:155030406 G>A maps to NM_207197.1 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:9666320 C>A maps to NM_003183.4 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:39535049 A>G maps to NM_014237.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr8:39525665 C>T maps to NM_014237.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:39587425 C>A maps to NM_014237.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:39502855 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:39581360 C>A maps to NM_014237.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:39486891 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:156915449 G>T maps to ENST00000430702 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:156917448 C>A maps to ENST00000430702 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:156957828 A>G maps to ENST00000430702 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156915443 G>T maps to ENST00000430702 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:156918896 C>T maps to ENST00000430702 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:156920070 C>A maps to ENST00000430702 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr5:156964974 T>G maps to ENST00000430702 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:156917427 G>T maps to ENST00000430702 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:156964935 G>C maps to ENST00000430702 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:156934147 C>A maps to ENST00000430702 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:156915333 G>T maps to ENST00000430702 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:156920136 G>C maps to ENST00000430702 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr5:156916127 C>T maps to ENST00000430702 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:39666958 T>G maps to NM_001464.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:39646226 G>T maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:39678646 G>A maps to NM_001464.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:39624683 G>T maps to NM_001464.3 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:39626919 C>A maps to NM_001464.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:39679166 G>T maps to NM_001464.3 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:39646226 G>A maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr8:39695677 G>A maps to NM_001464.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr8:39604092 A>C maps to NM_001464.3 L691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:39613318 C>T maps to NM_001464.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:70990219 C>A maps to NM_003814.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr14:70991354 T>C maps to NM_003814.4 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:70990476 A>T maps to NM_003814.4 L383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:70989766 C>A maps to NM_003814.4 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr14:70926036 G>C maps to NM_003813.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:87816013 T>C maps to NM_021722.4 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:87780626 G>A maps to NM_021723.3 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:87792440 C>T maps to NM_021723.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:87737564 C>T maps to NM_021723.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:87780636 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:87746059 G>T maps to NM_021723.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr7:87778373 T>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:87737539 C>G maps to NM_021723.3 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:207460797 C>A maps to NM_003812.2 C757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:207435495 C>G maps to NM_003812.2 Y509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:207482344 C>A maps to NM_003812.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:207452813 G>T did not map to a codon.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr2:207426991 A>G maps to NM_003812.2 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:207452096 C>T maps to NM_003812.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:207437888 T>C maps to NM_003812.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:207454131 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr2:207426946 G>C maps to NM_003812.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:175897287 C>G maps to NM_014269.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:175898482 G>T maps to NM_014269.4 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:175898085 T>A maps to NM_014269.4 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:175898628 C>A maps to NM_014269.4 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr4:175897107 G>A maps to NM_014269.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:120438008 A>G maps to NM_021794.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr1:120437939 C>G maps to NM_021794.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:39103642 G>A maps to NM_145004.5 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:39068731 G>T maps to NM_145004.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:39027464 A>T maps to NM_145004.5 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr8:39027458 G>A maps to NM_145004.5 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr8:39080569 A>T maps to NM_145004.5 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr20:3652101 C>T maps to NM_025220.2 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:3652889 G>T maps to NM_025220.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:3653451 C>T maps to NM_025220.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:3651941 G>T maps to NM_025220.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:3653514 G>T maps to NM_025220.2 C388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr20:3655457 G>T maps to NM_025220.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:3655285 G>T maps to NM_025220.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr20:3651738 G>A maps to NM_025220.2 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:24324369 G>T maps to ENST00000380789 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:24359040 G>A maps to ENST00000380789 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:24326278 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:24359023 G>T maps to ENST00000380789 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:24365021 C>T maps to ENST00000380789 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:24342861 C>A maps to ENST00000380789 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:24359004 C>A maps to ENST00000380789 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr8:24324449 C>A maps to ENST00000380789 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:135083893 C>A maps to NM_001109.4 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:38948861 A>G maps to NM_003816.2 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:38912023 G>T maps to NM_003816.2 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:38899495 G>T maps to NM_003816.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr8:24242040 A>T maps to NM_014479.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:28214864 G>T maps to NM_006988.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:28210755 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:28212699 C>A maps to NM_006988.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:8657673 C>T maps to NM_030957.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:8669980 C>T maps to NM_030957.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr19:8660967 G>A maps to NM_030957.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:8651344 G>T maps to NM_030957.2 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:33683975 G>T maps to NM_030955.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:33576959 G>T maps to NM_030955.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33658392 G>T maps to NM_030955.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:33658331 C>A maps to NM_030955.2 G383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:33891833 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:33576788 G>T maps to NM_030955.2 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:33637776 G>C maps to NM_030955.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33588880 C>T maps to NM_030955.2 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:33576395 G>T maps to NM_030955.2 A1245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:33546239 C>T maps to NM_030955.2 W1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:33576464 G>T maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:33662058 G>T maps to NM_030955.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr5:33616057 C>A maps to NM_030955.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33576821 C>T maps to NM_030955.2 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:33881487 G>A maps to NM_030955.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33527361 G>C maps to NM_030955.2 P1572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:33649001 G>T maps to NM_030955.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:33683992 C>A maps to NM_030955.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr5:33549398 G>T maps to NM_030955.2 C1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:33616097 C>A maps to NM_030955.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:33588843 G>A maps to NM_030955.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:33614445 A>G maps to NM_030955.2 Y808Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:33588886 G>A maps to NM_030955.2 C894C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:33588772 G>T maps to NM_030955.2 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:33630902 A>G maps to NM_030955.2 C668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:33549430 G>T maps to NM_030955.2 R1395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:33881250 C>A maps to NM_030955.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:33649756 C>A maps to NM_030955.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:33535097 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:33561188 A>T maps to NM_030955.2 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:33527373 G>T maps to NM_030955.2 C1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:33561209 C>A maps to NM_030955.2 A1349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:33624369 A>T maps to NM_030955.2 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:33576224 G>T maps to NM_030955.2 A1302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr5:33637844 C>T maps to NM_030955.2 K575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:33576470 C>A maps to NM_030955.2 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:33576452 G>C maps to NM_030955.2 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:33576929 C>T maps to NM_030955.2 W1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:33577136 A>G maps to NM_030955.2 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:33549335 C>T maps to NM_030955.2 A1426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:33630890 T>A maps to NM_030955.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:33684077 C>A maps to NM_030955.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr5:33546235 T>C maps to NM_030955.2 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:136321308 C>T maps to NM_139025.3 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:136324097 C>T maps to NM_139025.3 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr9:136313804 T>C maps to NM_139025.3 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr9:136307771 C>T maps to NM_139025.3 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:136310875 G>A maps to NM_139025.3 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:72434396 G>T maps to NM_139155.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:72490000 C>A maps to NM_139155.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:72511357 G>A maps to NM_139155.2 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:72434577 C>T maps to NM_139155.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr10:72495001 C>G maps to NM_139155.2 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:72511353 G>T maps to NM_139155.2 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:72492073 C>A maps to NM_139155.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:72509716 C>A maps to NM_139155.2 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:72520563 G>C maps to NM_139155.2 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:72468437 C>T maps to NM_139155.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr10:72489102 C>A maps to NM_139155.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130319698 C>A maps to NM_139055.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:130341206 C>T maps to NM_139055.2 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:130332081 C>T maps to NM_139055.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:130340917 C>T maps to NM_139055.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:130332434 C>A maps to NM_139055.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:130343038 C>T maps to NM_139055.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:130318936 G>T maps to NM_139055.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:130319287 C>T maps to NM_139055.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:130343101 G>T maps to NM_139055.2 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:130343025 G>T maps to NM_139055.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr11:130332467 C>T maps to NM_139055.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:5235285 C>A maps to NM_139056.2 Y670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:5319166 C>A maps to NM_139056.2 C1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:5146294 C>A maps to NM_139056.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:5237116 G>T maps to NM_139056.2 G687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:5306771 C>A maps to NM_139056.2 C1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:5303443 C>A maps to NM_139056.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:5235124 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:5239331 T>C maps to NM_139056.2 N741N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:5190085 A>G maps to NM_139056.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:5191804 A>T maps to NM_139056.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:5191879 C>A maps to NM_139056.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr5:5191904 T>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:5239792 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:100801841 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr15:100821538 G>A maps to NM_139057.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr15:100821544 G>A maps to NM_139057.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr15:100672324 C>A maps to NM_139057.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:77317891 G>T maps to NM_199355.2 Y1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:77317954 G>T maps to NM_199355.2 C1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:77327080 G>A maps to NM_199355.2 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:77317918 C>T maps to NM_199355.2 Q1200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr16:77369750 G>T maps to NM_199355.2 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:77325174 C>T maps to NM_199355.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:77375624 T>C maps to NM_199355.2 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:77396131 G>A maps to NM_199355.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:77398153 T>A maps to NM_199355.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr16:77334175 G>A maps to NM_199355.2 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:77327136 G>A maps to NM_199355.2 R1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:77331183 A>G did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr16:77401530 C>A maps to NM_199355.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr16:77389916 G>T maps to NM_199355.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr16:77401494 T>A maps to NM_199355.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:128984535 C>A maps to NM_133638.3 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:128994399 A>T maps to NM_133638.3 K793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:128797434 C>A maps to NM_133638.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:128983510 C>T maps to NM_133638.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:129019847 C>T maps to NM_133638.3 H894H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:129040071 T>A maps to NM_133638.3 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:129070803 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:178770884 C>T maps to NM_014244.4 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:178634681 G>A maps to NM_014244.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr5:178541011 G>A maps to NM_014244.4 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr5:178540918 G>T maps to NM_014244.4 I1195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr5:178551982 G>T maps to NM_014244.4 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:178548719 G>T maps to NM_014244.4 Y1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:178699959 G>T maps to NM_014244.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:178552141 A>T maps to NM_014244.4 C930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:43860486 G>A maps to ENST00000389420 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:43777381 C>A maps to ENST00000389420 V1592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:43945020 G>T maps to ENST00000389420 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:43822329 G>C maps to ENST00000389420 S1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:43777717 A>G maps to ENST00000389420 V1505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:43856733 C>T maps to ENST00000389420 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr12:43825132 A>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:43925970 C>A maps to ENST00000389420 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:43825161 A>G maps to ENST00000389420 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:43819415 A>G maps to ENST00000389420 D1395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr12:43944819 C>A maps to ENST00000389420 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:43886309 A>T maps to ENST00000389420 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:43945682 G>A maps to ENST00000389420 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:43945712 G>A maps to ENST00000389420 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:43925995 C>A maps to ENST00000389420 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:43858521 C>A maps to ENST00000389420 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:43770387 G>T maps to ENST00000389420 S1688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:43823487 C>A maps to ENST00000389420 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr12:43847711 A>T maps to ENST00000389420 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:43826425 C>T maps to ENST00000389420 W970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:43777519 T>C maps to ENST00000389420 S1546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr12:43846449 T>C maps to ENST00000389420 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:73179392 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:73188814 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:73188815 T>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:73181664 T>C maps to NM_014243.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:73184360 A>C maps to NM_014243.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr4:73179509 C>T maps to NM_014243.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:161165357 G>T maps to NM_005099.4 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161161116 C>T maps to NM_005099.4 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161165958 A>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:161165417 G>T maps to NM_005099.4 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:161166388 C>A maps to NM_005099.4 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:161163874 G>T maps to NM_005099.4 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr21:28296422 A>T maps to NM_007038.3 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:28302380 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:28296686 C>A maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:28296445 G>T maps to NM_007038.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr21:28306880 G>T maps to NM_007038.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:28306883 C>G maps to NM_007038.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr21:28302278 C>T maps to NM_007038.3 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr21:28304320 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:28296584 G>A maps to NM_007038.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:28315711 C>T maps to NM_007038.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:28306832 G>A maps to NM_007038.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:28315750 G>T maps to NM_007038.3 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr21:28338446 G>T maps to NM_007038.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr21:28337621 G>T maps to NM_007038.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr21:28296467 C>T maps to NM_007038.3 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:64747408 G>A maps to NM_197941.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:64748737 T>G maps to NM_197941.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:64766966 C>A maps to NM_197941.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79063992 G>A maps to ENST00000258883 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:79058499 G>A maps to ENST00000258883 S1251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:79057022 C>A maps to ENST00000258883 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:79058451 G>T maps to ENST00000258883 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:79059231 G>A maps to ENST00000258883 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:79051870 T>A maps to ENST00000258883 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:79066966 G>A maps to ENST00000258883 D625D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:79058523 C>T maps to ENST00000258883 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:79069872 G>T maps to ENST00000258883 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:130275919 G>A maps to NM_007037.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:130288956 G>T maps to NM_007037.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr11:130275453 C>T maps to NM_007037.4 *890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:130275911 C>A maps to NM_007037.4 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr11:130289019 C>T maps to NM_007037.4 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:130278465 G>T maps to NM_007037.4 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:130286091 G>T maps to NM_007037.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:64672543 C>T maps to NM_182920.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:64592755 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:64524896 G>A maps to NM_182920.1 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:64589669 C>G maps to NM_182920.1 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:64640125 C>A maps to NM_182920.1 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:64532514 G>T maps to NM_182920.1 G1661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr3:64601677 C>A maps to NM_182920.1 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:64582667 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:64619398 C>A maps to NM_182920.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:18777725 C>T maps to NM_001040272.4 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:18681847 G>C maps to NM_001040272.4 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:18574146 T>C maps to NM_001040272.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:18777139 C>T maps to NM_001040272.4 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:18777115 C>A maps to NM_001040272.4 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:18777149 A>C maps to NM_001040272.4 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:18795485 G>T maps to NM_001040272.4 G1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:18776905 G>T maps to NM_001040272.4 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:18622296 C>A maps to NM_001040272.4 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr9:18777001 G>T maps to NM_001040272.4 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:18829949 G>T maps to NM_001040272.4 L1408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr9:18721541 G>T maps to NM_001040272.4 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:18474250 A>T maps to NM_001040272.4 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:136403485 G>C maps to ENST00000393061 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:136405801 C>A maps to ENST00000393061 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr9:136406040 G>T maps to ENST00000393061 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:136405846 C>A maps to ENST00000393061 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr9:136403485 G>T maps to ENST00000393061 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:84651758 G>T maps to NM_207517.2 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:84611521 C>T maps to NM_207517.2 H764H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr15:84581867 C>T maps to NM_207517.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:84582126 G>T maps to NM_207517.2 G662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:84611387 G>T maps to NM_207517.2 G720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:84561543 G>T maps to NM_207517.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:84561544 G>T maps to NM_207517.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:84659932 G>T maps to NM_207517.2 G1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:84683292 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:84561558 C>A maps to NM_207517.2 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:84506902 C>T maps to NM_207517.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr15:84558924 T>C maps to NM_207517.2 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:84651628 A>T maps to NM_207517.2 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:84651166 C>A maps to NM_207517.2 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:84611739 C>A maps to NM_207517.2 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:84700169 T>C maps to NM_207517.2 C1580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr15:84539582 A>T maps to NM_207517.2 K278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:84442318 G>A maps to NM_207517.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:150531541 G>A maps to ENST00000369039 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:150525636 C>T maps to ENST00000369039 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:150529142 T>A maps to ENST00000369039 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr1:150531133 G>A maps to NM_025008.3 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:150525585 C>A maps to ENST00000369039 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:1506028 C>T maps to NM_213604.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:29281513 A>T maps to ENST00000394782 K281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:29283365 C>T maps to ENST00000394782 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:29280310 G>T maps to ENST00000394782 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154571061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154574328 G>A maps to ENST00000292205 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:154575012 G>A maps to ENST00000292205 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:154571061 C>G did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:154573641 G>A maps to ENST00000292205 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:46602545 A>G maps to NM_015833.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr21:46624491 G>T maps to NM_015833.3 G570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr21:46624487 C>T maps to NM_015833.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr21:46595733 C>T maps to NM_015833.3 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr21:46642090 C>T maps to NM_015833.3 D735D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr21:46604836 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr21:46603319 C>T maps to NM_015833.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr21:46600261 C>T maps to NM_015833.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr21:46642024 G>A maps to NM_015833.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:1229174 C>T maps to NM_018702.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:1313243 G>C maps to NM_018702.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr10:1405828 C>T maps to NM_018702.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:1405927 C>A maps to NM_018702.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:1405749 G>A maps to NM_018702.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:75652533 G>A maps to NM_012091.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:143754989 A>G maps to NM_182503.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:1913114 G>T maps to NM_138422.1 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:1912273 G>A maps to NM_138422.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:33562426 C>T maps to ENST00000373441 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:78399673 G>T maps to NM_020421.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:78392144 C>T maps to NM_020421.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr14:78353522 G>T maps to NM_020421.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr14:78398018 C>G maps to NM_020421.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:140373411 C>T maps to NM_052853.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:41206253 C>A maps to NM_024876.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:41216009 C>T maps to NM_024876.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:41211352 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:41216036 C>A maps to NM_024876.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:45614390 G>C maps to NM_021116.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:45743308 G>T maps to NM_021116.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr7:45719305 A>C did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr7:45719306 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45662260 G>T maps to NM_021116.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45726178 G>T maps to NM_021116.2 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:45719352 G>T maps to NM_021116.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr7:45614411 G>T maps to NM_021116.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:45753345 C>A maps to NM_021116.2 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr7:45747980 G>T maps to NM_021116.2 T950T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:45650000 G>T maps to NM_021116.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:45743058 C>T maps to NM_021116.2 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:45743341 C>T maps to NM_021116.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr7:45697355 G>C maps to NM_021116.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:45688396 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:45753345 C>A maps to NM_021116.2 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:167825401 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:167868674 G>A maps to NM_018417.4 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:167798555 C>A maps to NM_018417.4 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:167815047 C>G maps to NM_018417.4 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:167839516 G>A maps to NM_018417.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr1:167863153 C>T maps to NM_018417.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:167805753 G>A maps to NM_018417.4 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:7727278 C>A maps to NM_020546.2 Y592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:7520897 C>T maps to NM_020546.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:7789843 C>A maps to NM_020546.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626394 C>A maps to NM_020546.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:7626401 C>A maps to NM_020546.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr5:7626380 T>C maps to NM_020546.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:7709406 C>A maps to NM_020546.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:7626389 C>T maps to NM_020546.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:7773085 C>T maps to NM_020546.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:7804732 G>A maps to NM_020546.2 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr5:7706886 C>T maps to NM_020546.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr5:7520954 C>T maps to NM_020546.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:7690925 G>T maps to NM_020546.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:7727284 C>T maps to NM_020546.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:7820693 T>A maps to NM_020546.2 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:7626321 G>T maps to NM_020546.2 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:7789870 G>A maps to NM_020546.2 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:7789867 C>A maps to NM_020546.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr5:7709481 C>T maps to NM_020546.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr5:7757635 G>A maps to NM_020546.2 W677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:7695930 C>A maps to NM_020546.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:7743825 G>T maps to NM_020546.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:7695894 C>A maps to NM_020546.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:7690889 G>T maps to NM_020546.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:7414807 G>A maps to NM_020546.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:7784550 C>T maps to NM_020546.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:7773142 G>T maps to NM_020546.2 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:7766918 G>T maps to NM_020546.2 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:7789837 G>C maps to NM_020546.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:7706919 C>A maps to NM_020546.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:7757686 C>T maps to NM_020546.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:25061435 C>A maps to NM_004036.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:25044431 G>C maps to NM_004036.3 L1027L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-7907-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:25050871 G>A maps to NM_004036.3 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:25054602 A>G maps to NM_004036.3 Y661Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:24795298 C>T maps to NM_139247.3 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24800250 G>C maps to NM_139247.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr14:24801050 C>T maps to NM_139247.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:24801053 G>A maps to NM_139247.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:24798266 C>A maps to NM_139247.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:24787984 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:24799136 C>T maps to NM_139247.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:24788552 A>T maps to NM_139247.3 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:123021952 G>A maps to NM_183357.2 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:123019028 G>T maps to NM_183357.2 I946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:123166723 C>T maps to NM_183357.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:123051503 G>A maps to NM_183357.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:123003541 G>C maps to NM_183357.2 Y1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:123166345 G>T maps to NM_183357.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:123019010 G>A maps to NM_183357.2 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:123046596 G>A maps to NM_183357.2 H605H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:123049746 G>T maps to NM_183357.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:123066636 G>A maps to NM_183357.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:123166723 C>T maps to NM_183357.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:123014996 C>T maps to NM_183357.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49166295 C>A maps to NM_015270.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:49172025 C>A maps to NM_015270.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr12:49166146 C>A maps to NM_015270.3 A906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:50327263 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:131955632 G>T maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131796003 T>A maps to NM_001115.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:131848680 C>A maps to NM_001115.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:131797655 G>T maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:131826458 G>T maps to NM_001115.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:131797652 C>A maps to NM_001115.2 V1043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:131964214 C>A maps to NM_001115.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:131793006 G>T maps to NM_001115.2 R1129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:131848566 G>A maps to NM_001115.2 Y877Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:132002718 G>T maps to NM_001115.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr8:131792833 C>A maps to NM_001115.2 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:132051814 G>T maps to NM_001115.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:131812782 C>T maps to NM_001115.2 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:131955632 G>C maps to NM_001115.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:131792869 G>A maps to NM_001115.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:131922042 G>A maps to NM_001115.2 C517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:131916287 C>T maps to NM_001115.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:132051637 C>T maps to NM_001115.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:131833667 T>C did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr8:131955662 G>T maps to NM_001115.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:131964202 C>A maps to NM_001115.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr8:131922057 G>A maps to NM_001115.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr8:131792845 G>T maps to NM_001115.2 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:131861945 G>T maps to NM_001115.2 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr8:131861865 C>A maps to NM_001115.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:131792878 C>A maps to NM_001115.2 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:131896839 C>A maps to NM_001115.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:4057536 C>A maps to NM_001116.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr16:4057494 G>A maps to NM_001116.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr16:4164188 G>A maps to NM_001116.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:4042217 G>C maps to NM_001116.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr16:4016477 C>T maps to NM_001116.3 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:905425 C>A maps to NM_001117.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:905485 C>T maps to NM_001117.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:31126080 C>G maps to ENST00000409489 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:31132292 C>T maps to ENST00000409489 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:31125053 C>T maps to ENST00000409489 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:31104526 G>A maps to ENST00000409489 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:31125015 C>T maps to ENST00000409489 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr7:31124407 C>T maps to ENST00000409489 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:31126041 G>T maps to ENST00000409489 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:2901113 G>A maps to NM_014189.2 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr4:2886263 G>C maps to NM_014189.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr4:2877749 G>A maps to NM_014189.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:70900435 T>C maps to NM_017488.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:70901939 C>A maps to NM_001185054.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:70906009 C>G maps to NM_001185054.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:70933522 G>T maps to NM_001185054.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:70931504 G>T maps to NM_001185054.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:70910751 C>A maps to NM_001185054.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:70931555 C>T maps to NM_001185054.1 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:70933549 G>T maps to NM_001185055.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:70903945 G>A maps to NM_001185054.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:70890766 C>T maps to NM_001185054.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:70904013 G>T maps to NM_001185054.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:111876107 C>T maps to NM_016824.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr4:100205672 G>T maps to NM_000667.3 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:100205961 T>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr4:100208052 G>T maps to NM_000667.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:100235239 T>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:100235239 T>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:100239260 G>T maps to NM_000668.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:100239266 A>T maps to NM_000668.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:100237442 C>A maps to NM_000668.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:100231926 C>T maps to NM_000668.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:100235172 G>A maps to NM_000668.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:100063886 G>T maps to ENST00000505590 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr4:100062800 G>T maps to ENST00000505590 A70A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:100048405 T>C maps to ENST00000505590 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:99996200 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:100134760 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:100129926 G>C maps to NM_001102470.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:100131597 A>G maps to NM_001102470.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:100349700 C>T maps to NM_000673.4 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:100341785 G>T maps to NM_000673.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:100349331 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:100341785 G>T maps to NM_000673.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3504653 G>A maps to NM_018269.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:3502844 C>G maps to NM_018269.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:37214726 C>A maps to ENST00000416116 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:37210017 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr3:186570859 G>T maps to NM_004797.3 G5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr1:202912931 C>T maps to NM_015999.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:202920092 C>A maps to NM_015999.3 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr10:76158300 G>A maps to NM_006721.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr11:10327980 G>T maps to NM_001124.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:10327534 G>T maps to NM_001124.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:10327535 C>A maps to NM_001124.1 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:49510038 C>T maps to NM_181442.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr20:49510017 G>A maps to NM_181442.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr20:49510038 C>A maps to NM_181442.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:77895266 C>T maps to NM_014913.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:77894244 G>T maps to NM_014913.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr18:77896340 G>C maps to NM_014913.3 V1015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:77894746 C>G maps to NM_014913.3 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr10:64565040 A>G maps to NM_032804.5 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:203134619 C>T maps to NM_001048230.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:203134388 G>T maps to NM_001048230.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:112043034 G>C maps to NM_000677.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:112026353 C>T maps to NM_020683.6 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:112042961 G>T maps to NM_000677.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:112042823 A>G maps to NM_000677.3 V235V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:112028428 C>T maps to NM_020683.6 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr15:73048726 G>A maps to NM_031284.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:119306667 G>A maps to NM_001125.2 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:114077291 C>A maps to NM_138430.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36558941 A>G maps to NM_017825.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:26721658 G>T maps to ENST00000356368 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:159344181 C>T maps to NM_000679.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:159344454 C>A maps to NM_000679.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4202310 C>G maps to NM_000678.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:4202211 G>C maps to NM_000678.3 Y559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:4228884 G>T maps to NM_000678.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:112838896 G>A maps to NM_000681.3 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:112838173 C>T maps to NM_000681.3 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:112838131 G>T maps to NM_000681.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:96781456 C>A maps to NM_000682.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:3769637 C>A maps to NM_000683.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:115805006 C>T maps to NM_000684.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:148206921 C>T maps to NM_000024.5 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:148206481 G>T maps to NM_000024.5 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr5:148206583 C>T maps to NM_000024.5 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:67052854 G>T maps to NM_001619.3 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:67049756 C>T maps to NM_001619.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:67049199 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:67052427 G>T maps to NM_001619.3 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:26074882 G>C did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr22:26091115 G>T maps to NM_005160.3 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr22:26114345 C>A maps to NM_005160.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:244574691 G>A maps to NM_001126.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:244586217 C>T maps to NM_001126.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr14:105208278 C>T maps to NM_199165.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:44152431 C>T maps to NM_001129.3 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:44147456 G>A maps to NM_001129.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:44152608 C>T maps to NM_001129.3 Y863Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:44146463 C>T maps to NM_001129.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:44148745 C>T maps to NM_001129.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:44150654 C>A maps to NM_001129.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:44149662 C>T maps to NM_001129.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:19646918 A>G maps to NM_001114176.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr15:89173307 C>G maps to NM_022767.3 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr15:89169691 G>C maps to NM_022767.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:7870432 C>T maps to NM_001134647.1 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:7795472 C>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:7857262 G>A maps to NM_001134647.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:148709277 G>T maps to NM_152406.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:148695816 G>T maps to NM_152406.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:148712328 C>A maps to NM_152406.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:148691760 G>A maps to NM_152406.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:116075447 G>T maps to NM_001001936.1 Y161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:116064522 G>C maps to NM_001001936.1 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:88029316 A>T maps to NM_001166693.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:88035721 G>T maps to NM_001166693.1 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:88035586 G>T maps to NM_001166693.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:88029352 C>T maps to NM_001166693.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:88035844 C>T maps to NM_001166693.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr4:87968670 C>T maps to NM_001166693.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:148072806 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:147919179 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:148037651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:147743991 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:148038094 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:147967463 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:148059467 C>G did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:147919248 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:147743641 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:147743878 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:148037248 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:147924508 C>T did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:147744203 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:148048525 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:147743757 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr23:147743946 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:148072759 C>G did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:148038015 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:147743812 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:148037216 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:148038040 A>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:148037736 A>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:148059938 A>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:147744017 C>G did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr23:148037517 C>A did not map to a codon.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr23:148055036 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:148037466 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:148037341 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:148062277 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:148037332 G>T did not map to a codon.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr23:148037364 G>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:147985782 T>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:148037823 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:147967503 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:148068984 C>G did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:147743533 G>C did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:147733639 G>C did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:148055115 C>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:148048560 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:148035268 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:148035269 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:148037616 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:148048332 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:148035224 A>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:147743890 T>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:147733576 A>G did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:147743553 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:148037479 G>C did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:148055097 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:148048493 A>G did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:148037734 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:147743628 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:147743629 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:147919202 T>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:148035184 G>C did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:148037639 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:147743549 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:148037571 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:148038107 G>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:147743754 A>G did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:147891397 A>G did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:148069035 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:148068980 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:148039928 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr23:148072777 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:148035132 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:148068912 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:147743928 A>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:148037901 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:148048600 T>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:147924491 A>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:100623840 T>A maps to NM_001025108.1 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:100210238 C>T maps to NM_001025108.1 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:100181962 T>A maps to NM_001025108.1 T1060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:100210250 G>T maps to NM_001025108.1 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:100627996 T>C maps to NM_001025108.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:132270356 G>A maps to NM_014423.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:12340268 G>A maps to NM_006796.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr18:12367059 C>T maps to NM_006796.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:12348283 G>A maps to NM_006796.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:12371645 A>G maps to NM_006796.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr18:12358887 G>A maps to NM_006796.2 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:74361145 C>T maps to NM_001133.2 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:74349986 A>G maps to NM_001133.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:74357671 G>A maps to NM_001133.2 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:74351679 T>C maps to NM_001133.2 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:76202118 C>T maps to NM_001145526.1 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:76198622 C>T maps to NM_001145526.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:74308072 G>A maps to NM_001134.1 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:74318260 T>A maps to NM_001134.1 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64794784 G>A maps to ENST00000422803 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:64778626 C>T maps to ENST00000422803 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:64800102 A>G maps to ENST00000422803 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:64819084 C>T maps to ENST00000422803 D910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:178354501 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:178355579 G>A maps to NM_000027.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:178358559 A>T maps to NM_000027.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:236708123 G>A maps to NM_001037131.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:236706517 G>T maps to NM_001037131.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:236659076 G>A maps to NM_001037131.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:236706530 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:236877217 G>A maps to NM_001037131.1 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:236715887 G>C maps to NM_001037131.1 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:236957736 C>T maps to NM_001037131.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:88769445 G>A maps to NM_133447.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:88764093 G>A maps to NM_133447.1 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:88764084 G>C maps to NM_133447.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:58128444 G>A maps to NM_001122772.1 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:58126628 C>T maps to NM_001122772.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:58121758 G>A maps to NM_001122772.1 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:58124302 C>G maps to NM_001122772.1 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:58130937 G>A maps to NM_001122772.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:150814461 G>C maps to NM_031946.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:150817228 C>T maps to NM_031946.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:150817156 C>T maps to NM_031946.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr7:150841026 A>G maps to NM_031946.4 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:150815700 G>T maps to NM_031946.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr10:75457450 C>T maps to NM_001144000.1 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:51768802 C>T maps to NM_001077665.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr10:51769669 C>T maps to NM_001077665.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr10:51768775 G>T maps to NM_001077665.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:87089342 C>A maps to NM_152336.2 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:87089365 T>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:86807970 T>C maps to NM_152336.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:86838536 C>A maps to NM_152336.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:87099503 G>T maps to NM_152336.2 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr15:86814850 G>T maps to NM_152336.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:87089267 G>A maps to NM_152336.2 K861K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr15:86807973 G>T maps to NM_152336.2 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr15:86822926 T>G maps to NM_152336.2 Y665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47698821 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47712124 C>A maps to ENST00000357610 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr11:47711851 G>A maps to ENST00000357610 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:47681748 G>T maps to ENST00000357610 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:49128905 G>C maps to NM_032785.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:49511275 C>A maps to NM_032785.3 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:27292957 A>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:27278942 T>C maps to NM_021831.5 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:27280266 G>T maps to NM_021831.5 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr2:27278975 C>T maps to NM_021831.5 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr2:27281273 C>T maps to NM_021831.5 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:32150921 C>T maps to ENST00000375070 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:228384752 A>G maps to NM_001135187.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:228388580 G>A maps to NM_001135187.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr2:228384686 A>T maps to NM_001135187.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:100151828 C>T maps to NM_006076.4 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100151089 G>T maps to NM_006076.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:76359004 A>G maps to NM_018046.4 E691E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:141352705 C>T maps to NM_018238.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr7:141349061 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:100340790 C>G maps to ENST00000311030 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:100380943 G>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:100346960 C>A maps to ENST00000311030 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:100346945 A>T maps to ENST00000311030 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:100343332 C>T maps to ENST00000311030 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:100340949 C>T maps to ENST00000311030 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr6:32137743 C>T maps to NM_032741.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:45402210 G>T maps to NM_001037553.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr21:45389111 C>T maps to NM_001037553.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr21:45391371 G>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:161567585 C>T maps to NM_020133.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:161575191 C>A maps to NM_020133.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:161574501 G>A maps to NM_020133.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:41476484 G>A maps to NM_178819.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:84457903 G>C maps to NM_032717.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:84518668 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:84525895 T>C maps to NM_032717.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:78807395 C>T maps to NM_001013619.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:78825891 C>T maps to NM_001013619.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:178326700 C>T maps to NM_003659.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:178301780 A>T maps to NM_003659.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr2:178362493 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:178378633 C>T maps to NM_003659.3 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr7:16900124 T>A maps to NM_176813.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:957681 C>T maps to NM_198576.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:979210 G>T maps to NM_198576.2 G603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:981167 G>A maps to NM_198576.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:978999 G>A maps to NM_198576.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:985805 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:979594 G>T maps to NM_198576.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:979056 C>T maps to NM_198576.2 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:978963 C>G maps to NM_198576.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr16:67517005 G>C maps to NM_001138.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:230846287 G>A maps to NM_000029.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:230845984 C>A maps to NM_000029.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:230846485 G>A maps to NM_000029.3 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:230846206 C>A maps to NM_000029.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:230846467 G>A maps to NM_000029.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:88292349 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:88247824 T>C maps to ENST00000395847 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:88292464 T>A maps to ENST00000395847 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:88193912 T>C maps to ENST00000395847 V1088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148459391 C>T maps to NM_032049.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148459427 G>T maps to NM_032049.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr3:148458971 G>A maps to NM_032049.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr23:115304267 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:115303947 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:115304042 G>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:115304568 A>G did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:115303580 C>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:115304084 C>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:115304134 C>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:115303725 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:241808779 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:241817437 G>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr2:241815372 C>G maps to NM_000030.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:109681046 C>A maps to NM_031279.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:109684039 G>C maps to NM_031279.3 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:109681461 C>A maps to NM_031279.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:109664983 G>T maps to NM_031279.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:109667552 A>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:177642317 G>A maps to NM_153373.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:247063502 T>A maps to ENST00000428671 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247063771 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:247063772 T>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:247013697 C>T maps to ENST00000428671 R1908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr1:247013112 T>A maps to ENST00000428671 S2103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:247014497 C>A maps to ENST00000428671 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:247076618 A>T maps to ENST00000428671 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:247063717 C>A maps to ENST00000428671 G429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:32873371 C>T maps to NM_000687.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:32878561 G>A maps to NM_000687.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:32878140 C>T maps to NM_000687.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:32879308 C>A maps to NM_000687.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:110551753 C>T maps to NM_006621.4 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:129045718 G>C maps to NM_015328.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:129043236 G>C maps to NM_015328.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:129049314 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:27877828 T>C maps to NM_001029882.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:27874643 G>C maps to NM_001029882.2 S1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:27875155 C>A maps to NM_001029882.2 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:27875057 G>C maps to NM_001029882.2 S1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:135784320 G>A maps to NM_017651.4 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:135769451 T>A maps to NM_017651.4 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:62300196 G>A maps to NM_001620.1 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62288696 T>A maps to NM_001620.1 K4398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:62287344 C>T maps to NM_001620.1 K4848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:62287881 G>A maps to NM_001620.1 G4669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:62287884 C>T maps to NM_001620.1 E4668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr11:62292642 A>T maps to NM_001620.1 P3082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:62293286 C>A maps to NM_001620.1 E2868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:62284434 C>G maps to NM_001620.1 G5818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:62289393 G>A maps to NM_001620.1 I4165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:62298186 G>C maps to NM_001620.1 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:62288391 T>C maps to NM_001620.1 E4499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:62298828 C>A maps to NM_001620.1 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:62284241 G>A maps to NM_001620.1 L5883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:62297613 C>T maps to NM_001620.1 V1425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62293041 G>T maps to NM_001620.1 P2949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:62293113 G>C maps to NM_001620.1 V2925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:62286866 C>A maps to NM_001620.1 E5008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62294196 C>A maps to NM_001620.1 G2564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr11:62286884 C>A maps to NM_001620.1 E5002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:62300118 T>A maps to NM_001620.1 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr11:62288526 G>A maps to NM_001620.1 I4454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr11:62287120 A>T maps to NM_001620.1 L4923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:62288373 G>C maps to NM_001620.1 P4505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105415205 C>T maps to NM_138420.2 G2194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:105417680 C>T maps to NM_138420.2 G1369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:105410705 G>A maps to NM_138420.2 D3694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:105416669 G>T maps to NM_138420.2 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:105409426 G>A maps to NM_138420.2 L4121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:105416780 C>T maps to NM_138420.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:105410042 T>C maps to NM_138420.2 L3915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:105409859 C>T maps to NM_138420.2 P3976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:105412493 C>A maps to NM_138420.2 T3098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:105406156 C>A maps to NM_138420.2 G5211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:105418112 G>T maps to NM_138420.2 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr14:105418952 C>G maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:105413012 C>T maps to NM_138420.2 L2925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105420365 G>T maps to NM_138420.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105416309 G>C maps to NM_138420.2 P1826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105418991 C>T maps to NM_138420.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:105410771 C>G maps to NM_138420.2 V3672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:105415109 C>A maps to NM_138420.2 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr14:105416060 C>A maps to NM_138420.2 V1909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:105414140 C>T maps to NM_138420.2 V2549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr14:105411032 C>G maps to NM_138420.2 L3585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:105410090 G>T maps to NM_138420.2 V3899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr14:105412058 G>T maps to NM_138420.2 G3243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr14:105414908 G>A maps to NM_138420.2 A2293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr14:105415193 G>T maps to NM_138420.2 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr14:105405647 A>G maps to NM_138420.2 S5380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:105407963 C>A maps to NM_138420.2 A4608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:105416924 C>G maps to NM_138420.2 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr14:105412316 G>C maps to NM_138420.2 A3157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:105419326 G>A maps to NM_138420.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105408230 G>A maps to NM_138420.2 D4519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:105416867 C>G maps to NM_138420.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:105409426 G>A maps to NM_138420.2 L4121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:105417134 C>T maps to NM_138420.2 E1551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:105409121 G>T maps to NM_138420.2 P4222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr14:105419090 C>A maps to NM_138420.2 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr14:105413948 G>A maps to NM_138420.2 S2613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr14:105414089 C>A maps to NM_138420.2 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr14:105415471 C>A maps to NM_138420.2 E2106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:105410750 C>A maps to NM_138420.2 G3679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:105408446 C>T maps to NM_138420.2 G4447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:105421103 G>T maps to NM_138420.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr14:105414439 C>A maps to NM_138420.2 E2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:105409019 G>T maps to NM_138420.2 V4256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr14:105410606 G>A maps to NM_138420.2 P3727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr14:105414686 G>A maps to NM_138420.2 S2367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr14:105417185 C>T maps to NM_138420.2 G1534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr14:105415730 C>T maps to NM_138420.2 E2019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:105419213 C>G maps to NM_138420.2 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr14:105419027 C>T maps to NM_138420.2 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:105412519 G>A maps to NM_138420.2 L3090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:105419675 C>T maps to NM_138420.2 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:17382561 A>G maps to NM_001621.4 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:17378832 C>T maps to NM_001621.4 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:17349709 C>T maps to NM_001621.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:17379755 G>T maps to NM_001621.4 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:344052 G>A maps to NM_020731.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:434429 G>A maps to NM_020731.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:77935576 C>T maps to NM_012111.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:77935582 C>G maps to NM_012111.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:186338718 G>T maps to ENST00000273784 *369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:186331121 T>C maps to ENST00000273784 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:186338571 C>T maps to ENST00000273784 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:186335057 G>C maps to ENST00000273784 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:186338622 C>A maps to ENST00000273784 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:186335028 C>T maps to ENST00000273784 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186333532 G>T maps to ENST00000273784 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:31539816 G>C maps to NM_016633.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:8759493 G>C maps to NM_020661.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:222843270 A>T maps to NM_022831.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:133995666 A>T maps to NM_001185095.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr9:133986983 G>T maps to NM_001185095.1 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:129264137 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:129274512 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:129267392 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:129272582 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:129271087 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:129270035 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:129281759 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:129263559 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:129272641 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:129289202 A>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:129264008 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:129271159 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:129290566 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:129270700 C>A did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:129270621 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:129281787 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:129281501 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:129289262 T>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:71874071 G>A maps to NM_032797.5 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:21330811 G>T maps to NM_144704.2 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:21329083 C>A maps to NM_144704.2 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr22:21330058 G>T maps to NM_144704.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:143605318 G>T maps to NM_016108.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:106967308 G>C maps to NM_001624.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:106975227 A>G maps to NM_001624.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:106967351 G>T maps to NM_001624.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr6:106968958 G>T maps to NM_001624.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:106973006 G>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr6:106960437 G>A maps to NM_001624.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:106960401 G>T maps to NM_001624.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:26663746 C>G maps to NM_001039775.3 R1256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr1:26648745 G>A maps to NM_001039775.3 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:26664532 G>A maps to NM_001039775.3 C1159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:159036095 G>T maps to NM_004833.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:159035704 G>A maps to NM_004833.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:159035744 A>G maps to NM_004833.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159035798 C>A maps to NM_004833.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:159038399 G>A maps to NM_004833.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:159036038 C>T maps to NM_004833.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:159036023 G>T maps to NM_004833.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr7:6063249 C>T maps to NM_006303.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:67250703 C>T maps to NM_003977.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:6338337 G>A maps to NM_014336.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:6330022 C>A maps to NM_014336.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:6330283 G>T maps to NM_014336.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr21:45710772 G>C maps to NM_000658.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:45713742 C>G maps to NM_000383.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:45709651 G>T maps to NM_000383.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr21:45707005 C>T maps to NM_000383.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr21:45708261 T>A maps to NM_000383.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr21:45711087 C>A maps to NM_000383.2 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:4832528 C>A maps to NM_018836.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:4772523 G>T maps to NM_018836.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:4771989 C>A maps to NM_018836.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:4829964 A>T maps to NM_018836.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:4829946 C>T maps to NM_018836.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:4829937 C>A maps to NM_018836.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:130630758 G>A maps to ENST00000223836 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:130635070 G>A maps to ENST00000223836 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65691778 G>C maps to NM_013410.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:77752624 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:77763343 C>T maps to NM_174858.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:77806059 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:77763334 G>A maps to NM_174858.1 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:77752670 G>T maps to NM_174858.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr1:77759484 T>A maps to NM_174858.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:77752708 G>A maps to NM_174858.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:96875233 C>T maps to NM_152327.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr14:96916183 A>T maps to NM_152327.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr14:96953380 T>C maps to NM_152327.2 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:96944850 G>A maps to NM_152327.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr14:96949358 C>T maps to NM_152327.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr14:96944934 C>T maps to NM_152327.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr17:55184186 C>A maps to ENST00000427138 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr17:55193487 C>T maps to ENST00000427138 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr17:55193505 G>T maps to ENST00000427138 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:55194218 A>C did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr17:55193487 C>T maps to ENST00000427138 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:42869851 G>T maps to NM_016248.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr13:42888076 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr13:42876706 A>G maps to NM_016248.2 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr13:42882667 C>T maps to NM_016248.2 S1732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr13:42876872 C>T maps to NM_016248.2 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:151671919 C>G maps to NM_005100.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:151674268 C>T maps to NM_005100.3 H1581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:151669912 G>A maps to NM_005100.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:151673209 G>C maps to NM_005100.3 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:151674409 T>A maps to NM_005100.3 S1628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:151626886 A>G maps to NM_005100.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:151670161 T>G maps to NM_005100.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:151672171 G>A maps to NM_005100.3 K882K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:151670665 C>A maps to NM_005100.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:151673836 T>A maps to NM_005100.3 I1437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr15:86129054 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:86077001 A>T maps to NM_006738.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr15:86225437 T>A maps to NM_006738.4 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr15:86262349 C>T maps to NM_006738.4 I2019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr15:86122891 C>T maps to NM_006738.4 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:86205616 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:119053905 C>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:119048728 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:119053912 G>T did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr9:112900122 C>T maps to NM_007203.4 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112899607 C>G maps to NM_007203.4 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr9:112900056 C>T maps to NM_007203.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:112900793 C>T maps to NM_007203.4 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:4737206 G>A maps to NM_006422.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:4747356 T>C maps to NM_006422.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:4736588 G>C maps to NM_006422.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:4737737 G>C maps to NM_006422.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:49957632 A>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:49957153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:49958250 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:49957745 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:49961635 G>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:49958058 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:49958060 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:49958169 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:49955641 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:49957191 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:49957130 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:49957325 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:49957415 C>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:49962198 T>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:49955747 A>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:49958814 T>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:49957116 C>A did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:49961596 A>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:49955700 G>T did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:49962220 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:49958104 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:64935711 C>T maps to NM_004857.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:64935337 C>A maps to NM_004857.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:64935577 G>T maps to NM_004857.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:33293231 A>G maps to NM_004274.4 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:33242913 C>T maps to NM_004274.4 R1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:33290933 G>T maps to NM_004274.4 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:33068650 C>G maps to NM_004274.4 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:33242895 G>T maps to NM_004274.4 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:33015818 C>T maps to NM_004274.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:33004779 T>G maps to NM_004274.4 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:33165316 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:33205040 G>T maps to NM_004274.4 E1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:33014692 T>A maps to NM_004274.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:33292073 G>A maps to NM_004274.4 A1685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:33046385 G>T maps to NM_004274.4 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr14:32902813 G>T maps to NM_004274.4 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:33015050 G>T maps to NM_004274.4 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:33290674 G>A maps to NM_004274.4 W1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:33046324 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:33292193 A>T maps to NM_004274.4 S1725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:15483985 C>T maps to NM_005858.2 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:15484838 G>C maps to NM_005858.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:15484655 G>A maps to NM_005858.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:15483727 G>A maps to NM_005858.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:15483952 C>G maps to NM_005858.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:15512272 G>A maps to NM_014371.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:91714918 A>G maps to NM_005751.4 L2981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:91632044 A>C maps to NM_005751.4 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr7:91700232 A>G maps to NM_005751.4 K2174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:91645513 G>A maps to NM_005751.4 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:91708553 G>A maps to NM_005751.4 K2369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr7:91622329 A>G maps to NM_005751.4 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr7:91694635 G>A maps to NM_005751.4 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:91699438 G>A maps to NM_005751.4 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:91625026 C>T maps to NM_005751.4 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr7:91631978 C>G maps to NM_005751.4 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:91631163 G>T maps to NM_005751.4 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:91624936 G>A maps to NM_005751.4 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109819102 G>A maps to NM_001145128.2 D1704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:109962786 T>C maps to NM_001145128.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr6:109871391 G>A maps to NM_001145128.2 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr6:109965819 A>G maps to NM_001145128.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:117129924 G>A maps to NM_030767.4 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:117139108 C>G maps to NM_030767.4 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:117103958 G>A maps to NM_030767.4 S1307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:117119165 T>C maps to NM_030767.4 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:117122001 C>T maps to NM_030767.4 E788E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr9:117124076 G>A maps to NM_030767.4 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:109377549 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:109394791 G>T maps to NM_152763.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:46033773 G>T maps to NM_153326.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:134133179 C>A maps to NM_001628.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:134136346 G>A maps to NM_001628.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:134212695 C>A maps to NM_020299.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:134215411 G>T maps to NM_020299.4 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:134215481 G>T maps to NM_020299.4 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr7:134216763 A>G maps to NM_020299.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:134215441 A>G maps to NM_020299.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr7:134221870 T>A maps to NM_020299.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:5014793 G>T maps to NM_001353.5 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr10:5247725 G>T maps to NM_001818.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137776545 C>A maps to NM_005989.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:137792238 T>A maps to NM_005989.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:137761343 C>G maps to NM_005989.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:4879694 G>T maps to NM_001040177.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:4881967 C>T maps to NM_001040177.1 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:4872892 A>G maps to NM_001040177.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:4877970 C>G maps to NM_001040177.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:4872895 G>A maps to NM_001040177.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:4879673 C>T maps to NM_001040177.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:19634650 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:19630865 G>A maps to NM_003689.2 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:19630837 C>A maps to NM_003689.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:19612450 T>G maps to NM_012067.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:19610579 C>T maps to NM_012067.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:19610498 T>A maps to NM_012067.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:50373284 C>T maps to ENST00000391835 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr19:40745981 G>A maps to NM_001626.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr19:40748458 G>A maps to NM_001626.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:243736347 C>G maps to NM_005465.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:243736281 A>G maps to NM_005465.3 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:243778451 T>A maps to NM_005465.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:243708817 A>G maps to NM_005465.3 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:243663045 T>G maps to NM_181690.1 *466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:116151290 G>C maps to ENST00000277315 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:52236728 G>T maps to ENST00000441729 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:52246272 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:55052310 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:55047597 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:55040069 T>G did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:55052358 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:55050191 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:55047621 A>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:55041221 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:55043988 C>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:55047576 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:55042086 C>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:55041407 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:55040037 A>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:55052264 T>G did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:55042167 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:55052418 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:55052277 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:55052280 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:74277727 G>C maps to NM_000477.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:74277724 C>A maps to NM_000477.5 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:74283815 C>A maps to NM_000477.5 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:74285968 A>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:74285335 G>T maps to NM_000477.5 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:105266232 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:49967388 G>T maps to NM_153329.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:49964103 C>T maps to NM_153329.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:49965972 C>G maps to NM_153329.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:97373522 G>A maps to NM_002860.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:97380817 G>A maps to NM_002860.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr10:97388159 T>A maps to NM_002860.3 K300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr15:58247427 C>A maps to NM_003888.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr15:58285001 G>A maps to NM_003888.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:101447432 T>C maps to NM_000693.2 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr15:101434169 C>A maps to NM_000693.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:38396744 G>T maps to NM_000692.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:38396170 C>T maps to NM_000692.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:125877312 C>A maps to ENST00000273450 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:125876314 G>T maps to ENST00000273450 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:125872400 C>G maps to ENST00000273450 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:125876332 A>G maps to ENST00000273450 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:125877422 C>A maps to ENST00000273450 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr3:125828847 G>T maps to ENST00000273450 C772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:125879713 C>A maps to ENST00000273450 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:125844476 C>A maps to ENST00000273450 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:125826089 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:105420368 C>T maps to NM_001034173.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:105467759 C>T maps to NM_001034173.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:112235925 G>T maps to NM_000690.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr17:19645330 C>T maps to NM_000691.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:19645417 G>A maps to NM_000691.4 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:19645474 G>C maps to NM_000691.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:19555059 C>T maps to NM_001031806.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr17:19555089 A>G maps to NM_001031806.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr11:67789254 G>A maps to NM_001161473.1 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:67433011 G>A maps to NM_001031615.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:67432978 C>T maps to NM_001031615.1 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:67434390 G>T maps to NM_001031615.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:19199452 T>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:19209834 C>A maps to NM_003748.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:19208339 C>A maps to NM_003748.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:19211984 G>T maps to NM_003748.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:24503612 G>T maps to NM_170740.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr14:74551055 G>A maps to NM_005589.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:74531614 C>G maps to NM_005589.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr5:125912886 C>T maps to NM_001182.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:135239585 G>A maps to NM_022568.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr6:135254132 G>T maps to NM_022568.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:135263562 C>A maps to NM_022568.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:165667627 G>A maps to NM_000696.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr16:30080640 C>T maps to ENST00000395248 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:30080845 G>C maps to ENST00000395248 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:104189908 G>C maps to NM_000035.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:5128823 G>T maps to NM_019109.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:34179552 A>T maps to NM_032834.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:34179117 C>T maps to NM_032834.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:34179849 A>T maps to NM_032834.3 *474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr12:38714213 G>A maps to NM_001013620.3 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr22:50302924 G>A maps to NM_024105.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:110988102 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:110996019 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:110987963 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:110988104 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:110925491 C>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:110980040 A>G did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:110951606 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:110970073 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:110928265 C>T did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr23:110961490 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:110980034 A>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:110978349 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:110951509 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:110951466 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:125648219 G>T maps to NM_001195223.1 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr3:183960436 G>A maps to NM_005787.5 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:77832144 T>C maps to NM_024079.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr11:77823812 G>A maps to NM_024079.4 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111680425 A>G maps to ENST00000428306 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr11:111724369 A>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:111731268 C>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:111709014 C>A maps to ENST00000428306 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:29416584 G>T maps to NM_004304.3 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:29519835 T>G maps to NM_004304.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:30143132 G>A maps to NM_004304.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:29917880 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:29917778 C>A maps to NM_004304.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:29448339 G>T maps to NM_004304.3 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29754878 G>A maps to NM_004304.3 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:29455248 G>T maps to NM_004304.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:29940450 G>A maps to NM_004304.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:29451870 C>T maps to NM_004304.3 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498007 G>C maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:29498358 G>A maps to NM_004304.3 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:29754814 C>A maps to NM_004304.3 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr2:29543737 A>T maps to NM_004304.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr2:29606678 G>A maps to NM_004304.3 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:29443643 G>T maps to NM_004304.3 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:29498007 G>T maps to NM_004304.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29450488 C>A maps to NM_004304.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:29917833 A>T maps to NM_004304.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:29456481 A>G maps to NM_004304.3 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:29443604 G>C maps to NM_004304.3 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:29474107 C>A maps to NM_004304.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr2:29606634 A>T maps to NM_004304.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:29448357 G>T maps to NM_004304.3 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:29551273 C>G maps to NM_004304.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:29551312 G>A maps to NM_004304.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:29519815 G>T maps to NM_004304.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr2:29430079 C>A maps to NM_004304.3 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr2:29451801 G>A maps to NM_004304.3 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:29498274 G>T maps to NM_004304.3 Y635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:78142090 T>A maps to NM_006020.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:78161090 C>A maps to NM_006020.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:43908158 A>G maps to NM_139178.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:43908167 G>T maps to NM_139178.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:43940667 G>C maps to NM_139178.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:102097954 G>A maps to NM_017621.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:18087754 C>T maps to ENST00000261650 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:6374929 C>T maps to NM_032306.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:107427548 C>A maps to ENST00000417449 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:3744966 G>A maps to ENST00000403787 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:3726107 G>A maps to ENST00000403787 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr2:3743922 G>A maps to ENST00000403787 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:3749981 T>C maps to ENST00000403787 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:3727502 C>A maps to ENST00000403787 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:3750098 G>A maps to ENST00000403787 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:73679044 G>T maps to NM_015120.4 G1796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:73677379 A>T maps to NM_015120.4 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:73799764 C>T maps to NM_015120.4 T3586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73717354 G>T maps to NM_015120.4 E2756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:73678172 G>T maps to NM_015120.4 G1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:73651854 A>G maps to NM_015120.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:73830383 G>A maps to NM_015120.4 Q4104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:73717764 C>T maps to NM_015120.4 A2892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:73677808 A>G maps to NM_015120.4 T1384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:73678324 T>A maps to NM_015120.4 A1556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:73650099 G>C maps to NM_015120.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:73659340 G>T maps to NM_015120.4 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr2:73675264 C>T maps to NM_015120.4 L536L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-69-7979-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:7979493 T>A maps to NM_001139.2 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:4535474 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:4536574 C>G maps to NM_001140.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:45941035 C>A maps to NM_000698.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr10:45938490 C>T maps to NM_000698.2 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr10:45936814 C>T maps to NM_000698.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr10:45920486 G>A maps to NM_000698.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:8011888 C>A maps to ENST00000380149 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:8018292 A>G maps to ENST00000380149 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:8018968 C>A maps to ENST00000380149 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:233323381 G>T maps to NM_001631.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr2:233323438 C>T maps to NM_001631.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:233321706 A>T maps to NM_001631.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:233321082 G>A maps to NM_001631.3 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:233321769 G>T maps to NM_001631.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:233323044 G>A maps to NM_001631.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:113333029 G>T maps to NM_025144.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:113351752 G>A maps to NM_025144.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:113332984 G>C maps to NM_025144.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:113348781 C>T maps to NM_025144.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:113351863 G>T maps to NM_025144.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:113351657 G>T maps to NM_025144.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr4:113356392 A>T maps to NM_025144.3 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:113352043 T>C maps to NM_025144.3 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:113359730 G>T maps to NM_025144.3 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:56204295 A>T maps to NM_052947.3 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:56203479 G>A maps to NM_052947.3 S1313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr18:56246486 C>A maps to NM_052947.3 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr18:56247302 C>A maps to NM_052947.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:56205399 G>A maps to NM_052947.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:56202927 G>T maps to NM_052947.3 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr18:56171334 C>T maps to NM_052947.3 P2025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:56204799 C>A maps to NM_052947.3 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr18:56202747 C>T maps to NM_052947.3 T1557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr18:56171310 C>G maps to NM_052947.3 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:56247563 C>T maps to NM_052947.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr18:56247074 G>A maps to NM_052947.3 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:56205030 C>T maps to NM_052947.3 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:56247140 G>T maps to NM_052947.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr18:56246183 T>A maps to NM_052947.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr18:56246537 T>A maps to NM_052947.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:85383658 A>T maps to NM_020778.4 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:85406829 A>T maps to NM_020778.4 A1688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:85399756 G>A maps to NM_020778.4 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr15:85411402 C>T maps to NM_020778.4 Q1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr15:85383422 C>T maps to NM_020778.4 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:85383196 G>T maps to NM_020778.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:21902328 C>A maps to NM_000478.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr1:21902373 C>T maps to NM_000478.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:233244347 G>A maps to NM_001632.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:233244939 C>A maps to NM_001632.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:233244519 G>T maps to NM_001632.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:233245174 C>T maps to NM_001632.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr2:233245020 G>A maps to NM_001632.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7030-01A-11D-1945-08 chr2:233244592 C>T maps to NM_001632.3 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:233246360 C>A maps to NM_001632.3 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr2:233272675 G>A maps to NM_031313.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:202582932 C>A maps to NM_020919.3 G1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr2:202571684 C>A maps to NM_020919.3 P1488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:202611465 G>A maps to NM_020919.3 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:202603420 C>A maps to NM_020919.3 G797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:202572614 G>A maps to NM_020919.3 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:202611432 G>A maps to NM_020919.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:202588164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:46722808 G>A maps to NM_147129.3 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:46727830 C>T maps to NM_147129.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:46728571 C>A maps to NM_147129.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:202211398 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:202494489 G>A maps to ENST00000409099 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:203846374 C>T maps to NM_024744.14 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:85677429 C>A maps to NM_006982.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:85677632 G>A maps to NM_006982.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:110607490 G>A maps to NM_006492.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:44297152 C>A maps to NM_021926.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:44296989 G>A maps to NM_021926.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:44286577 C>T maps to NM_021926.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:33520878 C>A maps to NM_152462.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:33520885 G>A maps to NM_152462.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:33521119 C>A maps to NM_152462.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:33521100 G>T maps to NM_152462.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:33520747 A>T maps to NM_152462.2 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:33520612 G>T maps to NM_152462.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:11188890 C>T maps to NM_054028.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:11189586 A>C maps to NM_054028.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr8:11189307 G>T maps to NM_054028.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:7385377 C>A maps to NM_001102614.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:71471903 C>A maps to NM_016519.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr4:71464084 T>C maps to NM_016519.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:71459090 G>T maps to NM_016519.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:46568662 G>A maps to ENST00000458649 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:46563724 G>A maps to ENST00000458649 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:46455070 G>A maps to ENST00000458649 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr6:111214204 G>C maps to NM_001634.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:96361532 G>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:96350573 C>A maps to NM_152435.2 R141R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8614-01A-11D-2393-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-91-6848-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:2571042 C>T maps to NM_001145815.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:11316979 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:11316995 T>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:11316224 C>G did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:11316772 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:11316809 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:11316933 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:11316819 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:11316745 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:11316771 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:11316242 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:11316745 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr24:6736465 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr24:6736315 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr24:6736165 A>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr24:6736412 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr24:6736331 G>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr24:6736194 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr16:56439144 C>A maps to NM_001144.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56438862 G>A maps to NM_001144.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:2249447 C>T maps to NM_000479.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:53819600 A>G maps to NM_020547.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:53819600 A>T maps to NM_020547.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:118081210 C>A maps to NM_001098526.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:118071235 C>G maps to NM_001098526.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr1:110051192 G>T maps to NM_020703.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:47471975 A>G maps to NM_001143668.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:47472641 G>A maps to NM_001143668.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr12:47472392 C>T maps to NM_001143668.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:47471600 T>C maps to NM_001143668.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:49756556 G>A maps to NM_198722.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:49756817 C>A maps to NM_198722.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr3:49756820 G>A maps to NM_198722.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:109507779 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:109441768 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:109459810 G>C did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:109561257 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:109441766 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:109459749 C>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:109561126 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:109560902 A>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:128628474 G>A maps to NM_031445.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:112058718 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:112035188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:112022250 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:112024288 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:112054521 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:112024185 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:112058631 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:112024284 G>A did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:112024236 G>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:112022376 T>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:112035061 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:112058741 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:112022735 A>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:112033866 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:112048219 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:112024257 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:112022353 C>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:112024326 G>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:112024173 G>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:112033821 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:112024167 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:112022846 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:94602639 T>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:94533393 C>G maps to NM_130847.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:115220006 G>T maps to NM_000036.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:115220123 C>T maps to NM_000036.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:115220953 A>G maps to NM_000036.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:115217453 A>T maps to NM_000036.2 C606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:115220607 C>A maps to NM_000036.2 G416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:115222304 C>T maps to NM_000036.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:115226818 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:115223067 G>A maps to NM_000036.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr1:115218532 G>A maps to NM_000036.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:115217371 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:110168959 G>T maps to ENST00000393689 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:110172892 C>T maps to ENST00000393689 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:110168299 C>A maps to ENST00000393689 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:10500112 C>T maps to NM_000480.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr11:10514897 G>A maps to NM_000480.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:38514959 T>C maps to NM_001635.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:38462074 G>T maps to NM_001635.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr7:38431513 G>A maps to NM_001635.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:38431609 G>A maps to NM_001635.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:38433688 C>T maps to NM_001635.3 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:38431501 C>T maps to NM_001635.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr7:38431513 G>A maps to NM_001635.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:38530676 G>T maps to NM_001635.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:49458926 G>A maps to NM_000481.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:71384524 C>T maps to NM_212557.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:104234118 C>T maps to NM_001008219.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:104297219 T>C maps to NM_001008218.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:104297222 A>T maps to NM_001008218.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:104297233 G>A maps to NM_001008218.1 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:104121932 G>A maps to NM_020978.3 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:104116892 G>T maps to NM_020978.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:104120404 G>T maps to NM_020978.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:104122019 A>T maps to NM_020978.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:104116439 G>T maps to NM_020978.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:2740343 C>A maps to NM_133463.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:2740375 C>A maps to NM_133463.1 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:66250611 G>A maps to NM_016627.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr2:112601106 C>T maps to NM_022662.2 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:112540062 C>A maps to NM_022662.2 G1695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:73990157 T>C maps to NM_173473.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:140080783 C>A maps to NM_013366.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr9:140082024 C>T maps to NM_013366.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:25391838 A>T maps to ENST00000510092 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:25408817 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:121773444 G>A maps to NM_016237.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:121747579 T>C maps to NM_016237.4 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:121758193 G>A maps to NM_016237.4 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:121746476 C>A maps to NM_016237.4 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr12:121775092 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:110825554 G>A maps to NM_016238.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:110815422 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:77272896 C>A maps to NM_015305.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr14:77257080 C>A maps to NM_015305.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:77255731 C>A did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:213186477 G>A maps to NM_144567.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:108334177 G>A maps to NM_001146.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:108334268 G>C maps to NM_001146.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:6420407 G>T maps to NM_001147.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:6385118 A>G maps to NM_001147.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:870863 C>A maps to NM_015985.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr20:868991 G>A maps to NM_015985.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr20:896563 C>G maps to NM_015985.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:129851285 G>A maps to NM_012098.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:8429486 G>A maps to NM_139314.1 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:101762126 A>G maps to NM_178127.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:11253737 G>A maps to NM_021146.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:11253668 C>A maps to NM_021146.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:41543691 G>T maps to ENST00000415018 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:41547753 G>T maps to ENST00000415018 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:41585512 C>A maps to ENST00000415018 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:41581078 C>A maps to ENST00000415018 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:41519407 G>A maps to ENST00000415018 Q1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:41582017 G>A maps to ENST00000415018 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr8:41522414 C>A maps to NM_020478.4 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:41530128 G>T maps to ENST00000415018 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr8:41553938 C>A maps to ENST00000415018 E968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr8:41556968 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:41545683 G>C maps to ENST00000415018 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr8:41581055 G>T maps to ENST00000415018 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:41572556 G>A maps to ENST00000415018 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:41552782 C>G maps to ENST00000415018 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:41552166 C>T maps to ENST00000415018 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:41563705 T>C maps to ENST00000415018 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:41584820 C>A maps to ENST00000415018 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:41585467 C>A maps to ENST00000415018 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:41577304 G>T maps to ENST00000415018 Y327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:41585446 G>A maps to ENST00000415018 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr8:41551584 G>T maps to ENST00000415018 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:114275530 C>A maps to NM_001148.4 S1919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:114279550 C>A maps to NM_001148.4 S3259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:114257902 T>C maps to NM_001148.4 D1254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:114279343 A>T maps to NM_001148.4 V3190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:114294268 C>A maps to NM_001148.4 P3878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:114179249 C>T maps to NM_001148.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:114276238 G>A maps to NM_001148.4 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:114294556 C>A maps to NM_001148.4 S3937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:114280093 C>T maps to NM_001148.4 S3440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:114274541 G>T maps to NM_001148.4 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:114276797 G>T maps to NM_001148.4 G2342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:114279969 C>A maps to NM_001148.4 S3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:114278605 C>A maps to NM_001148.4 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:114170999 C>T maps to NM_001148.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:114286204 C>A maps to NM_001148.4 L3633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:114276895 C>A maps to NM_001148.4 A2374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:114275527 C>A maps to NM_001148.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:114294601 A>C maps to NM_001148.4 S3952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr4:114120255 A>T maps to NM_001148.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:114274601 G>T maps to NM_001148.4 E1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:114179282 T>A maps to NM_001148.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:114120177 C>A maps to NM_001148.4 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:114276280 A>T maps to NM_001148.4 V2169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:114277411 C>A maps to NM_001148.4 V2546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:114279121 C>T maps to NM_001148.4 A3116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr4:114279529 A>G maps to NM_001148.4 V3252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:114275785 T>C maps to NM_001148.4 S2004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:114278467 T>C maps to NM_001148.4 T2898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:114278764 C>G maps to NM_001148.4 S2997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:114278095 C>T maps to NM_001148.4 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:114278500 C>A maps to NM_001148.4 P2909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:114153408 T>A maps to NM_001148.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:114276757 A>T maps to NM_001148.4 T2328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr4:114257890 T>C maps to NM_001148.4 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:114199054 C>A maps to NM_001148.4 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr4:114251453 A>T maps to NM_001148.4 R985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:114280153 A>T maps to NM_001148.4 T3460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:114275487 C>A maps to NM_001148.4 S1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:114290744 T>A maps to NM_001148.4 P3798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:114278692 G>T maps to NM_001148.4 V2973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:114158753 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr4:114275989 C>G maps to NM_001148.4 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr4:114290745 G>T maps to NM_001148.4 E3799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:114277273 G>A maps to NM_001148.4 T2500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr4:114275389 G>A maps to NM_001148.4 S1872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:114203952 G>T maps to NM_001148.4 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:114286285 C>A maps to NM_001148.4 I3660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:114264291 T>C maps to NM_001148.4 F1414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:61832646 C>T maps to NM_020987.2 E2664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:61836087 G>A maps to NM_020987.2 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:61833744 C>A maps to NM_020987.2 S2298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:62038533 G>A maps to NM_020987.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr10:61958142 G>A maps to NM_020987.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:61874083 T>C maps to NM_020987.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr10:61829657 G>A maps to NM_020987.2 Q3661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr10:61946574 G>A maps to NM_020987.2 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:61836182 T>A maps to NM_020987.2 R1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:61840372 C>A maps to NM_020987.2 E1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr10:61829652 T>C maps to NM_020987.2 S3662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190606122 C>G maps to NM_144708.3 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:190541597 C>T maps to NM_144708.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:190554682 T>C maps to NM_144708.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr2:190541455 C>T maps to NM_144708.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:65242116 C>A maps to NM_182703.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr15:65219161 C>T maps to NM_182703.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:65209589 C>A maps to NM_182703.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:54559907 G>A maps to NM_153228.2 *764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:54450166 C>T maps to NM_153228.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:54431391 C>T maps to NM_153228.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:54517715 T>C maps to NM_153228.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:54558176 C>T maps to NM_153228.2 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr17:54428147 G>A maps to NM_153228.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:54534306 G>A maps to NM_153228.2 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr17:54535255 G>A maps to NM_153228.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:4085564 C>A maps to NM_016376.3 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:14769114 C>T maps to NM_054027.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:14769114 C>T maps to NM_054027.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:14769165 C>G maps to NM_054027.4 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:14741986 C>T maps to NM_054027.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:14749340 A>G maps to NM_054027.4 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:14769249 C>A maps to NM_054027.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr5:139907855 T>A maps to ENST00000253810 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:139905704 C>G maps to ENST00000253810 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:139928511 G>A maps to ENST00000253810 P2584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:92027977 C>T maps to NM_019004.1 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:91972512 C>A maps to NM_019004.1 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:91980362 A>C maps to NM_019004.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:92027962 A>T maps to NM_019004.1 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:92017134 T>C maps to NM_019004.1 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:92027593 T>C maps to NM_019004.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr7:92027911 C>T maps to NM_019004.1 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:113264439 G>T maps to NM_178510.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr11:113264460 G>T maps to NM_178510.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:113266828 C>T maps to NM_178510.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:113266927 G>A maps to NM_178510.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr19:17394673 G>T maps to NM_152363.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:133312077 G>C maps to NM_015114.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr12:133311157 C>T maps to NM_015114.1 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:133306799 C>A maps to NM_015114.1 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:241463552 C>A maps to ENST00000401804 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:241448842 T>C maps to ENST00000401804 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:241465251 G>A maps to ENST00000401804 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241439488 C>A maps to ENST00000401804 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr2:241494420 C>T maps to ENST00000401804 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr2:241465684 C>A maps to ENST00000401804 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:241452251 T>A maps to ENST00000401804 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:16666730 C>A maps to NM_020319.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr7:16666725 G>A maps to NM_020319.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr7:16649286 G>A maps to NM_020319.2 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr7:16664698 T>C maps to NM_020319.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:92677533 C>A maps to NM_014391.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:92679982 G>T maps to NM_014391.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:92678687 C>A maps to NM_014391.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr13:111545441 C>A maps to NM_017664.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89346598 C>A maps to NM_013275.4 P2117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:89351263 G>C maps to NM_013275.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:89351665 G>A maps to NM_013275.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:89349595 G>T maps to NM_013275.4 I1118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr16:89347438 C>A maps to NM_013275.4 P1837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:89347828 C>A maps to NM_013275.4 T1707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:89351074 C>T maps to NM_013275.4 E625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9256879 C>T maps to NM_015208.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:9257678 G>T maps to NM_015208.3 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr18:9258052 C>T maps to NM_015208.3 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:9254230 A>T maps to NM_015208.3 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr18:9255947 A>T maps to NM_015208.3 K895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr18:9256468 G>A maps to NM_015208.3 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr18:9255151 T>C maps to NM_015208.3 H629H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:27936420 G>A maps to NM_152345.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27935035 G>T maps to NM_152345.4 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:27937723 G>T maps to NM_152345.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:70728530 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:70819935 C>T maps to NM_030816.4 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:70742524 C>A maps to NM_030816.4 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:5922262 G>C maps to NM_001009941.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:74008401 C>G maps to NM_032217.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:73987353 T>G maps to NM_032217.3 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr4:73956678 C>T maps to NM_032217.3 S2222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr4:74019645 C>A maps to NM_032217.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:73941947 T>A maps to NM_032217.3 *2604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:73962874 A>C maps to NM_032217.3 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:73956684 T>C maps to NM_032217.3 L2220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:73984515 T>C maps to NM_032217.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:73942002 C>T maps to NM_032217.3 W2586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:99338070 C>A maps to NM_020349.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:67968448 A>T maps to NM_001012419.1 K670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr9:67968441 A>T maps to NM_001012419.1 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:69420406 C>T maps to NM_001098805.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:69420353 T>A maps to NM_001098805.1 L415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:90582698 T>G maps to NM_144590.2 *192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:97506547 T>G maps to NM_144994.7 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:97506535 A>G maps to NM_144994.7 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:97509717 G>A maps to NM_144994.7 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:4218087 C>T maps to ENST00000262970 N1067N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:4217037 C>T maps to ENST00000262970 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:4207604 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:4224483 C>A maps to ENST00000262970 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr10:27326210 T>C maps to NM_014915.2 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:27389204 C>A maps to NM_014915.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:27306604 A>G maps to NM_014915.2 C1444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:27389138 G>T maps to NM_014915.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:27294556 C>A maps to NM_014915.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr10:27328912 G>A maps to NM_014915.2 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33093032 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:33140659 G>T maps to NM_032139.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr19:33135265 G>A maps to NM_032139.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:33122399 C>A maps to NM_032139.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr3:15720996 T>A maps to NM_015199.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr18:21192079 C>A maps to NM_173505.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:37442577 G>T maps to ENST00000374660 G540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:37430989 G>T maps to ENST00000374660 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:37438727 T>A maps to ENST00000374660 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:37433953 G>A maps to ENST00000374660 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:37451741 C>G maps to ENST00000374660 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:37490203 C>T maps to ENST00000374660 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:37490185 G>A maps to ENST00000374660 Q997Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:37447479 C>A maps to ENST00000374660 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:37451601 C>T maps to ENST00000374660 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:37421190 A>C maps to ENST00000374660 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:37508734 C>G maps to ENST00000374660 L1428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr10:37508671 T>C maps to ENST00000374660 A1407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:37508663 A>T maps to ENST00000374660 K1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:37508450 G>T maps to ENST00000374660 G1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:37486216 G>T maps to ENST00000374660 E938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:37414906 C>T maps to ENST00000374660 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:37430750 T>A maps to ENST00000374660 L253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14799106 T>A maps to NM_001145029.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:14852040 C>A maps to NM_001145029.1 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:14851707 A>T maps to NM_001145029.1 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:14763928 A>G maps to NM_001145029.1 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr18:14763853 G>A maps to NM_001145029.1 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr18:14851639 G>T maps to NM_001145029.1 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:14782612 G>T maps to NM_001145029.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr18:14851980 G>A maps to NM_001145029.1 E1227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr18:14763796 G>A maps to NM_001145029.1 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr18:14763728 G>T maps to NM_001145029.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr18:14757861 C>T maps to NM_001145029.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:94014518 A>T maps to NM_032290.3 K612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:52283237 G>C maps to NM_182608.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:52282849 G>T did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr12:52282101 C>A maps to NM_182608.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:52284752 C>A maps to NM_182608.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:145473873 G>T maps to NM_001039888.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:79854330 A>T maps to NM_001004441.2 L503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:145563068 C>A maps to NM_144698.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:145561640 A>G maps to NM_144698.3 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:145563038 A>T maps to NM_144698.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:145560149 G>A maps to NM_144698.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:145562447 A>G maps to NM_144698.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:97845665 G>A maps to NM_001164315.1 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:97784158 G>T maps to NM_001164315.1 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:97875436 A>T maps to NM_001164315.1 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:98175298 T>A maps to NM_025190.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:82922341 C>G maps to ENST00000260047 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:82938903 T>C maps to ENST00000260047 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197943538 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:197943539 T>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:197873683 T>A maps to NM_001195144.1 K666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:197870517 G>A maps to NM_001195144.1 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:197964568 G>T maps to NM_001195144.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:198051746 C>A maps to NM_001195144.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:197872648 T>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr2:197946416 G>C maps to NM_001195144.1 S497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:10025082 G>T maps to NM_198798.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr20:10030697 C>G maps to NM_198798.1 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:125591731 C>G maps to NM_020337.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:125592016 T>G maps to NM_020337.2 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:125631201 G>A maps to NM_020337.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:56642587 A>T maps to NM_173595.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr12:56638475 C>A maps to NM_173595.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:56638526 C>T maps to NM_173595.3 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr12:56638553 C>T maps to NM_173595.3 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr22:38229003 A>G maps to NM_138797.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:55455693 G>T maps to NM_024669.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr5:55472080 A>G maps to NM_024669.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:55407116 G>T maps to NM_024669.2 C486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:55466582 G>A maps to NM_024669.2 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:77818207 A>G maps to NM_001029870.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:77817345 C>A maps to NM_001029870.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:77816877 G>A maps to NM_001029870.1 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:118893527 C>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:118893355 C>A did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr23:118893514 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:118893472 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr6:90333172 G>A maps to ENST00000339746 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:117876981 T>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:117876163 A>T maps to ENST00000357099 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:99837587 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr12:99640544 G>A maps to NM_152788.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:100200346 C>A maps to NM_152788.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:99478744 C>A maps to NM_152788.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:100048922 C>A maps to NM_152788.3 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:100169422 C>A maps to NM_152788.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:100200322 C>A maps to NM_152788.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr16:4751473 G>A maps to NM_133450.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:21261822 T>C maps to NM_145865.2 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:21261201 T>A maps to NM_145865.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:21262122 G>T maps to NM_145865.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:101552506 C>T maps to ENST00000375018 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr9:101544758 C>A maps to ENST00000375018 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:101536272 C>A maps to ENST00000375018 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:220100210 G>T maps to NM_001042410.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:220098103 A>T maps to NM_001042410.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:36438850 C>T maps to NM_018685.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:36438853 C>T maps to NM_018685.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:36445886 A>T maps to NM_018685.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:69933991 G>A maps to NM_018043.5 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:69933977 C>A maps to NM_018043.5 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:69978180 C>T maps to NM_018043.5 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr11:69933925 G>T maps to NM_018043.5 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:69972208 G>T maps to NM_018043.5 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:43618532 C>T maps to NM_018075.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:43618385 T>A maps to NM_018075.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:5724380 G>T maps to ENST00000356134 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr12:5841685 C>T maps to ENST00000356134 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr12:5963298 G>A maps to ENST00000356134 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:5853386 C>A maps to ENST00000356134 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:26463462 A>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:26538396 C>T maps to NM_031418.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:26552835 G>A maps to NM_031418.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:26463525 C>A maps to NM_031418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:26568987 C>T maps to NM_031418.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:26664730 T>C maps to NM_031418.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:26619957 C>A maps to NM_031418.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:26463610 C>T maps to NM_031418.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:26669337 C>A maps to NM_031418.2 Y837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr11:26463639 C>A maps to NM_031418.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:26556080 C>G maps to NM_031418.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:26664762 G>T maps to NM_031418.2 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:26677674 C>T maps to NM_031418.2 C860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:101480520 G>A maps to ENST00000392977 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:101436246 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:101504242 C>A maps to ENST00000392977 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:101472999 C>A maps to ENST00000392977 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:101477464 C>T maps to ENST00000392977 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:101491470 G>A maps to ENST00000392977 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:101490386 G>T maps to ENST00000392977 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:22281165 G>A maps to NM_213599.2 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:22272494 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:22281219 G>A maps to NM_213599.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:22257782 A>G maps to NM_213599.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:22257740 C>T maps to NM_213599.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:22294474 T>C maps to NM_213599.2 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr11:22294456 T>G maps to NM_213599.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:45744488 G>T maps to NM_001142679.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:45810525 C>T maps to NM_001142679.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr12:45803163 A>G maps to NM_001142679.1 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:45823075 A>G maps to NM_001025356.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr12:45725190 A>C maps to NM_001142679.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:242144349 G>T maps to NM_001001891.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:242163565 T>C maps to NM_001001891.3 *934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:242162663 C>T maps to NM_001001891.3 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:242155593 G>A maps to NM_001001891.3 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:242148971 G>A maps to NM_001001891.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:242144349 G>C maps to NM_001001891.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:242138774 C>T maps to NM_001001891.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:242140745 C>T maps to NM_001001891.3 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:242141709 C>A maps to NM_001001891.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:242129564 G>T maps to NM_001001891.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:242140751 C>T maps to NM_001001891.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17444343 C>A maps to NM_020959.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:17441756 G>A maps to NM_020959.2 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:17434397 G>C maps to NM_020959.2 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr11:433925 G>A maps to NM_001012302.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:48866731 A>G maps to NM_012404.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:150199077 C>G maps to NM_030920.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:90347592 C>T maps to NM_001150.2 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:90328732 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:90349373 G>T maps to NM_001150.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:90348374 C>G maps to NM_001150.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr15:90328671 C>A maps to NM_001150.2 E938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:90346961 G>A maps to NM_001150.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:90340925 C>A maps to NM_001150.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:69271871 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:69304604 A>G maps to NM_032208.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr2:69318049 A>G maps to NM_032208.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:69409623 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:69300230 G>T maps to NM_032208.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:69472354 A>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:69397402 C>A maps to NM_032208.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:80828600 G>A maps to NM_058172.5 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:46111910 A>G maps to NM_001128324.1 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:75778405 G>A maps to NM_000700.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr9:75777730 C>G maps to NM_000700.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:169049309 G>T maps to NM_007193.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:169102870 T>C maps to NM_007193.3 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:81926672 T>A maps to NM_145869.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:81926684 C>T maps to NM_145869.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:81929006 G>A maps to NM_145869.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:124748096 T>A maps to NM_001003954.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:124696963 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:60641387 C>T maps to NM_001002858.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:79503386 G>T maps to NM_005139.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr4:79503335 G>T maps to NM_005139.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:70047829 G>T did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr4:122607463 G>T maps to NM_001154.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:150509006 G>A maps to NM_001155.4 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:150957059 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:150967114 T>A maps to NM_003568.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:36561668 G>T maps to NM_001177506.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:36616224 T>A maps to NM_001177506.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:36552769 G>T maps to NM_001177506.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:36634037 T>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:36552858 C>A maps to NM_001177506.1 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:36579923 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:36571809 G>T maps to NM_001177506.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:40997102 G>T maps to NM_009590.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40997146 G>A maps to NM_009590.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:40997825 G>T maps to NM_009590.2 G395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr17:41001206 C>T maps to NM_009590.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:41004562 G>T maps to NM_003734.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:41004382 C>T maps to NM_003734.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr17:41004693 C>G maps to NM_003734.2 S445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr17:41008368 G>T maps to NM_003734.2 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:41003386 C>A maps to NM_003734.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr17:41003743 C>T maps to NM_003734.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:201464398 G>A maps to NM_001159.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:201488582 G>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:201515815 G>A maps to NM_001159.3 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:201523985 G>T maps to NM_001159.3 V1090V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:201477457 G>T maps to NM_001159.3 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:201485501 T>C maps to NM_001159.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:201534332 C>T maps to NM_001159.3 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:29737725 C>A maps to NM_001127.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:29726402 C>T maps to NM_001127.3 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr22:29735035 G>C maps to NM_001127.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:71780566 C>A maps to ENST00000423132 G575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:71807198 G>A maps to ENST00000423132 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:24028972 C>T maps to NM_003917.2 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:16338501 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:16339675 G>A maps to NM_001130524.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10692545 G>A maps to ENST00000453102 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:10692526 C>A maps to ENST00000453102 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:10692431 G>A maps to ENST00000453102 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:224642490 C>A maps to NM_001039569.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:50296348 G>T maps to NM_014203.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50302619 G>T maps to NM_014203.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:50306625 C>G maps to NM_014203.2 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:970220 C>T maps to ENST00000332231 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr11:1006606 C>T maps to ENST00000332231 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:34044367 G>T maps to NM_001030006.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:33935315 G>T maps to NM_001030006.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:33951558 G>A maps to NM_001030006.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:183896903 C>T maps to ENST00000411763 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:183894822 G>C maps to ENST00000411763 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:183899825 G>A maps to ENST00000411763 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:47342739 G>A maps to NM_004069.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:77385315 T>A maps to NM_003664.3 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:77409634 C>T maps to NM_003664.3 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:77409607 T>A maps to NM_003664.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:77523356 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:83333185 C>A maps to NM_004644.3 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:83350260 G>T maps to NM_004644.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:83332642 G>T maps to NM_004644.3 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:83333168 G>T maps to NM_004644.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:83328727 C>T maps to NM_004644.3 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:83330575 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:83332600 C>A maps to NM_004644.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr15:83331887 C>G maps to NM_004644.3 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:83328341 T>A maps to NM_004644.3 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:2115418 T>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2114282 C>T maps to ENST00000355272 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115313 C>T maps to ENST00000355272 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115340 C>T maps to ENST00000355272 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2115385 C>T maps to ENST00000355272 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:2120871 C>T maps to ENST00000355272 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:2132508 T>G maps to ENST00000355272 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:2102189 C>T maps to ENST00000355272 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:42012411 G>T maps to NM_006803.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:42025239 G>T maps to NM_006803.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:115205761 G>T maps to NM_001284.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:90378815 T>A maps to ENST00000398333 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:114442859 C>T maps to NM_006594.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:51294696 A>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr15:51250969 C>T maps to NM_007347.3 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr15:51250711 C>G maps to NM_007347.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr7:99700335 C>T maps to ENST00000429084 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:99704333 C>G maps to ENST00000429084 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:99106158 C>T maps to NM_181861.1 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:99056293 G>A maps to NM_181861.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:99102469 A>T maps to NM_181861.1 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:99053023 C>A maps to NM_181861.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:99059400 C>G maps to NM_181861.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr9:72055917 A>G maps to NM_001163.3 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:72086607 T>A maps to NM_001163.3 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr15:29390775 G>A maps to NM_005503.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr15:29346359 T>A maps to NM_005503.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:29397661 C>T maps to NM_005503.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:29346380 C>A maps to NM_005503.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:29346821 C>T maps to NM_005503.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:29386494 T>A maps to NM_005503.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr15:29347032 G>T maps to NM_005503.3 E316*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:6432501 G>A maps to ENST00000389906 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:6423817 C>A maps to ENST00000389906 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:26781305 A>T maps to NM_019043.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:26851279 C>A maps to NM_019043.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:26800824 A>G maps to NM_019043.3 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:26849031 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:26849657 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:26800732 C>A maps to NM_019043.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:40832536 A>G maps to NM_004307.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:40827943 G>A maps to NM_004307.1 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:139943780 C>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr5:139941698 C>T maps to ENST00000354402 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:139938170 T>A maps to ENST00000354402 *494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:139943800 G>A maps to ENST00000354402 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:112175323 G>T maps to NM_001127510.2 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:112174159 A>T maps to NM_001127510.2 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:112174893 A>G maps to NM_001127510.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:112178161 C>T maps to NM_001127510.2 Q2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:112111324 G>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr5:112164551 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:112173972 G>T maps to NM_001127510.2 V894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:112175949 A>G maps to NM_001127510.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:112177974 G>A maps to NM_001127510.2 R2228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:1462090 C>T maps to NM_005883.2 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:1470031 C>T maps to NM_005883.2 F2244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:1461076 C>T maps to NM_005883.2 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr19:1467097 G>A maps to NM_005883.2 E1266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:10471850 C>G maps to ENST00000423585 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr18:10468598 G>A maps to ENST00000423585 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr18:10487977 G>T maps to ENST00000423585 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:57036340 G>T maps to NM_153360.1 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr20:57035971 G>C maps to NM_153360.1 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:159558240 C>T maps to NM_001639.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:159558185 A>T maps to NM_001639.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:49720356 G>A maps to ENST00000438011 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:55028734 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:55029450 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:55033665 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:55033386 A>G did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:55033448 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:55033289 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:55033270 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:55033652 G>T did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:55033573 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:55033564 G>C did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr11:43333682 G>C maps to NM_001142930.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr11:34904942 T>A maps to NM_015957.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:68765341 T>A maps to NM_173545.2 Y381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:68772345 T>C maps to NM_173545.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:68753262 A>G maps to NM_173545.2 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57004349 G>A maps to NM_005161.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:57004322 G>T maps to NM_005161.4 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:36362524 C>T maps to NM_001024807.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:36362894 G>T maps to NM_001024807.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:129996649 A>T maps to NM_001642.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:129996638 G>T maps to NM_001642.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:129996685 G>A maps to NM_001642.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:130005575 C>T maps to NM_001642.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:161192311 C>T maps to NM_001643.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161192793 C>G maps to NM_001643.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:116691783 G>A maps to NM_000482.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:116691951 C>A maps to NM_000482.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:116692385 C>A maps to NM_000482.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:116692407 C>T maps to NM_000482.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:21238275 G>T maps to NM_000384.2 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:21233988 G>C maps to NM_000384.2 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:21235077 G>T maps to NM_000384.2 I1554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:21227176 G>A maps to NM_000384.2 D4017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:21255314 G>C maps to NM_000384.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:21225225 A>C maps to NM_000384.2 L4356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:21233631 G>T maps to NM_000384.2 I2036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:21236287 G>T maps to NM_000384.2 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:21255356 C>T maps to NM_000384.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21229929 G>A maps to NM_000384.2 F3270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:21232296 C>A maps to NM_000384.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21225813 G>A maps to NM_000384.2 G4160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:21229633 G>T maps to NM_000384.2 S3369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:21237342 G>T maps to NM_000384.2 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:21263871 A>C maps to NM_000384.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:21233784 G>A maps to NM_000384.2 T1985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:21239498 G>T maps to NM_000384.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:21224685 C>T maps to NM_000384.2 T4536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:21234456 G>T maps to NM_000384.2 G1761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:21225981 C>T maps to NM_000384.2 L4104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:21245792 G>T maps to NM_000384.2 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr2:21224709 G>A maps to NM_000384.2 Y4528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr2:21245797 G>A maps to NM_000384.2 H907H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:21235157 G>A maps to NM_000384.2 Q1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:21232044 T>A maps to NM_000384.2 A2565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:21238242 A>G maps to NM_000384.2 Y1169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:21242605 G>T maps to NM_000384.2 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:21229380 A>C maps to NM_000384.2 T3453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:21233667 A>T maps to NM_000384.2 I2024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:21251355 G>T maps to NM_000384.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:21234951 T>C maps to NM_000384.2 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:21233304 G>T maps to NM_000384.2 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:21234045 A>T maps to NM_000384.2 S1898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:21242731 T>A maps to NM_000384.2 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:21232871 C>A maps to NM_000384.2 E2290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:21230493 G>T maps to NM_000384.2 A3082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:21228597 G>T maps to NM_000384.2 P3714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:21236242 G>A maps to NM_000384.2 F1335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:21260889 G>A maps to NM_000384.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:21250864 A>G maps to NM_000384.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:21234525 G>C maps to NM_000384.2 L1738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr2:21228399 G>A maps to NM_000384.2 A3780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:21228221 G>A maps to NM_000384.2 L3840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:28507876 G>T maps to NM_018690.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28508885 G>T maps to NM_018690.2 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:28508140 G>A maps to NM_018690.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:28509317 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr16:28509652 A>G maps to NM_018690.2 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr16:28507606 G>A maps to NM_018690.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:7805421 G>T maps to NM_001644.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:7803639 C>A maps to NM_001644.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:7805355 G>A maps to NM_001644.3 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:41029441 G>T maps to NM_006789.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:41029081 C>A maps to NM_006789.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr22:39357576 G>A maps to NM_001193289.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr22:39358101 G>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr22:39414031 G>T maps to ENST00000396762 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr22:39413823 C>T maps to ENST00000396762 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:39425496 C>T maps to NM_152426.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:39445555 C>G maps to NM_145298.5 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:39441196 G>A maps to NM_145298.5 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:39440104 C>T maps to NM_001006666.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:39483020 A>T maps to NM_021822.3 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:183617679 C>A maps to NM_203454.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:183617856 G>T maps to NM_203454.2 Y20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:45419582 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:45452504 A>T maps to NM_000483.3 *102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:116701582 G>T maps to ENST00000360377 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:45448462 G>A maps to NM_001646.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:56755896 C>A maps to NM_001638.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:64216780 G>C maps to NM_000042.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:64208277 A>C maps to NM_000042.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr17:64216807 A>T maps to NM_000042.2 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:64210621 C>A maps to NM_000042.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:36661454 C>T maps to NM_145343.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:36537716 G>C maps to NM_145640.2 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr22:36537769 C>A maps to NM_145640.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr22:36587461 G>T maps to ENST00000332987 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:36123063 C>T maps to NM_030642.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr22:36122750 T>C maps to NM_030642.1 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr22:36123140 G>A maps to NM_030642.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr22:36122924 C>T maps to NM_030642.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr22:36122425 C>A maps to NM_030642.1 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr6:31625019 G>A maps to NM_019101.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:31625864 G>A maps to NM_019101.2 *189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:23897064 T>C did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:23897135 C>G did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:23876835 T>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:84329283 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:84342595 G>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:84329294 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:84342615 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:84258933 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr21:27284176 T>A maps to NM_000484.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr21:27327991 G>A maps to NM_000484.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:27269911 T>A maps to NM_000484.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:58571906 G>C maps to NM_006380.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:58524942 C>T maps to NM_006380.2 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:57294180 G>T maps to NM_012096.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:57274569 A>G maps to NM_012096.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:57272144 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:30963177 C>T maps to ENST00000509504 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:30963078 G>A maps to ENST00000509504 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:30951861 C>G maps to ENST00000509504 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154293723 G>A maps to NM_080429.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:154296866 G>T maps to NM_080429.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:154295747 G>T maps to NM_080429.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:77301177 C>T maps to NM_173039.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr11:77301279 C>T maps to NM_173039.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:241631350 C>T maps to ENST00000429564 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:241631603 G>T maps to ENST00000429564 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:241631419 A>G maps to ENST00000429564 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:241631678 G>C maps to ENST00000429564 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:241622086 C>G maps to NM_001102467.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr2:241622050 C>A maps to NM_001102467.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:241621948 G>A maps to NM_001102467.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:241621966 C>A maps to NM_001102467.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:241622122 C>A maps to NM_001102467.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:50349276 G>A maps to NM_000486.5 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:50348098 T>A maps to NM_000486.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:50344879 C>A maps to NM_000486.5 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:33443782 G>T maps to NM_004925.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr12:50355844 C>T maps to NM_001651.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:50367273 C>A maps to NM_001652.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:33386152 G>A maps to NM_001170.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:33386083 G>A maps to NM_001170.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:33386973 G>T maps to NM_001170.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:25235882 G>T maps to NM_001169.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:25235822 C>T maps to NM_001169.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr16:25235789 G>A maps to NM_001169.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:25238509 G>T maps to NM_001169.2 G242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:58465265 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:115298844 C>T maps to NM_173800.4 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:115335600 T>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:115361775 A>T maps to NM_173800.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr5:115350990 T>A maps to NM_173800.4 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:115361799 A>G maps to NM_173800.4 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:115351450 T>A maps to NM_173800.4 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:115298328 C>G maps to NM_173800.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:115336936 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:115336182 C>G maps to NM_173800.4 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr5:115298370 G>A maps to NM_173800.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:115351342 C>A maps to NM_173800.4 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:35192824 G>A maps to NM_014691.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:35168138 T>A maps to NM_014691.2 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr15:35162951 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:35166145 C>A maps to NM_014691.2 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr15:35222463 G>A maps to NM_014691.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:66941688 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:66765998 G>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:66863199 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:66941746 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:66788863 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:66931529 T>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:66863121 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:66765122 G>C did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:66863139 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:66931406 A>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:66937401 G>C did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:66765063 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:66765343 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:66931263 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:66766099 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:47426120 C>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:47426516 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:47430736 G>C did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:47426120 C>G did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:47426121 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:47426306 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:47424442 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:72406622 C>T maps to NM_001040118.2 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:72408100 G>C maps to NM_001040118.2 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:36163085 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:36230754 C>T maps to NM_015230.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:36093642 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:36179550 A>G maps to NM_015230.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:36118682 C>G maps to NM_015230.2 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:36160402 G>A maps to NM_015230.2 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr4:36149175 C>A maps to NM_015230.2 E1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:36148963 G>A maps to NM_015230.2 Q1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:36083908 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr4:36162125 G>A maps to NM_015230.2 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr4:36162148 G>A maps to NM_015230.2 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:36166625 C>A maps to NM_015230.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:36195268 T>A maps to NM_015230.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:36230837 T>A maps to NM_015230.2 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:141039357 G>A maps to NM_022481.5 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:141049580 T>C maps to NM_022481.5 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr5:141035759 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:141035434 C>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr5:141050082 C>A maps to NM_022481.5 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:141049580 T>C maps to NM_022481.5 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:143694572 C>A maps to NM_015193.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:118454054 G>T maps to ENST00000359415 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:118463521 G>T maps to ENST00000359415 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr11:118452184 T>A maps to ENST00000359415 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:49334842 C>G maps to NM_001659.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:127231283 C>T maps to NM_001662.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr7:127230160 C>T maps to NM_001662.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:61907552 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:61910346 G>T maps to NM_175609.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:68112720 G>A maps to NM_006421.3 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:68138278 T>C maps to NM_006421.3 K1352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr8:68165701 T>C maps to NM_006421.3 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:68200217 T>C maps to NM_006421.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:68138359 C>T maps to NM_006421.3 K1325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:68139488 G>A maps to NM_006421.3 Q1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr8:68152513 C>A maps to NM_006421.3 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:68179363 C>A maps to NM_006421.3 G592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:68188218 T>C maps to NM_006421.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:68170320 C>A maps to NM_006421.3 G814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:47611010 G>C maps to NM_006420.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:47611011 G>T maps to NM_006420.2 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr20:47592589 G>T maps to NM_006420.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:47601943 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:47607617 C>T maps to NM_006420.2 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:47569249 G>T maps to NM_006420.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr20:47587707 G>A maps to NM_006420.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:47591391 C>T maps to NM_006420.2 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:47587800 C>T maps to NM_006420.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr20:47589793 A>G maps to NM_006420.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr20:47587680 G>A maps to NM_006420.2 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:153750860 G>T maps to NM_001025595.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:153803942 C>A maps to NM_001025595.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:6500371 T>A maps to NM_012402.2 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:131894468 C>G maps to ENST00000356962 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:68112497 C>A maps to NM_001172.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:68114829 A>C maps to NM_001172.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:121305146 G>T maps to NM_001012659.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:121289634 G>C maps to NM_001012659.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:46700977 G>A maps to NM_004308.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:46702913 G>A maps to NM_004308.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46703731 C>T maps to NM_004308.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:148744108 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr4:148968052 T>C maps to NM_024605.3 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:148796290 C>T maps to NM_024605.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:148984304 C>A maps to NM_024605.3 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:148827869 T>A maps to NM_024605.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr15:32917433 A>T maps to NM_014783.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr15:32928864 G>T maps to NM_014783.3 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:32103261 C>A maps to NM_018287.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:143974008 A>G maps to NM_018460.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:143973997 G>T maps to NM_018460.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:143913187 C>A maps to NM_018460.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:144381792 G>T maps to NM_018460.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:144381786 T>A maps to NM_018460.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:144245001 T>G maps to NM_018460.3 L255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:144008084 T>C maps to NM_018460.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:144460992 C>T maps to NM_018460.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:143913137 A>T maps to NM_018460.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:24942255 C>T maps to NM_001006634.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:24975515 A>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr16:24980011 C>T maps to NM_001006634.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:24981853 C>A maps to NM_001006634.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr16:24942522 C>T maps to NM_001006634.1 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:129950632 C>A maps to NM_033515.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:129905143 G>A maps to NM_033515.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:129901276 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:99016089 G>A maps to NM_032900.4 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:99006076 C>A maps to NM_032900.4 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:110451558 G>T maps to NM_020809.2 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:110450209 G>A maps to NM_020809.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:110461421 C>A maps to NM_020809.2 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:110451844 G>A maps to NM_020809.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:110462718 A>G maps to NM_020809.2 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:24959145 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr10:24891011 T>A maps to NM_020824.3 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:24884929 C>A maps to NM_020824.3 E1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:24922389 G>C maps to NM_020824.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:24889619 T>A maps to NM_020824.3 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:24910188 G>T maps to NM_020824.3 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:49791024 G>T maps to ENST00000417912 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:49791159 C>A maps to ENST00000417912 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr10:49662177 C>T maps to ENST00000417912 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:49812823 G>A maps to ENST00000417912 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:86916249 G>T maps to NM_001025616.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:86491874 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:86893266 G>C maps to NM_001025616.2 A226A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-86-8359-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:69049694 C>A maps to NM_001007231.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:68962336 C>T maps to NM_001007231.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:69002464 C>A maps to NM_001007231.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:142437234 T>A maps to NM_015071.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:142586819 G>A maps to NM_015071.4 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr5:142513602 C>T maps to NM_015071.4 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr5:142500654 C>T maps to NM_015071.4 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:43473952 T>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43481668 C>T maps to ENST00000428638 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:43475383 C>G maps to ENST00000428638 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:6896571 C>T maps to ENST00000400091 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6889984 C>T maps to ENST00000400091 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:6890047 C>T maps to ENST00000400091 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr18:6873573 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:6859895 G>T maps to ENST00000400091 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:94643703 C>A maps to NM_004815.3 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:94649795 G>A maps to NM_004815.3 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:94685948 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:94639652 G>C maps to NM_004815.3 P1186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:161018083 A>G maps to NM_001025598.1 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:161024250 G>A maps to NM_001025598.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:161018913 G>A maps to NM_001025598.1 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:161018298 G>T maps to NM_001025598.1 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119133385 C>T maps to NM_020754.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:119128424 G>C maps to NM_020754.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:119133226 C>A maps to NM_020754.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:119120936 A>T maps to NM_020754.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:119133763 T>A maps to NM_020754.2 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:119134186 A>C maps to NM_020754.2 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:119134969 C>T maps to NM_020754.2 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:128842724 G>A maps to NM_001142685.1 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:128838969 C>A maps to NM_001142685.1 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:128846490 C>A maps to NM_001142685.1 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:128839515 C>T maps to NM_001142685.1 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:128868216 C>A maps to NM_001142685.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:128839602 G>T maps to NM_001142685.1 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:128839707 C>A maps to NM_001142685.1 G1786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:128839823 C>A maps to NM_001142685.1 E1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:36277798 A>G maps to ENST00000007510 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:36275139 G>T maps to ENST00000007510 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:36276335 G>A maps to ENST00000007510 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:36271849 C>T maps to ENST00000007510 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:130218248 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:130215685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:130222686 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:130215685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:130215893 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:130220348 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:130222673 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:130217882 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:130220360 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:130217847 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:130219599 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:130218649 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:130218275 A>G did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:130222677 C>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:130220002 C>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:130219590 C>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:130219637 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:130219638 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:130218975 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:130217847 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:130218649 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:130217874 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:130218268 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:130215840 T>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:130218993 C>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:130215644 T>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:130219646 G>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:130215869 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:130215717 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:130218252 A>T did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr23:130218911 C>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:130222713 C>G did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:130215822 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:130218635 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:130222705 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:145773605 C>T maps to NM_025251.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:153184453 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:153184317 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:153186251 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr23:153173205 C>G did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:153178192 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:153186129 C>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:153184608 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:153178970 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:153186550 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:153178173 C>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:153184316 C>A did not map to a codon.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr23:153184368 C>A did not map to a codon.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr23:153175376 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:153176038 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:32563252 A>G maps to NM_001030055.1 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:32560933 A>G maps to NM_001030055.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:32563471 A>T maps to NM_001030055.1 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr14:32624009 A>G maps to NM_001030055.1 V1455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr14:32561095 T>C maps to NM_001030055.1 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:32621726 C>T maps to NM_001030055.1 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:11162222 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:11196309 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:11162017 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:11187672 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:11207049 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:11204552 T>C did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:11197458 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:11157245 C>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:11682888 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:11682514 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:11197548 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:11187694 C>A did not map to a codon.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr23:11206860 C>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:11187774 G>C did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:11157574 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:11187743 G>T did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr23:11196286 C>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:11204540 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:11174648 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:11204420 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:11207001 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:45244879 C>T maps to ENST00000352766 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr22:45258348 G>A maps to ENST00000352766 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr22:45221401 G>A maps to ENST00000352766 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr22:45198038 G>T maps to ENST00000352766 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57872990 G>A maps to ENST00000393797 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:57866467 C>A maps to ENST00000393797 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:57871337 C>T maps to ENST00000393797 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:57872979 G>A maps to ENST00000393797 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:57869696 G>A maps to ENST00000393797 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57867884 G>T maps to ENST00000393797 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:57866308 G>C maps to ENST00000393797 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr17:79827719 G>A maps to NM_004309.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr12:15095500 G>A maps to NM_001175.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:332517 C>A maps to NM_001176.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:332522 C>G maps to NM_001176.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42392152 G>A maps to NM_199002.1 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr19:42396884 G>T maps to NM_199002.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:42407923 G>T maps to NM_199002.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:42410693 C>A maps to NM_199002.1 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:1808321 C>T maps to ENST00000398564 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:1844524 A>G maps to ENST00000398564 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:1893702 C>T maps to ENST00000398564 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr8:1877562 C>T maps to ENST00000398564 Y1036Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:1905110 A>T maps to ENST00000398564 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:1881964 G>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:1842737 G>T maps to ENST00000398564 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr8:1905155 C>T maps to ENST00000398564 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:1873469 G>A maps to ENST00000398564 W862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:17983153 G>A maps to NM_018125.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:17942587 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:17966798 T>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:17966695 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:156941608 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:156931504 C>T maps to NM_198236.1 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:156917215 G>A maps to NM_198236.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:156933009 C>T maps to NM_198236.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:156909459 C>A maps to NM_198236.1 E1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:156909460 C>A maps to NM_198236.1 L1325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:156910212 A>C maps to NM_198236.1 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:156911686 C>A maps to NM_198236.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156946816 C>T maps to NM_198236.1 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:120308015 G>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:120312487 T>C maps to NM_015313.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:120312503 C>A maps to NM_015313.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:120348934 G>A maps to NM_015313.2 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:8219339 C>T maps to NM_173728.3 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:8222369 C>A maps to NM_173728.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:8221892 C>A maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:8222141 G>T maps to NM_173728.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:73066630 C>T maps to NM_014786.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:73071466 G>T maps to NM_014786.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:73068349 G>T maps to NM_014786.3 L1355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:73021144 C>T maps to NM_014786.3 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7516152 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr19:7523432 C>T maps to NM_001130955.1 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:16525663 C>T maps to NM_153213.3 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:16535534 T>A maps to NM_153213.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:16528912 C>A maps to NM_153213.3 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:155935420 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:155932974 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:143884171 A>C maps to NM_001003702.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:148999940 G>T maps to NM_001001669.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr5:148989190 C>T maps to NM_001001669.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:149008499 C>T maps to NM_001001669.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:148989226 C>A maps to NM_001001669.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:148997776 G>T maps to NM_001001669.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:149001339 G>T maps to NM_001001669.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:131785527 T>C maps to NM_015320.2 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:131785624 G>T maps to NM_015320.2 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:131704164 G>A maps to NM_015320.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:144062359 G>T maps to NM_005435.3 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr7:144070343 C>T maps to NM_005435.3 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:135825840 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr23:135827449 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:135770095 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:135772778 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:135758847 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:135770131 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:135825772 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:135829671 G>A did not map to a codon.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr23:135762896 G>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:135757175 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:135770120 C>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:135764988 C>G did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:135863027 T>C did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:135825787 G>C did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:135767850 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:135827427 G>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:135829706 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:135770131 G>C did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:135764067 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:135863012 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:135750261 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:135761736 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:111896543 A>C did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:111767995 C>G maps to NM_001113511.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:111927997 G>A maps to NM_001113511.1 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:111862228 G>T maps to NM_001113511.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:62875605 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:62875606 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:62917185 T>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:62944519 C>A did not map to a codon.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr23:62944545 G>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:62885808 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:62857994 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:62893975 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:62898342 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:27105666 G>T maps to NM_006015.4 E1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr1:27056306 C>T maps to NM_006015.4 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:27088650 C>T maps to NM_006015.4 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:27097664 C>G maps to NM_006015.4 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:27102065 A>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27105722 A>G maps to NM_006015.4 E1778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:27106494 G>T maps to NM_006015.4 E2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:27056168 A>T maps to NM_006015.4 K389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:27101452 C>T maps to NM_006015.4 Q1579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:27089555 G>T maps to NM_006015.4 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:27101328 G>A maps to NM_006015.4 Q1537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr1:27106068 C>T maps to NM_006015.4 Q1894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:27105681 G>T maps to NM_006015.4 E1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr1:27087557 C>G maps to NM_006015.4 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr1:27056236 G>A maps to NM_006015.4 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:27087345 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:27057660 C>T maps to NM_006015.4 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:27092811 G>T maps to NM_006015.4 G945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:157528079 G>T maps to ENST00000367148 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:157469855 G>T maps to ENST00000367148 G871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:157527756 G>T maps to ENST00000367148 E1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:157522482 C>T maps to ENST00000367148 P1625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:46245319 G>T maps to NM_152641.2 G1138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:46211515 T>A maps to NM_152641.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:46244482 C>A maps to NM_152641.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:46233110 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:46233206 C>T maps to NM_152641.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:46244897 G>T maps to NM_152641.2 G998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr12:46298745 C>G maps to NM_152641.2 S1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:46245089 C>T maps to NM_152641.2 Q1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:46243557 A>T maps to NM_152641.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:46245825 C>G maps to NM_152641.2 S1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:46211528 G>T maps to NM_152641.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:46298745 C>A maps to NM_152641.2 S1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:46243559 G>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr12:46231200 G>A did not map to a codon.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr12:46240642 C>T maps to NM_152641.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:46246463 G>T maps to NM_152641.2 E1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr12:46230570 C>T maps to NM_152641.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:46245868 A>T maps to NM_152641.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:46254603 A>T maps to NM_152641.2 S1598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:74882170 C>T maps to ENST00000395077 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr15:74836318 A>G maps to ENST00000395077 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:34623452 G>T maps to NM_001017363.1 C278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:34627762 G>T maps to NM_001017363.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr9:34621487 G>T maps to NM_001017363.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:58817916 G>T maps to NM_002892.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:58772771 T>C maps to NM_002892.3 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:58785523 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:58832775 A>G maps to NM_002892.3 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:58827654 G>T maps to NM_002892.3 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:235377132 C>A maps to NM_016374.5 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:235418973 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:235383691 C>T maps to NM_016374.5 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:235384973 C>A maps to NM_016374.5 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:235341217 A>G maps to NM_016374.5 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:63852623 G>A maps to NM_032199.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:63852788 G>C maps to NM_032199.2 *1189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:63662048 G>C maps to NM_032199.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:63850815 G>T maps to NM_032199.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:72873112 T>C maps to NM_005744.3 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:48965033 G>T maps to NM_006321.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:101790283 G>A maps to NM_001177.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:50204759 G>A maps to NM_138450.5 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr13:50204834 C>A maps to NM_138450.5 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:100242378 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:100240689 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:93761926 G>A maps to NM_182896.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:160395201 C>G maps to NM_025047.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:79650120 T>C maps to NM_001040025.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr2:235404666 C>T maps to ENST00000339728 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:18810033 A>G maps to NM_015161.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:69153633 G>A maps to NM_006407.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr2:153575485 C>G maps to NM_152522.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr2:153575350 G>T maps to NM_152522.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:153575170 T>C maps to NM_152522.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:57377509 G>T maps to ENST00000360096 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:66539449 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:23270391 C>A maps to NM_173081.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:23257338 C>A maps to NM_173081.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:23321834 A>T maps to NM_173081.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr10:23287229 C>A maps to NM_173081.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:23248495 T>A maps to NM_173081.3 L177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:23248020 G>A maps to NM_173081.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:23244734 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:23235152 T>A maps to NM_173081.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:28276313 C>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:28233797 C>A maps to NM_018076.2 G494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:28260242 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr10:28224176 G>T maps to NM_018076.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:28233165 C>T maps to NM_018076.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:28233213 C>T maps to NM_018076.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:28233207 A>T maps to NM_018076.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:28260202 G>A maps to NM_018076.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31476155 T>C maps to ENST00000408912 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:31476035 A>T maps to ENST00000408912 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:31476281 A>G maps to NM_024742.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:31477279 G>T maps to ENST00000408912 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:31471320 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr16:31473824 C>T maps to ENST00000408912 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:31471243 C>T maps to ENST00000408912 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr19:19168364 C>T maps to ENST00000392336 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:73125036 C>T maps to NM_024585.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:137953877 G>T maps to ENST00000469044 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:137942329 C>T maps to ENST00000469044 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:232141471 C>G maps to ENST00000359743 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:232104711 G>T maps to ENST00000359743 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:232121318 C>T maps to ENST00000359743 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:232146779 G>A maps to ENST00000359743 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:232209772 C>T maps to ENST00000359743 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:100808045 A>G did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:100808176 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:100809209 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:100808214 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:100809148 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:100911042 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:100911626 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:100912508 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:100911667 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:100912024 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:100911062 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:100912145 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:100910688 A>G did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:100911976 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:100911241 T>C did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:100912525 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr23:100912443 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:100912144 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:100912118 T>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:100880241 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:100880275 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:100880494 G>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:100880025 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:101857108 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:101857514 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:101858563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:101858467 A>G did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:101857294 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:101857748 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:101857906 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:101857942 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:101857938 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:101857411 A>G did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:100871495 C>G did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr23:100871507 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:100871219 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:150789612 T>C maps to NM_001668.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:150811988 G>A maps to NM_001668.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:150804312 G>A maps to NM_001668.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:150801704 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:80750290 T>C maps to NM_014862.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:80750268 G>C did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr15:80767499 G>A maps to NM_014862.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869213 G>A maps to NM_014862.3 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:80869216 G>A maps to NM_014862.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:80767472 G>A maps to NM_014862.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:80767526 G>T maps to NM_014862.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:13378643 G>T did not map to a codon.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr12:27553497 T>A maps to NM_020183.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:27571019 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:98956025 C>T maps to NM_006409.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:98985773 G>A maps to NM_005720.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:98988656 G>C maps to NM_005720.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr7:98984356 C>T maps to NM_005720.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:98985701 C>A maps to NM_005720.2 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:110883274 C>A maps to NM_005719.2 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:9839446 G>A maps to NM_001198793.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:183596669 C>T maps to ENST00000294742 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr3:169485231 T>C maps to NM_032487.4 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr3:169485597 G>T maps to NM_032487.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr15:52844199 G>A maps to NM_006628.4 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:35723371 G>A maps to ENST00000458225 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:35778811 C>A maps to ENST00000458225 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:35785455 A>T maps to ENST00000458225 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:35750562 G>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr3:35763129 G>A maps to ENST00000458225 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:35785413 C>T maps to ENST00000458225 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr3:35763237 C>T maps to ENST00000458225 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:35770888 T>C maps to ENST00000458225 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr3:35780973 G>T maps to ENST00000458225 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:69496324 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:69500066 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:69497334 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:69497953 A>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:75001076 G>A maps to NM_004041.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:4621907 G>A maps to ENST00000412477 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:90669503 T>C maps to NM_020801.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr5:90678628 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:51065402 G>A maps to ENST00000395624 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:78181600 T>A maps to NM_000046.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:2825530 C>A did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr23:2825345 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:2828020 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:2840003 C>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:2825401 C>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:2835947 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:2871198 C>A did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:2867414 T>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:2867359 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:2873564 C>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:2856179 G>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:2856193 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:2990215 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:3030287 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:3028171 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:2990081 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:3002283 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:3002622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:3002384 G>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:3002329 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:2998959 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:3002622 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:3002589 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:2994710 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:3028248 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:3002689 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:3002583 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:3002484 T>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:3002300 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:3007539 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:3002443 C>G did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:3019231 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:2990162 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:3002503 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:3019198 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:66303648 T>C maps to NM_014960.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr17:66343279 G>T maps to NM_014960.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:2951227 T>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:2947340 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:2947328 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:2945414 G>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:2924701 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:2933192 G>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:2936698 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:2931178 G>C did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:2936657 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:2942083 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:2945507 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:2945370 G>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:2933092 C>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:2942078 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:2951416 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:2951417 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:149676787 G>A maps to NM_001012301.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:149681813 G>T maps to NM_001012301.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr5:149677247 G>A maps to NM_001012301.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:149677826 C>A maps to NM_001012301.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:114899798 C>T maps to NM_024590.3 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:114824020 G>A maps to NM_024590.3 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr4:114823912 C>G maps to NM_024590.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:94890988 C>T maps to NM_198150.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:94891011 A>T maps to NM_198150.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:94903723 G>T maps to NM_198150.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:3682644 T>A did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:3681249 C>T maps to NM_004314.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:3681075 C>G maps to NM_004314.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:3681264 C>A maps to NM_004314.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:77003161 T>C maps to NM_001130016.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr4:77025108 C>A maps to NM_001130016.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr4:77003392 T>A maps to NM_001130016.1 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:3660971 G>T maps to NM_001079536.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231115006 G>T maps to NM_022786.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:19965106 C>A maps to NM_001670.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:19968924 G>C maps to NM_001670.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr22:19959934 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr22:19960534 C>A maps to NM_001670.2 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr23:25033722 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:25028385 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:25033785 C>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:25031160 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:17942256 G>C maps to NM_004315.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr8:17918914 G>T maps to NM_004315.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:52008319 A>T maps to NM_019893.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr10:51974616 T>C maps to NM_019893.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr10:51978296 C>T maps to NM_019893.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:122953874 G>A maps to NM_024769.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:123065630 G>T maps to NM_024769.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:131130907 C>A maps to NM_018482.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:131073090 G>A maps to NM_018482.2 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr8:131414162 G>T maps to NM_018482.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:131130782 G>C maps to NM_018482.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr8:131226828 C>T maps to NM_018482.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:131073178 C>A maps to NM_018482.2 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:131138200 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:131128983 C>T maps to NM_018482.2 Q668Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:131200411 G>A maps to NM_018482.2 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:9437489 A>G maps to NM_003887.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:9540190 G>T maps to NM_003887.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:9463316 G>T maps to NM_003887.2 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:9468001 A>G maps to NM_003887.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150878457 C>A maps to ENST00000422024 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr7:150878439 C>A maps to ENST00000422024 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr7:150878358 G>A maps to ENST00000422024 D302D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-91-7771-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:150883747 T>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:15306058 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:15311351 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:15301746 T>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:15315772 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:15320870 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:15301711 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:15306041 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:15315769 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:63445160 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:63445198 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:63444977 G>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:63445330 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:63444306 G>C did not map to a codon.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr23:63444983 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:63444720 C>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:63445163 G>A did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:63445214 C>T did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:63445232 C>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:63444921 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:5683787 C>T maps to NM_024701.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:57310739 T>A maps to ENST00000295941 L2904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:123269433 G>A maps to NM_080928.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:123267197 G>T maps to NM_080928.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:123264717 G>T maps to NM_080928.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:123257663 C>A maps to NM_080928.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:123267194 G>T maps to NM_080928.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:123268938 A>T maps to NM_080928.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:123257733 G>T maps to NM_080928.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:42249612 C>A maps to NM_080863.4 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:76384714 G>T maps to NM_080868.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:76397585 G>A maps to NM_080868.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:76397865 C>T maps to NM_080868.2 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:237172865 C>T maps to NM_212556.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:237172850 C>T maps to NM_212556.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:237103580 G>T maps to NM_212556.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:94404125 G>A maps to ENST00000434324 Y563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr14:94401016 G>A maps to ENST00000434324 Y631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:94405651 C>T maps to ENST00000434324 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr14:94417426 G>T maps to ENST00000434324 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:95157270 C>T maps to NM_016116.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr7:95115330 A>G maps to NM_016116.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:177142721 A>T maps to NM_080874.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:177136780 C>A maps to NM_080874.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:177136755 G>A maps to NM_080874.3 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:177143571 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr4:177138029 C>T maps to NM_080874.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:132400146 G>C maps to NM_017873.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr9:132402829 G>A maps to NM_017873.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr15:101170137 C>T maps to NM_198243.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:15266878 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:15276995 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:15266946 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:15268583 T>C did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:15287937 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:15287909 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:15267023 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr10:73912658 G>A maps to NM_001198800.1 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30197041 A>G maps to NM_032204.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr22:30197037 C>A maps to NM_032204.3 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr22:30202279 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:101037628 C>A maps to NM_006828.2 E1811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:101090598 C>A maps to NM_006828.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:101103673 A>G maps to NM_006828.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:101166052 T>A maps to NM_006828.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr6:100957983 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:100964151 G>T maps to NM_006828.2 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:101053535 G>A maps to NM_006828.2 F1695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:101075567 G>A maps to NM_006828.2 R1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:100965955 C>G maps to NM_006828.2 L1946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:100964120 C>A maps to NM_006828.2 G2004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:101095321 T>A maps to NM_006828.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:101307033 C>A maps to NM_022091.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:8959543 C>A maps to NM_020646.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:8959614 C>A maps to NM_020646.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:8959438 G>T maps to NM_020646.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:108169003 G>T maps to NM_203436.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:119222018 C>A maps to NM_014034.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:14236935 G>A maps to NM_018154.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:7077010 C>G maps to NM_001671.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:7012166 G>A maps to NM_080912.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr17:7010562 G>C maps to NM_080912.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:155448828 G>A maps to ENST00000368346 Q1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155324276 C>G maps to ENST00000368346 G2405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:155452240 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:155451712 G>A maps to ENST00000368346 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155327183 C>T maps to ENST00000368346 E2331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:155448133 A>G maps to ENST00000368346 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:155452126 C>T maps to ENST00000368346 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155449758 T>A maps to ENST00000368346 K968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:155348314 G>A maps to ENST00000368346 L2073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:155451616 T>G maps to ENST00000368346 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:155451466 T>A maps to ENST00000368346 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:155451508 G>C maps to ENST00000368346 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:155408304 C>A maps to ENST00000368346 E1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr8:37993277 C>T maps to NM_004674.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:32848269 C>A maps to NM_001672.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:32848320 C>G maps to NM_001672.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:32848287 G>A maps to NM_001672.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr7:65546941 C>T maps to NM_000048.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:65552719 C>G maps to NM_000048.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:1748723 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:1743180 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:1746596 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:1743278 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:1755381 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:1742070 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:1748720 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:1746628 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:1742029 A>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:1752119 G>A did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:1743161 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:1742073 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:1748716 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:1752059 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:1755422 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:1755359 G>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:1746613 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:1546690 C>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:1553972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:1554610 T>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:1536941 G>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:1531624 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:97481663 G>A maps to NM_183356.3 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr7:97483917 G>A maps to NM_183356.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:97488525 T>G maps to NM_183356.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:190531043 C>G maps to NM_019048.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:190532187 C>A maps to NM_019048.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:190531350 G>T maps to NM_019048.2 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr2:190531770 G>T maps to NM_019048.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:3397734 C>T maps to NM_000049.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr17:3402306 C>T maps to NM_000049.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr17:3379591 G>T maps to NM_000049.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:104565239 G>A maps to NM_001080464.1 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:104552163 C>A maps to NM_001080464.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:104571735 C>A maps to NM_001080464.1 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:62550536 A>G maps to NM_004318.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:62430178 C>T maps to NM_004318.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:62465663 C>A maps to NM_004318.3 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:197072367 T>G maps to NM_018136.4 R2005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197101453 C>G maps to NM_018136.4 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:197072641 G>A maps to NM_018136.4 A1913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:197065249 C>T maps to NM_018136.4 V2955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:197074075 C>T maps to NM_018136.4 K1435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:197112564 C>A maps to NM_018136.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:197102669 A>T maps to NM_018136.4 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:197112505 C>T maps to NM_018136.4 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:197062286 T>A maps to NM_018136.4 I3063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:197073661 T>C maps to NM_018136.4 R1573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:197071423 C>T maps to NM_018136.4 Q2319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:197112094 C>T maps to NM_018136.4 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:197074086 T>G maps to NM_018136.4 R1432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:197070640 T>C maps to NM_018136.4 T2580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:197102651 C>T maps to NM_018136.4 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:197071288 G>A maps to NM_018136.4 I2364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:197069854 C>A maps to NM_018136.4 R2842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:197062324 G>T maps to NM_018136.4 R3051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:197059395 A>G maps to NM_018136.4 T3253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr9:95222018 G>A maps to NM_017680.4 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr9:95227213 G>T maps to NM_017680.4 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:70188283 G>A maps to NM_152792.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:70188226 G>C maps to NM_152792.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:79968733 C>A maps to ENST00000306729 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:62123878 A>G maps to NM_025080.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:62105604 C>A maps to NM_025080.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:62123818 A>G maps to NM_025080.3 T71T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5931-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:96795646 G>T maps to NM_001002036.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:96789753 A>G maps to NM_001002036.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:96789929 C>A maps to NM_001002036.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:96801131 G>T maps to NM_001002036.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:96799186 G>A maps to NM_001002036.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:96795627 G>T maps to NM_001002036.3 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:176903320 G>A maps to ENST00000281881 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:176918391 C>T maps to ENST00000281881 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:177030245 C>A maps to ENST00000281881 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176857283 G>T maps to ENST00000281881 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176983955 G>T maps to ENST00000281881 C506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:176853610 C>T maps to ENST00000281881 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176915132 C>A maps to ENST00000281881 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:177001816 G>T maps to ENST00000281881 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:176903308 C>A maps to ENST00000281881 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:177133767 C>A maps to ENST00000281881 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:176853570 C>A maps to ENST00000281881 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:176915099 C>T maps to ENST00000281881 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:177030246 T>C maps to ENST00000281881 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:176934373 C>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:176913025 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:177001625 G>T maps to ENST00000281881 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:176927593 G>T maps to ENST00000281881 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:177001652 G>T maps to ENST00000281881 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:177001598 G>T maps to ENST00000281881 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:177030276 G>A maps to ENST00000281881 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:176913068 C>A maps to ENST00000281881 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:176857322 G>T maps to ENST00000281881 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:176905465 C>A maps to ENST00000281881 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:177133754 G>A maps to ENST00000281881 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:176852121 G>A maps to ENST00000281881 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:176903321 C>G maps to ENST00000281881 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:177001858 C>A maps to ENST00000281881 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:176903302 C>A maps to ENST00000281881 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr1:176863925 G>A maps to ENST00000281881 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:176903320 G>T maps to ENST00000281881 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:176845700 G>A maps to ENST00000281881 C1153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:176993815 G>T maps to ENST00000281881 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:176934347 G>A maps to ENST00000281881 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:177133539 G>A maps to ENST00000281881 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:119770458 G>T maps to ENST00000313400 Y501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:119770370 C>A maps to ENST00000313400 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:119976721 G>T maps to ENST00000313400 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:119737556 C>A maps to ENST00000313400 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119976739 C>A maps to ENST00000313400 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:119977021 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:119976663 C>A maps to ENST00000313400 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:120176787 G>T maps to ENST00000313400 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr9:119976988 C>A maps to ENST00000313400 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:119382626 G>A maps to ENST00000313400 A1056A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-6983-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:119738457 G>T maps to ENST00000313400 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:119582942 C>A maps to ENST00000313400 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:119626012 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:119858356 G>T maps to ENST00000313400 Y414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:119382704 C>G maps to ENST00000313400 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr9:119770371 G>T maps to ENST00000313400 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:119976949 C>T maps to ENST00000313400 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:120053650 G>T maps to ENST00000313400 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:119625957 G>T maps to ENST00000313400 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr9:119188207 G>T maps to ENST00000313400 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr9:119977012 G>T maps to ENST00000313400 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:119858332 G>T maps to ENST00000313400 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr9:119567927 G>T maps to ENST00000313400 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr9:119976781 C>A maps to ENST00000313400 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:119488143 G>T maps to ENST00000313400 Y904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:119802224 C>T maps to ENST00000313400 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:119976694 G>T maps to ENST00000313400 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:120053685 C>A maps to ENST00000313400 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:31024004 G>T maps to ENST00000375687 G1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr20:31019450 G>A maps to ENST00000375687 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr20:31022684 C>T maps to ENST00000375687 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr20:31022608 G>T maps to ENST00000375687 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr20:31022449 T>G maps to ENST00000375687 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:31017710 G>T maps to ENST00000375687 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:31016031 T>G maps to ENST00000375687 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:31021428 G>T maps to ENST00000375687 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:25965338 G>A maps to NM_018263.4 F1289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:25966003 G>A maps to NM_018263.4 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:25973042 G>C maps to NM_018263.4 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:31325262 A>T maps to NM_030632.1 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:31323006 G>T maps to NM_030632.1 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr18:31325018 C>A maps to NM_030632.1 S1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:31319521 G>A maps to NM_030632.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31325272 A>T maps to NM_030632.1 R1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31324686 G>T maps to NM_030632.1 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31314323 G>T maps to NM_030632.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:31324968 T>A maps to NM_030632.1 A1719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:31250635 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr18:31326556 T>C maps to NM_030632.1 *2249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:31323339 G>T maps to NM_030632.1 R1176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr18:31318480 G>A maps to NM_030632.1 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:31320243 C>A maps to NM_030632.1 S959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:31323960 C>T maps to NM_030632.1 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:31319094 C>A maps to NM_030632.1 S576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:31324911 T>A maps to NM_030632.1 S1700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr18:31325446 C>T maps to NM_030632.1 L1879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:31314299 C>A maps to NM_030632.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr18:31323141 C>T maps to NM_030632.1 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr18:31326450 C>T maps to NM_030632.1 C2213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr18:31323159 T>A maps to NM_030632.1 A1116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:31226243 G>A maps to NM_030632.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr18:31323888 G>A maps to NM_030632.1 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr18:31323012 G>A maps to NM_030632.1 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr18:31323411 G>C maps to NM_030632.1 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr18:31263406 G>T maps to NM_030632.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr18:31325235 G>A maps to NM_030632.1 K1808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr18:31324782 C>A maps to NM_030632.1 P1657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr18:31325650 C>T maps to NM_030632.1 L1947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr18:31324548 T>C maps to NM_030632.1 F1579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:31325520 G>T maps to NM_030632.1 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr18:31323858 T>C maps to NM_030632.1 N1349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:117003754 T>C maps to NM_130768.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr7:117024806 C>T maps to NM_130768.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:117021088 G>A maps to NM_130768.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:124381403 G>A maps to NM_014109.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:124368697 G>C maps to NM_014109.3 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:124383142 C>A maps to NM_014109.3 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:124333374 C>T maps to NM_014109.3 *1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:24005765 C>A maps to NM_017552.1 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:1412651 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:1412681 G>T maps to NM_031921.4 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:1412654 T>C maps to NM_031921.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:1420548 C>T maps to NM_031921.4 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:1387813 G>T maps to NM_001039211.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:1403795 G>C maps to NM_001039211.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr1:1396237 G>T maps to NM_001039211.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr17:29219789 T>G maps to NM_024857.3 L1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:3909597 C>A maps to NM_033064.4 Y254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:123596232 C>T maps to NM_001001976.1 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:123670658 G>A maps to NM_001001976.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:123658376 G>C maps to NM_007041.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:175986269 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:175979487 G>A maps to NM_001880.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:175983097 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:175979527 G>A maps to NM_001880.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:175979563 T>A maps to NM_001880.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:175939546 A>G maps to NM_001880.2 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:50435871 A>C maps to NM_001193646.1 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161751776 C>T maps to NM_007348.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:161816262 A>G maps to NM_007348.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:161816293 A>C maps to NM_007348.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:32089084 G>T maps to NM_004381.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:32086643 C>T did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr6:32089111 C>T maps to NM_004381.4 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53994751 G>A maps to NM_001130059.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:14613955 G>T maps to NM_018179.3 G896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:14578063 T>C maps to NM_018179.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:14649277 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:14578094 G>T maps to NM_018179.3 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:14578049 G>T maps to NM_018179.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:14589179 C>T maps to NM_018179.3 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr12:14610229 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:14577287 G>T maps to NM_018179.3 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:14619497 A>T maps to NM_018179.3 K946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:14577229 T>C maps to NM_018179.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:14577230 G>T maps to NM_018179.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:14599920 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:10574811 T>C maps to NM_024997.2 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:81474312 G>C maps to NM_031482.4 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:234200894 C>T maps to ENST00000392018 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:64677291 C>A maps to ENST00000421419 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:64678616 C>A maps to ENST00000421419 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:64662452 G>A maps to ENST00000421419 Q1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:96807882 C>T maps to NM_018036.5 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:96794826 G>A maps to NM_018036.5 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:96761864 T>A maps to NM_018036.5 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:96784089 G>C maps to NM_018036.5 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:96775858 G>A maps to NM_018036.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:96811722 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:96807961 A>C maps to NM_018036.5 L274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:96809569 C>A maps to NM_018036.5 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:96788933 T>C maps to NM_018036.5 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:96794779 C>A maps to NM_018036.5 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:107381397 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:107377576 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr23:107381180 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:107381361 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:107369380 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:242607953 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:242610157 T>C maps to ENST00000337606 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:242590431 G>T maps to ENST00000337606 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:242594716 A>T maps to ENST00000337606 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10659646 C>T maps to NM_032885.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:10655477 G>T maps to NM_032885.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr6:106727554 G>A maps to NM_004849.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11382131 A>G maps to NM_006395.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:11389428 G>T maps to NM_006395.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:220090254 G>A maps to NM_024085.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:220087498 C>T maps to NM_024085.3 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:220087102 G>A maps to NM_024085.3 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:150718343 G>A maps to NM_173681.5 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:150715822 G>A maps to NM_173681.5 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:292926 C>T maps to ENST00000409479 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:293449 A>G maps to ENST00000409479 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:294190 G>T maps to ENST00000409479 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:216213879 G>T maps to NM_004044.6 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:51087336 A>T maps to ENST00000358385 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:51081229 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr11:63398538 A>G maps to NM_015459.3 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:108153532 C>T maps to NM_000051.3 Q1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:108183153 G>T maps to NM_000051.3 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr11:108236106 G>T maps to NM_000051.3 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:108218051 G>A maps to NM_000051.3 L2877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr11:108163368 C>A maps to NM_000051.3 S1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:108123622 C>T maps to NM_000051.3 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr11:108117854 G>C did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr11:108128264 G>T maps to NM_000051.3 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:108153445 A>T maps to NM_000051.3 K1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:108183143 T>A maps to NM_000051.3 L1975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:108115593 C>T maps to NM_000051.3 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:108143447 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:108160400 A>T maps to NM_000051.3 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:108121471 T>A maps to NM_000051.3 L427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:7050064 C>G maps to NM_001940.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:7043173 C>T maps to NM_001940.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:7045533 G>C maps to NM_001940.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:7045211 C>G maps to NM_001940.3 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:94750175 G>A maps to NM_005172.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:94750796 C>A maps to NM_005172.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr4:94750523 C>A maps to NM_005172.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:85981389 C>G maps to NM_032827.6 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr2:85981353 C>T maps to NM_032827.6 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:25958905 G>A maps to NM_024490.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:25925105 G>T maps to NM_024490.3 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:25924949 G>A maps to NM_024490.3 T1346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:25940068 G>A maps to NM_024490.3 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr15:25924556 T>C maps to NM_024490.3 S1477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr15:25940214 T>A maps to NM_024490.3 K947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr15:25953234 T>C maps to NM_024490.3 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160029652 C>A maps to NM_025153.2 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:160059374 C>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr5:159992642 C>T maps to NM_025153.2 Q1401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr5:160114889 C>T maps to NM_025153.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:160061466 G>T maps to NM_025153.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr5:159996663 G>A maps to NM_025153.2 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:160061535 A>T maps to NM_025153.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:159992722 G>A maps to NM_025153.2 Q1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr5:160033877 C>T maps to NM_025153.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:160049493 G>T maps to NM_025153.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:160061522 C>A maps to NM_025153.2 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:160047576 G>C maps to NM_025153.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr5:160044966 A>G maps to NM_025153.2 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:159992576 G>T maps to NM_025153.2 S1423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr5:160034072 G>C maps to NM_025153.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:160049535 C>A maps to NM_025153.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:47570993 T>A maps to NM_020453.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:47559750 G>A maps to NM_020453.3 W632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:47571098 G>C maps to NM_020453.3 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:47560210 C>T maps to NM_020453.3 H785H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr4:47560964 G>A maps to NM_020453.3 Q820Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473715 C>T maps to NM_032189.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:113473722 T>G did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:113439474 C>T maps to NM_032189.3 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:113536254 A>T maps to NM_032189.3 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr13:113514623 G>A maps to NM_032189.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr13:113481157 G>T maps to NM_032189.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:113490563 A>T maps to NM_032189.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:113530212 C>T maps to NM_032189.3 V1095V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:182605387 C>T maps to NM_014616.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:182635878 C>G maps to NM_014616.1 S1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182602613 C>G maps to NM_014616.1 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:182584168 A>T maps to NM_014616.1 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182616475 C>A maps to NM_014616.1 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:182590197 G>T maps to NM_014616.1 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:182591803 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:182597427 G>A maps to NM_014616.1 Q799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:138908906 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:138857045 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:138864751 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:138844232 T>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:138845532 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:138880884 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:138850586 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:138878614 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:138857034 T>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:138880429 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:138856884 A>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:138827965 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:138884471 A>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:138880903 T>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:138886709 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:138832248 C>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:138820081 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:138844208 T>A did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:138871609 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:138870480 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:138878529 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:138870420 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:138870463 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:138886698 T>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:25284698 G>C maps to NM_001185085.1 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:25265297 G>T maps to NM_001185085.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:25264845 A>C maps to NM_001185085.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:25283929 C>A maps to NM_001185085.1 Y915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr13:25281306 C>T maps to NM_001185085.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr13:25266577 G>A maps to NM_001185085.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr13:25262551 C>G maps to NM_001185085.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:25268627 C>A maps to NM_001185085.1 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr13:25264598 C>T maps to NM_001185085.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:25280510 G>T maps to NM_001185085.1 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr13:25264486 C>A maps to NM_001185085.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr13:25267034 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr13:25264848 G>T maps to NM_001185085.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19770476 G>A maps to NM_020410.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:19760427 G>A maps to NM_020410.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:19766433 C>A maps to NM_020410.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:19766206 G>A maps to NM_020410.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr19:19766875 G>A maps to NM_020410.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:17323578 C>A maps to NM_022089.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:194175079 T>A maps to NM_024524.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:194126746 G>T maps to NM_024524.3 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr3:194165452 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:193132539 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:193220353 G>T maps to NM_032279.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:193201779 G>A maps to NM_032279.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:193130048 C>T maps to NM_032279.2 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr3:193132462 G>C maps to NM_032279.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:193201779 G>C maps to NM_032279.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:193201743 G>A maps to NM_032279.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:193210949 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:193032854 C>A maps to NM_198505.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:193039468 C>G did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr3:193082036 C>G maps to NM_198505.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr3:193036808 C>A maps to NM_198505.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:116941612 C>T maps to NM_000701.7 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:116941624 G>A maps to NM_000701.7 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:116940557 C>G maps to NM_000701.7 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:160106719 C>T maps to NM_000702.3 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:160105633 C>T maps to NM_000702.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:160111105 C>A maps to NM_000702.3 Y1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:160098506 G>A maps to NM_000702.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:160106047 C>T maps to NM_000702.3 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:160098611 T>C maps to NM_000702.3 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160098581 C>A maps to NM_000702.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:160093740 G>C maps to NM_000702.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:160105659 C>A maps to NM_000702.3 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42489544 C>A maps to ENST00000441343 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:42480645 C>T maps to ENST00000441343 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42479786 C>A maps to ENST00000441343 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:42489243 G>T maps to ENST00000441343 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:42490069 C>T maps to ENST00000441343 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:42472956 C>T maps to ENST00000441343 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:42492225 C>T maps to ENST00000441343 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:160124870 C>A maps to NM_144699.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:160141393 G>C maps to NM_144699.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7030-01A-11D-1945-08 chr1:160147370 A>C maps to NM_144699.3 R885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:160147399 C>G maps to NM_144699.3 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:169100601 C>T maps to NM_001677.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr17:7558888 C>T maps to NM_001678.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:141622498 C>T maps to NM_001679.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:141632608 C>T maps to NM_001679.2 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:119509422 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:119500388 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:119513325 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:119509379 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:119512559 A>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:119505000 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:119510247 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:119504690 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:119513441 G>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:119505046 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:119512553 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:119496039 G>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:119500505 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:119513368 C>T did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr23:119505006 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:119500468 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:28914368 C>A maps to NM_173201.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:28912102 C>A maps to NM_173201.3 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr16:28913341 C>T maps to NM_173201.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:28909567 C>G maps to NM_173201.3 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:28898773 T>A maps to NM_173201.3 L220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:28906165 C>A maps to NM_173201.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:28909349 C>T maps to NM_173201.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:28913327 G>T maps to NM_173201.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:110777087 C>T maps to NM_170665.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:110783142 G>T maps to NM_170665.3 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:110765638 A>G maps to NM_170665.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z019-01A-01W-0746-08 chr17:3853825 G>A maps to NM_174953.1 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:3839651 C>A maps to NM_174953.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr17:3845944 G>A maps to NM_174953.1 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:3851059 C>G maps to NM_174953.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:89996905 T>A maps to ENST00000428670 K992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:90017983 C>A maps to ENST00000428670 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:10417182 C>A maps to NM_001001331.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:10392233 G>T maps to NM_001001331.2 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:10443871 G>T maps to NM_001001331.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:10444021 C>G maps to NM_001001331.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr3:10401702 G>T maps to NM_001001331.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:10380003 G>T maps to NM_001001331.2 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:10417305 C>A maps to NM_001001331.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr3:10392084 C>T maps to NM_001001331.2 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr3:10401723 C>T maps to NM_001001331.2 K581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:10413498 C>T maps to NM_001001331.2 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:152825204 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:152806952 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:152826287 C>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:152813360 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152825353 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:152806887 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:152825186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:152826266 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:152807849 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:152818573 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:152814196 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:152814179 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:152815040 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:152815041 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:152814988 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:152825272 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:152818718 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:152807813 A>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:152818634 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:152827614 G>T did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:152845594 G>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:152821830 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:152821566 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:152815030 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:152826335 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:152814968 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:152806835 T>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:152818491 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:152806851 A>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:152845649 T>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:152815536 T>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:152818578 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:152826252 G>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:152807166 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:152806814 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:152815551 A>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:203652428 C>A maps to NM_001001396.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:203652494 C>G maps to NM_001001396.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr1:203668678 C>T maps to NM_001001396.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:203682342 G>A maps to NM_001001396.1 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:203680133 G>T maps to NM_001001396.1 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:130714885 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr16:84402262 C>G maps to ENST00000416219 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:36050769 G>A maps to NM_000704.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:36045889 G>T maps to NM_000704.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:36050048 G>A maps to NM_000704.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:36050742 C>A maps to NM_000704.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36054336 C>A maps to NM_000704.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:36051325 G>T maps to NM_000704.2 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:36046179 C>T maps to NM_000704.2 K738K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:36053477 T>C maps to NM_000704.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:36047952 C>A maps to NM_000704.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36053417 G>T maps to NM_000704.2 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:36046362 G>A maps to NM_000704.2 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:36053345 G>T maps to NM_000704.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:36050967 C>T maps to NM_000704.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:36054405 C>T maps to NM_000704.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:114309243 C>T maps to NM_000705.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr18:43666457 G>T maps to NM_001001937.1 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:43664301 T>C maps to NM_001001937.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:57039069 C>A maps to NM_001686.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:57036522 G>A maps to NM_001686.3 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr12:57033787 G>A maps to NM_001686.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr20:57605378 C>T maps to NM_006886.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr20:57605428 C>A maps to NM_006886.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:111996839 C>T maps to NM_001688.4 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr12:54062981 A>C maps to NM_005176.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176043978 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:99063732 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:118279713 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:41939525 C>A maps to ENST00000417807 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:153664137 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153664220 T>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr23:153662570 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:153663817 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:153662610 C>G did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:153662713 G>T did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:153664065 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:153660667 A>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:81608633 G>T maps to NM_001017971.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:81614055 G>A maps to NM_001017971.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:81613923 G>T maps to NM_001017971.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:40464915 T>G did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:40458861 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:40456777 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:40652821 A>T maps to NM_001130020.1 K600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:124236930 A>G maps to NM_012463.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:124209238 C>T maps to NM_012463.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr12:124229214 C>G maps to NM_012463.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:124206995 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr12:124235709 C>T maps to NM_012463.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:138447659 G>T maps to NM_130840.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:138455935 C>G maps to NM_130840.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:138432217 C>T maps to NM_130840.2 W424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:138440502 G>T maps to NM_130840.2 C249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:138391431 C>T maps to NM_130840.2 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:44441770 G>A maps to NM_004047.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:87155155 A>G maps to NM_152565.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:87153746 A>T maps to NM_152565.1 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:87126053 G>T maps to NM_152565.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:87162417 C>G maps to NM_152565.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr5:172447276 C>G maps to NM_003945.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr3:113505203 C>T maps to NM_001690.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:113524372 G>T did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr3:113517287 G>T maps to NM_001690.3 G497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:20068140 C>T maps to NM_001693.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:104065050 G>T did not map to a codon.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr2:10914973 T>A maps to NM_001039362.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:10917754 G>A maps to NM_001039362.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:10911979 C>A maps to NM_001039362.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:10917754 G>A maps to NM_001039362.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr22:18082861 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr22:18096047 C>G maps to NM_001696.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:46739531 C>A maps to NM_080653.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:128505562 A>T maps to ENST00000492758 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr9:117359866 C>T maps to NM_004888.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:198509759 C>A maps to ENST00000489986 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:198492574 G>A maps to ENST00000489986 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:54714429 G>A maps to NM_015941.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:54714393 G>C maps to NM_015941.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:54714366 C>T maps to NM_015941.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:77301003 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:77245189 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:77296121 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:77254173 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:77289240 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:77286940 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:77266705 G>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:77264752 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:77298833 T>G did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:77244096 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:77245343 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:77301867 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:77301057 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:77287026 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:77243904 G>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:77302015 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:77284777 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:77243851 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:77275806 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:77245129 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:77284871 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:77284868 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr23:77298208 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:77275805 G>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:77267088 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:77270247 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:77275740 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:77268488 G>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:77244076 G>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:77267027 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:77298189 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:77286967 T>C did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:77245204 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:77245368 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:77244928 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:77296211 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:77264617 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:52548698 C>G maps to NM_000053.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr13:52513222 C>A maps to NM_000053.2 G1221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr13:52542717 C>T maps to NM_000053.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr13:52549172 T>A maps to NM_000053.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr13:52548951 G>C maps to NM_000053.2 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr13:52513210 C>T maps to NM_000053.2 K1225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52515215 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:52548749 A>G maps to NM_000053.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:52511719 C>A maps to NM_000053.2 V1265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:42583649 G>T maps to NM_006095.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:42590275 C>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:42576724 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr4:42509120 T>C maps to NM_006095.2 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:42509099 C>T maps to NM_006095.2 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:26148944 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr13:26411404 C>G maps to NM_016529.4 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:26343229 C>A maps to NM_016529.4 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr13:26043142 G>A maps to NM_016529.4 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:26138169 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr13:26273387 C>T maps to NM_016529.4 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:26043256 C>A maps to NM_016529.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr13:26535747 G>A maps to NM_016529.4 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr13:26127950 G>T maps to NM_016529.4 G360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr13:26153000 G>T maps to NM_016529.4 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr13:26343363 A>G maps to NM_016529.4 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:26273432 G>A maps to NM_016529.4 R778R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:55338752 C>A maps to NM_005603.4 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr18:55359070 G>A maps to NM_005603.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr18:55359139 G>A maps to NM_005603.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr18:55355660 G>A maps to NM_005603.4 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr18:55319832 G>A maps to NM_005603.4 F1048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:154318005 T>A maps to NM_020452.3 C926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154319196 G>T maps to NM_020452.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:1800442 G>A maps to NM_138813.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:1796076 C>T maps to NM_138813.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr19:1785673 C>A maps to NM_138813.2 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:50303040 C>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr15:50211113 G>A maps to NM_024837.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr15:50336853 G>A maps to NM_024837.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:50264908 A>T maps to NM_024837.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50154563 G>T maps to NM_024837.2 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:50158549 T>A maps to NM_024837.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr15:50168534 A>T maps to NM_024837.2 A989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr15:50168527 G>A maps to NM_024837.2 Q992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:50226372 C>A maps to NM_024837.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:50271824 G>A maps to NM_024837.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:50168681 G>T maps to NM_024837.2 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:50271904 C>A maps to NM_024837.2 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:50154486 T>C maps to NM_024837.2 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr15:50152669 G>A maps to NM_024837.2 I1100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr15:50168721 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:50215578 G>T maps to NM_024837.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:50171571 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr15:50303080 C>A maps to NM_024837.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:50224124 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:50235516 C>G maps to NM_006045.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:50346456 C>A maps to NM_006045.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:50310549 G>A maps to NM_006045.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:50305645 C>G maps to NM_006045.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:50244177 T>C maps to NM_006045.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr20:50329577 C>A maps to NM_006045.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr20:50234085 T>A maps to NM_006045.1 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr20:50241783 G>A maps to NM_006045.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:77133994 G>T maps to NM_198531.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:77067080 A>T maps to NM_198531.3 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr18:77107810 G>C maps to NM_198531.3 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:47124382 C>T maps to NM_022745.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:17931575 C>T maps to NM_145691.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:17921931 G>A maps to NM_145691.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:142253920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:142176507 A>C maps to NM_001184.3 L2531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:142178076 A>G maps to NM_001184.3 P2447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr3:142281216 T>A maps to NM_001184.3 K343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:142238584 G>A maps to NM_001184.3 N1436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:142272701 C>A maps to NM_001184.3 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:142272146 T>C maps to NM_001184.3 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:142281469 A>C maps to NM_001184.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:142188993 G>A maps to NM_001184.3 Q2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr3:48488254 G>A maps to NM_130384.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:3542926 G>A maps to NM_139321.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3527984 T>C maps to NM_139321.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr20:3571953 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:117185777 C>T maps to NM_207303.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:117040881 C>A maps to NM_207303.2 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:116919960 T>C maps to NM_207303.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:117309037 C>A maps to NM_207303.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr10:116889226 C>T maps to NM_207303.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:117026330 C>A maps to NM_207303.2 Y610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:117045738 A>G maps to NM_207303.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:117001357 A>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:117061392 C>T maps to NM_207303.2 C886C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:117059644 C>G maps to NM_207303.2 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr10:117026468 C>T maps to NM_207303.2 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:117607385 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:117075070 A>G maps to NM_207303.2 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:116919972 A>C maps to NM_207303.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:117024742 A>G maps to NM_207303.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:117185798 A>G maps to NM_207303.2 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr10:117607395 C>T maps to NM_207303.2 P1304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:117061365 T>A maps to NM_207303.2 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:117228683 G>T maps to NM_207303.2 G1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr10:117059671 A>G maps to NM_207303.2 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:76875946 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:76938363 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:76889170 C>A did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:76854956 G>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:76920134 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:76855269 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:76763964 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:76889200 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:76953070 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:76875877 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:76938717 G>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:76855001 C>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:76920160 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:76953082 G>A did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr23:76939964 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:76937080 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr23:76875915 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:76854924 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:76920184 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:76939994 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:76937731 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:76845316 G>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:76937394 T>C did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:76938253 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:76939374 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:76938068 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:76939597 T>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:76854905 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:76939419 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:76938076 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:76938717 G>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr23:76872167 A>G did not map to a codon.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr23:76939450 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:76845334 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:76920177 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:76920219 G>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:76891475 T>C did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr23:76778854 G>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:76938619 T>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:76907656 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:76855943 G>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:76890169 C>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr23:76874342 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:76890156 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:76907719 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr23:76776887 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:76939493 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:76938802 C>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:76972665 T>A did not map to a codon.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr23:76907620 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:76890136 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:76777776 C>A did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr6:16327155 G>A maps to NM_000332.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr6:16306817 G>A maps to NM_000332.3 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:16327488 C>A maps to NM_000332.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:16327968 C>G maps to NM_000332.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:111923111 C>T maps to NM_002973.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:111956119 T>G maps to NM_002973.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr12:111923132 A>C maps to NM_002973.3 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:111954042 C>A maps to NM_002973.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:111956182 G>A maps to NM_002973.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr16:28844382 C>T maps to NM_148414.1 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:28846895 G>A maps to NM_148414.1 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr16:28848096 G>A maps to NM_145714.1 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:28845863 A>T maps to NM_148414.1 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:13337045 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr23:13337401 C>G did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:13337343 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:13337397 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:13337380 C>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:13337383 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:13337039 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:13337404 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:13337275 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:13337593 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:13337311 G>C did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:63981399 G>A maps to NM_001177387.1 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:63965831 C>T maps to NM_001177387.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:110033960 A>G maps to NM_153340.4 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:110030426 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr9:94060302 A>G maps to NM_001698.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:74755111 G>A maps to ENST00000258081 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:1309388 T>C maps to NM_001127230.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:1309273 G>A maps to NM_001127230.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:8108671 G>A maps to NM_004217.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57743930 G>T maps to NM_001015878.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr19:57746649 G>T maps to NM_001015878.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:57743542 G>T maps to NM_001015878.1 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:57746677 A>T maps to NM_001015878.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:57744833 G>T maps to NM_001015878.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:57746746 C>T maps to NM_001015878.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:70231184 C>G maps to NM_015570.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:70231274 C>T maps to NM_015570.2 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:69599542 G>T maps to NM_015570.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:69364337 C>T maps to NM_015570.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:69364330 G>A maps to NM_015570.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr7:70228033 C>T maps to NM_015570.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:69064860 G>A maps to NM_015570.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:58191673 C>G maps to NM_006576.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:32598880 G>A maps to NM_015060.1 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:32598190 A>T maps to NM_015060.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:63544124 C>T maps to NM_000706.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:63543938 C>A maps to NM_000706.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63543872 G>A maps to NM_000706.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:63544088 C>A maps to NM_000706.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:206225036 C>T maps to NM_000707.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:206225297 C>T maps to NM_000707.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153171776 A>G did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:153172003 T>A did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:153171220 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153171743 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:153171597 T>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:153171638 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:153171804 T>G did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:153172068 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:69455987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:69460071 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:69455967 C>A did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:69455987 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:69459683 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:69459749 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:69264266 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:69262037 G>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:69261741 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:69261762 G>T did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr23:69269713 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:338151 C>T maps to NM_003502.3 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63554270 G>T maps to NM_004655.3 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:41765521 C>A maps to NM_021913.3 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:41727830 C>T maps to NM_021913.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:41758859 G>A maps to NM_021913.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:99569381 G>C maps to NM_001185.3 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:99565996 C>A maps to NM_001185.3 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:99564901 G>T maps to NM_001185.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:99569537 G>T maps to NM_001185.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:79169706 C>G maps to ENST00000269392 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:79165039 G>T maps to ENST00000269392 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:79166564 C>T maps to ENST00000269392 E803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:103845431 G>A maps to NM_148174.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:103846975 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:103841563 C>A maps to NM_148174.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:831732 C>T maps to NM_001700.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:831858 G>A maps to NM_001700.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:45007671 C>G maps to NM_004048.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:45003798 G>T maps to NM_004048.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr15:45007681 G>A maps to NM_004048.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:45007760 G>T maps to NM_004048.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:45007817 G>T maps to NM_004048.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:160804095 T>C maps to NM_033168.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:160804473 C>A maps to NM_033168.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:160804157 A>G maps to NM_033168.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:235617569 C>T maps to ENST00000366599 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:235613562 C>G maps to ENST00000366599 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:168726188 C>A maps to NM_020981.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:168726229 C>A maps to NM_020981.3 Y227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:193150638 G>T maps to NM_003783.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:193149615 G>T maps to NM_003783.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr21:41033154 C>T maps to NM_033172.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:31898025 C>T maps to NM_194318.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr13:31821176 C>G maps to NM_194318.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:31858869 G>A maps to NM_194318.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:134252845 G>T maps to NM_054025.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr11:134251866 T>A maps to NM_054025.2 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:134257514 G>A maps to NM_054025.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr11:134253971 G>T maps to NM_054025.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:71571615 G>A maps to NM_080742.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:71665880 G>A maps to NM_080742.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:71603882 A>T maps to NM_080742.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:62384572 G>T maps to NM_012200.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:62384542 C>T maps to NM_012200.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:62389347 C>A maps to NM_012200.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66114002 G>A maps to NM_006876.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66114502 C>A maps to NM_006876.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:66113530 G>T maps to NM_006876.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:62449631 C>T maps to NM_006577.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:17919024 C>A maps to NM_014256.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:76750774 G>A maps to ENST00000354301 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:232262810 G>C maps to NM_145236.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:232263210 G>T maps to NM_145236.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:41932626 G>C maps to NM_198540.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:81006547 A>G maps to NM_001009905.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:58024790 A>T maps to NM_001478.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:58022665 G>A maps to NM_001478.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:47243516 C>A maps to NM_153446.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:47247030 C>A maps to NM_153446.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:47236503 C>A maps to NM_153446.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:47247053 C>T maps to NM_153446.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr17:47241447 A>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:47237989 C>T maps to NM_153446.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr17:47241555 C>A maps to NM_153446.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr17:47219395 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:47236475 G>A maps to NM_153446.2 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:657407 C>T maps to NM_173593.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:654046 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:657268 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:379987 G>T maps to NM_178537.4 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr11:381702 C>T maps to NM_178537.4 R1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:379558 G>T maps to NM_178537.4 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:375892 C>A maps to NM_178537.4 C344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:379879 C>A maps to NM_178537.4 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:379893 G>A maps to NM_178537.4 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:379902 G>A maps to NM_178537.4 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:372747 G>T maps to NM_178537.4 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:376446 G>T maps to NM_178537.4 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:44450676 C>T maps to ENST00000309519 C259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:44450670 C>G maps to ENST00000309519 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:118937519 G>A maps to NM_212543.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:48252856 C>A maps to NM_004776.3 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr20:48273159 A>C maps to NM_004776.3 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr20:48330164 G>A maps to NM_004776.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:48330194 C>A maps to NM_004776.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:41860616 G>A maps to NM_030578.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:41863867 G>A maps to NM_030578.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:41860616 G>A maps to NM_030578.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:104240320 C>A maps to ENST00000297574 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:104125072 A>C maps to NM_001701.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:104125298 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:104133566 G>A maps to NM_001701.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr11:117186289 G>C maps to NM_012104.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:117163808 C>T maps to NM_012104.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:117163828 C>A maps to NM_012104.3 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:42613777 C>G maps to NM_012105.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr21:42622722 G>A maps to NM_012105.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr21:42647370 C>T maps to NM_012105.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr21:30698502 G>T maps to NM_206866.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr21:30699099 G>T maps to NM_206866.1 G319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr21:30715096 T>C maps to NM_206866.1 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:90661199 C>A maps to NM_001170794.1 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:90642500 G>A maps to NM_001170794.1 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:90642273 C>A maps to NM_001170794.1 G793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr6:90660231 G>A maps to NM_001170794.1 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:64037767 C>T maps to NM_032989.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:33264327 C>T maps to NM_004323.5 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr9:33264432 C>A maps to NM_004323.5 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:121431948 G>A maps to NM_004281.3 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr21:11097606 G>A maps to NM_182482.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:11058323 C>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr21:11049621 C>G did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr21:11049584 G>T maps to NM_182482.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:79419766 G>T maps to ENST00000436173 R1445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:79419841 G>T maps to ENST00000436173 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr17:79409907 G>A maps to ENST00000436173 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr17:79424529 G>T maps to ENST00000436173 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:40751730 G>T maps to NM_014952.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:40751680 C>T maps to NM_014952.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr15:40751538 C>T maps to NM_014952.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr15:40751632 C>T maps to NM_014952.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:143623434 G>T maps to NM_001702.2 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:143558744 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143561118 G>T maps to NM_001702.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:143570777 C>T maps to NM_001702.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr8:143559545 G>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:143607976 G>A maps to NM_001702.2 K1129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr8:143561099 G>A maps to NM_001702.2 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr8:143561105 G>A maps to NM_001702.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:143570747 G>A maps to NM_001702.2 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:143603423 G>T maps to NM_001702.2 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:32193110 G>T maps to NM_001703.2 P1556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:32203062 C>T maps to NM_001703.2 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:32203927 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:32222211 T>A maps to NM_001703.2 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:32198201 C>T maps to NM_001703.2 V1212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:32196625 A>T maps to NM_001703.2 A1385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:32206124 G>C maps to NM_001703.2 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:32203836 G>A maps to NM_001703.2 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:69348713 T>A maps to NM_001704.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:70040436 T>C maps to NM_001704.2 F1025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:69349324 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:70034898 T>C maps to NM_001704.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:70071277 A>G maps to NM_001704.2 E1371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:70071031 G>A maps to NM_001704.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:70092757 A>G maps to NM_001704.2 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70049261 C>T maps to NM_001704.2 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr6:70071184 A>G maps to NM_001704.2 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr6:69349229 C>A maps to NM_001704.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:70034870 T>A maps to NM_001704.2 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:69949084 C>A maps to NM_001704.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:70071379 A>T maps to NM_001704.2 S1405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:69944922 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:70049222 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:69640529 A>G maps to NM_001704.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:69653833 G>C maps to NM_001704.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:69666618 C>A maps to NM_001704.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr6:70070840 G>T maps to NM_001704.2 E1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:70049389 G>T maps to NM_001704.2 R1151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:69349202 G>A maps to NM_001704.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:70037782 T>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:70064177 A>G maps to NM_001704.2 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:69943232 C>A maps to NM_001704.2 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:70071352 A>T maps to NM_001704.2 A1396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr6:69684697 G>T maps to NM_001704.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:79058647 G>A maps to NM_017451.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr17:79031717 G>T maps to NM_017451.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:79073864 G>C maps to NM_017451.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:97949369 G>A maps to NM_018842.4 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:1394603 A>G maps to NM_003933.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:1394318 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:1396021 G>T maps to NM_003933.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:1391158 C>T maps to NM_003933.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:1389588 C>T maps to NM_003933.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:28971328 G>T maps to NM_012342.2 *261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr20:17705762 C>T maps to NM_001159495.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:102942738 A>G maps to NM_017935.4 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:102791746 A>T maps to NM_017935.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:102839229 C>T maps to NM_017935.4 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr4:102839312 C>T maps to NM_017935.4 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:102783750 A>C maps to NM_017935.4 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:88039713 G>T maps to NM_001173543.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:88052124 C>T maps to NM_001173543.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:52437180 G>A maps to NM_004656.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:52437151 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:52442491 G>A maps to NM_004656.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:215645721 C>T maps to NM_000465.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:215595193 C>A maps to NM_000465.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:135464767 C>A maps to NM_020064.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:135458477 C>A maps to NM_020064.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr9:135464782 G>T maps to NM_020064.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:135458234 G>A maps to NM_020064.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:91180206 G>C maps to NM_020063.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:91182494 G>A maps to NM_020063.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:91182131 G>T maps to NM_020063.1 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:91180089 G>T maps to NM_020063.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:129246010 C>T maps to NM_003658.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:129306859 C>A maps to NM_003658.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr11:129246034 C>A maps to NM_003658.4 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:17275855 G>T maps to NM_006317.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr5:17275900 G>A maps to NM_006317.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:17275960 G>T maps to NM_006317.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:31500579 G>A maps to ENST00000417556 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr6:31498559 G>C maps to ENST00000417556 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:31500658 C>A maps to ENST00000417556 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr6:31507048 G>A maps to ENST00000417556 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:31599435 G>T maps to NM_080686.2 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31592973 C>A maps to NM_080686.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:31603432 G>A maps to NM_080686.2 L1816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:31602528 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:31602684 T>G maps to NM_080686.2 P1697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:31599146 C>T maps to NM_080686.2 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr9:134351250 C>T maps to NM_013318.3 C1245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:134360131 C>T maps to NM_013318.3 I1840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:134351523 A>G maps to NM_013318.3 A1336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:134312025 C>T maps to NM_013318.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:134360137 C>T maps to NM_013318.3 L1842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:134351244 C>T maps to NM_013318.3 D1243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:134334682 G>C maps to NM_013318.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:134343085 G>A maps to NM_013318.3 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr9:134354713 G>T maps to NM_013318.3 E1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:134319584 A>C maps to NM_013318.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:171511179 A>G maps to ENST00000392078 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:171509979 C>T maps to ENST00000392078 N1125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:171482233 C>G maps to ENST00000392078 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:171504658 C>T maps to ENST00000392078 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:171510838 G>T maps to ENST00000392078 E1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:171501585 A>G maps to ENST00000392078 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:171510841 C>T maps to ENST00000392078 R1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:171544258 C>G maps to ENST00000392078 S2316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:171484873 A>T maps to ENST00000392078 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:171504669 G>T maps to ENST00000392078 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:171549010 G>A maps to ENST00000392078 L2439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:31614236 G>C maps to ENST00000404765 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:31612762 C>T maps to ENST00000404765 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:31608188 T>C maps to ENST00000404765 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:31609166 G>A maps to ENST00000404765 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:31608002 G>A maps to ENST00000404765 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:31612329 C>T maps to ENST00000404765 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:31631769 G>A maps to NM_033177.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:31657481 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:31671052 C>T maps to ENST00000375842 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:76012893 G>A maps to NM_006399.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:64756723 A>T maps to NM_138456.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:64757245 C>A maps to NM_138456.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49464212 C>G maps to NM_004324.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:49459547 G>T maps to NM_138761.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr14:35234328 C>A maps to NM_013448.2 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:72861645 C>T maps to NM_032408.3 E1264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:72903706 C>A maps to NM_032408.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:57007917 C>G maps to NM_013449.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:56992464 G>A maps to NM_013449.3 I1885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr12:57000042 C>T maps to NM_013449.3 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr12:56993822 C>G maps to NM_013449.3 R1652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:57009374 C>T maps to NM_013449.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160229597 G>A maps to NM_013450.2 Q1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:160205776 T>C maps to NM_013450.2 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:160294972 C>A maps to NM_013450.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:160295206 C>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr2:160204008 A>G maps to NM_013450.2 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:160189178 T>A maps to NM_013450.2 K1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:27148880 C>A maps to NM_003986.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:27077156 G>T maps to NM_003986.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:27141314 C>T maps to NM_003986.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:66297386 C>A maps to NM_024649.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:66282098 C>T maps to NM_024649.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:76742008 C>A maps to NM_024685.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:76739973 A>T maps to NM_024685.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:76740735 C>A maps to NM_024685.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:76740087 G>A maps to NM_024685.3 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:76740021 C>G maps to NM_024685.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:76740228 T>C maps to NM_024685.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:123663170 G>T maps to NM_152618.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr16:56544821 G>A maps to NM_031885.3 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:56536583 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr16:56545112 A>G maps to NM_031885.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr16:56545070 C>G maps to NM_031885.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:56553687 C>A maps to NM_031885.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:170359634 C>T maps to ENST00000419050 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:122774155 C>T maps to NM_176824.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:122768610 C>A maps to NM_176824.1 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:33397599 C>A maps to NM_198428.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:33545227 C>T maps to NM_198428.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:33644805 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:33217114 G>T maps to NM_198428.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:33545220 G>A maps to NM_198428.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:33185911 T>C maps to NM_198428.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:33217090 A>C maps to NM_198428.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:33313544 A>T maps to NM_198428.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:33545097 G>A maps to NM_198428.2 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:33427653 A>C maps to NM_198428.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:107491620 G>A maps to NM_001142568.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:107447682 C>A maps to NM_001142568.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:107493683 A>G maps to NM_001142568.1 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:107524267 G>T maps to NM_001142568.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:45317415 G>T maps to NM_005581.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156622223 T>A maps to NM_021948.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:156622658 T>C maps to NM_021948.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:156617895 C>T maps to NM_021948.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:156616746 G>T maps to NM_021948.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:156617351 T>G maps to NM_021948.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156618447 C>G maps to NM_021948.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:156621455 A>T maps to NM_021948.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156628464 C>A maps to NM_021948.3 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:156628465 C>A maps to NM_021948.3 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:156617789 C>A maps to NM_021948.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr1:156627539 C>G maps to NM_021948.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:156616665 C>A maps to NM_021948.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:156626862 A>C maps to NM_021948.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:156617403 C>T maps to NM_021948.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:152981070 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:152968479 C>A did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:152967485 C>G did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:152968500 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:152981133 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr16:75276841 G>T maps to NM_001170714.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr16:75263717 G>A maps to NM_001170714.1 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:75269173 A>T maps to NM_001170714.1 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr16:75263546 G>A maps to NM_001170714.1 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:94140198 C>T maps to NM_003567.2 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:52645230 C>A maps to NM_003657.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:52583537 G>A maps to NM_003657.2 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:52645452 C>A maps to NM_003657.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:52602017 G>T maps to NM_003657.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:59445832 G>T maps to ENST00000407086 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr17:59024578 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:58786658 T>C maps to ENST00000407086 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:59161842 C>T maps to ENST00000407086 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:59118182 G>T maps to ENST00000407086 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:58786578 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:59067345 C>T maps to ENST00000407086 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:58946044 G>T did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr17:58885362 A>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:49458379 C>T maps to NM_198799.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:24989519 C>T maps to NM_001178093.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:24989464 G>A maps to NM_001178093.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:25047339 C>A maps to NM_001178093.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:25047340 A>G maps to NM_001178093.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:165547327 C>A maps to NM_000055.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:165548501 G>T maps to NM_000055.2 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:165548008 C>A maps to NM_000055.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:165547480 G>T maps to NM_000055.2 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:165547891 A>T maps to NM_000055.2 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:165547906 T>A maps to NM_000055.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:165548103 C>A maps to NM_000055.2 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:165547327 C>A maps to NM_000055.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:165548725 G>T maps to NM_000055.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:80878645 G>T maps to NM_183050.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:80838876 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:80982856 G>C maps to NM_183050.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:31120693 C>T maps to NM_005881.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:85733445 G>C maps to NM_003921.4 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:60687790 C>T maps to NM_022893.3 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:60688843 G>A maps to NM_022893.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:60688269 C>A maps to NM_022893.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:60688978 C>G maps to NM_022893.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:60689359 C>A maps to NM_022893.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr2:60687847 G>A maps to NM_022893.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:60689437 G>A maps to NM_022893.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:60689419 C>A maps to NM_022893.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:60773316 C>G maps to NM_022893.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:60679769 G>T maps to NM_018014.3 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:99641150 C>G maps to NM_138576.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr14:99640498 C>A maps to NM_138576.2 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:99641357 G>A maps to NM_138576.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr14:99724030 C>A maps to NM_138576.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:99642482 G>A maps to NM_138576.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:99640724 C>A maps to NM_138576.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:99641921 C>A maps to NM_138576.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr14:99723931 G>A maps to NM_138576.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:99641942 C>T maps to NM_138576.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:60985524 G>A maps to NM_000633.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:60985503 C>A maps to NM_000633.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr18:60985566 G>A maps to NM_000633.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr18:60985346 G>A maps to NM_000633.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr18:60795971 G>A maps to NM_000633.2 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr15:80263322 C>A maps to NM_004049.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:80260010 A>T maps to NM_001114735.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr20:30309574 T>C maps to NM_138578.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr20:30309466 G>A maps to NM_138578.1 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr20:30309754 C>T maps to NM_138578.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr20:30253790 G>A maps to NM_138578.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:52404575 G>T maps to NM_020396.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:111907682 C>A maps to NM_138621.3 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr22:18178954 T>A maps to NM_015367.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr14:23778059 G>T maps to NM_004050.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:187447751 C>G maps to NM_001706.4 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:187447127 G>T maps to NM_001706.4 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:6929780 G>T maps to NM_181844.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:6930309 G>A maps to NM_181844.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:6927596 G>A maps to NM_181844.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr17:6927437 A>G maps to NM_181844.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr16:30905232 C>T maps to NM_004765.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:147092303 C>A maps to NM_004326.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:147092255 G>C maps to NM_004326.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118772870 G>C maps to NM_182557.2 Y527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:118769540 G>A maps to NM_182557.2 N1361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:118770824 T>C maps to NM_182557.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:136599730 G>T maps to NM_014739.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:136599244 A>C maps to NM_014739.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:136599568 A>G maps to NM_014739.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:136597525 T>C maps to NM_014739.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr6:136596724 T>C maps to NM_014739.2 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:136599607 C>T maps to NM_014739.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:136599511 A>T maps to NM_014739.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:136599625 C>A maps to NM_014739.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:136599484 C>A maps to NM_014739.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:136594295 G>A maps to NM_014739.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:136597096 T>G maps to NM_014739.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr6:136596997 A>T maps to NM_014739.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:81320985 G>A maps to NM_017429.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:81272545 A>G maps to NM_017429.2 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:112070549 G>T maps to NM_031938.4 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:39934314 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:39932962 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:39933725 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:39931719 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:39933625 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:39933626 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:39923698 C>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:39933359 T>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:39934248 T>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:39930368 T>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:39932116 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:39932117 T>G did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:39933350 T>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:39916425 C>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:39931883 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:39932704 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:39921531 G>A did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:39923083 T>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:39931976 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:39932575 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:39933591 G>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:129148735 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:129184715 G>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:129148379 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:129149332 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:129149327 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:129150087 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:129168529 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:129147340 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:129147050 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:129148881 A>T did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:129171499 C>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:129148344 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:129150033 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:129147030 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:129148662 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:129148565 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:129148821 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:129173178 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:129149564 T>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:129171500 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:129149754 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:129189898 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:129148295 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:129149295 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:129159249 G>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:129159036 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:129149883 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:129148235 C>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:129155079 C>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:129155072 G>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:129185892 A>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:129149222 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:129159059 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:129185862 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:129149295 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:129149580 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:129146953 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:129149416 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:129150092 G>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:129147582 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:129149724 C>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:129189974 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:129190076 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:129190042 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr22:23653922 C>T maps to NM_004327.3 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr22:23653913 G>T maps to NM_004327.3 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr22:23523710 G>C maps to NM_004327.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr22:23523152 G>T maps to NM_004327.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr22:23626285 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr22:23603637 G>T maps to NM_004327.3 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219527604 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:197241141 C>T maps to NM_203315.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:96730466 C>A maps to NM_000710.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:96706898 C>A maps to NM_000623.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:96707717 C>T maps to NM_000623.3 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr14:96707444 G>A maps to NM_000623.3 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:96707666 C>A maps to NM_000623.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:27679835 G>T maps to NM_001143810.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:27679715 A>T maps to NM_001143810.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:70797397 G>T maps to NM_018429.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:70793167 C>G maps to NM_018429.2 S624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:70818144 C>G maps to NM_018429.2 S1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr5:70856055 A>G maps to NM_018429.2 S2496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:70808255 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr5:70785480 G>C maps to NM_018429.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:70858314 C>T maps to NM_018429.2 Q2571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:70805603 C>T maps to NM_018429.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:40966603 A>G maps to NM_003766.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:40962837 G>A maps to NM_003766.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr17:40975820 C>T maps to NM_003766.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:101005478 G>A maps to NM_020836.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:18194093 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:18192349 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:18192295 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:18213465 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:18234698 T>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:18234841 T>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:18209220 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:18221736 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:18234681 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:18221853 C>G did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:18194203 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:18230761 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:18192331 G>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:18198676 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:18192212 C>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:18194205 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:18230694 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:18183162 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:18183129 C>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:18189250 G>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:18189124 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:18230736 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:18195791 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:18183168 G>C did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:107390627 C>T maps to NM_001080450.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:107391908 G>A maps to NM_001080450.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:107390009 C>T maps to NM_001080450.2 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:107390933 C>G maps to NM_001080450.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr6:107390362 C>A maps to NM_001080450.2 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:42122119 T>A maps to NM_207406.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:42145823 G>T maps to NM_207406.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:56857322 C>T maps to NM_152731.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:56857307 C>A maps to NM_152731.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:56880066 C>T maps to NM_152731.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr10:13541910 G>A maps to ENST00000396900 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:61725727 C>A maps to NM_001139443.1 V215V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5930-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61730374 C>G maps to NM_001139443.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:70070770 G>A maps to NM_032735.2 Y264Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-6982-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:70065290 G>A maps to NM_032735.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:70072551 G>A maps to NM_032735.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr12:70087508 C>T maps to NM_032735.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:70049364 G>A maps to NM_032735.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:70049061 G>A maps to NM_032735.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:70049229 G>C maps to NM_032735.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:102317842 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:102564633 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:102564881 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:102564740 C>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:102564743 C>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr16:14738322 C>T maps to NM_016561.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr16:14738323 C>T maps to NM_016561.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr20:17475129 C>T maps to NM_001195.3 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:133191317 C>T maps to NM_003571.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:133166198 G>C maps to NM_003571.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr3:133119188 C>T maps to NM_003571.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:133118938 G>A maps to NM_003571.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:152770112 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:152770113 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152770097 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152770099 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152770101 T>G did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:152773721 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:152772060 C>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:152773767 C>G did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:152773761 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:152772617 G>C did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr7:97841992 C>T maps to NM_177455.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:102004638 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:102004414 G>C did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:102005351 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:102004717 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:102004608 C>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:102005195 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:102005196 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:102005251 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:102004752 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:102004017 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:102003950 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:102005159 A>G did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:102005458 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:102005456 A>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:65494150 G>A maps to NM_152414.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:5025130 A>T maps to NM_003670.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr12:26276041 G>A maps to NM_030762.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:78426858 G>T maps to NM_001713.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:78421956 C>G maps to NM_001713.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:78416282 G>A maps to NM_001713.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr5:78376510 G>A maps to NM_017614.4 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:60588569 C>T maps to NM_001080512.1 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:60566791 G>A maps to NM_001080512.1 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:60577397 T>C maps to NM_001080512.1 N870N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:60548182 G>T maps to NM_001080512.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr10:60588534 C>T maps to NM_001080512.1 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:60559982 C>T maps to NM_001080512.1 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:60549173 T>A maps to NM_001080512.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr10:60546723 A>G maps to NM_001080512.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:32491767 G>T maps to NM_001714.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:32458938 G>C maps to NM_001714.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:32459004 C>T maps to NM_001714.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:32446999 C>A maps to NM_001714.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:32491885 G>T maps to NM_001714.2 E913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:95481864 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:127821173 C>T maps to NM_139343.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr2:127818194 C>T maps to NM_139346.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:127826586 C>A maps to NM_139343.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:127819725 G>A maps to NM_139343.1 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51693011 C>A maps to NM_016293.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:51693468 G>T maps to NM_016293.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:51717813 G>A maps to NM_016293.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:22481544 C>A maps to NM_018688.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:102239279 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:102221328 A>G maps to NM_001166.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:102201845 C>T maps to NM_182962.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:32740257 A>T maps to NM_016252.3 S3590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:32730165 C>T maps to NM_016252.3 S3198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:32735026 G>C maps to NM_016252.3 L3401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:32740149 A>G maps to NM_016252.3 P3554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr2:32664725 C>A maps to NM_016252.3 S1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:32774405 C>T maps to NM_016252.3 V4334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:32727860 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:32774453 G>T maps to NM_016252.3 G4350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:32673861 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:32678888 C>T maps to NM_016252.3 V1544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:32673982 A>C maps to NM_016252.3 S1535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:61869765 G>T maps to NM_139317.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:61870559 C>G maps to NM_139317.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr20:61870752 T>C maps to NM_139317.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr20:61870848 C>G maps to NM_139317.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr20:61870740 G>T maps to NM_139317.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:53793090 C>A maps to NM_033341.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:53793227 C>A maps to NM_033341.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:103492109 C>T maps to NM_017693.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr13:103460021 C>T maps to NM_017693.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:103468880 G>C maps to NM_017693.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr13:103459967 G>T maps to NM_017693.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr13:103473385 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr20:36147456 C>T maps to NM_006698.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:11412860 C>T maps to ENST00000427279 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:11405587 C>A maps to ENST00000427279 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:11406562 C>A maps to ENST00000427279 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:11414293 C>T maps to ENST00000427279 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:11406631 G>A did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr15:91341490 A>G maps to NM_000057.2 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:28616429 T>C maps to NM_000386.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:28576108 C>A maps to NM_000386.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:28612479 G>A maps to NM_000386.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:97960806 T>A maps to NM_013314.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:45683048 G>T maps to NM_212550.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:45682623 G>T maps to NM_212550.3 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr7:43846815 T>C maps to NM_000712.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:169346052 C>T maps to NM_003666.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:169338765 T>C maps to NM_003666.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr1:169349787 T>C maps to NM_003666.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:169347740 A>T maps to NM_003666.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:169345898 A>T maps to NM_003666.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr15:40396524 C>T maps to NM_001003940.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:22617984 C>T maps to NM_005180.6 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:22035416 G>T maps to NM_006129.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:22033771 G>T maps to NM_006129.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:22034500 C>T maps to NM_006129.4 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:69093485 C>A maps to NM_014482.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:69098253 C>A maps to NM_014482.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:69092864 G>T maps to NM_014482.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:69093071 G>A maps to NM_014482.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr2:69093005 C>T maps to NM_014482.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr23:50659037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:50658983 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:50659412 C>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:50659496 T>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:50658939 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:50654093 T>C did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:50654044 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:50659412 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:50659163 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:6759009 A>G maps to NM_001200.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr20:6750997 G>C maps to NM_001200.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:79832344 C>T maps to NM_198892.1 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr4:79832925 T>C maps to NM_198892.1 H1075H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:79832721 T>A maps to NM_198892.1 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:79792102 G>A maps to NM_198892.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:79831812 C>G maps to NM_198892.1 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:79833081 C>A maps to NM_198892.1 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr4:79832089 G>T maps to NM_198892.1 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:79831903 A>T maps to NM_198892.1 K735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr4:79831883 C>G maps to NM_198892.1 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:81967523 G>T maps to NM_001201.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr4:81952497 G>T maps to NM_001201.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:81967360 C>T maps to NM_001201.2 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55659146 C>A maps to NM_021073.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55739648 T>C maps to NM_021073.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:55739582 T>A maps to NM_021073.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:55638876 G>A maps to NM_021073.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:7862663 G>T maps to NM_001718.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:7862667 C>A maps to NM_001718.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:55758868 G>T maps to NM_001719.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:55758883 C>T maps to NM_001719.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:55758936 G>T maps to NM_001719.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:55758945 G>A maps to NM_001719.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:55803292 G>A maps to NM_001719.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr20:55758793 C>A maps to NM_001719.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr20:55758924 G>A maps to NM_001719.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:39988105 C>G maps to NM_181809.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:34182961 G>A maps to NM_133468.3 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:34085916 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:34085925 G>A maps to NM_133468.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:34118559 G>A maps to NM_133468.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:34085916 G>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:34085917 G>T maps to NM_133468.3 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:34118586 G>A maps to NM_133468.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr7:34085928 A>T maps to NM_133468.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:34182919 C>G maps to NM_133468.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:34118541 G>T maps to NM_133468.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:34086017 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:34097699 T>C maps to NM_133468.3 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:34118553 C>A maps to NM_133468.3 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:34118541 G>T maps to NM_133468.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:88677024 C>T maps to NM_004329.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:88683406 C>T maps to NM_004329.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:88677013 G>T maps to NM_004329.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:96025610 C>A maps to ENST00000440890 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:96075790 C>A maps to ENST00000440890 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:96051153 A>T maps to ENST00000440890 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:203242241 A>G maps to NM_001204.6 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:203424546 G>T maps to NM_001204.6 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:43288496 G>T maps to NM_014753.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:43287085 G>T maps to NM_014753.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:43292651 G>T maps to NM_014753.3 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:43289421 G>A maps to NM_014753.3 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:43288462 T>G maps to NM_014753.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:43315872 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:43297665 G>T maps to NM_014753.3 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:43280018 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:15554497 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:15574208 G>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:15568066 C>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:15560165 T>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:15560197 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:15540711 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:83931884 C>G maps to NM_001717.3 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:83932934 C>T maps to NM_001717.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:83933225 T>C maps to NM_001717.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:83926397 G>T maps to NM_001717.3 P927P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr15:83933129 A>G maps to NM_001717.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:83931830 G>A maps to NM_001717.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr15:83932043 G>A maps to NM_001717.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:83935590 C>T maps to NM_001717.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:83935601 C>A maps to NM_001717.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr15:83926688 C>A maps to NM_001717.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:16552764 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:16436589 A>T maps to NM_017637.5 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:16437285 C>T maps to NM_017637.5 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:16738390 G>T maps to NM_017637.5 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:16727920 C>T maps to NM_017637.5 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr9:16436508 A>C maps to NM_017637.5 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:16552725 G>T maps to NM_017637.5 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr9:16727854 T>A maps to NM_017637.5 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr9:16437285 C>T maps to NM_017637.5 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr9:16419244 G>A maps to NM_017637.5 S1014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:172573919 A>T maps to NM_013979.2 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:172590833 G>T maps to NM_013979.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:59961503 T>A maps to NM_004330.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr15:59971851 C>A maps to NM_004330.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:112991431 G>A maps to ENST00000273395 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:112969438 C>T maps to ENST00000273395 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:112998135 C>T maps to ENST00000273395 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112987218 C>A maps to ENST00000273395 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:112998276 C>G maps to ENST00000273395 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:113002306 C>A maps to ENST00000273395 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr3:112991469 C>G maps to ENST00000273395 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:112993294 C>A maps to ENST00000273395 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:112998716 G>A maps to ENST00000273395 E690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:13605301 C>T maps to NM_148894.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:13610218 G>A maps to NM_148894.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:13606444 C>T maps to NM_148894.2 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:13603789 T>C maps to NM_148894.2 A1578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:13604518 T>A maps to NM_148894.2 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:13605955 A>G maps to NM_148894.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr4:13604662 C>T maps to NM_148894.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:13602199 G>T maps to NM_148894.2 T2108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr4:13601179 T>C maps to NM_148894.2 G2448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:13604344 C>A maps to NM_148894.2 V1393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr2:242511797 C>T maps to NM_032515.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr2:198646502 G>A maps to NM_197970.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:3129349 A>T maps to NM_004332.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr20:36935978 G>A maps to NM_001725.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr20:36952396 G>A maps to NM_001725.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:36954746 C>A maps to NM_001725.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:36932693 C>A maps to NM_001725.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:36965552 C>T maps to NM_001725.2 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31604873 G>A maps to NM_025227.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr20:31608183 G>T maps to NM_025227.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:31607498 G>T maps to NM_025227.1 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr20:31609538 C>A maps to NM_025227.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr20:31606156 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:31601729 G>T maps to NM_025227.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr22:32841967 C>A maps to NM_174932.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:32841871 G>T maps to NM_174932.2 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr22:32838715 G>T maps to NM_174932.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr22:32829707 G>T maps to NM_174932.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr22:32841928 G>A maps to NM_174932.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:31624323 C>T maps to NM_174897.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr20:31627262 C>A maps to NM_174897.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:31630679 C>A maps to NM_174897.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr20:31625516 C>A maps to NM_174897.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:220236272 C>A maps to NM_006085.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:220253149 G>T maps to NM_006085.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:65928064 G>C maps to ENST00000321892 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:65928031 C>T maps to ENST00000321892 I2178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:65908724 C>T maps to ENST00000321892 V1701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr17:65850860 G>A maps to ENST00000321892 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:65909150 G>A maps to ENST00000321892 K1843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr17:65971936 G>A maps to ENST00000321892 L2989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr17:65887990 G>T maps to ENST00000321892 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:140434504 G>A maps to NM_004333.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:140494267 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:140482953 G>C maps to NM_004333.4 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr7:140481402 C>A maps to NM_004333.4 G469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:140476710 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:112093414 G>A maps to NM_006768.3 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr17:41245543 G>A maps to ENST00000471181 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:41244213 C>A maps to ENST00000471181 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:41245944 C>A maps to ENST00000471181 G535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:41246509 G>T maps to ENST00000471181 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:41219651 C>A maps to ENST00000471181 E1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:41243907 C>A maps to ENST00000471181 E1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:41258528 G>T maps to ENST00000471181 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr17:41222992 G>A maps to ENST00000471181 V1668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:41234511 C>A maps to ENST00000471181 G1422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr17:41243707 A>G maps to ENST00000471181 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:32914848 C>T maps to NM_000059.3 N2119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr13:32906433 A>T maps to NM_000059.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:32914806 A>C maps to NM_000059.3 I2105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr13:32972776 C>G maps to NM_000059.3 S3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr13:32953975 A>T maps to NM_000059.3 K3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr13:32913246 C>T maps to NM_000059.3 I1585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr13:32937422 C>A maps to NM_000059.3 S2695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr13:32911849 G>T maps to NM_000059.3 E1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:154348414 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:154299835 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:154344445 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:154348317 C>T did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:154348403 A>G did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:154344387 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:154299834 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:50192204 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:50197938 G>A maps to ENST00000342989 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr22:50192226 C>G maps to ENST00000342989 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr22:50216779 T>G maps to ENST00000342989 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr22:50217641 G>A maps to ENST00000342989 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:32944373 C>T maps to ENST00000395289 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr9:136917481 G>A maps to NM_007371.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:136918439 G>A maps to NM_007371.3 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:15350201 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:15367951 C>A maps to NM_058243.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:15367041 G>C maps to NM_058243.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:50368764 A>T maps to NM_001173984.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:137500093 A>G maps to NM_139199.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:137480930 G>A maps to NM_139199.1 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:137501759 C>A maps to NM_139199.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:137504272 T>A maps to NM_006696.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:137481527 C>T maps to NM_139199.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:137497801 C>T maps to NM_139199.1 Q707Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr5:137503764 G>A maps to NM_139199.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:870663 G>A maps to NM_001009877.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:876251 G>A maps to NM_001009877.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:878500 C>A maps to NM_001009877.2 G361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:878489 T>C maps to NM_001009877.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:92447220 G>A maps to ENST00000347608 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:92445139 G>A maps to ENST00000347608 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:92459755 A>G maps to ENST00000347608 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28464260 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:28467645 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:37707162 C>A maps to NM_018310.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:37704487 C>A maps to NM_018310.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:59820496 T>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:59938840 T>C maps to NM_032043.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:59924470 C>T maps to NM_032043.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:59858277 G>A maps to NM_032043.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:59858313 G>A maps to NM_032043.2 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:59878763 C>T maps to NM_032043.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:59763347 G>A maps to NM_032043.2 T918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr17:59885878 G>A maps to NM_032043.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:34925007 C>A maps to NM_018321.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:66108314 C>A maps to NM_001024957.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr11:66109629 C>A maps to NM_001024957.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr14:36304126 G>T maps to NM_032352.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:9785986 G>A maps to NM_001003694.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:9781177 G>T maps to NM_001003694.1 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:9787289 C>T maps to NM_001003694.1 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:9781261 C>T maps to NM_001003694.1 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:36168791 C>T maps to NM_015695.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:36196765 G>T maps to NM_015695.2 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:36182092 G>A maps to NM_015695.2 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:36182134 G>A maps to NM_015695.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:135574142 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:135572293 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:135574130 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:135570362 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:135570276 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:135574443 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:135570597 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:135574141 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:135572418 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:55814151 G>A maps to NM_032430.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:55816253 G>A maps to NM_032430.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55805584 C>A maps to NM_032430.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:55816899 A>G maps to NM_032430.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr19:55800958 G>C maps to NM_032430.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:55816695 C>A maps to NM_032430.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:55816284 C>T maps to NM_032430.1 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:55814217 C>A maps to NM_032430.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:55798405 G>T maps to NM_032430.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr19:55815432 T>C maps to NM_032430.1 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:1466884 C>A maps to NM_003957.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:1467068 C>T maps to NM_003957.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:1463776 C>T maps to NM_003957.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1475796 C>T maps to NM_003957.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr11:1462056 C>T maps to NM_003957.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr21:40559156 G>C maps to NM_018963.3 S2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:40571249 G>A maps to NM_018963.3 Q1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:40601362 C>A did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr21:40569300 G>A maps to NM_018963.3 S1898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:79973079 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:79932141 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:79936892 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:79975017 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:80001180 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:79936969 T>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:79960238 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:79951406 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:79951408 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:79937525 C>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:79932260 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:79980528 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:80001180 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:79937521 C>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:79978261 T>A did not map to a codon.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr23:79938051 C>G did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:79978182 G>C did not map to a codon.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr23:80047409 G>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:79951431 T>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:79951432 T>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:79939644 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:79978128 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:79991525 A>T did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:79965004 T>C did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:79999688 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:79936986 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:79932534 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:79939514 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:79945591 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:79975053 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:79962958 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:79932288 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:79947449 C>G did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:79932687 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:79947424 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:79932440 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:80001217 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:79932310 T>G did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:79989633 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:79978179 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:79999659 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:79952242 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:79960190 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:79984376 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:79962988 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:79932146 T>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:62459864 C>G maps to NM_001130702.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:62472927 G>A maps to NM_001130702.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:62457841 G>A maps to NM_001130702.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:32842118 C>G maps to NM_001143888.1 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:32842196 C>T maps to NM_001143888.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr19:572651 C>T maps to NM_001728.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:49694956 C>T maps to NM_003458.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:49691857 A>T maps to NM_003458.3 A1623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:49689124 G>T maps to NM_003458.3 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:49689787 C>A maps to NM_003458.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:49692178 C>G maps to NM_003458.3 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:49694473 G>A maps to NM_003458.3 L2495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:49693066 C>T maps to NM_003458.3 G2026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:49691788 G>T maps to NM_003458.3 P1600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:49692640 G>A maps to NM_003458.3 A1884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:49694656 G>T maps to NM_003458.3 R2556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:49695121 G>A maps to NM_003458.3 G2711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:49698361 C>T maps to NM_003458.3 P3028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr3:49698497 G>T maps to NM_003458.3 G3074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:55474246 C>A maps to NM_057176.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:55472786 C>T maps to NM_057176.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr9:116130560 T>C maps to NM_017688.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:116132007 C>T maps to NM_017688.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr4:15716985 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:15724521 G>C maps to ENST00000382346 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:17516357 G>T maps to NM_004335.2 C9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:122850097 G>T maps to NM_001098169.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:93776186 A>T maps to NM_003972.2 K1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:93711233 G>T maps to NM_003972.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:93695416 A>G maps to NM_003972.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:93788544 A>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr10:93743989 G>T maps to NM_003972.2 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr10:93767939 C>A maps to NM_003972.2 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:93741961 G>T maps to NM_003972.2 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:83725257 T>G maps to NM_025238.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:83735783 C>A maps to NM_025238.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:13427329 G>C maps to NM_032320.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:108051443 C>G maps to NM_001018072.1 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:108010912 C>A maps to NM_001018072.1 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:108051372 C>T maps to NM_001018072.1 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:107713181 C>A maps to NM_001018072.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:108034178 A>G maps to NM_001018072.1 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:107914367 G>T maps to NM_001018072.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:107937904 C>A maps to NM_001018072.1 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr12:107914363 C>A maps to NM_001018072.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr12:107713769 G>A maps to NM_001018072.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:108042980 A>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr12:107937910 G>C maps to NM_001018072.1 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:108051464 C>T maps to NM_001018072.1 H1095H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:107712989 G>T maps to NM_001018072.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr12:108012087 G>T maps to NM_001018072.1 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:3632582 C>A maps to NM_032444.2 A1755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:3640109 C>A maps to NM_032444.2 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:3632492 C>T maps to NM_032444.2 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr16:3645674 G>A maps to NM_032444.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr16:3647556 T>C maps to NM_032444.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr16:3634822 C>T maps to NM_032444.2 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:3640875 C>T maps to NM_032444.2 E921E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr16:3640067 G>A maps to NM_032444.2 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:124036379 G>T maps to ENST00000368994 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:124049434 A>T maps to ENST00000368994 K134*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-97-7554-01A-11D-2036-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MN-A4N5-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-NJ-A4YI-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:11903468 C>T maps to NM_014962.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr20:11899000 C>G maps to NM_014962.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr14:105716558 G>A maps to NM_033271.2 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:93723642 C>A maps to NM_001002860.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:93761035 T>C maps to NM_001002860.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr14:93760231 C>G maps to NM_001002860.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr14:93717917 C>A maps to NM_001002860.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:92554450 C>T maps to NM_183242.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:38548124 T>C maps to NM_052893.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr6:38560591 T>A maps to NM_052893.1 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr6:38545425 T>C maps to NM_052893.1 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:38560522 T>A maps to NM_052893.1 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:75681103 G>A maps to NM_001729.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:15677045 G>T maps to NM_000060.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:15686793 G>A maps to NM_000060.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr12:92538098 A>G maps to NM_001731.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:92538059 G>A maps to NM_001731.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr11:111369486 A>G maps to NM_017589.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:100613309 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:100626676 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:100630241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:100617170 T>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr23:100609682 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:100615128 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:100617574 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:100617166 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:100613357 C>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:100615556 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:100608221 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:100615598 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:100617216 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:100611117 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:100611143 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:100617623 C>G did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:100611179 A>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:100613364 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:100615742 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:100617634 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:100630265 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:100617597 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:100617611 G>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:100608945 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:100625026 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:100612561 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr6:26509305 C>A maps to NM_001732.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:26509111 G>T maps to NM_001732.2 G431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:26509122 C>G maps to NM_001732.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:26501821 C>G maps to NM_001732.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:26508187 G>C maps to NM_001732.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr6:26509080 C>A maps to NM_001732.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26468737 C>T maps to NM_007049.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:26388251 A>T maps to NM_001197237.1 K152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:26388373 C>G maps to NM_001197237.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr6:26384102 C>G maps to NM_001197237.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr6:26405814 C>A maps to NM_007048.5 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr6:26408109 G>T maps to NM_007048.5 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:26370769 A>T maps to NM_001197246.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:26444522 A>T maps to NM_006994.4 K142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:26452056 A>C maps to NM_006994.4 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:26448953 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:26451939 C>T maps to NM_006994.4 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr6:32374894 C>T maps to ENST00000468270 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr6:32370841 G>T maps to ENST00000468270 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:32370727 C>A maps to ENST00000468270 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:32362584 G>A maps to ENST00000468270 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:32370751 G>A maps to ENST00000468270 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:32372944 G>T maps to ENST00000468270 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:180338528 C>A maps to NM_001040462.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:180338441 G>A maps to NM_001040462.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:180486690 G>C maps to NM_152547.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr5:180477369 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:180481245 C>T maps to NM_152547.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:180477289 G>A maps to NM_152547.4 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:180486750 C>T maps to NM_152547.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:103221744 C>A maps to NM_033637.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:103294513 C>T maps to NM_033637.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr10:103190199 A>T maps to NM_033637.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:111395585 A>G maps to NM_004336.3 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:111395636 C>T maps to NM_004336.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:111425234 G>C maps to NM_004336.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr2:111399325 T>A maps to NM_004336.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr2:111395736 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:116633960 G>C maps to NM_032725.3 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:116636084 A>T maps to NM_032725.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:116629058 G>A maps to NM_032725.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:105581377 T>A maps to NM_007073.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr6:105577253 C>T maps to NM_007073.4 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:41897939 G>T maps to NM_004053.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:56385037 C>A maps to NM_004758.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:56386582 T>A maps to NM_004758.2 A1350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:56386311 C>A maps to NM_004758.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr17:56400699 C>A maps to NM_004758.2 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:56386668 G>A maps to NM_004758.2 Q1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:56389622 C>T maps to NM_004758.2 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:56387345 G>A maps to NM_004758.2 I1291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:56389901 C>A maps to NM_004758.2 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:56384266 G>A maps to NM_004758.2 Y1682Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr17:56389735 C>A maps to NM_004758.2 E816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr17:56400736 C>A maps to NM_004758.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:56386680 C>A maps to NM_004758.2 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:56400037 C>A maps to NM_004758.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr17:56389367 G>A maps to NM_004758.2 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:201683038 C>T maps to ENST00000452790 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:16721014 C>A maps to NM_014038.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:16734616 C>T maps to NM_014038.2 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:16736595 G>A maps to NM_014038.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr10:77542780 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:78316965 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:78317042 C>T maps to NM_032024.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:21784771 C>A maps to NM_001010911.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr10:21784723 G>A maps to NM_001010911.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr10:21784582 G>A maps to NM_001010911.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr10:115891845 C>A maps to NM_018017.2 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:98741602 G>A maps to NM_015652.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:98741553 C>G maps to NM_015652.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:98741315 G>T maps to NM_015652.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:98743639 A>G maps to NM_015652.2 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:124457440 C>A maps to NM_001010912.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:124459150 C>G maps to NM_001010912.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:124459224 C>A maps to NM_001010912.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr10:50396339 C>A maps to ENST00000374148 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:127426973 C>T maps to ENST00000356792 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr10:127429727 C>T maps to ENST00000356792 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:127426554 A>T maps to ENST00000356792 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:127414292 A>T maps to ENST00000356792 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:127442260 A>G did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr10:127414385 A>G maps to ENST00000356792 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:127434402 G>T maps to ENST00000356792 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:127429681 T>C maps to ENST00000356792 N761N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:127436205 T>C maps to ENST00000356792 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:5788149 G>T maps to NM_017782.4 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:5782211 G>A maps to NM_017782.4 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr10:5777378 G>A maps to NM_017782.4 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr10:5799598 G>A maps to NM_017782.4 V2283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:5788305 A>G maps to NM_017782.4 Q974Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr10:102748607 C>G maps to NM_021830.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr10:102748095 G>A maps to NM_021830.4 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:45496130 G>T maps to NM_001039380.2 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:45496148 G>A maps to NM_001039380.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:104557799 A>T maps to NM_001083913.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr10:104569674 C>A maps to NM_001083913.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:72536982 G>A maps to NM_152710.2 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72541682 G>T maps to NM_152710.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr10:99968659 C>T maps to ENST00000314594 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr10:99968824 A>T maps to ENST00000314594 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:11908753 G>A maps to NM_153256.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:11911909 G>T maps to NM_153256.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50902608 G>A maps to NM_001042427.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:73515146 G>C maps to NM_022153.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:73515223 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:73511557 G>A maps to NM_022153.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:82187221 G>A maps to NM_032333.4 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:82182200 A>T maps to NM_032333.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr10:33103368 A>T maps to ENST00000375025 K364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50532447 G>T maps to NM_001135196.1 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50531555 C>A maps to NM_001135196.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:50532341 T>G maps to NM_001135196.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:103761773 C>A maps to NM_024541.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr10:103773782 T>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:105883605 C>T maps to ENST00000336358 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:105883586 C>G maps to ENST00000336358 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr10:105883632 A>G maps to ENST00000336358 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:105942138 G>A maps to ENST00000389588 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:105939595 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:105971911 C>A maps to ENST00000389588 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:105971860 A>G maps to ENST00000389588 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:115534716 C>A maps to NM_182601.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr10:115534041 A>C maps to NM_182601.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr10:115526173 A>G maps to NM_182601.1 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:115529574 C>A maps to NM_182601.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:118425118 C>A maps to ENST00000388884 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr10:118424321 G>A maps to ENST00000388884 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:128118365 G>A maps to NM_001004298.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:128147645 G>T maps to NM_001004298.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:128114598 G>A maps to NM_001004298.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:128192772 G>A maps to NM_001004298.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:128193339 C>T maps to NM_001004298.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:128192663 C>A maps to NM_001004298.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr10:134261354 G>A maps to NM_173541.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr10:134755106 C>T maps to ENST00000368586 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:118101713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:118138000 A>G maps to NM_198515.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:118101645 T>C maps to NM_198515.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr10:118137967 T>C maps to NM_198515.2 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:118084851 G>A maps to NM_198515.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:111750307 C>T maps to NM_022761.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:111754493 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:64878980 G>A maps to NM_013265.2 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr11:64875836 C>T maps to NM_013265.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:64875962 C>T maps to NM_013265.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:68029451 C>A maps to NM_022338.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr11:76257079 A>G maps to ENST00000393457 P1172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:76169295 G>T maps to ENST00000393457 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:76183702 G>A maps to ENST00000393457 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:76256989 T>C maps to ENST00000393457 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:76169286 G>A maps to ENST00000393457 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:57509595 G>A maps to NM_170746.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:557580 G>A maps to NM_173573.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:33628274 T>A maps to ENST00000389726 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:33596336 C>A maps to ENST00000389726 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:33667500 G>C maps to ENST00000389726 G1602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:33604899 G>T maps to ENST00000389726 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:33564326 T>C maps to ENST00000389726 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:33564920 C>A maps to ENST00000389726 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:33564734 C>A maps to ENST00000389726 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:33667314 C>A maps to ENST00000389726 G1540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:33565439 A>T maps to ENST00000389726 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:33682505 G>A maps to ENST00000389726 Q1744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:33572680 G>C maps to ENST00000389726 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:33572766 G>A maps to ENST00000389726 W937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:33596252 G>T maps to ENST00000389726 V1121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:33604986 C>T maps to ENST00000389726 C1211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:6231696 C>T maps to NM_173525.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:6231613 C>T maps to NM_173525.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:6231319 C>A maps to NM_173525.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:128774401 C>T maps to NM_145013.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:62430600 C>G maps to ENST00000431002 *290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62435065 G>C maps to ENST00000431002 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr11:62437221 C>A maps to ENST00000431002 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:47179381 T>A maps to NM_001003677.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:111156777 G>C maps to NM_198498.1 *237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:93488501 C>T maps to ENST00000354421 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:16760378 A>T maps to NM_014267.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:122830080 G>T maps to NM_024806.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:122817440 G>T maps to NM_024806.2 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:122756811 G>T maps to NM_024806.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:108263935 C>A maps to NM_152587.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:108277821 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:61254451 G>C maps to NM_145017.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr11:61257978 G>T maps to NM_145017.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:61249828 C>A maps to NM_145017.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:61254045 C>A maps to NM_145017.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr11:65685010 G>C maps to NM_001135635.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:65684940 C>A maps to NM_001135635.1 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101953854 T>G maps to NM_032930.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:101946660 G>T maps to NM_032930.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:36657642 G>T maps to NM_138787.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:82644075 G>T maps to NM_145018.3 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:82645328 T>G maps to NM_145018.3 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:82644263 C>T maps to NM_145018.3 C628C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr11:82643009 A>G maps to NM_145018.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62439291 C>T maps to NM_001085372.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:63586319 C>A maps to NM_138471.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:63585544 G>A maps to NM_138471.1 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr11:109294740 G>T maps to NM_207645.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:109294787 T>A maps to NM_207645.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:109294919 C>A maps to NM_207645.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:109294457 G>A maps to NM_207645.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:109294691 T>A maps to NM_207645.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:61539136 G>A maps to NM_001127392.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:61541489 G>T maps to NM_001127392.1 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:61551039 C>T maps to NM_001127392.1 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:111166915 C>A maps to ENST00000355430 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:53693950 G>A maps to NM_021640.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:27078780 G>A maps to NM_018164.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:27070631 G>T maps to NM_018164.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:27066580 G>A maps to NM_018164.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:91347826 G>A maps to NM_152638.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:91348366 C>G maps to NM_152638.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:91347477 C>A maps to NM_152638.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:91347781 C>T maps to NM_152638.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:91347990 C>A maps to NM_152638.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr12:91348429 G>C maps to NM_152638.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr12:110925705 C>T maps to NM_013300.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:82850503 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:82871107 C>T maps to NM_032230.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:110206855 G>A maps to NM_032829.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:32134159 G>T maps to NM_018169.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:32134158 A>G maps to NM_018169.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:32135454 G>A maps to NM_018169.3 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:32135901 A>G maps to NM_018169.3 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr12:32138265 G>A maps to NM_018169.3 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr12:32137351 G>T maps to NM_018169.3 G1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:32134999 A>T maps to NM_018169.3 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:32138250 G>A maps to NM_018169.3 K1454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:32134432 G>T maps to NM_018169.3 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr12:32134630 C>T maps to NM_018169.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:32138463 G>A maps to NM_018169.3 Q1525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:32137258 C>T maps to NM_018169.3 Q1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr12:32137641 A>G maps to NM_018169.3 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:13526176 C>G maps to ENST00000318426 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:13526239 C>T maps to ENST00000318426 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr12:21679860 G>T maps to NM_030572.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:4645225 T>C maps to NM_020374.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:4614498 C>A maps to NM_020374.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:40040215 G>T maps to NM_001031748.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:40077280 C>T maps to NM_001031748.2 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:40076659 G>T maps to NM_001031748.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr12:40044123 A>G maps to NM_001031748.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:49073615 C>A maps to NM_017822.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:103699928 C>A maps to NM_001099336.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:121442168 C>T maps to NM_022895.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:52470567 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:102589844 A>T maps to NM_017915.3 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:102589774 T>C maps to NM_017915.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr12:102572512 C>T maps to NM_017915.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:117175636 G>A maps to NM_024738.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:4460458 G>T maps to NM_020375.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr12:4461604 A>T maps to NM_020375.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:88379803 T>A maps to NM_152589.1 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:88381708 T>A maps to NM_152589.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:88391904 G>A maps to NM_152589.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:112622800 G>T maps to NM_001109662.2 S3151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:112607316 G>C maps to NM_001109662.2 V3894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:112605159 C>A maps to NM_001109662.2 A3993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:112622470 G>A maps to NM_001109662.2 Y3261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:112717029 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:112600870 C>T maps to NM_001109662.2 K4193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:112717041 T>C maps to NM_001109662.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:112711488 C>A maps to NM_001109662.2 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:112638547 G>A maps to NM_001109662.2 R2649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:112608230 C>T maps to NM_001109662.2 V3814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:112688181 C>A did not map to a codon.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr12:112600843 A>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:112673515 T>C maps to NM_001109662.2 Q1667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:112616995 C>T maps to NM_001109662.2 L3559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:6806546 G>T maps to NM_153685.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:10339081 C>T maps to NM_153022.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:10339129 C>A maps to NM_153022.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:14976096 A>C maps to NM_175874.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:97087504 G>T maps to ENST00000342887 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:97147596 G>T maps to ENST00000342887 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:97114181 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr12:97078968 C>A maps to ENST00000342887 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr12:97052064 A>T maps to ENST00000342887 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:97084913 T>C maps to ENST00000342887 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:80707372 G>T maps to NM_173591.3 E1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:80762068 G>T maps to NM_173591.3 G2190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:80633154 C>T maps to NM_173591.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:80658871 C>T maps to NM_173591.3 C693C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:80615943 C>A maps to NM_173591.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:80615886 C>T maps to NM_173591.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:80623120 C>T maps to NM_173591.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:80707359 C>A maps to NM_173591.3 Y1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:80714281 G>T maps to NM_173591.3 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:80761503 A>C maps to NM_173591.3 S2156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:80658967 C>T maps to NM_173591.3 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:80626845 C>T maps to NM_173591.3 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr12:80750657 C>T maps to NM_173591.3 R1986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:80658853 G>A maps to NM_173591.3 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:80663932 T>A maps to NM_173591.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:80704476 C>A maps to NM_173591.3 Y1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:80707382 C>G maps to NM_173591.3 S1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:80735800 A>T maps to NM_173591.3 I1699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:80749651 G>C maps to NM_173591.3 T1901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr12:64588289 G>A maps to ENST00000311915 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr12:27234390 G>A maps to ENST00000398815 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:93100911 C>T maps to NM_001037671.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:93100823 T>A maps to NM_001037671.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:25148751 C>T maps to NM_001101339.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:25149231 G>T maps to NM_001101339.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr13:50502072 C>A maps to NM_020456.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr13:46942866 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr13:46946332 G>T maps to NM_025113.2 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr13:39587156 C>A maps to NM_025138.3 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:39586309 C>A maps to NM_025138.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr13:39588170 G>A maps to NM_025138.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:39596462 C>A maps to NM_025138.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr13:39605734 C>A maps to NM_025138.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:39586280 G>T maps to NM_025138.3 S884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:31526831 C>A maps to NM_152325.1 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr13:31540435 C>T maps to NM_152325.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:31506869 C>A maps to NM_152325.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr13:31513829 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr13:113052420 A>G maps to NM_145248.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:44455681 A>T maps to NM_153218.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:31495226 C>A maps to NM_032849.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31495870 A>T maps to NM_032849.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:31480657 G>T maps to NM_032849.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr13:31498490 A>T maps to NM_032849.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:31495910 C>T maps to NM_032849.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:73320850 G>T maps to ENST00000377815 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:73317702 T>A maps to ENST00000377815 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:113333726 C>T maps to NM_207440.1 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr13:37269430 C>A maps to NM_203451.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:103338685 G>A maps to NM_001010977.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:103346734 G>T maps to NM_001010977.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:76121287 G>A maps to NM_007176.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:57083898 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:57083899 G>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr14:57085395 C>A maps to NM_017799.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:57101670 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90764711 C>A maps to NM_017970.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:90744787 G>A maps to NM_017970.2 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr14:90770362 G>A maps to NM_017970.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr14:90756951 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:50092640 A>C maps to NM_018139.2 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:50100256 G>A maps to NM_018139.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr14:50100867 G>A maps to NM_018139.2 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr14:57949820 G>A maps to NM_018168.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr14:45687539 T>C maps to NM_018353.4 K929K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:74824463 G>T maps to NM_018228.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:74825220 G>T maps to NM_018228.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:74823803 C>A maps to NM_018228.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:74823624 C>A maps to NM_018228.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr14:74823664 C>A maps to NM_018228.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr14:74824664 G>T maps to NM_018228.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:76638253 C>T maps to NM_017926.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:96848613 A>T maps to NM_016472.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:50583009 G>A maps to NM_024558.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:93673328 C>T maps to NM_032490.4 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:90397946 G>A maps to NM_145231.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:81259232 C>T maps to NM_152446.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr14:81251328 C>A maps to NM_152446.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:81380709 G>A maps to NM_152446.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:80971347 G>A maps to NM_152446.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:81259283 C>G maps to NM_152446.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:77880277 C>A maps to NM_001113475.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:77889076 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:59939766 T>C maps to NM_144581.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:59942717 T>A maps to NM_144581.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:104056516 G>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:104056598 G>A maps to NM_032374.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:104056610 G>A maps to NM_032374.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:91626658 G>T maps to NM_001102368.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:91633605 C>T maps to NM_001102368.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr14:77327094 G>A maps to NM_194287.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:77844782 C>G maps to NM_001010860.1 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr14:78234806 A>G maps to NM_174943.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:76549610 G>T maps to NM_052873.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:50550443 G>A maps to NM_001014830.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:50550583 G>A maps to NM_001014830.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:50550572 G>A maps to NM_001014830.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr14:24774177 C>T maps to NM_174913.1 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr14:24771456 C>T maps to NM_174913.1 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:45373678 G>A maps to NM_001017923.1 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:58604954 T>G maps to ENST00000438670 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:58599889 C>A maps to ENST00000438670 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:58471882 C>A maps to ENST00000438670 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr14:58605803 C>G maps to ENST00000438670 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:60903700 T>A maps to NM_174978.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:60928087 C>A maps to NM_174978.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:74206174 C>A maps to NM_001043318.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:74206048 G>A maps to NM_001043318.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:74196469 C>A maps to NM_001043318.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:74206147 C>T maps to NM_001043318.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr14:95932464 G>A maps to NM_152592.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr14:95934166 C>T maps to NM_152592.3 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:95932315 G>C maps to NM_152592.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:95884364 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:95942059 C>A maps to NM_152592.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:95912419 C>A maps to NM_152592.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:95912350 G>T maps to NM_152592.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:95910831 G>C maps to NM_152592.3 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:95932296 C>A maps to NM_152592.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:95922040 G>A maps to NM_152592.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:95942071 G>T maps to NM_152592.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:65019537 C>T maps to NM_172365.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr14:65054902 C>T maps to NM_172365.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:100795347 G>T maps to NM_207117.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr14:100795205 C>A maps to NM_207117.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:103566612 T>A maps to NM_001077594.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr14:105960173 C>T maps to ENST00000392523 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:23468205 G>A maps to NM_021944.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:24923773 A>C maps to NM_018958.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:24921529 G>A maps to NM_018958.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:24922504 C>T maps to NM_018958.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:24922492 C>G maps to NM_018958.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:24923266 G>A maps to NM_018958.2 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:24924111 C>G maps to NM_018958.2 S1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr15:24922792 A>T maps to NM_018958.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:24921595 C>A maps to NM_018958.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:24923235 C>A maps to NM_018958.2 S741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr15:24924481 G>T maps to NM_018958.2 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr15:24923785 A>T maps to NM_018958.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr15:24922198 C>G maps to NM_018958.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:24924298 C>A maps to NM_018958.2 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:24922546 C>A maps to NM_018958.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24921211 C>A maps to NM_018958.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:24923341 C>A maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:24923218 C>A maps to NM_018958.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr15:24921415 G>T maps to NM_018958.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:24921760 C>A maps to NM_018958.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:24922345 T>A maps to NM_018958.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:24923530 C>T maps to NM_018958.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr15:24923546 G>T maps to NM_018958.2 E845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:24922264 T>A maps to NM_018958.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:24922351 C>T maps to NM_018958.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:24924331 C>A maps to NM_018958.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:24922255 C>G maps to NM_018958.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:24922624 C>T maps to NM_018958.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr15:24923185 C>G maps to NM_018958.2 Y724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr15:24922996 C>A maps to NM_018958.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:40678593 C>A maps to NM_033286.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:40675158 C>A maps to NM_033286.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:40675204 G>T maps to NM_033286.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:40675062 G>T maps to NM_033286.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:81428996 G>A maps to ENST00000458088 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:81440835 C>A maps to ENST00000458088 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr15:81428948 G>T maps to ENST00000458088 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:81440245 G>C maps to ENST00000458088 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:81440789 C>A maps to ENST00000458088 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:76496244 C>T maps to NM_152335.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:76496118 C>A maps to NM_152335.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr15:49903437 C>A maps to NM_152647.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:49907320 G>T maps to NM_152647.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr15:49800504 C>G maps to NM_152647.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr15:49800492 G>A maps to NM_152647.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:49800545 C>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:75499771 C>T maps to NM_015492.4 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:75498944 C>T maps to NM_015492.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:75503330 C>T maps to NM_015492.4 F1006F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:90135398 G>A maps to NM_152259.3 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:90162952 C>T maps to NM_152259.3 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:90138747 G>T maps to NM_152259.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr15:90167026 A>C maps to NM_152259.3 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr15:90168094 T>A maps to NM_152259.3 P1518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:65888104 G>C maps to ENST00000420799 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:65899625 T>A maps to ENST00000420799 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr15:65871943 C>T maps to ENST00000420799 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:65890719 G>A maps to ENST00000420799 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:40631026 C>T maps to NM_207380.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr15:40630015 G>T maps to NM_207380.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:40630768 C>T maps to NM_207380.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34648155 C>A maps to ENST00000438749 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:34640215 C>T maps to ENST00000438749 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:34648890 C>A maps to ENST00000438749 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:34647927 T>C maps to ENST00000438749 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:34640602 C>A maps to ENST00000438749 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr15:34648998 C>T maps to ENST00000438749 N920N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:34648926 T>A maps to ENST00000438749 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr15:40855223 G>C maps to NM_001080791.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr15:40855097 G>A maps to NM_001080791.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:74032390 G>T maps to NM_001039614.1 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr15:74032287 G>T maps to NM_001039614.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:74032374 G>T maps to NM_001039614.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:73766252 G>A maps to NM_001042367.1 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:614004 C>A maps to ENST00000293874 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr16:613533 C>T maps to ENST00000293874 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr16:614976 C>T maps to ENST00000293874 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:90095675 C>T maps to NM_001214.3 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr16:90095615 G>T maps to NM_001214.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr16:15675107 G>A maps to NM_033201.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:15677093 C>A maps to NM_033201.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:81097425 G>A maps to NM_152337.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:29830978 G>A maps to NM_024516.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89735692 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2511048 C>A maps to NM_025108.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:19702684 C>T maps to NM_020314.5 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:19656205 A>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:19639972 A>G maps to NM_020314.5 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:19663356 C>A maps to NM_020314.5 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:19661757 A>C maps to NM_020314.5 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:19644487 C>T maps to NM_020314.5 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:8722678 G>T maps to NM_024109.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr16:67168096 T>C maps to NM_025187.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67154013 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr16:4790575 G>A maps to NM_139170.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr16:4790575 G>A maps to NM_139170.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:1889351 G>A maps to NM_001163560.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:11444628 A>G maps to NM_152308.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:49433158 G>T maps to NM_144602.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49430385 A>G maps to NM_144602.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:49433131 C>A maps to NM_144602.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr16:58148722 G>A maps to NM_013242.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:67702292 C>T maps to NM_001012984.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19725532 C>T maps to NM_001012991.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr16:5110369 G>C maps to ENST00000350219 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3544800 G>A maps to NM_001080524.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:3544668 G>T maps to NM_001080524.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:1479268 G>T maps to NM_001010878.1 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:30771728 C>T maps to NM_001014979.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:80361845 C>A maps to NM_175902.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:80373370 C>G maps to NM_175902.4 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:80352342 C>T maps to NM_175902.4 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:32906101 G>T maps to NM_207454.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:42745036 T>C maps to NM_001145080.2 N586N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:42745404 T>A maps to NM_001145080.2 L709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:42745462 T>C maps to NM_001145080.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42744679 T>G maps to NM_001145080.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:72955007 T>A maps to NM_030630.2 K383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:43333281 C>T maps to NM_152343.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr17:43333146 C>G maps to NM_152343.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43333140 G>A maps to NM_152343.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:56620019 G>A maps to NM_001038704.1 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:56621439 G>A maps to NM_001038704.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:56620083 T>C maps to NM_001038704.1 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10608453 C>T maps to NM_020233.4 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr17:10614343 A>T maps to NM_020233.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:42232033 T>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr17:42228408 A>G maps to NM_024032.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr17:42230075 G>T maps to NM_024032.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:79202796 C>T maps to NM_144679.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:45492280 C>T maps to NM_152347.4 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr17:45452189 G>A maps to NM_152347.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:65989226 G>A maps to NM_181655.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:65989127 A>T maps to NM_181656.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:8092735 G>A maps to NM_017622.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:8092891 C>A maps to NM_017622.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:7306507 G>A maps to NM_152766.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:58506770 C>A maps to NM_181707.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:58506877 C>A maps to NM_181707.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:58506910 C>A maps to NM_181707.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr17:58506880 G>T maps to NM_181707.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:34191866 G>A maps to NM_152781.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr17:34192361 C>T maps to NM_152781.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr17:34185256 C>A maps to NM_152781.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:54892330 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:8141518 C>A maps to NM_025099.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:8139420 C>T maps to NM_025099.5 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:8146358 C>T maps to NM_025099.5 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8135133 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:8138500 G>A maps to NM_025099.5 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr17:8134632 G>C maps to NM_025099.5 S877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:8135235 G>A maps to NM_025099.5 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:8139593 G>A maps to NM_025099.5 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr17:79514391 G>A maps to NM_025161.5 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:79512906 G>A maps to NM_025161.5 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr17:57288785 G>A maps to NM_018149.6 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr17:57287712 G>T maps to NM_018149.6 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:7330140 C>A maps to NM_175734.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:7329777 A>G maps to NM_175734.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:30668303 C>A did not map to a codon.
Alternatively spliced codon TCGA-55-7724-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:72588361 C>T maps to NM_152460.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:72588733 C>A maps to NM_152460.2 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:30179858 C>T maps to NM_018405.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:7155865 G>A maps to NM_203414.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr17:59489801 G>T maps to NM_203425.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:3721735 G>C maps to NM_001114118.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr17:5126670 C>A maps to NM_207103.2 L34L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-97-8172-01A-11D-2284-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:74729618 G>T maps to ENST00000317409 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:74729666 G>T maps to ENST00000317409 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:74729740 C>G maps to ENST00000317409 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr17:74729629 C>G maps to ENST00000317409 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:36991510 G>A maps to NM_001080465.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr18:13621149 C>T maps to NM_181481.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr18:13645127 C>A maps to NM_181481.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:13645451 A>T maps to NM_181481.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:13645526 C>T maps to NM_181481.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr18:34385370 G>A maps to NM_015476.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:34378462 C>A maps to NM_015476.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:13671872 A>G maps to NM_152352.3 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:33557476 C>G maps to NM_031446.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:77798590 C>T maps to NM_024805.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:77805851 G>T maps to NM_024805.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr18:77797372 C>G maps to NM_024805.2 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43796092 C>A maps to NM_145055.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:43796478 G>T maps to NM_145055.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr18:43820130 A>G maps to NM_145055.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr18:52265099 C>G maps to NM_173629.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr18:52265216 G>C maps to NM_173629.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr18:52262227 C>A maps to NM_173629.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:30950109 G>A maps to NM_001105528.1 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr18:30928851 A>G did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30806758 G>A maps to NM_001105528.1 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr18:30791979 T>A maps to NM_001105528.1 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr18:30977172 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:30554588 C>A maps to NM_001105528.1 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:30903459 G>T maps to NM_001105528.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr18:30926279 C>A maps to NM_001105528.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr18:30950012 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr18:30926184 A>T maps to NM_001105528.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:20878011 C>A maps to NM_032933.4 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr18:20945619 C>A maps to NM_032933.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr18:21106649 A>G maps to NM_013326.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr18:21109654 C>T maps to NM_013326.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:30199320 C>A maps to NM_001031726.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr19:30477229 C>T maps to NM_003796.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:758715 C>A maps to NM_173481.2 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:757677 G>T maps to NM_173481.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:757002 C>T maps to NM_173481.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr19:901460 G>A maps to NM_138774.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:1235048 C>A maps to ENST00000382477 E130*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-5428-01A-01D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-44-3919-01A-02D-1458-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-50-8460-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:3623982 T>C maps to NM_021231.1 A115A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-78-7158-01A-11D-2036-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:2276203 G>C maps to NM_198532.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:2099251 A>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:11486599 C>T maps to NM_175871.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:33464468 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50657930 C>A maps to NM_152358.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:50666244 C>A maps to NM_152358.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:16611990 A>T maps to NM_032207.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:7571040 G>T maps to NM_198534.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:36496282 C>T maps to ENST00000455847 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:36497348 G>C maps to ENST00000455847 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:40832376 C>A maps to ENST00000357884 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:40832337 C>A maps to ENST00000357884 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:40832385 C>G maps to ENST00000357884 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:18672928 A>G maps to NM_024069.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:55672122 T>C maps to ENST00000301249 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55677956 C>T maps to ENST00000301249 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:55672062 C>A maps to ENST00000301249 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:55672062 C>A maps to ENST00000301249 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:13885475 C>T maps to NM_014047.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:13996796 A>T maps to ENST00000454313 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:14006309 G>A maps to ENST00000454313 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:14006294 G>C maps to ENST00000454313 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:14000996 T>A maps to ENST00000454313 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:7742569 C>T maps to NM_174918.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:7742604 G>T maps to NM_174918.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:1011100 G>A maps to NM_001033026.1 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr19:51768792 G>A maps to NM_173635.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:7278081 C>T maps to NM_020156.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:119760087 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:119760064 T>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:119760948 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:22964186 C>A maps to NM_015991.2 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:22965740 C>A maps to NM_015991.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22986050 C>A maps to NM_000491.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22986095 C>A maps to NM_000491.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:22987743 C>A maps to NM_000491.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr1:22986050 C>A maps to NM_000491.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:22987662 G>T maps to NM_000491.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:22970581 G>C maps to NM_172369.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:22974095 C>A maps to NM_172369.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:22974074 C>T maps to NM_172369.3 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:43045020 G>A maps to NM_006688.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr12:49730236 G>A maps to NM_001008223.1 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr17:77043764 C>A maps to ENST00000392445 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:159797577 C>A maps to NM_031908.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:34035751 C>A maps to NM_181435.4 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:34028928 G>A maps to NM_181435.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:34043215 C>T maps to NM_181435.4 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:37578326 C>A maps to NM_182486.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr22:37578449 C>A maps to NM_182486.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:15444287 C>A maps to NM_001135170.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:15443996 C>A maps to NM_001135170.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr4:15437421 C>A maps to NM_001135170.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr16:1143911 G>T maps to NM_207419.3 Y116*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-A47A-01A-21D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr13:24895530 G>T maps to NM_178540.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr13:24895902 G>A maps to NM_178540.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr13:24471068 T>C maps to NM_001007537.1 S19S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-NJ-A4YF-01A-12D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:7188192 C>A maps to ENST00000290575 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:244538727 G>T maps to NM_001012970.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:244724028 C>T maps to NM_001130957.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr1:244640841 G>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:244715641 A>G maps to NM_001130957.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:111494008 T>C maps to NM_018372.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:111495394 C>A maps to NM_018372.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr1:111495202 G>A maps to NM_018372.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:172425553 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:172425553 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:200880664 G>A maps to NM_018265.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:200882702 G>T maps to NM_018265.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:200880739 C>T maps to NM_018265.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:200860812 A>C maps to NM_018265.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:210010462 C>A maps to NM_014388.6 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:210014249 G>T maps to NM_014388.6 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:210004185 A>G maps to NM_014388.6 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:210010462 C>G maps to NM_014388.6 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38155360 C>A maps to NM_017850.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr1:38155303 G>T maps to NM_017850.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:38155369 C>A maps to NM_017850.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:162829264 G>A maps to NM_178550.4 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:162824950 G>C maps to NM_178550.4 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:162825462 C>T maps to NM_178550.4 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:162344229 C>A maps to NM_182581.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:169801584 C>T maps to NM_018186.2 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:169812835 C>T maps to NM_018186.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:36786291 C>A maps to NM_001162530.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:36785388 G>A maps to NM_001162530.1 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:169390791 G>A maps to ENST00000367806 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:169391212 A>C maps to ENST00000367806 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:220870012 C>T maps to NM_024709.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:231474215 G>T maps to NM_032018.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:231474237 G>T maps to NM_032018.4 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:231488890 C>T maps to NM_032018.4 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:179364231 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr1:179504079 C>G maps to NM_144696.4 S1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:179460857 C>A maps to NM_144696.4 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:179348611 T>C maps to NM_144696.4 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:179460857 C>A maps to NM_144696.4 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:11009695 G>A maps to NM_001170754.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:11008658 C>A maps to NM_001170754.1 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:24112858 C>T maps to NM_020362.4 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170964570 C>A maps to NM_001163629.1 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:170965730 G>A maps to NM_001163629.1 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:170967492 C>A maps to NM_025063.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:170934322 C>A maps to NM_001163629.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:170931104 A>C maps to NM_001163629.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:170964615 T>C maps to NM_001163629.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:170928656 C>A maps to NM_001163629.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr1:170967370 A>T maps to NM_001163629.1 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr1:170931112 T>G maps to NM_001163629.1 L124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:170927672 G>C maps to NM_001163629.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:170955787 C>A maps to NM_001163629.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:170965719 G>A maps to NM_001163629.1 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:170965720 G>T maps to NM_001163629.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:26162281 G>A maps to NM_024037.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:182920509 A>G maps to ENST00000287709 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:182873350 A>T maps to ENST00000287709 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:67591502 A>T maps to NM_001013674.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:67558975 T>A maps to NM_001013674.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:67560953 G>A maps to NM_001013674.1 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247737488 C>G maps to NM_145278.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247737458 C>A maps to NM_145278.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:247737560 C>T maps to NM_145278.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:12820862 G>A maps to NM_152290.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:12820844 G>A maps to NM_152290.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:116666736 C>A maps to NM_152367.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:116670875 G>A maps to NM_152367.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr1:116675910 C>A maps to NM_152367.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57209874 A>G maps to NM_001004303.4 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57252873 C>A maps to NM_001004303.4 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:57252851 C>A maps to NM_001004303.4 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:57192182 C>A maps to NM_001004303.4 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:57216867 G>C maps to NM_001004303.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:57233535 G>A maps to NM_001004303.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:27278133 C>T maps to NM_152365.2 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038354 A>T maps to NM_001002912.4 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75038801 T>C maps to NM_001002912.4 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:75038450 G>T maps to NM_001002912.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:75038497 T>A maps to NM_001002912.4 R966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:75102077 T>C maps to NM_001002912.4 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:75107013 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75072441 C>T maps to NM_001002912.4 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75042609 T>A maps to NM_001002912.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:75097612 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:75086427 T>C maps to NM_001002912.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr1:75038849 G>T maps to NM_001002912.4 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:75037301 C>T maps to NM_001002912.4 E1364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:75038557 C>A maps to NM_001002912.4 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:75086562 A>G maps to NM_001002912.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75037409 C>T maps to NM_001002912.4 K1328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:75086593 G>C maps to NM_001002912.4 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:75038905 C>A maps to NM_001002912.4 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:75055644 T>A maps to NM_001002912.4 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:75037805 C>G maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:75037595 G>A maps to NM_001002912.4 V1266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:75037334 G>A maps to NM_001002912.4 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:75078488 G>C maps to NM_001002912.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:75107023 C>T maps to NM_001002912.4 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:75055735 G>A maps to NM_001002912.4 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:75107037 C>A maps to NM_001002912.4 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:75037636 C>A maps to NM_001002912.4 G1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:75038039 G>T maps to NM_001002912.4 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:75038363 C>T maps to NM_001002912.4 E1010E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:75038768 A>G maps to NM_001002912.4 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:75037802 G>T maps to NM_001002912.4 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:75038365 C>A maps to NM_001002912.4 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:75037589 T>A maps to NM_001002912.4 L1268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:75072506 C>A maps to NM_001002912.4 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:75055723 A>G maps to NM_001002912.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:55167806 G>A maps to ENST00000454855 K1139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:55161093 C>T maps to ENST00000454855 Y994Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:55134562 C>T maps to ENST00000454855 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:55158163 G>T maps to ENST00000454855 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:55145069 C>T maps to ENST00000454855 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:55166823 G>A maps to ENST00000454855 K1067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:55136509 G>T maps to ENST00000454855 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:55139466 C>T maps to ENST00000454855 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr1:55148430 C>T maps to ENST00000454855 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:55277778 C>T maps to NM_001110533.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:206239420 A>T maps to NM_001007544.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:11769500 C>G maps to NM_198545.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:11766489 C>A maps to NM_198545.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:11769434 G>A maps to NM_198545.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:154173059 G>A maps to NM_001010979.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:154172962 A>T maps to NM_001010979.1 L59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:46685387 C>A maps to NM_001013615.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:109649723 G>A maps to NM_001122961.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:24706265 T>C maps to ENST00000374409 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:24687416 G>A maps to ENST00000374409 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:184446684 T>C maps to NM_030806.3 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:23696035 G>A maps to ENST00000507744 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:23695807 C>G maps to ENST00000507744 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:36181805 G>C maps to NM_152374.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:213009320 G>C maps to NM_001024601.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:185109210 C>A maps to NM_030934.4 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:185153947 A>G maps to NM_001105518.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:185153462 A>G maps to NM_001105518.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:186375224 A>G maps to NM_017847.5 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:28209154 C>T maps to NM_001105556.1 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:28203186 C>A maps to NM_001105556.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:154192835 C>T maps to NM_001098616.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr1:178485001 C>G maps to NM_032126.4 L56L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-NJ-A4YQ-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:43233240 C>T maps to NM_024097.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:43239265 C>T maps to NM_024097.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:85718350 G>T maps to NM_198077.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:85724261 T>C maps to NM_198077.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:150245264 G>T maps to NM_024579.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:150249040 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:226175778 C>A maps to NM_152608.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226176061 T>G maps to NM_152608.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:151020577 C>G maps to NM_017860.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:151020364 G>A maps to NM_017860.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:151020761 G>T maps to NM_017860.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:151020973 C>A maps to NM_017860.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:151021309 G>A maps to NM_017860.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr1:233105692 C>T maps to NM_032324.1 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:109191436 G>T maps to ENST00000370031 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:109191325 C>A maps to ENST00000370031 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:109191531 C>A maps to ENST00000370031 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:109191483 C>A maps to ENST00000370031 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156384529 C>G maps to ENST00000357975 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:25573268 G>A maps to NM_020317.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:223567017 C>A maps to NM_152610.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:223568334 G>A maps to NM_152610.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:223567833 G>T maps to NM_152610.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:223567449 G>A maps to NM_152610.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:156703952 G>T maps to NM_015997.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:156704033 G>C maps to NM_015997.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:228363177 A>G maps to NM_001010867.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:209956172 G>C maps to NM_152485.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:209956700 C>A maps to NM_152485.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:209956823 T>A maps to NM_152485.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:209956457 C>A maps to NM_152485.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:153615716 C>A maps to NM_015607.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:153615793 G>C maps to NM_015607.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:54562016 C>T maps to ENST00000371331 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:156264221 G>A maps to NM_144580.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:60505797 G>A maps to NM_152377.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:60538213 T>A maps to NM_152377.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:16560260 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:172571919 C>T maps to ENST00000367723 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:172554998 A>T maps to ENST00000367723 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:32682935 C>A maps to NM_019118.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:32687572 C>A maps to NM_019118.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:156897533 C>T maps to NM_144702.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34663387 C>A maps to NM_001134734.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:34663080 C>T maps to NM_001134734.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:34663380 G>T maps to NM_001134734.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:226784575 C>G maps to ENST00000366788 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:226784512 C>A maps to ENST00000366788 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:226784530 G>T maps to ENST00000366788 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:31903836 A>G maps to NM_000063.4 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:31911285 C>T maps to ENST00000437789 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr6:31911242 C>G maps to ENST00000437789 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr6:31901426 G>T maps to ENST00000437789 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:31901507 G>A maps to ENST00000437789 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr6:31896515 C>T maps to ENST00000477310 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:9498867 C>T maps to NM_012261.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:9496976 G>C maps to NM_012261.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr20:9496232 T>C maps to NM_012261.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:9496199 G>T maps to NM_012261.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:9498708 G>C maps to NM_012261.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:55100930 C>A maps to NM_001012971.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:55111382 T>A maps to NM_001013646.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:61576188 C>T maps to NM_017896.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:31044010 C>T maps to NM_080616.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:31873971 C>T maps to NM_033197.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:31876595 G>A maps to NM_033197.2 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:31889127 G>T maps to NM_033197.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:35433299 A>G maps to NM_080627.2 N975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:35434279 C>A maps to NM_080627.2 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:35509140 C>A maps to NM_080628.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:35504604 C>A maps to NM_080628.1 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35737067 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:35802494 C>A maps to ENST00000343811 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr20:35752145 G>A maps to ENST00000343811 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:35740726 A>G maps to ENST00000343811 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:35749390 C>T maps to ENST00000343811 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:62493318 C>A maps to NM_080622.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:2795874 G>T maps to NM_080739.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:34572614 C>T maps to ENST00000373973 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:34596255 C>A maps to ENST00000373973 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:34611600 G>A maps to ENST00000373973 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr20:34583045 T>C maps to ENST00000373973 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:34572667 G>A maps to ENST00000373973 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30617579 C>A maps to ENST00000300415 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:30602735 G>T maps to ENST00000300415 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30602723 C>A maps to ENST00000300415 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr20:31643258 C>T maps to NM_182658.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:31661395 G>T maps to NM_182658.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr20:31644415 C>A maps to NM_182658.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:31649630 G>A maps to NM_182658.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:31644492 G>A maps to NM_182658.1 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:31647282 C>T maps to NM_182658.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:31671170 A>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:31685499 G>A maps to NM_182519.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:31672766 G>A maps to NM_182519.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31671450 C>A maps to NM_182519.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:31672751 C>T maps to NM_182519.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr20:31685466 C>A maps to NM_182519.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:31671677 G>T maps to NM_182519.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:31672737 C>A maps to NM_182519.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:31671269 C>T maps to NM_182519.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3234370 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr20:3324333 T>A maps to NM_001009984.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:3340198 C>T maps to NM_001009984.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr20:3321200 C>A maps to NM_001009984.1 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:62187725 C>A maps to NM_024059.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:62187705 C>T maps to NM_024059.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:5843982 C>A maps to NM_152504.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:58645680 C>G maps to NM_173644.1 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:61428021 C>T maps to NM_018270.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:35238009 C>T maps to NM_018840.4 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:20232313 C>T maps to ENST00000389655 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:20051545 C>A maps to ENST00000389655 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr20:20243766 C>T maps to ENST00000389655 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:20140012 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr20:20177350 G>A maps to ENST00000389655 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr20:20258059 C>A maps to ENST00000389655 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr20:20258002 G>C maps to ENST00000389655 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:20037344 C>A maps to ENST00000389655 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr20:20243671 C>A maps to ENST00000389655 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:3802910 C>T maps to NM_018347.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:34843633 G>T maps to NM_015511.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:34832712 A>T maps to NM_015511.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:34828452 G>A maps to NM_015511.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr20:55092257 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:55088421 G>T maps to ENST00000357348 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:1161881 G>A maps to NM_018354.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:1162052 C>T maps to NM_018354.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:1161656 G>T maps to NM_018354.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:746286 G>A maps to NM_033409.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr20:746118 C>T maps to NM_033409.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:744287 G>A maps to NM_033409.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:742373 G>A maps to NM_033409.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr20:13765722 G>A maps to NM_024120.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr20:31811752 G>A maps to NM_178466.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:17950903 C>A maps to NM_052865.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:18794669 C>T maps to NM_178483.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:18794879 C>T maps to NM_178483.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:56735844 A>T maps to NM_178456.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:56728653 G>A maps to NM_178456.2 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:56735868 C>A maps to NM_178456.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:56728598 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:56726070 G>A maps to NM_178456.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:56728612 A>T maps to NM_178456.2 K28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:56728611 G>A maps to NM_178456.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:10603339 G>C maps to NM_001009608.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr20:10579400 G>T did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr20:10603597 G>A maps to NM_001009608.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:10603871 G>T maps to NM_001009608.1 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr20:257908 G>A maps to NM_153269.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr21:45941909 G>A maps to ENST00000443468 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:45941861 C>A maps to ENST00000443468 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr21:45987863 C>T maps to ENST00000443468 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr21:45948416 C>T maps to ENST00000443468 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr21:45953698 C>A maps to ENST00000443468 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:45947288 G>C maps to ENST00000443468 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr21:45563122 G>C maps to NM_004649.6 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:33651132 C>A maps to NM_018944.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr21:47706940 G>C maps to NM_058181.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr21:47735386 C>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr21:30521559 C>T maps to NM_020152.2 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr21:30547128 G>T maps to NM_020152.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr21:19168901 C>A maps to NM_001100420.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:19165869 C>T maps to NM_001100420.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:32795631 G>A maps to NM_014306.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:19839363 C>A maps to NM_024627.5 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr22:19839739 G>A maps to NM_024627.5 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr22:32108283 G>T maps to NM_173566.2 T1847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:32097682 T>C maps to NM_173566.2 P2022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr22:32108336 C>A maps to NM_173566.2 G1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr22:24982372 C>T maps to NM_207644.2 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:32546304 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr22:32547533 G>T maps to NM_001010859.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45598868 A>C did not map to a codon.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr22:45599788 G>A maps to NM_001009880.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:45598963 G>A maps to NM_001009880.1 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr21:43321742 T>A maps to NM_015500.1 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr21:43319228 G>T maps to NM_015500.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:118986935 G>A maps to NM_014807.3 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr11:118984559 A>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:118982043 A>T maps to NM_014807.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:73850837 G>A maps to ENST00000334126 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:73765700 C>A maps to ENST00000334126 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:73768560 C>A maps to ENST00000334126 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:73748714 G>A maps to ENST00000334126 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:73803557 T>G maps to ENST00000334126 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:99767206 G>C maps to NM_144706.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:27805000 C>G maps to NM_032266.3 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:27805333 C>A maps to NM_032266.3 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:27804469 C>T maps to NM_032266.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:27805276 T>C maps to NM_032266.3 P1946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:27803383 T>A maps to NM_032266.3 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:27800824 G>T maps to NM_032266.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:27801983 C>T maps to NM_032266.3 R849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr2:27800980 A>G maps to NM_032266.3 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:27804736 T>C maps to NM_032266.3 H1766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:27802027 C>T maps to NM_032266.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:27001192 G>T maps to NM_017877.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:101879005 C>T maps to NM_017546.4 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:101881337 G>T maps to NM_017546.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:44993591 A>T maps to NM_024766.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:26671556 A>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:26677519 C>A maps to NM_145038.2 S642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:26663340 A>G maps to NM_145038.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26678074 C>T maps to NM_145038.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:26624937 C>T maps to NM_145038.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:26667615 G>A maps to NM_145038.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:26652620 C>G maps to NM_145038.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:106694259 C>A maps to NM_032411.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:106690423 G>T maps to NM_032411.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:70408787 C>G maps to NM_017880.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:20990126 T>G maps to ENST00000381090 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:24255710 C>A maps to NM_025203.2 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:10350512 G>T maps to NM_182626.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr2:105959427 G>A maps to NM_024093.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:11273690 G>A maps to NM_182500.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:27360749 C>A maps to NM_178553.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:27360546 G>T maps to NM_178553.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:99448924 C>A maps to NM_207362.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:37463237 G>C did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:232457721 A>T maps to NM_152614.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:232458228 C>T maps to NM_152614.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:47357381 C>T maps to NM_001163561.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:47382369 G>A maps to NM_001163561.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:219222788 G>T maps to NM_198559.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:219231791 C>T maps to NM_198559.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr2:55403123 T>G did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:210993810 G>A maps to NM_152519.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:26798826 C>A maps to NM_001105519.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:29295577 G>C maps to NM_001029883.1 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:29295618 A>T maps to NM_001029883.1 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:29294982 G>T maps to NM_001029883.1 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:29295087 C>T maps to NM_001029883.1 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:29293998 G>T maps to NM_001029883.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:29295785 A>G maps to NM_001029883.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:29296485 C>A maps to NM_001029883.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:54587620 C>T maps to NM_001100396.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:54571010 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:120069236 G>A maps to NM_001017927.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:170502614 A>T maps to NM_001085447.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74043092 C>A maps to NM_001080474.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:74042528 C>A maps to NM_001080474.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:74041003 T>A maps to NM_001080474.1 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:74040676 A>T maps to NM_001080474.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:74043869 G>A maps to NM_001080474.1 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr2:74043577 C>A maps to NM_001080474.1 S743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:209049756 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:209046028 C>A maps to NM_001099334.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr2:209051686 C>T maps to NM_001099334.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:228476172 T>G maps to NM_020161.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:228497783 C>A maps to NM_020161.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:24406433 C>T maps to NM_001040710.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:24398403 A>C maps to NM_001040710.1 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:24413445 C>A maps to NM_001040710.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:242815329 C>T maps to NM_173821.2 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:242814381 T>A maps to NM_173821.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:242814573 C>T maps to NM_173821.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:242814846 C>T maps to NM_173821.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:63631786 C>A maps to NM_015910.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85049049 G>T maps to ENST00000409520 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:85051249 C>T maps to ENST00000409520 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:85059219 G>T maps to ENST00000409520 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:85049163 C>A maps to ENST00000409520 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr19:6696468 C>A maps to NM_000064.2 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:8212739 G>T maps to NM_004054.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:8212490 G>T maps to NM_004054.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:8211785 G>T maps to NM_004054.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr12:8212562 G>T maps to NM_004054.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:119236106 C>T maps to NM_016589.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:119236072 G>A maps to NM_016589.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:119217732 G>A maps to NM_016589.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:119217753 C>T maps to NM_016589.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:119466714 C>T maps to NM_033364.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:119466072 G>T maps to NM_033364.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:119426273 C>T maps to NM_033364.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:119445163 G>T maps to NM_033364.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:112736345 G>T maps to NM_015412.3 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:14756869 G>A maps to NM_032137.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:14769947 C>T maps to NM_032137.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:14763189 G>T maps to NM_032137.4 G489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:14798904 C>A maps to NM_032137.4 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:14813694 C>T maps to NM_032137.4 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:194790680 C>A maps to NM_152531.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr3:126268893 C>A maps to NM_152533.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:10145978 G>A maps to NM_001164839.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr3:99890703 A>G maps to NM_032359.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:99897181 G>T maps to NM_032359.3 G264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:99891179 G>A maps to NM_032359.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:99891161 C>T maps to NM_032359.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr3:128292392 G>A maps to NM_007354.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:118865122 C>A maps to NM_152539.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865704 T>C maps to NM_152539.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:118865773 G>A maps to NM_152539.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:118866367 C>A maps to NM_152539.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:118865569 C>A maps to NM_152539.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:118865971 C>A maps to NM_152539.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:118865731 C>A maps to NM_152539.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:118865770 A>G maps to NM_152539.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:118865773 G>A maps to NM_152539.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr3:8672547 A>C maps to NM_015931.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:37458916 G>T maps to NM_178339.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr3:37476506 G>A maps to NM_178339.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:133647317 C>A maps to NM_025041.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:129009526 T>A maps to NM_001006109.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:88202560 G>A maps to NM_173824.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:88205655 G>T maps to NM_173824.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:43121363 C>G maps to NM_032806.4 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:43122518 C>A maps to NM_032806.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr3:43121447 C>T maps to NM_032806.4 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:43121602 C>A maps to NM_032806.4 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr3:43122491 G>C maps to NM_032806.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:143691783 C>T maps to NM_173552.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:143708571 G>T maps to NM_173552.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr3:192516719 G>A maps to NM_178496.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:192516573 C>T maps to NM_178496.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:192516396 G>T maps to NM_178496.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:192516993 G>A maps to NM_178496.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:192516438 G>A maps to NM_178496.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:192635484 G>T maps to NM_178496.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:192516573 C>A maps to NM_178496.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:56667419 G>C maps to ENST00000447900 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:56695041 A>G maps to ENST00000447900 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:56674033 C>T maps to ENST00000447900 W915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:69026884 T>A maps to ENST00000383701 K490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:58817567 C>T maps to ENST00000482387 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:58855171 C>A maps to ENST00000482387 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:184800917 T>C maps to NM_001025266.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:184801038 G>C maps to NM_001025266.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:48955835 G>A maps to NM_001123040.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:138669284 G>C maps to NM_001040061.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:47543342 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:47539856 C>T maps to NM_001031703.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:207317923 C>A maps to NM_000715.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:207297524 A>T maps to NM_000715.3 K174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:207314563 C>T maps to NM_000715.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:207286462 A>G maps to NM_000715.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:207307857 A>C maps to NM_000715.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:207271572 C>A maps to NM_001017367.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:207265091 C>T maps to NM_001017367.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:57843022 C>T maps to NM_032313.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:57843073 C>G maps to NM_032313.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:100458875 T>A maps to NM_032149.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:100458827 C>A maps to NM_032149.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:100434273 C>A maps to NM_032149.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr4:100463154 C>A maps to NM_032149.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:37591709 C>T maps to NM_018302.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:113479456 C>A maps to NM_018392.4 G1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:113541201 G>A maps to NM_018392.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:113533733 T>G maps to NM_018392.4 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:113524822 C>A maps to NM_018392.4 G945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:113530549 T>A maps to NM_018392.4 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:113538964 G>A maps to NM_018392.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:120221743 G>T maps to NM_001170330.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:71200917 T>A maps to NM_033122.3 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:71200776 C>A maps to NM_033122.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:71201632 G>T maps to NM_033122.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:71201475 C>A maps to NM_033122.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:87808957 C>G maps to NM_144645.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:98762071 C>A maps to NM_174952.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:98865109 A>G maps to NM_174952.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:98480249 T>A maps to NM_174952.2 K447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr4:98761944 C>A maps to NM_174952.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:165878523 C>G maps to NM_153027.1 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr4:165878575 T>C maps to NM_153027.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:71024466 T>G maps to NM_214711.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:71024280 C>A maps to NM_214711.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:184605295 A>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:184606246 G>A maps to NM_021942.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:184626182 G>T maps to NM_021942.4 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:184612551 A>C maps to NM_021942.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:184614123 G>T maps to NM_021942.4 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:184606485 G>A maps to NM_021942.4 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:3254981 C>G maps to NM_001042690.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:140196472 T>A maps to ENST00000260011 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:5961119 C>G maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:5975501 C>A maps to ENST00000324058 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:5981914 C>A maps to ENST00000324058 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:5975559 T>A maps to ENST00000324058 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:5966831 G>T maps to ENST00000324058 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:146617752 G>A maps to NM_001080531.1 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr4:71099894 C>T maps to NM_152997.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:123731376 G>A maps to NM_001735.2 Y1394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr9:123716129 C>T maps to NM_001735.2 E1593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr9:123776292 A>C maps to NM_001735.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr19:47823816 G>A maps to ENST00000355085 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:47823414 G>T maps to ENST00000355085 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:47823226 G>T maps to ENST00000355085 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:47824024 G>T maps to ENST00000355085 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:133295281 G>C maps to NM_020199.2 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr5:134782573 G>T maps to NM_130848.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr5:134782289 G>T maps to NM_130848.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:31541485 A>G maps to NM_018356.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:175763869 C>G maps to ENST00000443967 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:43446491 C>A maps to NM_022483.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr5:36211992 T>A maps to NM_001085411.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:36197707 G>A maps to NM_001085411.1 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:36225699 C>A maps to NM_001085411.1 A168A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-7662-01A-11D-2063-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:154210375 G>A maps to NM_032385.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:156769986 C>T maps to NM_001001343.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:156770406 G>T maps to NM_001001343.3 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:172539306 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:37169219 C>A maps to NM_023073.3 T2302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr5:37186459 C>A maps to NM_023073.3 E1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr5:37169396 T>A maps to NM_023073.3 T2243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:37169084 C>A maps to NM_023073.3 G2347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:37180960 C>T maps to NM_023073.3 L1856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:37180986 G>A maps to NM_023073.3 Q1848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:37169411 G>A maps to NM_023073.3 P2238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:41904477 C>G maps to NM_175921.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:159822491 C>T maps to NM_022090.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:159821567 T>A maps to NM_022090.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr5:442604 C>T maps to NM_138464.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:41160436 G>T maps to NM_001115131.1 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:41181562 C>A maps to NM_001115131.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:41201791 G>T maps to NM_001115131.1 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:41161793 C>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:41181493 G>A maps to NM_001115131.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:41154098 C>A maps to NM_001115131.1 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:41199957 C>T maps to NM_001115131.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:41158799 A>T maps to NM_001115131.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:41154095 C>A maps to NM_001115131.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:41195922 G>T maps to NM_001115131.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:41160463 G>T maps to NM_001115131.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr5:41176733 G>C maps to NM_001115131.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:41195936 G>T maps to NM_001115131.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:41199915 G>A maps to NM_001115131.1 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr5:41201722 G>T maps to NM_001115131.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:41154083 C>T maps to NM_001115131.1 K706K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:41160349 G>T maps to NM_001115131.1 C526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:41149361 A>T maps to NM_001115131.1 Y868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:41196021 G>T maps to NM_001115131.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr5:41149523 G>T maps to NM_001115131.1 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:32260790 T>A maps to ENST00000447241 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:32261492 C>T maps to ENST00000447241 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:32260880 A>T maps to ENST00000447241 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:32323446 C>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:11768562 T>C maps to NM_001143948.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:34614530 C>A maps to NM_024294.2 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr6:34614501 C>G maps to NM_024294.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:34574443 C>T maps to NM_024294.2 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:34614552 C>A maps to NM_024294.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:43197173 C>A maps to ENST00000509253 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:139363913 C>T maps to NM_021243.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:165711482 G>T maps to NM_144980.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:165715540 G>T maps to NM_144980.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:165703509 A>T maps to NM_144980.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:165715669 C>A maps to NM_144980.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:165723068 C>A maps to NM_144980.3 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:165715240 G>A maps to NM_144980.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:165715300 T>C maps to NM_144980.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:165713954 C>T maps to NM_144980.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:165713954 C>A maps to NM_144980.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr6:165715645 G>A maps to NM_144980.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:165715711 T>C maps to NM_144980.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:165715189 G>T maps to NM_144980.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:165712973 G>T maps to NM_144980.3 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:165715273 C>A maps to NM_144980.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:170102857 G>A maps to ENST00000439249 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:33669172 G>A maps to NM_032340.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:30596122 G>A maps to ENST00000376485 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:30617663 C>G maps to NM_001161376.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr6:30619069 G>A maps to NM_001161376.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:47846856 G>A maps to NM_001013732.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:47976477 G>A maps to NM_001013732.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:47846938 T>A maps to NM_001013732.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:47976770 G>C maps to NM_001013732.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47846146 G>A maps to NM_001013732.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:47846230 T>G maps to NM_001013732.3 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:48036172 C>T maps to NM_001013732.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr6:47846203 C>A maps to NM_001013732.3 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:47846656 G>T maps to NM_001013732.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr6:47847082 C>A maps to NM_001013732.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:47847064 G>T maps to NM_001013732.3 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:47847487 C>A maps to NM_001013732.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:54025354 C>G maps to ENST00000502396 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:54095708 C>A maps to ENST00000502396 C972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:53989476 A>T maps to ENST00000502396 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:53883844 G>T maps to ENST00000514921 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:54066940 C>A maps to ENST00000502396 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:53986315 C>A maps to ENST00000502396 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:53989455 C>T maps to ENST00000502396 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:54095672 G>A maps to ENST00000502396 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:3738374 A>T maps to NM_183373.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:3723970 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:3751615 C>A maps to NM_183373.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:4077606 C>A maps to NM_173563.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:31080012 C>A maps to NM_014070.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:31079508 C>T maps to NM_014070.2 W209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:31079655 T>A maps to NM_014070.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:43477340 G>T maps to NM_001012974.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:88138501 G>A maps to NM_001031743.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:97676906 C>A maps to NM_198468.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:97597754 C>T maps to NM_198468.2 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr6:97616093 T>C maps to NM_198468.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr6:97627326 C>T maps to NM_198468.2 G831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:97720633 T>C maps to NM_198468.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:97634565 C>T maps to NM_198468.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:97677143 C>T maps to NM_198468.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr6:99797119 G>T maps to NM_032511.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:121615755 A>G maps to ENST00000275159 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:121563385 A>G maps to ENST00000275159 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:121402009 C>T maps to ENST00000275159 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:121563370 G>A maps to ENST00000275159 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:121577381 C>A maps to ENST00000275159 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr6:121615714 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:121563450 G>A maps to ENST00000275159 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr6:127796878 G>A maps to NM_001012279.2 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr6:127836122 G>A maps to NM_001012279.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:109484116 C>T maps to NM_173830.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:133118162 G>A maps to NM_052831.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:133091438 T>C maps to NM_052831.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:107372259 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:118803035 T>A maps to NM_001042475.2 K551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:118801676 C>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:118812917 T>C maps to NM_001042475.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:151789866 G>A maps to NM_024573.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:74072903 G>T maps to NM_001017361.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:43970829 G>T maps to NM_153246.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:112420549 G>T maps to NM_001033564.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:31737523 G>A maps to NM_025258.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:31743833 C>T maps to NM_025258.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:31737787 G>C maps to NM_025258.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:31741101 G>A maps to NM_025258.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:127898551 T>G maps to NM_001010905.1 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:127898458 C>A maps to NM_001010905.1 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:127911456 G>T maps to NM_001010905.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:39082789 G>A maps to NM_018322.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:170160822 A>G maps to NM_018341.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:170179307 G>A maps to NM_018341.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:35715159 G>T maps to NM_145028.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:35705825 G>A maps to NM_145028.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:35715381 G>T maps to NM_145028.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:151917627 G>T maps to ENST00000367290 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:151917628 G>T maps to ENST00000367290 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:151859247 G>A maps to ENST00000367290 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:151869437 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:151936690 G>A maps to ENST00000367290 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr6:151917606 C>A maps to ENST00000367290 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:40945337 T>C maps to NM_000587.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:40981597 G>T maps to NM_000587.2 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr5:40945414 C>A maps to NM_000587.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr5:40937761 G>T maps to NM_000587.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:40981623 G>T maps to NM_000587.2 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:40959644 C>A maps to NM_000587.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:40498718 T>A maps to NM_001193311.1 L310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:40277288 G>T maps to NM_001193311.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr7:40277288 G>C maps to NM_001193311.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:40723698 T>C maps to NM_001193311.1 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:31735161 G>A maps to NM_006658.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:31735206 G>T maps to NM_006658.4 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:42950255 G>A maps to NM_001099858.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:6631426 G>T maps to NM_024067.2 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:2577813 C>A maps to NM_152743.3 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr7:6862973 C>T maps to NM_198097.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:150027588 A>G maps to NM_138434.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:150027822 T>C maps to NM_138434.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:25194711 C>G maps to NM_138811.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:148311162 G>T maps to NM_145304.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:142637619 G>C maps to NM_178829.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:142636717 C>A maps to NM_178829.4 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:142636750 A>G maps to NM_178829.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:39606022 G>T maps to NM_020192.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:39611873 A>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:66410079 C>T maps to NM_017994.4 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:99752720 G>C maps to NM_018275.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr7:129847875 G>T maps to NM_145268.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:100033310 G>T maps to NM_145030.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr7:100033015 G>C maps to NM_145030.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr7:1049626 G>A maps to NM_032350.5 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:100085976 G>A maps to ENST00000423930 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100085859 C>A maps to ENST00000423930 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:100086912 G>T maps to ENST00000423930 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100086048 T>C maps to ENST00000423930 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:100086412 C>T maps to ENST00000423930 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:100087212 C>A maps to ENST00000423930 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:100086357 G>T maps to ENST00000423930 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:100817806 C>T maps to NM_198571.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:112124998 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr7:139030420 C>T maps to NM_197964.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:48086055 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:120704290 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:120767241 C>T maps to NM_024913.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:120911453 A>T maps to NM_024913.4 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:120876790 A>T maps to NM_024913.4 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:120782110 G>C maps to NM_024913.4 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:120767203 G>T maps to NM_024913.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr7:120906324 T>C maps to NM_024913.4 Y785Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:120773889 G>T maps to NM_024913.4 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr7:99746598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:89887464 T>C maps to NM_001039706.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:89891301 G>T maps to NM_001039706.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:89874782 C>T maps to NM_001039706.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:89874755 C>G maps to NM_001039706.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:108524274 G>T maps to NM_001024607.1 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:47859103 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:6370131 G>A maps to NM_001037163.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:57349152 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:57351622 C>T maps to NM_000562.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:57351649 G>A maps to NM_000562.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:57347231 C>T maps to NM_000562.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:57347291 G>A maps to NM_000562.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:57372338 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:57333305 C>G maps to NM_000562.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:57431534 G>T maps to NM_000066.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:57411653 G>T maps to NM_000066.2 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:57417780 C>A maps to NM_000066.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:49986615 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:49986621 C>T maps to NM_001007176.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:144126079 C>T maps to NM_173687.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:144124452 C>A maps to NM_173687.2 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr8:144124453 A>G maps to NM_173687.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:146279401 A>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr8:69351820 G>T maps to NM_052958.2 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr8:96281312 G>A maps to NM_177965.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:42407750 A>G maps to NM_001135675.1 *108W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:67422389 C>T maps to NM_152765.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:67422361 G>A maps to NM_152765.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr8:99101610 G>A maps to NM_173549.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr8:99102181 C>T maps to NM_173549.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10555359 G>T maps to NM_001040032.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10557833 C>A maps to NM_001040032.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:10555136 C>A maps to NM_001040032.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:10555133 G>T maps to NM_001040032.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:10555223 C>T maps to NM_001040032.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:10555334 C>A maps to NM_001040032.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:10555358 C>T maps to NM_001040032.1 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr8:124253514 C>T maps to NM_032847.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:124251333 G>C maps to NM_032847.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:124243669 C>A maps to NM_032847.1 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:124250157 A>G maps to NM_032847.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:12878739 A>C maps to NM_020844.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:27922221 G>A maps to ENST00000341513 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:27925798 G>A maps to ENST00000341513 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:27927170 T>C maps to ENST00000418860 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:38385957 T>A maps to NM_207412.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:39288978 G>A maps to NM_001737.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:39316032 A>C maps to NM_001737.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:39341263 G>A maps to NM_001737.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:39342282 T>A maps to NM_001737.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:39341330 C>T maps to NM_001737.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr5:39306814 C>T maps to NM_001737.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:39311440 C>A maps to NM_001737.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:39311242 C>A maps to NM_001737.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:39341775 A>G maps to NM_001737.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:98691074 A>G maps to NM_001010895.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:98669550 C>T maps to NM_001010895.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr9:86258487 C>G maps to NM_001001551.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr9:86258453 C>A maps to NM_001001551.2 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132084685 T>C maps to NM_001012715.3 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:27289706 G>A maps to NM_020641.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:104238431 C>A maps to NM_032342.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:104238915 A>G maps to NM_032342.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:104238674 C>A maps to NM_032342.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:35825242 C>T maps to NM_001012446.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:96080694 G>C maps to NM_001098808.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:35045841 C>A maps to NM_203299.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr9:35044908 C>A maps to NM_203299.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:35043339 G>A maps to NM_203299.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr9:139929106 C>A maps to NM_207511.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:139960770 G>C maps to NM_178448.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139959972 C>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:139887561 G>A maps to NM_183241.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr9:12775854 T>C maps to NM_203403.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:100678465 T>A maps to NM_016481.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:139379064 G>C maps to NM_152571.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:89771609 T>C maps to NM_001001709.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:135447818 G>A maps to NM_207417.1 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:135285780 C>T maps to NM_207417.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:135285843 C>T maps to NM_207417.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr9:139740227 C>A maps to NM_001080482.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:34385779 C>G did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr9:97717495 G>T maps to NM_001193329.1 G567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:97823055 C>A maps to NM_001193329.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr9:97522730 T>A maps to NM_001193329.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:97522563 C>T maps to NM_001193329.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr9:77567245 T>A maps to NM_017998.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr9:77598774 C>A maps to NM_152420.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr9:77598700 C>T maps to NM_152420.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:116191476 C>A maps to ENST00000451722 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:116187351 A>G maps to ENST00000451722 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:5431904 G>A maps to NM_018465.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr9:5361758 C>A maps to NM_018465.2 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr9:111819470 C>A maps to NM_032012.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:132375844 G>T maps to NM_199350.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr9:111701691 G>A maps to NM_017832.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:86570402 C>A maps to NM_032307.3 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr9:86554605 C>A maps to NM_032307.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:4661976 G>A maps to ENST00000454239 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:136330482 C>T maps to NM_017586.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:71152288 G>A maps to NM_153237.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:27556698 C>T maps to NM_018325.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr9:27562474 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:27561599 A>G maps to NM_018325.2 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:90502662 A>G maps to NM_178828.4 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:90499920 C>A maps to NM_178828.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:90502200 C>A maps to NM_178828.4 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr9:90501057 C>A maps to NM_178828.4 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:90502474 C>T maps to NM_178828.4 Q1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:90497973 G>A maps to NM_178828.4 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:90503532 C>A maps to NM_178828.4 C1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:26886164 T>A maps to NM_024828.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr9:26842343 C>G maps to NM_024828.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:114467645 T>G did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr9:114520997 G>T maps to NM_173521.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:114538245 A>G maps to NM_173521.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:74526691 G>A maps to NM_182505.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:74526698 C>T maps to NM_182505.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr9:139718064 C>T maps to NM_001173988.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:135763713 G>T maps to ENST00000372136 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:117405508 G>T maps to ENST00000374049 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:15721813 G>T maps to NM_173550.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr9:15695283 G>T maps to NM_173550.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:136251402 G>A maps to NM_153710.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr9:136260872 G>A maps to NM_153710.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr9:136269059 G>A maps to NM_153710.3 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr9:136249641 G>A maps to NM_153710.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:136268869 C>A maps to NM_153710.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:136253250 C>A maps to NM_153710.3 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:136245974 C>A maps to NM_153710.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:135602878 C>T maps to NM_152572.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:86242061 G>T maps to NM_001738.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:86249254 G>A maps to NM_001738.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:86240797 A>T maps to NM_001738.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:86244717 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:50008361 C>A maps to NM_001082534.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:50008442 C>A maps to NM_001082534.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:49713293 C>T maps to NM_001082534.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:50235098 G>T maps to NM_001082534.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:49142168 G>T maps to NM_001217.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:49147767 C>T maps to NM_001217.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:63618489 G>A maps to NM_001218.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:86163065 C>T maps to NM_198584.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:86193559 G>T maps to NM_198584.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150235521 C>A maps to NM_012113.1 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:150233897 G>A maps to NM_012113.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr8:86392931 G>T maps to NM_000067.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:86357416 C>T maps to NM_005181.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:86352058 T>C maps to NM_005181.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:86354305 G>A maps to NM_005181.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:58236673 G>T maps to NM_000717.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:58234888 A>T maps to NM_000717.3 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:58236700 G>T maps to NM_000717.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:87921827 C>T maps to NM_001739.1 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:87936057 A>T maps to NM_001739.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:15794884 A>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:15768255 A>T did not map to a codon.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr23:15800701 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:9009427 C>A maps to ENST00000413627 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:9009397 A>G maps to ENST00000413627 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:66880939 G>T maps to NM_005182.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61144929 C>T maps to NM_004056.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:61137141 C>A maps to NM_004056.4 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:35674214 G>T maps to NM_001216.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:49906178 T>A maps to NM_001079670.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:227152831 G>A maps to NM_020247.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:227170665 C>T maps to NM_020247.4 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:227149097 A>T maps to NM_020247.4 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:24509554 C>T maps to NM_012295.3 A1380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24458475 A>T maps to NM_012295.3 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:24445598 C>T maps to NM_012295.3 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:24451494 C>A maps to NM_012295.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr22:24447323 G>T maps to NM_012295.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr22:24452751 C>A maps to NM_012295.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr22:24561545 C>T maps to NM_012295.3 F1653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr22:24509644 G>A maps to NM_012295.3 K1410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr22:24483437 G>T maps to NM_012295.3 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:20716571 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr20:60967530 C>T maps to NM_031215.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr20:60966385 C>T maps to NM_031215.2 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:121098633 T>A maps to NM_001033677.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:121098585 C>T maps to NM_001033677.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr12:121093915 C>A maps to ENST00000453000 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:48533814 C>T maps to NM_019855.3 *174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:21735703 T>A maps to NM_138644.1 L80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:21735968 C>G maps to NM_138644.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:21739820 C>T maps to NM_138644.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:21735743 T>C maps to NM_138644.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr18:21736784 T>C maps to NM_012189.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr1:65107575 G>A maps to ENST00000371073 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:13395963 C>A maps to NM_023035.2 E1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:13419010 G>T maps to NM_023035.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:13325396 G>A maps to NM_023035.2 D1923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:13397779 T>C maps to NM_023035.2 K1034K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:13476191 T>A maps to NM_023035.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:13365935 G>A maps to NM_023035.2 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:13335574 C>T maps to NM_023035.2 R1883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:13335576 G>T maps to NM_023035.2 R1883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:13414674 G>A maps to NM_023035.2 N671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:13470425 G>T maps to NM_023035.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:13410156 G>A maps to NM_023035.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:13323473 G>T maps to NM_023035.2 P2011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:13418935 G>T maps to NM_023035.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:140852089 G>A maps to ENST00000277549 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:140777194 G>C did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr9:140953580 C>T maps to ENST00000277549 I1509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr9:140968457 G>T maps to ENST00000277549 L1600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr9:140777251 C>T maps to ENST00000277549 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr9:140952656 G>A maps to ENST00000277549 E1422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:140772561 C>A maps to ENST00000277549 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:140907687 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:140972590 G>T maps to ENST00000277549 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:140850263 G>T maps to ENST00000277549 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr9:140938286 G>A maps to ENST00000277549 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr9:140952584 G>T maps to ENST00000277549 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:141010080 G>C maps to ENST00000277549 R1910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:140880888 G>T maps to ENST00000277549 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:140919613 G>T maps to ENST00000277549 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:140968056 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr9:140953544 C>A maps to ENST00000277549 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr9:140953544 C>T maps to ENST00000277549 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr9:140953136 C>A maps to ENST00000277549 Y1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:2614018 C>G maps to NM_199460.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:2721097 C>A maps to NM_199460.2 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:2775888 C>A maps to NM_199460.2 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:2797764 C>A maps to NM_199460.2 S2062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:2794919 C>T maps to NM_199460.2 D1947D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:2786942 G>A maps to NM_199460.2 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:2675716 C>T maps to NM_199460.2 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:2714277 C>T maps to NM_199460.2 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:2788839 C>A maps to NM_199460.2 A1822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:2778096 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:2786311 C>A maps to NM_199460.2 Y1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:2705066 C>T maps to NM_199460.2 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:2613702 C>T maps to ENST00000399634 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:2775902 G>A maps to NM_199460.2 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr12:2224660 G>A maps to NM_199460.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:2621975 A>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:2566831 C>T maps to NM_199460.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr12:2694554 G>T maps to NM_199460.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr12:2224519 G>T maps to NM_199460.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:2659169 C>A maps to NM_199460.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:2694619 G>A maps to NM_199460.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:2797641 C>A maps to NM_199460.2 L2021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:2716161 C>T maps to NM_199460.2 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr12:2602398 G>A maps to NM_199460.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:2763056 C>A maps to NM_199460.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:2760807 C>T maps to NM_199460.2 N1364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:2224441 G>T maps to NM_199460.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:2229538 C>A maps to NM_199460.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:2692049 C>A maps to NM_199460.2 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:53785858 C>G maps to NM_001128840.1 Y1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:53694291 A>T maps to NM_001128840.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:53694252 C>T maps to NM_001128840.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:53700465 G>C maps to NM_001128840.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr3:53699685 G>T did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr3:53808687 G>T maps to NM_001128840.1 A1395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:53820924 A>G maps to NM_001128840.1 K1623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:181705561 C>T maps to ENST00000357570 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181701954 G>C maps to ENST00000357570 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:181745259 C>A maps to ENST00000357570 V1721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:181701819 C>T maps to ENST00000357570 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:181752855 G>T maps to ENST00000357570 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181546993 C>A maps to ENST00000357570 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:181705571 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:181727928 G>C maps to ENST00000357570 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:181702005 A>T maps to ENST00000357570 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:181701771 C>T maps to ENST00000357570 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:181763997 A>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:181767573 C>T maps to ENST00000357570 I2182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:181708383 T>A maps to ENST00000357570 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:181741333 C>A maps to ENST00000357570 Y1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:181690943 C>G maps to ENST00000357570 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr1:181732648 C>A maps to ENST00000357570 T1599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:181745280 C>A maps to ENST00000357570 Y1728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:181727922 G>A maps to ENST00000357570 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:181620520 C>T maps to ENST00000357570 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:181548221 T>C maps to ENST00000357570 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:181767567 C>A maps to ENST00000357570 G2180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:181687189 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:181620523 C>T maps to ENST00000357570 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:181726249 G>T maps to ENST00000357570 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:181689447 C>T maps to ENST00000357570 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:181702857 C>T maps to ENST00000357570 D1078D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:181735734 C>A maps to ENST00000357570 I1623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:181702612 G>T maps to ENST00000357570 G997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:181693669 C>A maps to ENST00000357570 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:181764046 G>C maps to ENST00000357570 R2025R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:181480506 G>T maps to ENST00000357570 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:181705534 C>T maps to ENST00000357570 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:181546974 C>A maps to ENST00000357570 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:181707531 G>T maps to ENST00000357570 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:181689991 G>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:181767763 G>T maps to ENST00000357570 E2246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:181754454 C>A maps to ENST00000357570 A1860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr1:181702134 A>C maps to ENST00000357570 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:49068405 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:49063080 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:49063212 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:49063288 C>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:49088146 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:49079431 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:49083470 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:49070668 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:49072003 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:49068425 C>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:49067063 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:49086700 C>G did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:49084727 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:49079279 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:49070319 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:49068418 T>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:49079434 G>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:49083419 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:49065116 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:49077498 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:49067839 C>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:49076961 C>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:49068379 G>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:49066114 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:49067054 A>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:49067056 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:49070314 C>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:49063211 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:49070709 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:49070710 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:49065125 G>T did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:49066185 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:49063299 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:49063316 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:49084715 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:48649378 C>T maps to NM_018896.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:48646275 G>A maps to NM_018896.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:48655738 C>A maps to NM_018896.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:48699018 A>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:48655861 C>A maps to NM_018896.3 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:48680440 C>T maps to NM_018896.3 D1350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:48683416 G>T maps to NM_198397.1 V1485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:48696026 G>A maps to NM_018896.3 R1813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:48697132 G>T maps to NM_018896.3 G1957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:48696098 G>A maps to NM_018896.3 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr17:48699155 G>C did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:48701338 G>T maps to NM_018896.3 T2044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:1251718 G>T maps to NM_021098.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr16:1250432 C>T maps to NM_021098.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:1260866 G>T maps to NM_021098.2 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:1261983 C>T maps to NM_021098.2 F1535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr16:1261986 C>T maps to NM_021098.2 I1536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:1260935 C>A maps to NM_021098.2 R1396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:1255175 G>A maps to NM_021098.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:1270531 C>T maps to NM_021098.2 D2200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr22:40066958 G>C maps to NM_021096.3 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:40055838 G>T maps to NM_021096.3 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:39996547 C>T maps to NM_021096.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr22:39966876 G>A maps to NM_021096.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr22:40066943 C>T maps to NM_021096.3 H1508H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:40080421 T>A maps to NM_021096.3 T1982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr22:40055835 G>T maps to NM_021096.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:40068256 G>A maps to NM_021096.3 V1531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr22:40066859 C>A maps to NM_021096.3 I1480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr22:40066161 G>A maps to NM_021096.3 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:40036943 G>T maps to NM_021096.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr22:40061946 C>A maps to NM_021096.3 S1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:40036946 G>T maps to NM_021096.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:40055064 C>A maps to NM_021096.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:40060148 C>A maps to NM_021096.3 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr22:40030582 G>T maps to NM_021096.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr22:40059773 C>A maps to NM_021096.3 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr22:40036946 G>T maps to NM_021096.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:201028376 C>A maps to NM_000069.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:201044701 C>A maps to NM_000069.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:201030580 G>T maps to NM_000069.2 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:201043677 G>T maps to NM_000069.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:201052308 G>A maps to NM_000069.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:201044650 G>A maps to NM_000069.2 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:201054579 A>C maps to NM_000069.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:201061157 G>T maps to NM_000069.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:201079290 C>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:201054079 G>A maps to NM_000069.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:201030556 C>T maps to NM_000069.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:201019617 G>T maps to NM_000069.2 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:201047119 G>A maps to NM_000069.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:201028355 G>T maps to NM_000069.2 T1162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:201036049 C>A maps to NM_000069.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:201046248 C>T maps to NM_000069.2 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:201030408 G>A maps to NM_000069.2 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:81643765 T>C maps to NM_000722.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:81634804 G>A maps to NM_000722.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:81693627 C>A maps to NM_000722.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:81714109 G>C maps to NM_000722.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:81612628 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:81765971 G>A maps to NM_000722.2 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:81579776 C>A maps to NM_000722.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:81579741 C>T maps to NM_000722.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:82072744 G>A maps to NM_000722.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:81598290 T>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:81611923 T>A maps to NM_000722.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:81603858 G>T maps to NM_000722.2 C655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:81593627 C>A maps to NM_000722.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:81964567 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:50431584 A>C maps to ENST00000435965 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:54872615 G>T maps to NM_018398.2 G498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:54913115 G>T maps to NM_018398.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:54604085 C>G maps to NM_018398.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:54615853 G>T maps to NM_018398.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:54871257 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:54798281 G>A maps to NM_018398.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:2016648 C>T maps to NM_172364.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:1949932 G>T maps to NM_172364.4 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:2024089 C>T maps to NM_172364.4 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:2022227 G>A maps to NM_172364.4 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:1965187 T>A maps to NM_172364.4 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:1965193 C>T maps to NM_172364.4 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:2024043 G>T maps to NM_172364.4 Y95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:1969333 C>G maps to NM_172364.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:1994017 G>T maps to NM_172364.4 C396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:2027606 G>C maps to NM_172364.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:1965175 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:2022272 G>T maps to NM_172364.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:1919485 G>A maps to NM_172364.4 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:1910244 C>T maps to NM_172364.4 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:1967761 C>T maps to NM_172364.4 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37343839 T>C maps to NM_000723.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:37341403 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:37340311 A>T maps to NM_000723.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:37343116 G>A maps to NM_000723.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:37331622 C>T maps to NM_000723.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr17:37343068 C>T maps to NM_000723.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:18439904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:18825106 A>G maps to NM_201596.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:18787303 G>C maps to NM_201596.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:18803261 C>A maps to NM_201596.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:18789787 T>A maps to NM_201596.2 C168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:18439884 C>G maps to NM_201596.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:18789835 G>T maps to NM_201596.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr10:18825058 G>T maps to NM_201596.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:49220591 G>T maps to NM_000725.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:49221498 C>T maps to NM_000725.2 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:49217130 C>G maps to NM_000725.2 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:152954855 G>A maps to NM_000726.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:152739885 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65040955 C>A maps to NM_000727.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr17:65040853 C>A maps to NM_000727.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:24373039 C>A maps to NM_006539.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr16:24366256 C>T maps to NM_006539.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:24372670 A>T did not map to a codon.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr16:24358137 C>T maps to NM_006539.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr16:24268206 T>A maps to NM_006539.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:24373033 C>A maps to NM_006539.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:24268275 C>A maps to NM_006539.3 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:64961110 C>T maps to NM_014405.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr17:65026855 A>T maps to NM_014405.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:64875162 G>A maps to NM_014404.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:64873632 C>A maps to NM_014404.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:64881045 G>T maps to NM_014404.1 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:64880888 G>A maps to NM_014404.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:64881146 G>T maps to NM_145811.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:64873599 C>A maps to NM_014404.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:64873599 C>A maps to NM_014404.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:64881119 G>T maps to NM_145811.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:64880786 C>A maps to NM_014404.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:64873632 C>A maps to NM_014404.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:64881146 G>T maps to NM_145811.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:64875123 T>A maps to NM_014404.1 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:54502969 C>A maps to NM_145814.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:54515440 T>A maps to NM_145814.1 *261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:54502939 C>A maps to NM_145814.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:54515346 G>T maps to NM_145814.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:54444823 C>T maps to NM_031896.4 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:54445372 C>T maps to NM_031896.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:54417827 G>T maps to NM_031896.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:54418757 G>T maps to NM_031896.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:54466476 C>G maps to NM_031895.5 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:54485394 G>A maps to NM_031895.5 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:54466458 G>T maps to NM_031895.5 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr19:54483187 C>A maps to NM_031895.5 C145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:27458429 G>T maps to NM_004341.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:27457405 T>A maps to NM_004341.3 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:27459688 C>T maps to NM_004341.3 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr2:27463182 C>T maps to NM_004341.3 F1849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:27456886 G>A maps to NM_004341.3 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:27462632 A>C maps to NM_004341.3 P1821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:27461928 G>A maps to NM_004341.3 E1694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:27466161 T>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:27455009 G>T maps to NM_004341.3 G855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:27462665 G>T maps to NM_004341.3 T1832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:27465739 G>T maps to NM_004341.3 E2127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:27446490 G>A maps to NM_004341.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:115080336 G>A maps to NM_014333.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:86010711 G>A maps to NM_153184.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:86115878 C>A maps to NM_153184.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:85932593 G>T did not map to a codon.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr3:85932501 C>A maps to NM_153184.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:85932529 C>T maps to NM_153184.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:86115872 C>A maps to NM_153184.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:86028410 T>A maps to NM_153184.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:85961611 G>T maps to NM_153184.3 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:86010618 G>T maps to NM_153184.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:159163315 G>T maps to NM_021189.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:159170654 C>T maps to NM_021189.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:159166235 C>A maps to NM_021189.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:159166836 C>A maps to NM_021189.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:159163810 T>A maps to NM_021189.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:159169550 G>T maps to NM_021189.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:159170597 C>A maps to NM_021189.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:159166833 C>A maps to NM_021189.3 Y346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:159166199 G>A maps to NM_021189.3 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:159162392 G>T maps to NM_021189.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:159163771 G>C maps to NM_021189.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:159162410 C>T maps to NM_021189.3 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:159161786 C>T maps to NM_021189.3 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:159161787 C>T maps to NM_021189.3 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:62739207 G>A maps to ENST00000383709 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:62751547 C>A maps to ENST00000383709 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:62478118 G>T maps to ENST00000383709 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:62860686 G>A maps to ENST00000383709 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:62636554 G>T maps to ENST00000383709 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:62423880 G>T maps to ENST00000383709 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:62631518 C>A did not map to a codon.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr3:62385095 G>A maps to ENST00000383709 D1354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr3:62464058 C>T maps to ENST00000383709 W1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:62503855 T>A maps to ENST00000383709 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:62739366 T>A maps to ENST00000383709 K213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:62860635 C>A maps to ENST00000383709 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:122261606 T>C maps to NM_001167940.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:122091529 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:122261579 C>T maps to NM_001167940.1 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:122221322 G>A maps to NM_001167940.1 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:7356308 G>C maps to NM_001170692.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:7334276 T>A maps to NM_001170692.1 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:7365745 G>T maps to NM_001170692.1 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr6:7370187 A>G maps to NM_001170692.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr6:7378909 A>C maps to NM_001170692.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:91090663 A>T maps to NM_004929.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:91094280 G>T maps to NM_004929.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:71417905 T>C maps to NM_001740.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:71418736 A>T maps to NM_001740.4 K209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr16:71423650 G>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr16:71423651 G>T maps to NM_001740.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:71418247 G>C maps to NM_001740.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:71411574 G>T maps to NM_001740.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:14990344 T>C maps to NM_001741.2 *142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:14992651 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr11:14991611 C>G maps to NM_001741.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:15098939 C>A maps to NM_000728.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:15096642 C>A maps to NM_000728.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:15098834 C>G maps to NM_000728.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:54110042 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:54109681 C>A maps to NM_020898.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:54109066 G>A maps to NM_020898.2 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:93065407 G>T maps to NM_001164737.1 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:93065483 T>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:93065452 G>A maps to NM_001164737.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:93065290 G>T maps to NM_001164737.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:93067544 G>T maps to NM_001164737.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:93063563 C>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:93065449 C>A maps to NM_001164737.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:93101688 T>A maps to NM_001164737.1 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr7:93055879 G>A maps to NM_001164737.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:93108765 C>T maps to NM_001164737.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr7:93055668 C>G maps to NM_001164737.1 *509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:93116257 C>A maps to NM_001164737.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:188225373 G>T maps to NM_005795.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:188243734 C>A maps to NM_005795.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:188223967 G>A maps to NM_005795.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:188243759 T>A did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr7:134645357 G>A maps to NM_033138.3 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:134632510 C>G maps to NM_033138.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:134552501 T>A maps to NM_033138.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr7:134644744 T>A maps to NM_033138.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:105215147 C>A maps to NM_001001412.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:105215318 G>T maps to NM_001001412.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr10:105218097 T>G maps to NM_001001412.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:105209506 G>A maps to NM_015916.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:105209245 G>T maps to NM_015916.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:105209689 G>T maps to NM_015916.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90870297 C>T maps to NM_006888.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:47112164 G>A maps to NM_005184.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:5567425 C>A maps to NM_005185.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:5541245 G>T maps to NM_017422.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr1:1848604 G>A maps to NM_138705.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:71275384 G>T maps to NM_031468.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:71488746 G>T maps to NM_031468.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:71571171 C>A maps to NM_031468.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr7:71488668 C>T maps to NM_031468.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:71252834 G>T maps to NM_031468.3 C237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13050437 C>T maps to NM_004343.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:16595991 C>T maps to NM_145046.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:135140379 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149631369 C>A maps to NM_015981.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:149636357 G>T maps to NM_015981.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:149644578 C>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:149633052 G>A maps to NM_015981.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:44282849 A>T maps to NM_001220.4 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:44259816 G>T maps to NM_001220.4 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:44272447 G>A maps to NM_001220.4 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:44268413 T>A maps to NM_001220.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:44266241 G>C maps to NM_001220.4 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:114386722 C>T maps to ENST00000515496 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:75607835 G>T maps to ENST00000423381 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:110814168 C>A maps to NM_001744.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr5:110782424 A>T maps to NM_001744.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:110730452 C>G maps to NM_001744.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:110730480 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:110730468 G>T maps to NM_001744.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr5:110784899 C>A maps to NM_001744.4 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:3785656 C>T maps to ENST00000381771 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr17:3788921 C>A maps to ENST00000381771 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:3779707 G>A maps to ENST00000381771 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:121687628 G>A maps to NM_006549.3 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:49899270 C>T maps to NM_024046.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:49897038 G>A maps to NM_024046.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:134077086 G>T maps to NM_001745.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:134077173 T>C maps to NM_001745.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:138714661 C>G maps to ENST00000409386 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:138713800 C>A maps to ENST00000409386 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:138710462 C>A did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr9:138719299 C>T maps to ENST00000409386 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr9:138714220 G>A maps to ENST00000409386 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:200817727 G>T maps to ENST00000236925 G622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:200817336 A>G maps to ENST00000236925 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:200819109 A>G maps to ENST00000236925 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:200818116 G>T maps to ENST00000236925 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:200816774 T>C maps to ENST00000236925 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:200818569 G>A maps to ENST00000236925 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:200730087 C>G maps to ENST00000236925 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:200818378 G>T maps to ENST00000236925 G839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr1:200730066 A>G maps to ENST00000236925 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:7797433 G>T maps to NM_015215.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:7527930 C>T maps to NM_015215.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr1:7700569 G>A maps to NM_015215.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr1:7792637 G>T maps to NM_015215.2 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:7724187 C>T maps to NM_015215.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:7797499 G>A maps to NM_015215.2 Q1176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:7737719 G>T maps to NM_015215.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:7724661 G>T maps to NM_015215.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:7724721 C>T maps to NM_015215.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7792505 A>G did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:7737752 C>A maps to NM_015215.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr1:7723641 C>T maps to NM_015215.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:7724157 C>A maps to NM_015215.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:7527939 G>C maps to NM_015215.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr17:4873762 G>A maps to NM_015099.3 F959F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-78-8662-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:67698482 A>T maps to NM_018448.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:67699248 G>T maps to NM_018448.3 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:67675716 G>T maps to NM_018448.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:67696223 C>T maps to NM_018448.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:67696181 A>C maps to NM_018448.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:12854498 G>C maps to NM_001162499.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:12845082 G>T maps to NM_001162499.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr3:12858984 C>T maps to NM_001162499.1 Q852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:76993506 G>A maps to NM_138793.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:40529939 C>A maps to NM_001105530.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:17539604 G>T maps to NM_006366.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:64974040 C>T maps to NM_005186.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64950963 G>T maps to NM_005186.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr2:241534097 G>A maps to NM_023083.3 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:241534568 G>T maps to NM_023083.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:241536199 G>T maps to NM_023083.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:241528797 A>T maps to NM_023083.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:241537462 A>C maps to NM_023083.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:44144682 C>T maps to NM_007058.3 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:30975917 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:30974118 T>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr2:30966340 C>A maps to ENST00000295055 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:30955325 C>A maps to ENST00000295055 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:30993186 G>C maps to ENST00000295055 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:30977171 C>A maps to ENST00000295055 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:30977172 C>A maps to ENST00000295055 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:223940635 G>T maps to NM_001748.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:223947006 C>T maps to NM_001748.4 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr15:42680048 G>A maps to NM_000070.2 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:42678467 G>A maps to NM_000070.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:42695110 C>T maps to NM_000070.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:42676730 C>T maps to NM_000070.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr15:42676713 G>T maps to NM_000070.2 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:76823720 C>T maps to ENST00000360841 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76834861 G>A maps to ENST00000360841 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:76833669 C>A maps to ENST00000360841 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:110494844 C>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr23:110496279 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:110489965 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:110497564 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:110489961 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:110494828 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:110494201 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:110494908 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:110494869 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:110494895 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:110490608 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:110494470 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:110497516 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:110490675 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:110494309 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:110494159 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:110490683 G>C did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:110495655 A>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:110489914 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:110495658 G>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:110497505 C>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:110497506 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:110492208 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:110490690 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:110494263 T>C did not map to a codon.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr23:110495621 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:110494190 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:110494153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230916349 C>T maps to NM_006615.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:230910378 T>A did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:230904924 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:36633999 C>T maps to NM_001749.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55601072 G>A maps to NM_032330.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:34113551 C>T maps to NM_005898.4 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:34118026 G>T maps to NM_005898.4 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:34097943 A>G maps to NM_005898.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:30863315 A>T maps to NM_001002259.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:30888022 C>A maps to NM_001002259.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:30872087 T>C maps to NM_001002259.1 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:30883195 G>A maps to NM_001002259.1 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr12:30881635 G>A maps to NM_001002259.1 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:30872147 G>A maps to NM_001002259.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:5915066 C>G maps to ENST00000394521 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:75676094 G>A maps to NM_032606.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:75692560 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:35921165 G>T maps to NM_144647.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:35910560 G>T maps to NM_144647.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr5:35904742 G>A maps to NM_144647.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:35910465 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr5:35910140 G>A maps to NM_144647.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:35921197 G>T maps to NM_144647.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:116552134 G>T maps to NM_006136.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:18891235 G>T maps to NM_033328.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:18891414 C>A maps to NM_033328.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr12:18892100 A>G maps to NM_033328.2 *300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:37906347 C>A maps to NM_014550.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr22:37913978 G>A maps to NM_014550.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr22:37902245 G>A maps to NM_014550.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:2959088 C>T maps to NM_032415.4 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr7:2985558 C>T maps to NM_032415.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:2949712 C>T maps to NM_032415.4 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:2962897 C>G maps to NM_032415.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:2972220 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:2987299 C>A maps to NM_032415.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr7:2987386 C>T maps to NM_032415.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:2946433 G>T maps to NM_032415.4 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:2966388 G>A maps to NM_032415.4 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:2954904 C>G maps to NM_032415.4 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:2987265 G>A maps to NM_032415.4 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:78162252 G>C maps to NM_024110.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:78156488 C>T maps to NM_024110.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr17:78163583 C>T maps to NM_024110.2 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:78169366 G>T maps to NM_024110.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:78175556 C>A maps to NM_024110.2 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr17:78163549 A>T did not map to a codon.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr11:104912155 A>G maps to NM_001017534.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:104915303 A>C maps to NM_001017534.1 L30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:104912369 T>A maps to NM_001017534.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:104912186 T>C maps to NM_001017534.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:104970148 C>G did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:105009605 G>T maps to NM_021571.3 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:105009614 G>T maps to NM_021571.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:40853101 C>T maps to NM_032587.3 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:40854019 A>G maps to NM_032587.3 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:40843719 A>T maps to NM_032587.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:40853443 C>T maps to NM_032587.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:40852496 A>T maps to NM_032587.3 K355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr5:40852461 C>G maps to NM_032587.3 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:48734061 G>A maps to NM_001184900.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr9:139261261 G>C maps to NM_052813.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr9:139265295 C>A maps to NM_052813.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:8949173 C>T maps to NM_014316.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:111274656 T>A maps to NM_018210.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:111277565 C>T maps to NM_018210.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:11032405 G>A maps to NM_199141.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr19:11024704 C>T maps to NM_199141.1 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr19:11032423 C>T maps to NM_199141.1 Y606Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-86-8674-01A-21D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:3038338 C>T maps to NM_001014437.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:111353783 C>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr13:111340149 C>G maps to NM_024537.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr13:111340149 C>A maps to NM_024537.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:25272229 G>C maps to NM_018272.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:25302608 C>A maps to NM_018272.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:25261484 G>T maps to NM_018272.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr17:38318121 C>T maps to NM_007359.4 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr17:38319154 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr17:38297832 G>T maps to NM_007359.4 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:38319961 G>T maps to NM_007359.4 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:44581415 G>A maps to NM_138423.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:44620905 G>T maps to NM_138423.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:44630105 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:40912854 T>C maps to NM_170589.3 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:40917838 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:40902475 G>C maps to NM_170589.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr15:40916160 C>T maps to NM_170589.3 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:40949551 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:94180651 A>T maps to NM_022900.4 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:41519761 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:41519768 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:41448844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:41604854 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:41495913 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:41390394 T>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:41524662 T>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:41646517 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:41419064 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:2229899 G>T maps to NM_020764.3 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:2239497 C>G maps to NM_020764.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr16:2237440 G>A maps to NM_020764.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr16:2233718 C>T maps to NM_020764.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr16:2239497 C>A maps to NM_020764.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:73500775 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:73499757 C>T maps to NM_020753.3 W554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr17:73498481 C>T maps to NM_020753.3 E891E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:104901056 C>A maps to NM_033292.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:104901095 C>A maps to NM_033292.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:104905106 C>T maps to NM_033292.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:104899950 A>G maps to NM_033292.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:104905201 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:104901910 C>T maps to NM_033292.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:202074064 C>T maps to NM_032977.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:15166239 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:142989753 G>A maps to NM_032982.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:142997068 G>T maps to NM_032982.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:142991329 G>T maps to NM_032982.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:143000938 G>T maps to NM_032982.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:185552920 G>A maps to NM_032991.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:104871219 A>G maps to NM_001136112.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:104872880 G>A maps to NM_001136112.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:104872925 G>T maps to NM_001136112.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:104868129 G>A maps to NM_001136112.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:110612132 G>A maps to NM_001226.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:115481471 C>T maps to NM_033338.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:202131374 G>T maps to NM_001080125.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:90576191 A>G maps to NM_012115.3 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:90576932 A>T maps to NM_012115.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:90577103 G>T maps to NM_012115.3 G1365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90573713 C>T maps to NM_012115.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:90577241 G>T maps to NM_012115.3 V1411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:15819509 C>T maps to NM_001229.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:15834373 T>A maps to NM_001229.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:160163609 T>C maps to NM_001231.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:160165727 C>T maps to NM_001231.4 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:160164818 G>A maps to NM_001231.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:160160606 G>T maps to NM_001231.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:160160687 G>C maps to NM_001231.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:160171073 C>T maps to NM_001231.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:116269692 T>C maps to NM_001232.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:116243866 C>A maps to NM_001232.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr1:116310961 T>C maps to NM_001232.3 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:121994735 G>A maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:122002777 C>T maps to NM_001178065.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:122002642 C>T maps to NM_001178065.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:121980613 C>G maps to NM_001178065.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr3:122003063 G>T maps to NM_001178065.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:121980793 G>C maps to NM_001178065.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:122003779 G>T maps to NM_001178065.1 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:121980670 G>A maps to NM_001178065.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:122003455 C>A maps to NM_001178065.1 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:122002828 G>T maps to NM_001178065.1 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:55027542 G>T maps to NM_020356.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:55012272 G>T maps to NM_020356.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:55012263 T>A maps to NM_020356.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:55025689 C>A maps to NM_020356.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr20:55012296 G>T maps to NM_020356.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr20:55033748 G>A maps to NM_020356.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:55033538 C>T maps to NM_020356.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:55020993 G>A maps to NM_020356.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:55026873 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:55026918 C>T maps to NM_020356.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:10714190 G>A maps to NM_001079843.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:10713920 C>A maps to NM_001079843.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:10711080 C>A maps to NM_001079843.1 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:34473747 C>T maps to NM_001752.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:65789114 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:65793535 G>C maps to NM_053054.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:65787786 C>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:65788968 G>C maps to NM_053054.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:43927613 C>T maps to NM_172095.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:43939635 C>A maps to NM_172095.1 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:43939615 C>A maps to NM_172095.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:134345147 C>T maps to NM_178019.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:26527427 C>T maps to NM_198137.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:26517183 C>A maps to NM_198137.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:26517186 G>T maps to NM_198137.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:92083976 T>A maps to NM_024764.2 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:92136301 G>T maps to NM_024764.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr14:92150219 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr14:92150223 C>A maps to NM_024764.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:38849156 G>A maps to NM_021185.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:38858711 G>T maps to NM_021185.4 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:38845473 C>T maps to NM_021185.4 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:38858212 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:38850211 G>A maps to NM_021185.4 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr7:116199022 A>G maps to NM_001753.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:8787363 C>A maps to NM_001234.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:32210931 C>T maps to NM_005093.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:88952472 G>T maps to NM_005187.5 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:119144583 A>T maps to NM_005188.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:119170449 G>T maps to NM_005188.2 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:105464840 C>A maps to NM_170662.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:105400604 C>T maps to NM_170662.3 K753K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:105378047 G>A maps to NM_170662.3 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:107398941 A>G maps to NM_024814.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:107399463 G>C maps to NM_024814.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:49315226 G>A maps to NM_004352.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr16:49313329 C>A maps to NM_004352.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:70209224 G>A maps to NM_182511.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr18:70209164 G>C maps to NM_182511.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr18:70205886 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr18:70209305 G>T maps to NM_182511.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:24897057 C>A maps to NM_001039771.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:54573762 C>A maps to NM_080617.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:54579044 C>A maps to NM_080617.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr20:54579039 G>T maps to NM_080617.4 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:37444819 C>T maps to NM_001757.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37518590 G>C maps to NM_001236.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr21:37518644 G>T maps to NM_001236.3 V223V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-J2-8194-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:44483092 G>A maps to ENST00000398168 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr21:44486389 G>A maps to ENST00000398168 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr21:44479403 G>A maps to ENST00000398168 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr21:44485370 G>A maps to ENST00000398168 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:154767 G>C maps to NM_018491.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:114202562 G>T maps to NM_172003.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:114220011 C>G maps to NM_172003.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:77757745 C>T maps to NM_005189.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:77757820 G>T maps to NM_005189.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr17:77758642 G>A maps to NM_005189.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:77755611 C>T maps to NM_032647.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:77755713 G>A maps to NM_032647.3 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:77755767 C>T maps to NM_032647.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr7:26242642 G>A did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr7:26246106 C>T maps to NM_016587.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr7:26251376 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:77807853 C>G maps to NM_003655.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr12:54645823 C>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:54635661 A>T maps to NM_012117.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:77768511 C>G maps to NM_020649.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr22:39069239 G>A maps to NM_015373.3 *127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:14024010 G>T maps to NM_017721.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:14031677 G>A maps to NM_017721.4 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:52819277 C>A maps to NM_032449.2 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:15581638 C>T maps to NM_001080522.2 Q1274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:97776051 T>A maps to NM_001159747.1 L168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:97779093 T>C maps to NM_001159747.1 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:97773579 T>C maps to NM_001159747.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr10:70532743 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:70516154 C>G maps to NM_018237.2 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr10:70548066 T>C maps to NM_018237.2 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:70516188 G>A maps to NM_018237.2 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:57106908 C>T maps to NM_133459.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:57134022 C>A maps to NM_133459.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:57115239 G>T maps to NM_133459.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr18:57106777 A>C maps to NM_133459.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:131596096 C>A maps to NM_004059.4 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:89401928 C>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:89434415 A>G maps to NM_001008661.2 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr3:42906617 C>T maps to NM_001296.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr18:66504395 A>G maps to NM_024781.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:66504560 T>C maps to NM_024781.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:66721317 G>T maps to NM_024781.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:66504518 A>G maps to NM_024781.2 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:15131384 C>A maps to NM_173482.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:15121887 T>A maps to NM_173482.2 L84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:15132451 C>T maps to NM_173482.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr9:35658645 G>C maps to NM_174923.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:219893020 G>T maps to NM_194302.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:219894145 C>T maps to NM_194302.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219870196 C>T maps to NM_194302.2 Q1670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:219886502 G>T maps to NM_194302.2 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:219869056 G>A maps to NM_194302.2 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:219885895 G>T maps to NM_194302.2 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219896344 C>T maps to NM_194302.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:219903120 A>G maps to NM_194302.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr2:219892557 G>T maps to NM_194302.2 C675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:219896376 C>A maps to NM_194302.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:219890812 C>A maps to NM_194302.2 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:219895921 A>G maps to NM_194302.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:219890791 G>A maps to NM_194302.2 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:219870855 G>A maps to NM_194302.2 C1603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:219892500 G>A maps to NM_194302.2 C694C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:219874158 C>T maps to NM_194302.2 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:74628614 G>C maps to NM_138357.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:74631208 C>G maps to NM_138357.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr18:47753780 G>A maps to NM_145020.3 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr18:47778105 C>T maps to NM_145020.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:114607026 G>C maps to NM_001040440.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr16:58301477 A>G maps to NM_014157.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr19:48807228 C>A maps to NM_144577.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:21988399 C>T maps to NM_152612.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr22:21991355 C>A maps to NM_152612.2 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr22:21989500 A>G maps to NM_152612.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:21991044 C>T maps to NM_152612.2 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:48923038 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:48921446 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:48920018 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:48920061 G>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:48919855 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:48924953 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:48921476 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:48924720 C>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:44411448 G>T maps to NM_144974.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:44442841 C>G maps to NM_144974.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr13:44442841 C>G maps to NM_144974.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:33392155 G>A maps to NM_032816.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:33370118 G>A maps to NM_032816.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:33439178 T>C maps to NM_032816.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:33450885 G>T maps to NM_032816.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33424516 T>A maps to NM_032816.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr19:18054499 C>T maps to NM_001136203.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:68578627 C>T maps to NM_176816.3 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr7:23682709 G>A maps to NM_138771.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:205500 T>G maps to NM_145265.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:206056 C>T maps to NM_145265.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:205458 C>A maps to NM_145265.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:31592659 G>T maps to NM_194300.2 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:31617852 A>G maps to NM_194300.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:31682504 G>T maps to NM_194300.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:31682378 C>A maps to NM_194300.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:31683377 C>A maps to NM_194300.2 C798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:31691582 T>A maps to NM_194300.2 R914R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-8119-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:31683039 C>T maps to NM_194300.2 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:31617510 G>T maps to NM_194300.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:31683323 C>T maps to NM_194300.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:31617612 C>T maps to NM_194300.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:31683158 C>A maps to NM_194300.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:42784549 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:42777197 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:42781128 G>A maps to NM_144719.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:42750504 C>T maps to NM_144719.3 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:92978025 A>G maps to NM_017667.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:42209752 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:57765152 C>T maps to NM_032269.5 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:57765097 G>T maps to NM_032269.5 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr16:57734100 C>T maps to NM_032269.5 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:128454718 G>T maps to NM_022742.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:128446837 G>T maps to NM_022742.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:79639109 G>C maps to NM_199287.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109408184 A>G maps to NM_144978.1 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109415039 G>T maps to NM_144978.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:109432410 G>A maps to NM_144978.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:123633787 A>G maps to NM_022757.4 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:123633772 A>C maps to NM_022757.4 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:123634224 T>A maps to NM_022757.4 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:223168735 C>T maps to NM_153038.1 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:179718291 T>C maps to NM_173648.3 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:179701636 C>A maps to NM_173648.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:179701811 G>T maps to NM_173648.3 T1378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:179742774 C>A maps to NM_173648.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr2:179736894 G>A maps to NM_173648.3 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179714840 T>A maps to NM_173648.3 K1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr2:179733927 G>A maps to NM_173648.3 H770H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-NJ-A4YQ-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:74708962 C>G maps to ENST00000393965 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:16664736 A>T did not map to a codon.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr17:16612934 C>T maps to NM_014695.1 Q522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:16612579 C>T maps to NM_014695.1 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:16593878 A>G maps to NM_014695.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:16612466 G>T maps to NM_014695.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:76891543 A>T maps to NM_020879.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:106152063 C>A maps to NM_001008723.1 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:106121899 G>C maps to NM_001008723.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:106139942 C>A maps to NM_001008723.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr10:106214272 C>A maps to NM_001008723.1 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr10:106121911 A>T maps to NM_001008723.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:159166147 C>A maps to NM_138803.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:159166102 G>A maps to NM_138803.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:159033119 T>C maps to NM_138803.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:24838914 C>A maps to NM_001130726.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:124857202 C>T maps to NM_025004.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:124857316 G>T maps to NM_025004.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:197565879 G>T maps to NM_001080539.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr2:197584363 A>T maps to NM_001080539.1 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:11531871 G>T maps to NM_145045.4 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:49894163 G>A maps to NM_144688.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr22:30762168 C>T maps to NM_001017437.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr22:30771483 C>T maps to NM_001017437.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77290614 G>T maps to NM_001042784.1 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:77300478 A>G maps to NM_001042784.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:77283378 T>C maps to NM_001042784.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:77288728 A>G maps to NM_001042784.1 N516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:77274332 T>A maps to NM_001042784.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:133378843 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:46087338 G>A maps to NM_001114938.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:93672777 G>A maps to NM_206886.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:159860279 G>T maps to NM_012337.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:159858144 G>A maps to NM_012337.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:159858260 C>A maps to NM_012337.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:26603782 G>A maps to NM_022778.2 *763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:49093591 C>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:49093592 A>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:49105345 C>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:49093572 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:49106112 A>G did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr1:44461718 C>T maps to NM_152499.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:27610104 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:27598008 C>A maps to NM_018246.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:27606080 C>A maps to NM_018246.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:3669281 G>T maps to NM_152492.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3669110 G>T maps to NM_152492.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:3679922 C>A maps to NM_152492.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:3669272 G>T maps to NM_152492.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:3669131 C>A maps to NM_152492.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr1:3679970 C>T maps to NM_152492.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:3677975 C>A maps to NM_152492.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:3669224 C>T maps to NM_152492.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr10:12940463 C>T maps to NM_031455.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:43111811 A>T maps to NM_001080850.2 K633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43021929 C>T maps to NM_001080850.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:43111804 G>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119528 C>T maps to NM_001080850.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43119550 C>G maps to NM_001080850.2 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:43032145 G>A maps to NM_001080850.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:74554834 G>C maps to ENST00000321288 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:74574129 G>C maps to ENST00000321288 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:74573105 C>T maps to ENST00000321288 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:74559017 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:74623567 C>T maps to ENST00000321288 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr15:74610980 C>A maps to NM_182791.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:74554861 C>T maps to ENST00000321288 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:74560765 C>A maps to ENST00000321288 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:27379045 C>T maps to NM_030771.1 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:27371932 T>C maps to NM_030771.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:27378961 C>T maps to NM_030771.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr3:49293878 G>T maps to NM_178173.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr3:126153080 C>T maps to ENST00000505024 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr3:126138958 A>G maps to ENST00000505024 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:126152007 C>A maps to ENST00000505024 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:126132991 C>G maps to ENST00000505024 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:96292379 C>A maps to NM_182496.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:96284692 G>C maps to NM_182496.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:180366129 C>A maps to NM_181426.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:180378510 G>T maps to NM_181426.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:180372600 A>T maps to NM_181426.1 C293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:180381657 T>A maps to NM_181426.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:180381774 C>A did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr3:180377313 C>A maps to NM_181426.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:180359853 C>A maps to NM_181426.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:78063607 G>A maps to NM_017950.2 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:78073487 C>A maps to NM_017950.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:78022508 C>T maps to NM_017950.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr17:78055572 C>T maps to NM_017950.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:78063584 A>T maps to NM_017950.2 K912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78013807 T>C maps to NM_017950.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:78063593 C>T maps to NM_017950.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:94805586 G>A maps to NM_001042399.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:8638458 C>T maps to NM_144681.2 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:8647023 G>A maps to NM_144681.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:63898445 C>A maps to NM_145036.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:64125896 G>A maps to NM_145036.3 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr17:61843459 C>A maps to NM_020198.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61833628 C>A maps to NM_020198.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr17:61833644 G>A maps to NM_020198.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:128758689 G>A maps to NM_024768.2 *599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:128758556 G>T maps to NM_024768.2 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:128758689 G>A maps to NM_024768.2 *599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr3:191092899 A>G maps to NM_178335.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:191093118 C>G maps to NM_178335.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:48476262 G>C maps to NM_024661.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr3:48474183 C>T maps to NM_024661.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr3:48476459 C>A maps to NM_024661.3 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:113187948 T>G maps to NM_144718.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:113212133 A>C maps to NM_144718.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr3:113207813 G>A maps to NM_144718.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:113188062 C>A maps to NM_144718.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:107096824 G>T maps to NM_032600.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:107096574 T>A maps to NM_032600.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:107097330 C>A maps to NM_032600.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:107097303 C>G maps to NM_032600.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:107096856 A>G maps to NM_032600.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:107097304 C>T maps to NM_032600.2 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:80159586 G>A maps to ENST00000445854 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:80137052 C>T maps to ENST00000445854 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr10:61666020 G>A maps to ENST00000395341 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:119909873 G>A maps to NM_178499.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:119961557 C>T maps to NM_178499.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:119909846 G>C maps to NM_178499.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:119942924 C>A maps to NM_178499.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:46506740 G>T maps to NM_001080402.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:46521385 C>T maps to NM_001080402.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:111318978 G>A maps to NM_152591.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:49314777 G>T maps to NM_033124.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr12:49312206 G>A maps to NM_033124.4 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr3:56627032 G>C maps to NM_001141947.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:56647648 C>T maps to NM_001141947.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:93118682 C>A maps to NM_181645.3 C303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:32806871 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:52439952 C>A maps to NM_031290.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr13:52439609 C>T maps to NM_031290.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:52439603 G>C maps to NM_031290.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52439525 G>A maps to NM_031290.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr13:52439615 C>T maps to NM_031290.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr3:49200930 C>T maps to NM_022903.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr3:49200969 C>A maps to NM_022903.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:32657259 C>T maps to NM_001008391.2 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:32724417 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:32657325 G>T maps to NM_001008391.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:32636434 G>A maps to NM_001008391.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:32657240 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:32635142 G>A maps to NM_001008391.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:132288182 C>T maps to NM_138770.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr2:132288371 C>T maps to NM_138770.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr2:132290276 C>T maps to NM_138770.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:132290206 G>T maps to NM_138770.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr2:132290880 A>G maps to NM_138770.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:130897885 G>A maps to NM_207310.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:130899946 G>T maps to NM_207310.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr2:130897880 G>T maps to NM_207310.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:130897507 G>T maps to NM_207310.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:130899922 G>A maps to NM_207310.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:130899724 G>C maps to NM_207310.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:130899727 A>T maps to NM_207310.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:130897180 G>A maps to NM_207310.1 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:130897862 C>A maps to NM_207310.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:547536 C>T maps to NM_032358.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:46915350 C>G maps to NM_032040.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:46915989 G>C maps to NM_032040.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:46916051 C>A maps to NM_032040.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:46914993 G>A maps to NM_032040.3 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:112358550 C>A maps to ENST00000447230 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:112324419 C>A maps to ENST00000447230 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr3:112357657 C>T maps to ENST00000447230 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:112358038 C>T maps to ENST00000447230 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:112358067 C>A maps to ENST00000447230 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr3:112358288 G>C maps to ENST00000447230 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr3:112356937 C>G maps to ENST00000447230 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:86130968 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:85630435 G>A maps to NM_173556.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:85584274 C>A maps to NM_173556.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:85606378 C>A maps to NM_173556.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:118886113 C>T maps to NM_198489.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr2:56420010 A>T maps to NM_001080433.1 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr2:56419616 C>T maps to NM_001080433.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:56420276 G>T maps to NM_001080433.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:60609860 C>T maps to NM_024098.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:60610349 G>A maps to NM_024098.3 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:60610190 A>G maps to NM_024098.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:60615505 G>T maps to NM_024098.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66359145 C>A maps to NM_018219.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:66357993 C>A maps to NM_018219.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:55563917 G>A maps to ENST00000436346 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:55555428 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:55562249 G>A maps to ENST00000436346 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr2:55615933 G>A maps to ENST00000436346 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:55523084 C>T maps to ENST00000436346 R1733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:55582734 T>A maps to ENST00000436346 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:55601998 G>A maps to ENST00000436346 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:55646153 C>T maps to ENST00000436346 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:64121276 C>A maps to NM_032251.5 P1308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:64122798 T>A maps to NM_032251.5 P1411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:64109509 G>A maps to NM_032251.5 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64120218 C>T maps to NM_032251.5 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:64111771 G>T maps to NM_032251.5 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:91779573 C>G maps to NM_001080414.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr14:91739805 G>T maps to NM_001080414.2 Y1750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr14:91804432 C>T maps to NM_001080414.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr14:91755659 G>A maps to NM_001080414.2 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr14:91770193 C>A maps to NM_001080414.2 A1162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:85396369 G>A maps to NM_152723.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:85397122 C>T maps to NM_152723.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:82996953 G>C maps to NM_021825.3 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:28459851 G>T maps to NM_018318.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:28702078 A>T maps to NM_018318.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:28603338 A>T maps to NM_018318.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:28458597 T>C maps to NM_018318.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:28458613 G>T maps to NM_018318.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:124421889 C>A maps to NM_025140.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:118766201 G>C maps to NM_019044.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:118706926 G>A maps to NM_019044.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:118716039 A>G maps to NM_019044.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:4267770 G>T maps to NM_018074.4 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:4249229 C>G maps to NM_018074.4 Y10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7043209 C>A maps to NM_153376.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:41822538 G>T maps to NM_052848.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:41828557 G>T maps to NM_052848.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:41822728 C>T maps to NM_052848.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:169021408 A>T maps to NM_017785.4 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:31112686 G>A maps to NM_001105564.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:31112815 G>A maps to NM_001105564.1 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr6:31116423 C>A maps to NM_001105564.1 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:31112827 C>A maps to NM_001105564.1 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:36169748 C>T maps to NM_005893.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr4:26490873 C>T maps to NM_000730.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:26483501 C>A maps to NM_000730.2 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:26490978 G>A maps to NM_000730.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr4:26483655 C>A maps to NM_000730.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr4:26483451 G>T maps to NM_000730.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:26487329 A>G maps to NM_000730.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:6292376 C>T maps to NM_176875.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:6292658 C>A maps to NM_176875.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:6291447 G>T maps to NM_176875.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:6292586 C>T maps to NM_176875.2 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:6292376 C>T maps to NM_176875.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:6291423 C>T maps to NM_176875.2 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:6291106 C>T maps to NM_176875.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:6292010 C>A maps to NM_176875.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32688817 G>A maps to NM_002981.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:32683574 G>T maps to NM_005408.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:32685122 C>A maps to NM_005408.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:34311468 T>A maps to NM_032962.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr17:34304602 C>A maps to NM_004590.2 *121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:34308429 A>T maps to NM_004590.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:34709817 G>C maps to NM_002989.2 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:34340788 A>C maps to NM_005064.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:34340338 G>C maps to NM_005064.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr7:75441235 C>A maps to NM_002991.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr19:8121117 G>A maps to NM_005624.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:43381990 C>A maps to NM_148672.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:43388578 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr17:32598249 C>G maps to ENST00000378569 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:32598261 C>T maps to ENST00000378569 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:32646552 G>T maps to ENST00000394620 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:45104117 G>C maps to NM_001029835.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:45109546 G>T maps to NM_001029835.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:45108138 G>T maps to NM_001029835.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:45113930 C>A maps to NM_001029835.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:122741886 T>A maps to NM_001237.3 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:122743557 C>A maps to NM_001237.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:68473355 C>T maps to NM_031966.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:20781909 G>A maps to NM_182849.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr14:20781942 G>C maps to NM_182849.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr15:59406797 T>C maps to NM_004701.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:50053544 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:50053794 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:50052411 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:50053673 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:50089665 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:50053798 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:50052404 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:50090715 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:50056875 T>G did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr23:50054190 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:50052962 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:50089804 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:50051723 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:50094638 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:50051955 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:50051957 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:50054332 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:50053788 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:50052995 G>C did not map to a codon.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr23:50094700 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:50053311 G>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:50056881 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:50053714 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:50094342 A>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:50053319 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:50053405 A>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:50085245 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:50052922 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:50094259 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:50094322 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:50094665 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:50085235 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:50053608 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:50054015 A>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:50052226 A>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:50053079 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:50053080 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:50053962 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:50051709 T>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:50054321 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:50051912 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:50053978 C>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:50053711 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:50051843 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:50089772 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:99994323 G>A maps to NM_005190.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:99997441 C>T maps to NM_005190.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:69458697 G>T maps to NM_053056.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:69458748 C>T maps to NM_053056.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:4385190 C>A maps to NM_001759.3 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:4387952 T>C maps to NM_001759.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:4383220 C>A maps to NM_001759.3 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr12:4383337 C>T maps to NM_001759.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:30303883 G>A maps to NM_001238.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:30308448 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:2481128 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:2489404 C>T maps to NM_001761.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:78081896 C>T maps to NM_004354.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:86705174 C>A maps to NM_001239.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:77977477 T>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:132085053 C>G maps to NM_001039780.2 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:97810017 G>A maps to NM_001134375.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr14:99976638 G>C maps to ENST00000437596 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr14:99959892 C>T maps to ENST00000437596 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:156866173 C>A maps to NM_020307.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr1:1322673 C>T maps to NM_030937.4 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:1325634 C>T maps to NM_030937.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:54527327 C>A maps to NM_021147.3 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:49089836 G>A maps to NM_001240.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:49099549 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr12:49086992 G>A maps to NM_001240.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr12:49087119 G>C maps to NM_001240.2 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:35841975 A>T maps to NM_145012.4 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr10:35842026 C>T maps to NM_145012.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55653055 T>A maps to ENST00000442196 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:46245042 G>T maps to NM_001295.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:46245636 G>C maps to NM_001295.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:46400067 C>A maps to NM_001123396.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:46401301 C>A maps to NM_001123041.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr3:46306672 T>A maps to NM_178328.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:46414425 C>T maps to NM_001100168.1 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr6:167550347 G>A maps to NM_004367.5 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:38711509 C>T maps to NM_001838.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:45942345 A>C maps to NM_031200.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66368019 G>T maps to NM_005125.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:69993721 G>C maps to NM_006431.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:69983323 C>G maps to NM_006431.2 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:156290752 G>C maps to NM_005998.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr1:156280402 C>T maps to NM_005998.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:62112168 C>A maps to NM_006430.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:10254822 G>T maps to NM_012073.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258363 G>C maps to NM_012073.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:10258620 G>T maps to NM_012073.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:56126390 G>T maps to NM_001762.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:56127300 G>T maps to NM_001762.3 G345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:33266229 A>T maps to NM_006584.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:33259505 A>T maps to NM_006584.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:73467574 A>C maps to NM_006429.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:73471670 G>A did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:73467658 C>A maps to NM_006429.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:73467589 G>T maps to NM_006429.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:73476216 C>T maps to NM_006429.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:73476213 C>A maps to NM_006429.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:17072375 C>G maps to NM_014406.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:17073110 C>T maps to NM_014406.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:17072297 G>T maps to NM_014406.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:17072654 A>G maps to NM_014406.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:17072912 G>T maps to NM_014406.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr22:17072105 C>A maps to NM_014406.4 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:17072822 G>T maps to NM_014406.4 C206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr22:17073299 G>T maps to NM_014406.4 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:17072114 G>T maps to NM_014406.4 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr22:17073397 G>A maps to NM_014406.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr22:17073398 C>A maps to NM_014406.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr22:17072540 G>A maps to NM_014406.4 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:17073011 G>C maps to NM_014406.4 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:17073416 G>T maps to NM_014406.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr22:17073350 C>T maps to NM_014406.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr22:17073317 C>T maps to NM_014406.4 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:17073041 C>A maps to NM_014406.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:117559874 G>A maps to NM_004258.3 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:117561103 A>C maps to NM_004258.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:117554556 C>T maps to NM_004258.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:117552673 C>T maps to NM_004258.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:117552697 A>T maps to NM_004258.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:117568279 A>T maps to NM_004258.3 K860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:74440083 A>T maps to NM_133493.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:74519731 A>T maps to NM_133493.3 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:74497099 G>T maps to NM_133493.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:74528209 G>T maps to NM_133493.3 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:74497135 C>A maps to NM_133493.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr6:74497175 G>T did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr6:74521962 C>G maps to NM_133493.3 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:74407140 A>T maps to NM_133493.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:140012310 G>T maps to NM_001174105.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:838173 C>G maps to NM_139030.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:145699073 T>A maps to NM_007053.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:145698986 C>T maps to NM_007053.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:7636211 C>A maps to NM_004244.4 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:7654058 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:7639557 G>T maps to NM_004244.4 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:7632482 C>T maps to NM_004244.4 K1151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:7639557 G>T maps to NM_004244.4 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:7640162 T>A maps to NM_004244.4 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:7640234 G>T maps to NM_004244.4 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:7656239 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:7651465 G>T maps to NM_004244.4 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:7639096 G>T maps to NM_004244.4 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:7653944 C>A maps to NM_004244.4 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:7656273 T>G maps to NM_004244.4 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:7637773 A>T maps to NM_004244.4 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:7531613 A>T maps to ENST00000416109 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:7522157 G>T maps to ENST00000416109 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7522231 C>A maps to ENST00000416109 E1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr12:7586287 C>A maps to ENST00000416109 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:7527332 T>C maps to ENST00000416109 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:7559188 T>C maps to ENST00000416109 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:7586275 C>A maps to ENST00000416109 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:7548877 A>T maps to ENST00000416109 C631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:7559353 G>T maps to ENST00000416109 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:7585996 C>A maps to ENST00000416109 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:7551109 G>C maps to ENST00000416109 Y503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr12:7586009 A>G maps to ENST00000416109 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:27709013 C>A maps to NM_207397.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:43859867 G>T maps to NM_020406.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:43858497 C>T maps to NM_020406.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr19:43858092 C>A maps to NM_020406.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:43866342 G>A maps to NM_020406.2 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr19:43858434 G>T maps to NM_020406.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:43866473 T>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:43864549 A>T maps to NM_020406.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66480331 C>G maps to NM_005582.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:66492421 G>T maps to NM_005582.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:66479857 G>C maps to NM_005582.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:66480250 G>A maps to NM_005582.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:66480256 G>T maps to NM_005582.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:28947910 C>T maps to NM_001178098.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:28948592 C>A maps to NM_001178098.1 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:28948975 G>T maps to NM_001178098.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:28947868 C>A maps to NM_001178098.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr16:28943359 C>T maps to NM_001178098.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:158225117 C>A maps to NM_001763.2 Y101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158225932 G>T maps to NM_001763.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:158225792 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:158226843 C>A maps to NM_001763.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:158226573 A>T did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:158225792 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:158300742 G>T maps to NM_001764.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158300658 C>T maps to NM_001764.2 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:158299699 G>T maps to NM_001764.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:158299788 C>A maps to NM_001764.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:158299244 C>A maps to NM_001764.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:158299875 C>A maps to NM_001764.2 G125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:158300724 G>T maps to NM_001764.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158299391 G>T maps to NM_001764.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:158299852 C>G maps to NM_001764.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158261155 G>A maps to NM_001765.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:158261063 C>T maps to NM_001765.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:158262515 G>C maps to NM_001765.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:158262458 C>A maps to NM_001765.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:158262416 C>A maps to NM_001765.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:158153921 C>T maps to NM_001766.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:158151904 G>T maps to NM_001766.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:158152890 G>T maps to NM_001766.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:158152740 A>T maps to NM_001766.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158152752 A>T maps to NM_001766.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:158152897 C>A maps to NM_001766.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:158151987 G>T maps to NM_001766.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:158153930 C>T maps to NM_001766.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:158324239 C>A maps to NM_030893.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:158325614 A>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:158325756 C>A maps to NM_030893.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:158324233 T>G maps to NM_030893.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158324256 G>A maps to NM_030893.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:158326333 T>A maps to NM_030893.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:158326315 C>A maps to NM_030893.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr1:158324372 G>T maps to NM_030893.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158326381 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:158325716 G>A maps to NM_030893.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:158326381 G>C did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:158324170 C>A maps to NM_030893.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158325306 T>A maps to NM_030893.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:158325348 G>A maps to NM_030893.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:117303198 C>T maps to NM_001767.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr1:117311353 A>C maps to NM_001767.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:117311267 C>T maps to NM_001767.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:112064004 C>A maps to NM_001004196.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:112648057 C>A maps to NM_138806.3 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:112643969 G>T maps to NM_138806.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:112648322 T>G maps to NM_138806.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:112666766 C>T maps to NM_138806.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr3:112643993 G>T maps to NM_138806.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr3:112648253 C>A maps to NM_138806.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:112648337 A>T maps to NM_138806.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:112647834 C>A maps to NM_138806.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:112564524 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:112546460 A>G maps to NM_001008784.2 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:112545957 C>T maps to NM_001008784.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr3:112538704 C>A maps to NM_001008784.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71058201 G>C maps to NM_015717.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:71058893 T>A maps to NM_015717.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:7809832 C>T maps to NM_021155.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:7808994 G>T maps to NM_021155.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:35832041 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:35829248 C>G maps to NM_001771.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:35836515 C>A maps to NM_001771.3 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:35832309 G>T maps to NM_001771.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:35827244 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:35832318 C>T maps to NM_001771.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:35831820 C>A maps to NM_001771.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:35823582 C>T maps to NM_001771.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:35831820 C>T maps to NM_001771.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr18:67563078 T>A maps to NM_006566.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:160811266 C>A maps to NM_001166663.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr1:160808807 G>T maps to NM_001166663.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:160808239 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:160811392 C>A maps to NM_001166663.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:160803840 C>T maps to NM_001166663.1 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:160808276 G>C maps to NM_001166663.1 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:66084210 C>A maps to NM_020404.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:66082935 A>T maps to NM_020404.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:66083346 G>T maps to NM_020404.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:66082509 A>G maps to NM_020404.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:6560158 C>T maps to NM_001242.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr9:5457193 T>C maps to NM_014143.3 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:73995329 G>A maps to NM_001024736.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr15:73994710 C>T maps to NM_001024736.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr15:73994860 G>T maps to NM_001024736.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:204599580 C>G maps to NM_006139.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:204591548 G>T maps to NM_006139.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:47471031 G>A maps to NM_012120.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr6:47549736 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30364597 C>T maps to NM_006110.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:72470715 C>G maps to NM_007261.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:72462877 C>A maps to NM_007261.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:72469994 G>T maps to NM_007261.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:72470011 G>T maps to NM_007261.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:72541057 G>T maps to NM_006678.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72540856 C>T maps to NM_006678.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr17:72541912 G>A maps to NM_006678.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:72608824 C>T maps to ENST00000426295 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr17:72608913 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:72522082 G>A maps to NM_174892.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:72522106 G>T maps to NM_174892.2 C87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:72518918 G>T maps to NM_174892.2 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr17:72518978 G>A maps to NM_174892.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:72584764 G>A maps to NM_001115152.1 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:72578358 G>T maps to NM_001115152.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:72584839 G>A maps to NM_001115152.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:72700892 A>G maps to ENST00000412086 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:72694569 A>T maps to ENST00000412086 L181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:41939275 G>C maps to NM_145273.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:41939257 C>T maps to NM_145273.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:41934470 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:41931256 C>A maps to NM_145273.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr17:41926223 C>T maps to NM_145273.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:160636570 C>T maps to NM_001198759.1 W1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:51729249 C>T maps to NM_001772.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51728726 T>C maps to NM_001772.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:51738912 C>A maps to NM_001772.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:51728597 C>A maps to NM_001772.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:51729317 C>G maps to NM_001772.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:51738460 T>A maps to NM_001772.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:208062809 C>A maps to NM_001025109.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:208070867 G>A maps to NM_001025109.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:208062944 C>A maps to NM_001025109.1 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:208084383 C>T maps to NM_001025109.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:208084356 C>T maps to NM_001025109.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:208062963 C>T maps to NM_001025109.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:80302096 C>T maps to NM_001127444.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr7:80290447 C>G maps to NM_001127444.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:49843569 C>A maps to NM_001774.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:15780138 C>A maps to NM_001775.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:15839728 C>A maps to NM_001775.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:15841732 A>G maps to NM_001775.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:118209936 G>A maps to NM_000732.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:118210616 G>A maps to NM_000732.4 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:45912707 T>G maps to ENST00000423698 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr19:45911840 G>A maps to ENST00000423698 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:6923305 A>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:6926293 A>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:6923320 G>A maps to NM_000616.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:44757606 T>G maps to NM_001250.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr20:44751318 G>A maps to NM_001250.4 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:135741285 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:135730549 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:135730548 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:135732555 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:135730459 C>G did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:135738525 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:135741548 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:135741381 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:35211478 G>A maps to NM_000610.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:35223311 G>A maps to NM_000610.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:160651120 C>A maps to NM_001778.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:160654838 T>A maps to NM_001778.2 K75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:160654848 G>A maps to NM_001778.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:60885645 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:60886853 C>A maps to NM_014207.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr11:60887036 C>T maps to NM_014207.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:26644546 C>A maps to NM_001803.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:117078850 C>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:157804199 C>A maps to NM_005894.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:157803125 T>A maps to NM_005894.2 K299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:157805681 C>A maps to NM_005894.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157804206 G>C maps to NM_005894.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:157805888 C>A maps to NM_005894.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr1:157804212 C>T maps to NM_005894.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:157805894 G>T maps to NM_005894.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:60785468 C>A maps to NM_006725.3 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:60739345 C>A maps to NM_006725.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:60785402 C>A maps to NM_006725.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:60777207 A>T maps to NM_006725.3 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:60777113 G>A maps to NM_006725.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:60783218 C>A maps to NM_006725.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80273285 G>T maps to NM_006137.6 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:80274795 G>A maps to NM_006137.6 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:80274702 A>C maps to NM_006137.6 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:6586183 C>A maps to NM_001252.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:6590995 C>A maps to NM_001252.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:6590932 G>T maps to NM_001252.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:6590911 G>C maps to NM_001252.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:35618282 G>T maps to NM_001782.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr9:35616192 G>C maps to NM_001782.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:35611862 T>C maps to NM_001782.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:149782840 G>A maps to NM_001025159.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:119263472 G>T maps to NM_005191.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:119248737 A>G maps to NM_005191.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr11:2398820 C>T maps to NM_004356.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:2417124 G>C maps to NM_004356.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:44640630 C>A maps to NM_002231.3 C253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:44626731 G>T maps to NM_002231.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:44626732 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:14135349 G>T maps to NM_004233.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr6:14135361 C>T maps to NM_004233.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:160535277 C>A maps to NM_001184879.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160523868 T>A maps to NM_001184879.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:160520772 G>T maps to NM_001184879.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:160535530 C>A maps to NM_001184879.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:160520760 C>T maps to NM_001184879.1 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:121838341 G>C maps to NM_175862.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:121828230 C>A maps to NM_175862.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121825184 G>T maps to NM_175862.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:121822389 C>T maps to NM_175862.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:121822510 G>T maps to NM_175862.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:121838356 C>A maps to NM_175862.3 C322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:87017616 C>T maps to ENST00000456996 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:87017547 C>G maps to ENST00000456996 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:87017793 C>T maps to ENST00000456996 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:87073891 T>A maps to NM_172213.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:23066262 C>T maps to NM_012072.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:23066265 G>T maps to NM_012072.3 C188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:23065955 G>T maps to NM_012072.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:23066781 G>T maps to NM_012072.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:23065770 G>T maps to NM_012072.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr20:23065922 G>T maps to NM_012072.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:111342669 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:111356048 C>G maps to NM_198196.2 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:111325561 C>A maps to NM_198196.2 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:111297998 C>T maps to NM_198196.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:14501734 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:2640678 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr23:2635665 A>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:2632485 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:149944649 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:149945945 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:149962191 A>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:149944723 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:149999766 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:149945921 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:149963905 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:149984520 G>T did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:20915691 G>T maps to NM_001785.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:20915673 C>T maps to NM_001785.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr15:43027804 C>G maps to NM_138477.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr15:43021261 G>A maps to NM_138477.2 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr15:43020851 C>T maps to NM_138477.2 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:43025384 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr10:12292307 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:100960421 G>T maps to NM_033312.2 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr1:100928315 C>T maps to NM_033312.2 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr9:99327124 T>A maps to NM_033331.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr9:99286008 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:115002122 C>T maps to NM_003903.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr13:115037764 A>G maps to NM_003903.3 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:115037914 G>T maps to NM_003903.3 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:43828708 G>A maps to NM_001255.2 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr1:43826789 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:54429306 A>G maps to NM_001170402.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:54415662 G>T maps to NM_001170402.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54415704 T>G maps to NM_001170402.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:137525546 G>A maps to NM_004661.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr5:137527958 G>A maps to NM_004661.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:137542337 G>A maps to NM_004661.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:48207329 A>T maps to NM_001789.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:3781941 C>T maps to NM_021873.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:137626351 C>A maps to NM_001790.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr5:137622941 C>A maps to NM_001790.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:45214546 G>A maps to NM_001114091.1 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr17:45214645 T>C maps to NM_001114091.1 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:10504033 G>A maps to NM_007065.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr6:110501724 C>T maps to NM_015891.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:110551181 G>T maps to NM_015891.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:22405021 A>C maps to NM_001039802.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:227441854 A>G maps to ENST00000366766 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:227381577 C>A maps to ENST00000366766 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:227219082 T>G maps to ENST00000366766 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:227223258 A>C maps to ENST00000366766 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:103440445 C>G maps to NM_006035.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:103412023 G>C maps to NM_006035.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:103406195 G>A maps to NM_006035.3 V1560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:103442277 G>A maps to NM_006035.3 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr14:103410339 G>A maps to NM_006035.3 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:64604409 C>T maps to NM_017525.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:64606194 A>G maps to NM_017525.2 Y352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:64599135 C>A maps to NM_017525.2 E1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:64606678 C>T maps to NM_017525.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:64600142 G>A maps to NM_017525.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37964469 C>T maps to NM_152243.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:71282453 G>A maps to NM_012121.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:71282495 C>T maps to NM_012121.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:71281796 C>A maps to NM_012121.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr17:71282615 C>A maps to NM_012121.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr22:19504396 C>T maps to NM_001178010.1 H571H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:44374185 A>G maps to NM_001253.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:44387331 C>T maps to NM_001253.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:44371572 A>G maps to NM_001253.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr6:44397513 C>G maps to NM_001253.2 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:91967323 C>G maps to NM_001134420.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:193218894 C>T maps to NM_024529.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr8:25337498 A>C maps to ENST00000434814 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:25318020 C>G maps to ENST00000434814 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr8:25325814 G>A maps to ENST00000434814 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr14:105477867 G>C maps to NM_145701.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:64846929 G>A maps to ENST00000404147 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:174223565 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:174231036 G>A maps to NM_031942.4 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr2:174231030 C>T maps to NM_031942.4 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:38168929 C>T maps to NM_018101.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr1:38168971 G>A maps to NM_018101.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:45127528 C>G maps to NM_022842.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr3:45134847 G>T maps to NM_022842.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:45153866 G>A maps to NM_022842.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:45153842 G>C maps to NM_022842.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:54606876 G>T maps to NM_201546.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:54605348 G>A maps to NM_201546.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr16:68862084 C>T maps to NM_004360.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:24511576 G>T maps to NM_006727.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:24488131 G>T maps to NM_006727.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:24537755 C>A maps to NM_006727.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:24488152 A>T maps to NM_006727.3 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:24491685 C>A maps to NM_006727.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:24491816 G>A maps to NM_006727.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:24487846 G>C maps to NM_006727.3 Y764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:24535923 A>T maps to NM_006727.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:24487943 G>T maps to NM_006727.3 S732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:24537747 G>T maps to NM_006727.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:24491712 G>T maps to NM_006727.3 A616A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5942-01A-21D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:24491733 G>A maps to NM_006727.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr5:24511450 G>A maps to NM_006727.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:24488008 G>T maps to NM_006727.3 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:24509738 C>A maps to NM_006727.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:24509922 G>T maps to NM_006727.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:24487842 G>T maps to NM_006727.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:24537618 A>T maps to NM_006727.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:24488005 C>A maps to NM_006727.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:24509756 C>A maps to NM_006727.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr5:24487801 A>G maps to NM_006727.3 Y779Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:24487792 C>T maps to NM_006727.3 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:24593574 G>A maps to NM_006727.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:24493034 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:24487954 G>A maps to NM_006727.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:24535842 C>G maps to NM_006727.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:24537581 C>A maps to NM_006727.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:24509871 G>T maps to NM_006727.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:24491721 G>T maps to NM_006727.3 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr5:24537545 C>A maps to NM_006727.3 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:24488173 C>T maps to NM_006727.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:65032651 G>T maps to NM_001797.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:65026937 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:65016162 T>A maps to NM_001797.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:65026827 T>C maps to NM_001797.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:64981712 T>C maps to NM_001797.2 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:65006840 G>T maps to NM_001797.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:64981946 G>T maps to NM_001797.2 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:64981814 T>C maps to NM_001797.2 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:65022182 A>G maps to NM_001797.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr16:65022082 C>A maps to NM_001797.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:21975200 C>A maps to NM_004061.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:21752202 C>A maps to NM_004061.3 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:21817108 A>T maps to NM_004061.3 L316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21975281 G>T maps to NM_004061.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:21975416 G>T maps to NM_004061.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:21854831 G>T maps to NM_004061.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:21751847 A>T maps to NM_004061.3 *795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:21755774 C>A maps to NM_004061.3 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr5:21752318 G>A maps to NM_004061.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:21802307 A>G maps to NM_004061.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:21755940 C>A maps to NM_004061.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr5:21752202 C>A maps to NM_004061.3 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:21751992 G>A maps to NM_004061.3 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr5:22078728 G>A maps to NM_004061.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr5:21751881 G>A maps to NM_004061.3 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr5:21842392 C>A maps to NM_004061.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr5:21752006 C>A maps to NM_004061.3 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr5:21975482 G>A maps to NM_004061.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:21765113 G>T maps to NM_004061.3 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:21752094 G>A maps to NM_004061.3 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:83378606 C>A maps to ENST00000268613 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:83251005 G>A maps to ENST00000268613 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:83065759 C>A maps to ENST00000268613 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:82891971 G>T maps to ENST00000268613 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:83378558 G>C maps to ENST00000268613 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:83711847 G>T maps to ENST00000268613 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr16:83816884 C>T maps to ENST00000268613 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:83378553 C>A maps to ENST00000268613 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr16:83704552 C>T maps to ENST00000268613 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr16:89261325 C>T maps to NM_004933.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:66943245 G>T maps to NM_004062.2 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:66949150 C>G maps to NM_004062.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr16:66947160 C>T maps to NM_004062.2 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:95164220 C>T maps to NM_001144663.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:95158252 A>G maps to NM_001144663.1 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:95183093 T>C maps to NM_001144663.1 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:95188783 G>A maps to NM_001144663.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:95172197 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:95158219 G>A maps to NM_001144663.1 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:19591213 T>A maps to NM_004934.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:19520858 T>A maps to NM_004934.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:19612582 G>C maps to NM_004934.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr5:19612605 C>A maps to NM_004934.3 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:19838915 G>A maps to NM_004934.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:19571710 A>T maps to NM_004934.3 P410P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8208-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr5:19839002 G>A maps to NM_004934.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr5:19571779 G>A maps to NM_004934.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:19473825 C>G did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:19571796 G>A maps to NM_004934.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:19543985 G>T maps to NM_004934.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:19612600 A>G maps to NM_004934.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:19747264 A>T maps to NM_004934.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:64178898 C>A maps to NM_021153.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:64197150 G>A maps to NM_021153.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr18:64218474 T>A maps to NM_021153.2 K211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:64172147 G>C maps to NM_021153.2 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:64211251 G>T maps to NM_021153.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:64172378 G>A maps to NM_021153.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr18:64172342 G>A maps to NM_021153.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:25532210 G>T maps to NM_001792.3 S876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:25568620 T>C maps to NM_001792.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:25593715 C>T maps to NM_001792.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:25583116 G>T maps to NM_001792.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr18:25591899 G>T maps to NM_001792.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:25582999 A>C maps to NM_001792.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr18:25565500 G>T maps to NM_001792.3 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:25543367 G>T maps to NM_001792.3 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr18:25565084 C>A maps to NM_001792.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:25565563 C>A maps to NM_001792.3 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:25570185 T>A maps to NM_001792.3 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:59206353 C>A maps to NM_031891.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:59195339 C>A maps to NM_031891.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:59206372 G>T maps to NM_031891.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:59221421 G>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr18:59157923 C>G maps to NM_031891.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr18:59221666 G>T maps to NM_031891.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr18:59221612 G>A maps to NM_031891.2 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr18:59206378 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:59221444 C>A maps to NM_031891.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:59221903 G>T maps to NM_031891.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr18:59174759 C>A maps to NM_031891.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr18:59221513 C>T maps to NM_031891.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr18:59217331 G>T maps to NM_031891.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:59221630 C>A maps to NM_031891.2 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44815275 C>T maps to NM_021248.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:44815503 G>A maps to NM_021248.1 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:44828104 C>T maps to NM_021248.1 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:44815305 G>T maps to NM_021248.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:44856176 C>A maps to NM_021248.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:44828101 C>T maps to NM_021248.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr20:44839088 C>G maps to NM_021248.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:44839088 C>A maps to NM_021248.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:44839163 C>A maps to NM_021248.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:44828146 C>A maps to NM_021248.1 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr20:44869743 C>A maps to NM_021248.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:73558955 C>A maps to ENST00000398860 P2386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:73544805 C>T maps to ENST00000398860 T1892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:73574860 C>T maps to ENST00000398860 L3302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:73569656 C>T maps to ENST00000398860 R2940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:73326638 C>A maps to ENST00000398860 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548713 G>C maps to ENST00000398860 L1951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:73548779 G>A maps to ENST00000398860 V1973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:73544709 C>A maps to ENST00000398860 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:73406355 C>T maps to ENST00000398860 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr10:73567646 C>T maps to ENST00000398860 L2874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr10:73551075 A>G maps to ENST00000398860 L2084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr10:73468897 C>A maps to ENST00000398860 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:73567651 C>A maps to ENST00000398860 A2875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr10:73553353 G>T maps to ENST00000398860 L2228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr10:73560448 G>T maps to ENST00000398860 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:23517503 G>C maps to NM_022478.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:23522739 G>C maps to NM_022478.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:23521745 T>C maps to NM_022478.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr14:23517524 C>G maps to NM_022478.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:23517599 G>A maps to NM_022478.3 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr20:58560057 C>T maps to NM_177980.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:58564176 G>T maps to NM_177980.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:58567502 G>T maps to NM_177980.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:68712777 C>T maps to NM_001793.4 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:68713831 G>T maps to NM_001793.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:68714951 G>T maps to NM_001793.4 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:60499427 C>T maps to NM_001794.2 H555H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr20:60503479 C>T maps to NM_001794.2 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr20:60448883 G>A maps to NM_001794.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:60498690 C>T maps to NM_001794.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:60504808 C>T maps to NM_001794.2 N716N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:60419725 C>A maps to NM_001794.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr20:60504877 C>T maps to NM_001794.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr20:60509268 C>T maps to NM_001794.2 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr20:60419731 C>A maps to NM_001794.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:66424345 C>A maps to NM_001795.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:66432426 G>A maps to NM_001795.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:66436897 G>T maps to NM_001795.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr16:66436570 C>T maps to NM_001795.3 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr16:66437038 C>A maps to NM_001795.3 Y774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:31323228 C>A maps to NM_004932.2 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:31317987 G>T maps to NM_004932.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31294152 G>T maps to NM_004932.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:31322998 A>T maps to NM_004932.2 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:31294305 G>T maps to NM_004932.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:31323216 G>C maps to NM_004932.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:31323243 C>G maps to NM_004932.2 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:31317543 T>C maps to NM_004932.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:31294066 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:31299712 C>T maps to NM_004932.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:31302381 G>T maps to NM_004932.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:31317492 C>A maps to NM_004932.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:31323123 C>G maps to NM_004932.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:31322949 G>C maps to NM_004932.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:31299685 C>A maps to NM_004932.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:31294295 C>A maps to NM_004932.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:31267594 C>T maps to NM_004932.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:31299688 G>A maps to NM_004932.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:31302386 G>T maps to NM_004932.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr5:31323057 T>C maps to NM_004932.2 F672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:31302239 T>A maps to NM_004932.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:31302236 T>C maps to NM_004932.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:63492009 C>A maps to NM_004361.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:63477088 C>A maps to NM_004361.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:63477089 C>A maps to NM_004361.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:63548087 C>A maps to NM_004361.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr18:63525117 C>T maps to NM_004361.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:63511182 G>T maps to NM_004361.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:63511298 G>C maps to NM_004361.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:63529992 A>T maps to NM_004361.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr18:63529900 G>C did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr18:63430200 G>T maps to NM_004361.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:63547682 C>A maps to NM_004361.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr18:63477199 A>G maps to NM_004361.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr18:63526254 C>T maps to NM_004361.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr18:63547761 G>T maps to NM_004361.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr18:63547760 G>T maps to NM_004361.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr18:63547761 G>T maps to NM_004361.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr18:63477115 C>A maps to NM_004361.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:62055058 G>T maps to NM_001796.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:61687697 G>T maps to NM_001796.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:61687544 G>C maps to NM_001796.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:61823357 C>A maps to NM_001796.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:61689396 A>T maps to NM_001796.2 L628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:61859036 C>T maps to NM_001796.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:61761003 G>T maps to NM_001796.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr16:62055274 A>G maps to NM_001796.2 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:61851500 C>A maps to NM_001796.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:61854976 G>T maps to NM_001796.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr16:61823352 C>T maps to NM_001796.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr16:61935283 C>A maps to NM_001796.2 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr16:61823325 C>A maps to NM_001796.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:61851474 A>T maps to NM_001796.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:61859042 G>T maps to NM_001796.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:61689617 G>T maps to NM_001796.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr16:61687616 G>T maps to NM_001796.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr16:61689413 G>A maps to NM_001796.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:26881388 C>T maps to NM_016279.3 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:26885732 G>T maps to NM_016279.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:26988224 T>C maps to NM_016279.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:26881505 A>T maps to NM_016279.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:26890028 G>A maps to NM_016279.3 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:26906107 C>A maps to NM_016279.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:26906095 G>A maps to NM_016279.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:26881640 G>T maps to NM_016279.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr5:26903856 G>A maps to NM_016279.3 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:26915771 T>C maps to NM_016279.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr5:26881625 G>C maps to NM_016279.3 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr5:26881670 T>A maps to NM_016279.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:26890651 A>T maps to NM_016279.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:26916032 C>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:26881682 A>T maps to NM_016279.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr5:26915836 C>A maps to NM_016279.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:26915867 T>A maps to NM_016279.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:26881412 C>G maps to NM_016279.3 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:26886150 G>T maps to NM_016279.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:26915966 G>A maps to NM_016279.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:26902673 G>T maps to NM_016279.3 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:26916032 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:26915924 A>T maps to NM_016279.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr5:26885834 G>T maps to NM_016279.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:26881403 C>T maps to NM_016279.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr5:26881246 A>T maps to NM_016279.3 *790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:26885729 T>A maps to NM_016279.3 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:26988329 T>A maps to NM_016279.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr5:26906190 C>A maps to NM_016279.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr5:26902730 C>A maps to NM_016279.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:26890659 G>T maps to NM_016279.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:26881322 A>G maps to NM_016279.3 Y764Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85972974 C>A maps to NM_033100.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr10:85968012 C>T maps to NM_033100.2 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr10:85973959 C>A maps to NM_033100.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:85972036 C>T maps to NM_033100.2 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:176017473 G>A maps to NM_001171976.1 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:176016153 C>A maps to NM_001171976.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:175995736 G>C maps to NM_001171976.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:176017661 C>A maps to NM_001171976.1 T1171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:176002324 C>A maps to NM_001171976.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:176002179 C>T maps to NM_001171976.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr5:176022671 G>A maps to NM_001171976.1 *1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:175995989 C>T maps to NM_001171976.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:176011846 G>T maps to NM_001171976.1 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr5:175995995 C>T maps to NM_001171976.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:105660901 G>C maps to NM_152750.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:105656439 C>T maps to NM_152750.4 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:105664963 C>T maps to NM_152750.4 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:105672971 G>C maps to NM_152750.4 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:618106 G>A maps to NM_021924.4 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:620374 G>C maps to NM_021924.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:29874030 C>T maps to NM_006319.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr10:62544478 G>C maps to NM_001786.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr16:89762018 C>T maps to NM_052988.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:1573206 C>A maps to ENST00000401097 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:37650801 G>A maps to NM_016507.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:37676280 A>G maps to NM_016507.2 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:40037170 G>T maps to NM_003718.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:40102634 G>T maps to NM_003718.4 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr7:40027314 A>C maps to NM_003718.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:90377055 G>T maps to NM_012395.2 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:202736999 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:202677285 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:202737049 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:202755506 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:202700487 T>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:202755520 T>C maps to NM_139158.1 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:202698677 C>A maps to ENST00000450471 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:202672347 G>A maps to ENST00000450471 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:47087979 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:47083884 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:47086815 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:47086598 G>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:47083103 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:96694098 A>G maps to NM_002595.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:96704919 G>T maps to NM_002595.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:96707212 T>C maps to NM_002595.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:205495284 G>A maps to NM_212503.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:205495239 C>T maps to NM_212503.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:205495549 C>T maps to NM_212503.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:205496950 C>T maps to NM_212503.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:110988771 A>G maps to NM_015076.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:90588910 G>T maps to NM_001039803.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:58144536 G>C maps to NM_000075.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:150752433 C>A maps to NM_004935.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr2:219825609 C>A maps to NM_003936.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:219824751 G>T maps to NM_003936.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:31973518 C>A maps to ENST00000357886 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr20:31984819 T>A maps to ENST00000357886 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:123201726 G>A maps to NM_018249.4 F1224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123215790 C>A maps to NM_018249.4 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:123253682 T>A maps to NM_018249.4 K462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:123170667 C>T maps to NM_018249.4 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:123169401 G>A maps to NM_018249.4 S1617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr9:123220759 G>A maps to NM_018249.4 F781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:123202071 T>C maps to NM_018249.4 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:123165238 G>A maps to NM_018249.4 L1718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:46052625 A>T maps to NM_176096.1 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:46054188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:92247457 A>G maps to NM_001145306.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:92244465 C>T maps to NM_001145306.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:26975641 G>T maps to NM_001260.1 G384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:26927935 G>T maps to NM_001260.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:130550578 C>T maps to ENST00000373265 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:130551527 G>T maps to ENST00000373265 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:50801306 A>G maps to NM_004196.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:76525508 C>T maps to ENST00000307465 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:76551106 C>T maps to ENST00000307465 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:76532443 C>A maps to ENST00000307465 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:39406333 G>T maps to ENST00000395035 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:39411789 T>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:39411788 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:18668586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:18622561 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:18646664 C>A did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:18622570 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:18668698 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:18606110 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:18627663 C>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:18622842 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:18622581 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:18622686 A>G did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:18646678 G>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:18600058 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:12870965 C>T maps to NM_004064.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:12870830 C>T maps to NM_004064.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:2905951 G>A maps to NM_000076.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr9:21971024 G>A maps to NM_001195132.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:21971002 C>A maps to NM_001195132.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:21970913 C>T maps to NM_001195132.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:21994144 T>C maps to ENST00000361570 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:22008862 C>T maps to NM_004936.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr9:22008886 C>T maps to NM_004936.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr9:22006054 G>A maps to NM_004936.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr1:51436087 G>A maps to NM_078626.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:10677772 G>A maps to NM_079421.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:10677814 G>C maps to NM_079421.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr14:54884581 A>G maps to NM_005192.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:125864221 T>A maps to ENST00000392693 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:125851150 T>A maps to ENST00000392693 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:125891245 C>A maps to ENST00000392693 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr11:125887046 A>G maps to ENST00000392693 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:125848197 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:125864824 C>A maps to ENST00000392693 G829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:125888240 T>G maps to ENST00000392693 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:125853845 C>A maps to ENST00000392693 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:125889634 T>C maps to ENST00000392693 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:125864181 C>A maps to ENST00000392693 E883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:139866269 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:139866014 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:139866322 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:139865752 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:139866393 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:139865923 C>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:139866349 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:139866479 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:139865803 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:139866215 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:139866216 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:139865924 A>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:139866375 C>A did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:139866086 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:139865905 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:139866051 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:22358636 C>T maps to NM_001802.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:22358862 G>C maps to NM_001802.1 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:22358582 C>T maps to NM_001802.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:22359092 A>C maps to NM_001802.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15516138 T>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:15499941 C>T maps to ENST00000455584 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:15522457 A>G maps to ENST00000261644 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:14140071 G>A maps to NM_001007530.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr4:85566416 A>C maps to NM_001263.3 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5170849 G>C maps to NM_003818.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:5167437 C>T maps to NM_003818.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:5170745 A>G did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:31083933 A>T maps to NM_001264.4 C486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:88873712 C>T maps to NM_030928.3 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr16:88872176 G>T maps to NM_030928.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr16:88870298 C>T maps to NM_030928.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:133302941 A>G maps to NM_017548.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149563051 C>T maps to NM_001804.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:28537311 G>T maps to NM_001265.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr13:28542987 T>A maps to NM_001265.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr13:28542666 G>T maps to NM_001265.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr13:28542717 G>T maps to NM_001265.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:72667132 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:72667474 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:72667279 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:72667526 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:72674385 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:72673393 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:72667505 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:72667367 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:72667094 C>A did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:72667108 T>C did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:72667543 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:72667442 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:72674300 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:72667490 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:72667207 C>G did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:72667549 A>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:72673479 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:72667225 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:72673428 T>A did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:72673396 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:72674377 G>T did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr6:4892237 G>T maps to ENST00000328908 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:4892411 G>T maps to ENST00000328908 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:4935981 G>T maps to ENST00000328908 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:80638383 C>T maps to NM_152342.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:80642133 T>A did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr16:80718847 G>C maps to NM_152342.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:45206811 T>A maps to ENST00000396750 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51983902 C>A maps to NM_001080405.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:51984863 A>T maps to NM_001080405.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:51986391 C>A maps to NM_001080405.1 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:51986377 C>T maps to NM_001080405.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:51983827 C>T maps to NM_001080405.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:45033479 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:45015706 C>T maps to NM_001102597.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:45029167 G>A maps to NM_001102597.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:45026872 C>A maps to NM_001102597.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:45010245 G>T maps to NM_001102597.1 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:45017235 G>T maps to NM_001102597.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:42312899 C>A maps to NM_001815.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:42132220 C>A maps to NM_001817.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:42132074 C>A maps to NM_001817.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42231193 C>T maps to NM_004363.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:42219635 C>A maps to NM_004363.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:42213866 C>T maps to NM_004363.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr19:42259610 G>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:42190823 C>A maps to NM_006890.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr19:42187791 G>A maps to NM_006890.3 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:43097711 A>T maps to NM_001816.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr19:43093606 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:43097972 C>A maps to NM_001816.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:48808466 G>A maps to NM_005194.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48650523 G>A maps to NM_005195.3 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:23587853 C>A maps to NM_001805.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:23588230 G>T maps to NM_001805.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr14:23588249 T>A maps to NM_001805.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:33870448 G>T maps to NM_001806.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:37455420 C>T maps to NM_005760.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr2:37430152 T>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:37455251 T>A maps to NM_005760.2 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:17688151 G>A maps to NM_017424.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:17672610 A>G maps to NM_017424.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr22:18020341 C>T maps to ENST00000400579 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:17978516 G>T maps to ENST00000400579 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:18022492 G>C maps to ENST00000400579 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:18028663 G>A maps to ENST00000400579 Q1208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr22:18028015 G>T maps to ENST00000400579 A992A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr22:18018335 C>T maps to ENST00000400579 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:135940544 C>T maps to NM_001807.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:135947048 C>A maps to NM_001807.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:135945961 C>T maps to NM_001807.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr9:135940487 C>G maps to NM_001807.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:51733775 C>G maps to NM_001971.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:51723584 C>G maps to NM_001971.5 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr12:51733745 G>T maps to NM_001971.5 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:15788108 C>A maps to ENST00000375924 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:15783626 G>T maps to ENST00000375924 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:15793990 C>A maps to ENST00000375924 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:22336214 C>A maps to NM_005747.4 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:22310739 A>G maps to NM_007352.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:22313088 C>A maps to NM_007352.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:11363182 G>C maps to NM_006561.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:151677545 G>T maps to NM_007185.4 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:151681767 G>T maps to NM_007185.4 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:34853035 G>A maps to NM_020180.3 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:34854815 G>C maps to NM_020180.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:34855076 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:3273913 C>T maps to NM_021938.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:72582474 G>A maps to NM_052840.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr22:46795763 G>A maps to NM_014246.1 H1754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr22:46760541 C>G maps to NM_014246.1 L2882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr22:46807545 G>A maps to NM_014246.1 I1574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr22:46760128 G>A maps to NM_014246.1 V2933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:46787141 C>T maps to NM_014246.1 W2064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:46760116 C>A maps to NM_014246.1 P2937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr22:46780485 G>A maps to NM_014246.1 S2279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:46860000 G>A maps to NM_014246.1 F1262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:109801501 G>T maps to NM_001408.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:109807586 C>T maps to NM_001408.2 T1854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:109793579 G>A maps to NM_001408.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:109815629 C>G maps to NM_001408.2 P2773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:109810585 C>T maps to NM_001408.2 V2074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:48696794 T>G maps to NM_001407.2 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:48697116 G>C maps to NM_001407.2 S984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:48685885 C>T maps to NM_001407.2 L2262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48697760 T>A maps to NM_001407.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:48697066 G>A maps to NM_001407.2 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:48690479 C>G maps to NM_001407.2 R1863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr3:48697250 T>C maps to NM_001407.2 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:2580776 G>A maps to NM_001048212.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:27016113 G>T maps to NM_001809.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:3767007 C>A maps to NM_001810.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr20:3766047 G>A maps to NM_001810.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:3766565 G>A maps to NM_001810.5 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:90038267 C>G maps to NM_145039.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:90038108 C>G maps to NM_145039.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:68374580 C>A maps to NM_001812.2 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:68380365 C>T maps to NM_001812.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:68379792 C>G maps to NM_001812.2 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:104061194 C>G maps to NM_001813.2 V1985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr4:104084359 C>T maps to NM_001813.2 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:104070552 G>A maps to NM_001813.2 Q1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr4:104065531 C>A maps to NM_001813.2 E1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:104082499 C>A maps to NM_001813.2 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr4:104116369 G>A maps to NM_001813.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:104101485 C>A maps to NM_001813.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr4:104103945 A>G maps to NM_001813.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:214791960 A>T maps to NM_016343.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:214818771 C>T maps to NM_016343.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:214818475 G>T maps to NM_016343.3 E1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:214788287 C>G maps to NM_016343.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:214819596 A>G maps to NM_016343.3 E2228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:214826277 C>T maps to NM_016343.3 L2756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:214815961 G>A maps to NM_016343.3 Q1427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:214788296 A>G maps to NM_016343.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:214836932 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr1:214794038 C>T maps to NM_016343.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:214787201 G>A maps to NM_016343.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:214814635 C>T maps to NM_016343.3 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:214820451 C>A maps to NM_016343.3 G2513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:214818159 G>A maps to NM_016343.3 L1749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:214819354 G>T maps to NM_016343.3 E2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:214818018 C>G maps to NM_016343.3 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:214830291 C>T maps to NM_016343.3 T2834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:214832298 C>T maps to NM_016343.3 S3023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:214818283 G>T maps to NM_016343.3 E1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:214832292 G>T maps to NM_016343.3 A3021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:214816615 A>G maps to NM_016343.3 L1645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:214822110 G>T maps to NM_016343.3 E2642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:214828618 G>A maps to NM_016343.3 K2786K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:214818843 G>T maps to NM_016343.3 L1977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:214811234 T>C maps to NM_016343.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:100417902 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:100403106 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:100402978 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:100364526 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:100357330 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:100402799 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:100402992 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:100382592 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:100381697 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:100364528 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:100403111 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:100403112 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:100356186 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:100381765 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:100401266 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr13:25458535 C>T maps to NM_018451.3 V1181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr13:25466833 T>A maps to NM_018451.3 R1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:25457508 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64824355 C>A maps to NM_022145.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:64824278 C>T maps to NM_022145.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:173772115 A>C maps to NM_001127181.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:173780305 T>A maps to NM_001127181.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:81053853 G>C maps to NM_001100624.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr16:81061789 C>T maps to NM_001100624.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:81056209 A>T maps to NM_001100624.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:25040608 C>T maps to NM_024322.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:95375391 A>G maps to NM_001012267.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr9:95142054 A>C maps to NM_001012267.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:95099902 G>T maps to NM_001012267.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr9:95142086 G>T maps to NM_001012267.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:67862625 A>G maps to NM_025082.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:67864377 G>A maps to NM_025082.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr16:67863680 G>A maps to NM_025082.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr6:126661424 G>T maps to ENST00000368325 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:123924433 C>A maps to NM_007018.4 R1770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:123898152 G>T maps to NM_007018.4 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:123920101 A>C maps to NM_007018.4 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123877465 A>T maps to NM_007018.4 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:123907592 G>T maps to NM_007018.4 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:123911010 C>G maps to NM_007018.4 S1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr9:123922512 G>A maps to NM_007018.4 K1674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:122685674 G>T maps to NM_153223.3 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:122729124 C>A maps to NM_153223.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:56858233 A>G maps to NM_025009.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr4:56830456 A>C maps to NM_025009.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr4:56851485 G>T maps to NM_025009.3 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:56847391 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:56865570 G>T maps to NM_025009.3 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:49031026 C>A maps to NM_001194998.1 G1518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr15:49059640 G>A maps to NM_001194998.1 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr15:49073535 T>C maps to NM_001194998.1 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr15:49083486 G>A maps to NM_001194998.1 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:49061269 T>A maps to NM_001194998.1 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:49044593 C>A maps to NM_001194998.1 G1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:117267986 A>G maps to NM_014956.4 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117265079 G>T maps to NM_014956.4 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:117279604 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:117280535 C>T maps to NM_014956.4 S1317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:117234157 C>G maps to NM_014956.4 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:243336058 A>G maps to NM_014812.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:243327604 T>C maps to NM_014812.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:243349109 C>A maps to NM_014812.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:243327829 G>T maps to NM_014812.2 I1144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:243327841 T>G maps to NM_014812.2 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:243385064 C>T maps to NM_014812.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr18:13049049 G>T maps to NM_032142.3 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr18:13071109 A>G maps to NM_032142.3 S1749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr18:13030462 G>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr18:13105056 G>A maps to NM_032142.3 L2342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:34061701 G>T maps to NM_007186.3 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr20:34067213 C>T maps to NM_007186.3 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:34079133 C>T maps to NM_007186.3 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr20:34090952 C>T maps to NM_007186.3 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr12:88486597 G>T maps to NM_025114.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:180047643 A>G maps to NM_014810.4 L1938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:180013209 T>G maps to NM_014810.4 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:180006107 G>T maps to NM_014810.4 E1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:179982979 A>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:179982980 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:179965880 T>C maps to NM_014810.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:179989821 C>T maps to NM_014810.4 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:180063552 A>G maps to NM_014810.4 Q2771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr10:95276915 G>T maps to NM_018131.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:95564351 C>T maps to NM_014679.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:134278006 G>A maps to NM_025180.3 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:134255996 G>T maps to NM_025180.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:134278165 T>C maps to NM_025180.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:134250709 A>G maps to NM_025180.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr3:138244342 C>T maps to NM_024491.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr3:138219358 G>A maps to NM_024491.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:138291754 G>A maps to NM_024491.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:639205 G>A maps to NM_018140.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:640628 C>G maps to NM_018140.3 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr5:639250 G>T maps to NM_018140.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr9:80869843 G>A maps to NM_001098802.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:101477063 C>G maps to ENST00000327230 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:101443555 C>T maps to ENST00000327230 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:101477084 T>C maps to ENST00000327230 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:14720333 G>T maps to NM_005454.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:14722637 G>T maps to NM_005454.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:14722418 G>T maps to NM_005454.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:131193497 G>A maps to NM_016174.4 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr9:131191102 G>T maps to NM_016174.4 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:182413480 C>T maps to NM_001030311.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:182409476 G>T maps to NM_001030311.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:182423392 G>T maps to NM_001030311.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:182438564 T>C maps to NM_001030311.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:55862794 C>A maps to NM_001025195.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:55862836 C>G maps to NM_001025195.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55844546 G>T maps to NM_001025195.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:66975440 G>T maps to NM_003869.5 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:66974561 C>T maps to NM_003869.5 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr16:66975425 C>T maps to NM_003869.5 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:67006789 C>T maps to NM_024922.5 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:67006320 A>T maps to NM_024922.5 K452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr16:66998527 C>T maps to NM_024922.5 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr16:66998346 C>T maps to NM_024922.5 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:55903521 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:55895371 C>T maps to NM_001143685.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr16:55903593 G>T maps to NM_001143685.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:55893497 G>A maps to NM_001143685.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr16:55903557 G>T maps to NM_001143685.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr16:55895335 C>T maps to NM_001143685.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:55880392 G>T maps to NM_001143685.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:55880440 G>A maps to NM_001143685.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:67034818 C>G maps to ENST00000326686 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr18:580695 G>A maps to NM_004066.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr18:580908 G>A maps to NM_004066.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr18:580860 G>T maps to NM_004066.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:151997691 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:151997692 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:151998261 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:151996440 C>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:151997125 G>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr16:56995953 C>A maps to NM_000078.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:57005004 G>A maps to NM_000078.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:31919701 G>A maps to ENST00000437789 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:31918139 C>T maps to ENST00000437789 F1030F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr6:31914201 G>C maps to ENST00000437789 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr6:31916605 G>C did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:131356278 C>G maps to NM_032545.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr2:131356266 G>A maps to NM_032545.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:196654311 G>T maps to NM_000186.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:196714945 G>T did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:196706689 G>C maps to NM_000186.3 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:196646636 G>A maps to NM_000186.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:196709746 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:196645148 T>C maps to NM_000186.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:196648784 G>T maps to NM_000186.3 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:196712627 G>T maps to NM_000186.3 V1060V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:196716442 G>A maps to NM_000186.3 *1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:196711059 G>A maps to NM_000186.3 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:196645128 C>T maps to NM_000186.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:196659292 C>A maps to NM_000186.3 Y420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:196796070 C>T maps to NM_002113.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:196797376 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:196794685 T>C maps to NM_002113.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:196799681 T>C maps to NM_002113.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:196794713 G>T maps to NM_002113.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:196928065 G>A maps to ENST00000367421 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:196927061 G>T maps to ENST00000367421 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:196762603 G>A maps to NM_021023.5 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:196749042 C>T maps to NM_021023.5 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:196762641 A>T maps to NM_021023.5 *331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:196749103 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:196871740 C>A maps to NM_006684.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:196871707 C>A maps to NM_006684.2 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:196887424 A>T maps to NM_006684.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196881878 C>G maps to NM_006684.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr1:196887534 A>C maps to NM_006684.2 *332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:196963385 G>T maps to ENST00000367414 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:196967402 C>T maps to ENST00000367414 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr1:196973881 G>A maps to ENST00000367414 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:196963357 G>A maps to ENST00000367414 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:196964991 T>A maps to ENST00000367414 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr1:196952084 C>T maps to ENST00000367414 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:196963357 G>A maps to ENST00000367414 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:202000804 A>G maps to NM_001127183.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:201994632 A>C maps to NM_001127183.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:202025624 C>T maps to NM_001127183.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:47489072 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:47485814 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:47487499 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:47486199 G>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:47487634 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:47487551 C>A did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:47486575 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:117243606 G>T maps to NM_000492.3 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:117235030 G>A maps to NM_000492.3 W846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:117282537 C>G maps to NM_000492.3 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:117232611 C>A maps to NM_000492.3 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr7:117231993 C>G maps to NM_000492.3 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:117149132 T>A maps to NM_000492.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:87795509 C>T maps to NM_000735.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:87796105 C>A maps to NM_000735.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:87796135 C>A maps to NM_000735.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:87796135 C>T maps to NM_000735.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:87796048 T>A maps to NM_000735.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:88104802 C>A maps to NM_001195308.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr3:88105072 A>G maps to NM_001195308.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151499484 G>T maps to NM_020770.2 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:151504913 C>T maps to NM_020770.2 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:57730400 G>T maps to NM_032866.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr15:57730632 C>T maps to NM_032866.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:57743762 G>A maps to NM_032866.3 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr2:27324378 C>T maps to ENST00000404694 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:54976776 G>T maps to NM_006568.2 G34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:55004778 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:55004893 T>G maps to NM_006568.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:55004903 G>T maps to NM_006568.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:54976676 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:53999057 G>A maps to NM_001008708.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr17:48545502 C>T maps to NM_001267.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:4432136 G>A maps to NM_005483.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:37775117 C>T maps to NM_005441.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:37758466 C>T maps to NM_005441.2 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:50872956 T>C maps to NM_020549.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:50833699 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:50827904 C>A maps to NM_020549.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50863272 T>A maps to NM_020549.4 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:50857552 G>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:50856617 C>T maps to NM_020549.4 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:50856564 C>A maps to NM_020549.4 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr10:50835766 A>T maps to NM_020549.4 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:50870701 G>T maps to NM_020549.4 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:50835817 G>C maps to NM_020549.4 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:50859998 G>A maps to NM_020549.4 Q527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr10:50863281 A>T maps to NM_020549.4 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:98236530 C>T maps to NM_001270.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr5:98192266 C>A maps to NM_001270.2 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr5:98224785 G>C maps to NM_001270.2 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:146758076 G>A maps to NM_004284.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:146747842 G>A maps to NM_004284.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:146759401 G>T maps to NM_004284.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:93496622 A>T maps to NM_001271.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr15:93499826 C>T maps to NM_001271.3 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:93515118 G>T maps to NM_001271.3 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:93558023 C>T maps to NM_001271.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7801418 C>T maps to NM_001005271.2 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:7807239 C>T maps to NM_001005271.2 D1334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:7803212 G>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:7797907 A>G maps to NM_001005271.2 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:6709106 C>A maps to ENST00000309577 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:6702760 G>A maps to ENST00000309577 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr12:6697034 C>T maps to ENST00000309577 E1182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:6680115 T>G maps to ENST00000309577 P1908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:6696923 G>C maps to ENST00000309577 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:6697583 C>A maps to ENST00000309577 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:6709381 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:6710493 C>A maps to ENST00000309577 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:6196656 C>G maps to NM_015557.2 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:6194274 C>A maps to NM_015557.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:6196605 G>T maps to NM_015557.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:6202512 C>A maps to NM_015557.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:6206462 C>A maps to NM_015557.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6173019 G>A maps to NM_015557.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6185834 C>A maps to NM_015557.2 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:6203991 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:6204157 G>A maps to NM_015557.2 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:6196889 G>T maps to NM_015557.2 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:6196844 G>A maps to NM_015557.2 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr1:6186806 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:6188907 G>A maps to NM_015557.2 D1203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:6194813 G>T maps to NM_015557.2 C992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:6171839 G>A maps to NM_015557.2 I1748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:6190296 G>A maps to NM_015557.2 Y1118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:6214762 G>A maps to NM_015557.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:6194861 G>T maps to NM_015557.2 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:6203989 C>A maps to NM_015557.2 E646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:40049591 C>A maps to NM_032221.3 E1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:40049592 C>A maps to NM_032221.3 T1894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40033946 C>T maps to NM_032221.3 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40049654 C>A maps to NM_032221.3 E1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:40102042 C>A maps to NM_032221.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:40053840 G>A maps to NM_032221.3 L1441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:40042044 C>T maps to NM_032221.3 E2350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr20:40040831 C>G maps to NM_032221.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr20:40161983 C>A maps to NM_032221.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr20:40033727 C>A maps to NM_032221.3 P2551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:40033716 G>T maps to NM_032221.3 S2555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr20:40126141 C>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr20:40033716 G>C maps to NM_032221.3 S2555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:40116399 C>A maps to NM_032221.3 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr20:40049349 G>A maps to NM_032221.3 I1975I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr20:40102030 C>A maps to NM_032221.3 G865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:61769147 G>T maps to NM_017780.2 G2437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:61765655 C>T maps to NM_017780.2 F2124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:61654704 G>T maps to NM_017780.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:61655553 G>A maps to NM_017780.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:61750661 G>T maps to NM_017780.2 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:61774814 C>T maps to NM_017780.2 R2631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:61707559 C>T maps to NM_017780.2 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr8:61774826 A>T maps to NM_017780.2 K2635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr8:61774807 T>C maps to NM_017780.2 H2628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:61655604 A>T maps to NM_017780.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:61765694 A>T maps to NM_017780.2 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:61777732 G>T maps to NM_017780.2 L2745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr8:61765932 G>T maps to NM_017780.2 E2217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:61767074 G>A maps to NM_017780.2 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr8:61748803 C>T maps to NM_017780.2 R1317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:61766019 G>T maps to NM_017780.2 E2246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:61769401 A>G maps to NM_017780.2 G2521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:21864051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr14:21859723 C>A maps to NM_001170629.1 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:21876960 C>T maps to NM_001170629.1 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:21868346 C>A maps to NM_001170629.1 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:21870663 T>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr14:21867830 T>C maps to NM_001170629.1 Q1617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:21862292 G>C maps to NM_001170629.1 L1887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:21860106 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21878144 G>A maps to NM_001170629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr14:21862130 C>A maps to NM_001170629.1 G1941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr14:21860938 G>A maps to NM_001170629.1 L2166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr14:21873478 C>A maps to NM_001170629.1 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr14:21897346 G>A maps to NM_001170629.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr14:21870211 G>A maps to NM_001170629.1 G1322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:53338271 T>G maps to ENST00000219084 S2118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:53281337 C>T maps to ENST00000219084 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr16:53191329 T>C maps to ENST00000219084 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:125499161 A>T maps to NM_001274.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:16633868 G>A maps to NM_006387.5 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:16630438 C>T maps to NM_006387.5 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:133428309 G>A maps to NM_001161344.1 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr14:93397925 G>A maps to NM_001275.3 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:5903185 G>A maps to NM_001819.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:5903865 G>A maps to NM_001819.2 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:5897566 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr20:5903170 C>T maps to NM_001819.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:5905682 C>T maps to NM_001819.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:203151967 C>A maps to NM_001276.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:203149612 G>C maps to NM_001276.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:203149636 G>T maps to NM_001276.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:111861778 G>A maps to NM_201653.2 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:72783353 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:72797280 C>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:54880042 C>A maps to NM_012110.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:883185 C>T maps to NM_001142676.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:203191395 G>T maps to NM_003465.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:203192351 G>A maps to NM_003465.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:203192737 G>T maps to NM_003465.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:203186906 C>T maps to NM_003465.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:67864557 A>T maps to NM_001277.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:67832050 T>C maps to NM_001277.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr22:51018793 G>T maps to NM_005198.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:369945 G>T maps to NM_006614.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:424292 G>T maps to NM_006614.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:440828 C>G maps to NM_006614.2 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:384664 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:404926 G>T maps to NM_006614.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:383703 T>A maps to NM_006614.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:447321 C>A maps to NM_006614.2 Y1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:423917 C>A maps to NM_006614.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:424283 C>A maps to NM_006614.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:424235 C>T maps to NM_006614.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr3:396329 T>C maps to NM_006614.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:386356 G>A maps to NM_006614.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr3:391200 T>G maps to NM_006614.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:419518 T>A maps to NM_006614.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr3:396434 C>A maps to NM_006614.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr3:396416 C>T maps to NM_006614.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:405043 C>A maps to NM_006614.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:403380 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:447381 C>A maps to NM_006614.2 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr3:424295 C>T maps to NM_006614.2 N706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr3:447261 C>G maps to NM_006614.2 V1181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr3:370038 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:447381 C>A maps to NM_006614.2 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:432414 G>A maps to NM_006614.2 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr3:424203 G>T maps to NM_006614.2 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:85233801 T>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:85233808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:85211369 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:85128135 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:85156167 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:85302485 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:85213878 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:85211304 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:85119679 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:85218820 T>C did not map to a codon.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr23:85218782 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:85233834 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:85119743 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:85213884 C>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr23:85219007 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:85149240 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:85211156 C>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:85218722 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:85218724 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:85211188 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241798501 G>A maps to NM_001821.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:241797472 C>T maps to NM_001821.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr18:11852091 C>T maps to NM_020412.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:87302614 T>C maps to NM_014043.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:24682633 G>C maps to NM_014169.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:24679975 T>C did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:32440004 A>G maps to NM_176812.4 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:32438872 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:82667719 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:82665452 G>A maps to NM_152284.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr9:33270624 G>T maps to NM_016410.5 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:78968446 G>T maps to NM_024591.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:78972163 A>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr2:175742789 G>A maps to NM_001822.4 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr2:175664885 C>A maps to NM_001822.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:175677109 C>T maps to NM_001822.4 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:29546842 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:19638269 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr21:19638303 T>A maps to NM_024944.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr21:19629021 A>T maps to NM_024944.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:89936514 T>A maps to NM_012124.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:23767748 C>A maps to NM_022097.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:220404715 G>A maps to NM_024536.5 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:150932244 C>A maps to NM_019015.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr7:150935688 C>T maps to NM_019015.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr12:102110586 T>A maps to NM_020244.2 Y215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:184104848 T>C maps to NM_003741.2 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:184104518 G>T maps to NM_003741.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:184103925 C>G maps to NM_003741.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr3:184104389 G>T maps to NM_003741.2 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:184104631 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:184105720 G>T maps to NM_003741.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr3:184099528 G>A maps to NM_003741.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:184103931 G>T maps to NM_003741.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:109931882 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:109937400 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:109919535 T>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:109943925 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:109922563 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:109924710 C>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:110005942 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:109924843 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:109937399 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:109964751 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:109963061 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:109919542 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:109964653 G>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:110035357 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:109924832 C>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:109964629 T>A did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:109924727 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr23:109924727 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:109924722 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:109963073 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:74413893 G>T maps to NM_015424.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:74441864 G>A maps to NM_015424.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:62677633 G>A maps to NM_000738.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:62678509 A>T maps to NM_000738.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:62677483 C>A maps to NM_000738.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:136700961 C>A maps to NM_001006628.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:136700550 C>A maps to NM_001006628.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:136700124 G>T maps to NM_001006628.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr7:136700367 C>T maps to NM_001006628.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:136700193 C>A maps to NM_001006628.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:136699779 C>G maps to NM_001006628.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:136700859 C>A maps to NM_001006628.1 C416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:136700752 C>A maps to NM_001006628.1 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:136700976 C>T maps to NM_001006628.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:136699779 C>A maps to NM_001006628.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:136700014 C>A maps to NM_001006628.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:136700958 G>A maps to NM_001006628.1 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr7:136699632 C>A maps to NM_001006628.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:136699743 C>A maps to NM_001006628.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:136700134 G>T maps to NM_001006628.1 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:136700010 C>A maps to NM_001006628.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:240070931 G>T maps to NM_000740.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:240071332 C>A maps to NM_000740.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:240072433 C>A maps to NM_000740.2 C561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:240071405 G>T maps to NM_000740.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:240071236 C>A maps to NM_000740.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240070780 G>T maps to NM_000740.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:240070930 G>A maps to NM_000740.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:240070813 A>T maps to NM_000740.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240071723 G>T maps to NM_000740.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:240071053 G>T maps to NM_000740.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:240071785 C>T maps to NM_000740.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:240071140 C>T maps to NM_000740.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:46408020 C>T maps to NM_000741.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:46407201 G>T maps to NM_000741.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:46408002 A>G maps to NM_000741.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:46408005 G>A maps to NM_000741.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:46407287 C>A maps to NM_000741.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34356222 C>G maps to NM_012125.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:34355793 C>A maps to NM_012125.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:34355598 G>T maps to NM_012125.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr15:34355379 C>A maps to NM_012125.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:34355841 C>A maps to NM_012125.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:175622694 C>T maps to NM_001039523.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:175624090 G>A maps to NM_001039523.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:175618339 G>T maps to NM_001039523.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:175629092 A>G maps to NM_001039523.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr2:175618426 C>A maps to NM_001039523.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr2:175618414 G>T maps to NM_001039523.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:3688460 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:27321176 G>A maps to NM_000742.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr15:78893786 G>A maps to NM_000743.4 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:61981901 G>C maps to NM_000744.5 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:61981751 C>A maps to NM_000744.5 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:61981847 G>T maps to NM_000744.5 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr20:61990926 G>C maps to NM_000744.5 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:61978134 C>T maps to NM_000744.5 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:61990971 G>T maps to NM_000744.5 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:61991019 G>T maps to NM_000744.5 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:78882621 C>T maps to NM_000745.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:42611339 C>T maps to NM_004198.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:42611417 C>G maps to NM_004198.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:42611333 T>A maps to NM_004198.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:42611771 G>A maps to NM_004198.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:42612117 G>A maps to NM_004198.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr8:42612090 G>A maps to NM_004198.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:42612177 G>T maps to NM_004198.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr8:42612117 G>A maps to NM_004198.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:42611933 T>C maps to NM_004198.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:32393543 G>T maps to NM_001190455.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr4:40339330 C>T maps to NM_017581.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:154544066 C>T maps to NM_000748.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:154543727 C>T maps to NM_000748.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr1:154542284 C>T maps to NM_000748.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:154544243 C>T maps to NM_000748.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:154544087 C>T maps to NM_000748.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:42552715 C>A maps to NM_000749.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:42586929 C>T maps to NM_000749.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:42586824 C>T maps to NM_000749.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:42591709 G>T maps to NM_000749.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:42563857 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:78921764 G>A maps to NM_000750.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:78921929 G>A maps to NM_000750.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr15:78921881 G>T maps to NM_000750.3 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:233396060 G>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:233394808 C>T maps to NM_000751.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:233398754 G>T maps to NM_000751.1 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:233393273 G>T maps to NM_000751.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:233394802 G>A maps to NM_000751.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:233391330 G>T maps to NM_000751.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:4804384 G>A maps to NM_000080.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:233409176 C>A maps to NM_005199.4 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:233409291 T>G did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr2:233408312 G>A maps to NM_005199.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:45671312 G>A maps to NM_003654.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:45672158 G>T maps to NM_003654.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:45671408 G>T maps to NM_003654.4 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr11:45671710 G>T maps to NM_003654.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:45671422 G>T maps to NM_003654.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:45671387 G>A maps to NM_003654.4 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:101012005 C>T maps to NM_004854.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:101010244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:105151494 G>T maps to NM_018413.5 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:105150923 C>T maps to NM_018413.5 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:105151068 C>T maps to NM_018413.5 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:2473293 G>A maps to NM_018641.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:2472402 G>A maps to NM_018641.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:2473086 C>T maps to NM_018641.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:126261141 C>G maps to NM_152889.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:126261333 C>T maps to NM_152889.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:40763897 G>A maps to NM_130468.3 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr10:125798149 G>T maps to NM_015892.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:125798089 G>A maps to NM_015892.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:125805371 G>A maps to NM_015892.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:142841088 G>T maps to NM_004267.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:142840701 C>T maps to NM_004267.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr10:73767037 C>A maps to NM_004273.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr10:73767094 C>T maps to NM_004273.4 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr10:73767292 C>T maps to NM_004273.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71571551 C>A maps to NM_001166395.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:71570874 C>A maps to NM_001166395.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:75563280 G>A maps to NM_024533.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:75513021 G>A maps to NM_021615.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr16:75512952 G>C maps to NM_021615.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:75513168 C>T maps to NM_021615.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:75513270 C>A maps to NM_021615.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr16:75512742 G>A maps to NM_021615.4 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:75512559 G>T maps to NM_021615.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:75512649 C>A maps to NM_021615.4 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:75513168 C>T maps to NM_021615.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:46433944 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:46433843 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:34263295 C>A maps to NM_022467.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr19:34263625 C>T maps to NM_022467.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:34263841 C>T maps to NM_022467.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:34180191 C>A maps to NM_022467.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:34263535 G>A maps to NM_022467.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:34263061 G>T maps to NM_022467.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr18:24496402 G>A maps to NM_031422.4 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr18:24496408 C>T maps to NM_031422.4 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:101717775 T>G maps to NM_014918.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:101717883 C>A maps to NM_014918.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:101719143 C>T maps to NM_014918.4 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:129520887 G>T maps to NM_175856.4 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr5:129520241 G>C maps to NM_175856.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr16:840383 C>G maps to ENST00000317063 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:101964957 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101959778 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:101982737 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:101977790 T>A maps to NM_001278.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:101978566 C>T maps to NM_001278.3 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:101978829 C>A maps to NM_001278.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr10:101960515 C>A maps to NM_001278.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr10:101980342 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:96936995 G>T maps to NM_004804.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:96933113 G>T maps to NM_004804.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr16:57473208 T>A maps to NM_020313.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:57464214 C>T maps to NM_020313.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:78416081 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:16280509 G>T maps to NM_054113.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:16278975 G>A maps to NM_054113.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:26852374 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:26864167 C>T maps to NM_001029881.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:42791819 G>T maps to NM_015125.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:42798341 G>T maps to NM_015125.3 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:12274207 C>A maps to ENST00000342845 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:24775612 C>T maps to NM_014430.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:9911573 G>A maps to ENST00000430427 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr3:9911904 C>A maps to ENST00000430427 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:11002978 C>T maps to NM_000246.3 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:10996624 G>T maps to NM_000246.3 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:11000998 G>T maps to NM_000246.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:65494367 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:65497679 C>G maps to NM_003613.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:65491150 G>A maps to NM_003613.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr15:65490211 G>A maps to NM_003613.3 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:19654862 C>T maps to NM_153221.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:19654683 G>T maps to NM_153221.2 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:19655450 C>A maps to NM_153221.2 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:19655918 G>A maps to NM_153221.2 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:19654529 C>G maps to NM_153221.2 Y392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:19656624 G>T maps to NM_153221.2 E1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:19656542 T>C maps to NM_153221.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:102825901 C>A maps to NM_001177611.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr14:102822164 C>A maps to NM_001177611.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:102825811 G>A maps to NM_001177611.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr19:1270961 T>G maps to ENST00000413636 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr16:69184597 G>A maps to NM_032830.2 A299A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-49-6742-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr3:50645181 C>A maps to NM_013324.5 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:120146112 C>A maps to ENST00000392521 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:120221782 C>A maps to ENST00000392521 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:120166384 A>G maps to ENST00000392521 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:120166314 G>A maps to ENST00000392521 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:120135606 C>A maps to ENST00000392521 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr12:120156086 C>T maps to ENST00000392521 P1377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:120142200 G>A maps to ENST00000392521 Y1757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:120295394 C>A maps to ENST00000392521 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr12:120135821 G>A maps to ENST00000392521 N1887N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:120152001 C>A maps to ENST00000392521 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr12:120306959 G>T maps to ENST00000392521 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:120135561 C>T maps to ENST00000392521 A1928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:71522721 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:139695042 G>A maps to NM_006079.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:139694817 G>A maps to NM_006079.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr6:139694475 G>A maps to NM_006079.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:130941552 G>A maps to NM_012127.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:130942799 G>A maps to NM_012127.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:130941407 G>A maps to NM_012127.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:130941293 C>A maps to NM_012127.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:113514404 T>C maps to NM_152515.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr2:113514764 G>C maps to NM_152515.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr2:113500347 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:106633562 G>A maps to NM_006825.3 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:106633388 C>A maps to NM_006825.3 G408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr12:106633721 G>A maps to NM_006825.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr12:106633455 G>A maps to NM_006825.3 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr12:106632897 C>T maps to NM_006825.3 E571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:46772988 G>A maps to ENST00000415402 F1743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:46812052 C>T maps to ENST00000415402 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr11:46831349 T>C maps to ENST00000415402 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:46774957 A>G maps to ENST00000415402 S1653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:46785063 C>T maps to ENST00000415402 Q1218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:103986585 G>A maps to NM_001823.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr14:103987646 C>T maps to NM_001823.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr14:103988638 C>T maps to NM_001823.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:45810790 G>A maps to NM_001824.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:45811714 C>G maps to NM_001824.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:45810856 G>A maps to NM_001824.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:43890470 C>T maps to ENST00000413657 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:80553611 C>A maps to NM_001825.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:154950547 C>T maps to NM_001826.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:122363411 T>A maps to NM_015282.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:122206697 T>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:122216415 C>G maps to NM_015282.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:33540176 T>G maps to ENST00000359576 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:33586291 G>A maps to ENST00000359576 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:33614642 G>A maps to ENST00000359576 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:86960012 G>T maps to NM_001285.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:86939170 C>T maps to NM_001285.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:86952402 G>T maps to NM_001285.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:86965586 A>G maps to NM_001285.3 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:86959281 G>A maps to NM_001285.3 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:86951147 T>A maps to NM_001285.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:86954770 C>T maps to NM_001285.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:86939559 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:86960042 C>A maps to NM_001285.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:86964327 C>T maps to NM_001285.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:86913415 G>T maps to NM_006536.5 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:86891152 T>A maps to NM_006536.5 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:86905996 C>A maps to NM_006536.5 S457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:86904632 G>T maps to NM_006536.5 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:86919205 T>A maps to NM_006536.5 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:86921202 T>A maps to NM_006536.5 L942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:87029452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:87041100 T>A maps to ENST00000263723 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:87012867 C>A maps to ENST00000263723 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:87045772 A>G maps to ENST00000263723 E836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:87040314 C>G maps to ENST00000263723 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:87012921 T>C maps to ENST00000263723 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:87041234 C>A maps to ENST00000263723 S635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:87031609 C>A maps to ENST00000263723 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:87043669 G>T maps to ENST00000263723 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:87045091 C>A maps to ENST00000263723 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:87045265 A>G maps to ENST00000263723 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:109479737 T>C maps to NM_001048210.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:67132762 G>T maps to NM_013246.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:143029824 C>A maps to NM_000083.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:143047737 C>T maps to NM_000083.2 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:143039109 G>A maps to NM_000083.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143017865 C>A maps to NM_000083.2 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:143016924 T>C maps to NM_000083.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:143016942 T>C maps to NM_000083.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:143039112 C>A maps to NM_000083.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:143016968 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:143039236 T>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:143028406 C>A maps to NM_000083.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:143048739 C>A maps to NM_000083.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:143036383 C>T maps to NM_000083.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:143039181 C>T maps to NM_000083.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:143043747 C>A maps to NM_000083.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:143028328 C>A maps to NM_000083.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr7:143047472 C>A maps to NM_000083.2 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:143049056 G>C maps to NM_000083.2 *989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:143027940 G>T maps to NM_000083.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:143028322 A>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr3:184071085 T>C maps to NM_004366.4 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:170618823 G>A maps to NM_173872.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:170613431 C>G maps to NM_173872.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:170610314 A>T maps to NM_173872.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:10174599 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:10188800 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:10174803 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:10176536 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:10181881 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:10176256 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:10155565 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:10165982 C>G did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:10182001 G>A did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr23:10182100 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:10181854 A>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:10176260 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:10180533 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:49853405 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:49845312 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:49853483 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:49837206 G>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:49854898 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:49834575 G>C did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:49853489 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:49846436 G>T did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:49840595 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:49854784 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:11889328 C>T maps to ENST00000376496 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:11896113 G>A maps to ENST00000376496 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:11866327 G>A maps to ENST00000376496 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:11896119 C>T maps to ENST00000376496 H630H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:11867186 G>C did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:1507712 C>A maps to ENST00000382745 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr16:1498463 C>G maps to ENST00000382745 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:16358321 C>T maps to NM_004070.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:16351312 C>T maps to NM_004070.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:16353089 G>T maps to NM_004070.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:16358737 G>T maps to NM_004070.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:16375010 C>T maps to NM_000085.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:16378693 G>T maps to NM_000085.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:190027980 G>A maps to NM_021101.4 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:190026066 C>T maps to NM_021101.4 *212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:190026122 G>A maps to NM_021101.4 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:96086269 C>A maps to NM_182848.3 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:96205171 C>T maps to NM_006984.4 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:170140989 C>A maps to NM_005602.5 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:90042181 C>T maps to NM_001185072.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr7:90042544 G>C maps to NM_001185072.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr21:37833633 G>T maps to NM_001146077.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr21:37833636 G>T maps to NM_001146077.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:100876127 C>T maps to NM_014343.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:190126220 G>A maps to NM_006580.3 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31538560 G>A maps to NM_012131.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:31538608 G>A maps to NM_012131.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:31538716 G>A maps to NM_012131.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:137742561 C>T maps to NM_016369.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:137717892 C>A maps to NM_001002026.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:137749853 C>A maps to NM_016369.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr3:137717826 C>A maps to NM_001002026.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:137742521 C>A maps to NM_016369.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:106171517 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:106171886 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:106171684 A>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:106171706 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:106171780 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:106171473 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:8560234 C>A maps to NM_194284.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr11:113650991 C>A maps to NM_001101389.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:113650516 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7164149 G>A maps to NM_001185022.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr17:7163725 G>A maps to NM_001185022.1 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr21:31587928 G>C maps to NM_199328.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:3063830 C>T maps to NM_020982.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:3063923 G>A maps to NM_020982.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:51871756 G>C maps to NM_152353.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:6978390 G>T maps to NM_182906.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51226832 C>T maps to NM_002975.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:51228645 G>T maps to NM_002975.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr19:51228603 C>T maps to NM_002975.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:10124249 G>T maps to ENST00000355690 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr12:10168266 A>T maps to NM_001129998.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:38724678 G>A maps to NM_175060.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:38724381 G>A maps to NM_175060.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr14:38724576 C>A maps to NM_175060.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:38724114 G>T maps to NM_175060.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:38724627 G>A maps to NM_175060.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr16:11118743 G>C maps to ENST00000409790 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:11114170 G>A maps to ENST00000409790 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr16:11260248 C>T maps to ENST00000409790 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:11038616 A>T maps to ENST00000409790 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:14707959 G>T maps to ENST00000417570 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14710888 C>G maps to ENST00000417570 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr19:14698429 C>A maps to ENST00000417570 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:74446938 G>T maps to NM_001011880.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:10226011 T>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:10228147 A>C maps to NM_016511.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr12:10233992 G>A maps to NM_016511.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:10150959 G>A maps to NM_016509.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr12:10010224 G>A maps to NM_005127.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:78064458 C>A maps to NM_005752.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr16:78064471 G>T maps to NM_005752.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:45077112 G>A maps to NM_003278.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:8288250 A>G maps to NM_016184.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:8670778 A>C maps to NM_080387.4 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:8673749 T>A maps to NM_080387.4 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:8688714 C>T maps to NM_014358.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:71043248 G>A maps to NM_173535.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:71043306 G>A maps to NM_173535.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:71046532 T>G maps to NM_173535.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:71044164 G>A maps to NM_173535.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:71043261 G>A maps to NM_173535.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:71044011 C>T maps to NM_173535.2 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr2:71043960 C>T maps to NM_173535.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:7828196 G>A maps to NM_014257.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:7832416 C>T maps to NM_014257.4 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:7830593 G>A maps to NM_014257.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:141629975 G>A maps to NM_013252.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:10205372 T>C maps to NM_207345.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:10217377 C>A maps to NM_207345.2 Y173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10218182 G>T maps to NM_207345.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:31701436 C>T maps to NM_001288.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:154508496 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:154507269 A>G did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:154508585 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:154508455 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:25167380 G>T maps to NM_013943.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:45870992 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:36080996 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr21:36079666 G>T maps to ENST00000360731 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:157233055 C>A maps to NM_001195555.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:157232888 A>T maps to NM_001195555.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:157216485 G>A maps to NM_001195555.1 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:157232901 G>C maps to NM_001195555.1 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:122862098 G>C maps to ENST00000302528 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:122862286 C>A maps to ENST00000302528 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr12:122845559 G>A maps to ENST00000302528 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr12:122803777 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:122862307 G>A maps to ENST00000302528 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:73753333 G>T maps to NM_003388.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:73768238 G>T maps to NM_003388.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:73771659 C>A maps to NM_003388.4 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:73790269 C>A maps to NM_003388.4 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr7:73795167 G>T maps to NM_003388.4 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:73790473 C>A maps to NM_003388.4 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:36517902 G>A maps to NM_015526.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:36508344 C>A maps to NM_015526.2 G487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:36509847 G>T maps to NM_015526.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:29390369 G>T maps to ENST00000379543 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:29358411 A>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:29375677 G>T maps to ENST00000379543 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:29404701 G>C maps to ENST00000379543 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:29375644 C>T maps to ENST00000379543 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:201718133 G>C maps to NM_001162407.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:201726035 A>G maps to NM_001162407.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:155233107 C>A maps to ENST00000368361 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr15:74919992 G>A maps to NM_001130028.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:178050303 T>C maps to NM_020666.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:92818630 C>A maps to NM_001025233.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:95682071 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:95677188 C>G maps to NM_024734.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr14:95670314 C>T maps to NM_024734.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:28498849 G>A maps to NM_000086.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:28488911 G>T maps to NM_000086.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:28488845 C>T maps to NM_000086.2 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569227 T>G maps to NM_006493.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:77569332 A>G maps to NM_006493.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr13:77566283 G>T maps to NM_006493.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr13:77570218 C>T maps to NM_006493.2 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr15:68500741 C>A maps to NM_017882.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:68504015 C>A maps to NM_017882.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:10492114 G>T maps to NM_052964.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr4:10542119 G>C maps to NM_052964.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:10566321 G>T maps to NM_052964.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:10509588 C>T maps to NM_052964.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:77333671 T>C maps to NM_001293.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:56344979 A>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:57428833 C>T maps to NM_006831.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:57427352 C>T maps to NM_006831.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:57428601 G>A maps to NM_006831.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:72012962 C>A maps to NM_030813.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:72145269 G>A maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:72145269 G>C maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:35763531 G>A maps to NM_001832.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:35765032 G>T maps to NM_001832.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr6:35762923 C>G maps to NM_001832.2 *113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr19:45488521 G>T maps to NM_001294.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:45477824 G>T maps to NM_001294.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:45477748 G>C maps to NM_001294.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:1323906 A>G maps to NM_030782.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr5:1339045 C>T maps to NM_030782.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:1318498 C>T maps to NM_030782.3 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:1323948 G>C maps to NM_030782.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:65447221 C>T maps to NM_006660.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:150690384 A>T maps to NM_001195794.1 T37T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-95-7567-01A-11D-2063-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:17528599 C>T maps to NM_001079827.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:17524643 C>A maps to NM_001079827.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:17524556 C>G maps to NM_001079827.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:17528581 C>T maps to NM_001079827.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:17528452 G>C maps to NM_001079827.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:129676622 G>A maps to NM_152311.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:129690841 T>G maps to NM_152311.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:36226020 C>A maps to NM_022111.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:36226021 C>A maps to NM_022111.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:36209100 T>A maps to NM_022111.3 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:9801203 C>A maps to NM_001009566.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:9811564 G>A maps to NM_001009566.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:9791825 C>T maps to NM_001009566.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:140277557 C>A maps to NM_022131.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:140285093 A>G maps to NM_022131.2 *956W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:140285094 G>T maps to NM_022131.2 *956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:140265369 C>A maps to NM_022131.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:140277664 C>T maps to NM_022131.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:140122645 A>T maps to NM_022131.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:140251314 C>T maps to NM_022131.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140178588 C>A maps to NM_022131.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:140277676 C>A maps to NM_022131.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:140167391 C>T maps to NM_022131.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:140275474 C>A maps to NM_022131.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:140282885 C>A maps to NM_022131.2 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:7288096 C>G maps to NM_014718.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:7295904 C>A maps to NM_014718.3 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:7288871 G>A maps to NM_014718.3 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:36197558 G>T maps to NM_007096.3 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:57725718 C>A maps to NM_004859.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:57762457 T>C maps to NM_004859.3 N1492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:57746154 G>T maps to NM_004859.3 G716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:57721647 G>C maps to NM_004859.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:57741252 A>G maps to NM_004859.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:19171031 G>A maps to NM_007098.3 F1566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:19196444 T>C maps to NM_007098.3 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:19183810 C>T maps to NM_007098.3 W1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr22:19230339 G>C maps to NM_007098.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:27462597 G>A maps to NM_001831.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:641486 G>A maps to NM_199167.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:633425 C>T maps to NM_199167.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr8:62371044 C>T maps to NM_173519.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:62212571 C>G maps to NM_173519.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:62371092 G>T maps to NM_173519.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:62212460 T>C maps to NM_173519.2 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:62212448 C>A maps to NM_173519.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:62289212 C>T maps to NM_173519.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:123319272 G>A maps to NM_001010852.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:123319299 G>A maps to NM_001010852.2 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:123369764 A>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:123376973 G>T maps to NM_001010852.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:123332168 T>C maps to NM_001010852.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:123377168 G>A maps to NM_001010852.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:100543591 G>T maps to NM_206808.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:100518492 G>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr13:100511245 G>T maps to NM_206808.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:24976617 A>G maps to NM_001836.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:24974787 G>T maps to NM_001836.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:24976665 G>T maps to NM_001836.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:24975308 G>A maps to NM_001836.2 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:22208544 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:22208540 G>T maps to NM_018686.3 G186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:22211631 C>T maps to NM_018686.3 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:10288613 C>T maps to NM_138809.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:10288574 G>A maps to NM_138809.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:81730227 G>T maps to NM_198390.2 G532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:108686655 C>T maps to NM_001142344.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr12:108686690 C>A maps to NM_001142344.1 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:6991648 C>T maps to NM_207315.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:6991687 C>A maps to NM_207315.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:7003595 C>A maps to NM_207315.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:66613614 G>A maps to NM_144673.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr16:66621856 C>A maps to NM_144673.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr16:66651242 G>A maps to NM_178818.2 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:23847664 C>T maps to ENST00000339180 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:79029480 G>T maps to NM_153610.3 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:79028949 A>T maps to NM_153610.3 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79028115 A>T maps to NM_153610.3 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:79034901 A>T maps to NM_153610.3 S3438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:79032561 A>G maps to NM_153610.3 V2658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:79029780 T>C maps to NM_153610.3 S1731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:79030941 G>A maps to NM_153610.3 E2118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:79026484 G>T maps to NM_153610.3 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:79084792 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr5:79029021 A>G maps to NM_153610.3 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr5:79030788 T>C maps to NM_153610.3 S2067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88249303 A>G maps to NM_173538.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:88249283 G>T maps to NM_173538.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr8:88365913 C>A maps to NM_173538.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:88249150 T>A maps to NM_173538.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:88249219 G>A maps to NM_173538.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:87917311 G>C maps to NM_173538.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:87951935 A>T maps to NM_173538.2 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:88218366 G>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr8:88296947 C>T maps to NM_173538.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:72238503 C>T maps to NM_032649.5 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:72250878 C>T maps to NM_032649.5 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72250893 G>T maps to NM_032649.5 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr18:72176087 G>A maps to NM_018235.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:72183516 G>T maps to NM_018235.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr18:72180860 G>T maps to NM_018235.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47942861 A>T maps to NM_001142564.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:150912785 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:150908125 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:150912359 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:150912052 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:150912096 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:150912747 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:150911088 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:150911820 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:150911914 G>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:150912289 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:150907048 C>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:150911607 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:150912020 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:150912465 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:150912759 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:150912076 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:150912331 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:150911607 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:150912083 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:150906978 G>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:150906968 C>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:150912484 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:99012829 G>T maps to NM_001298.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:98999889 C>T maps to NM_001298.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99012598 T>C maps to NM_001298.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:99013353 C>A maps to NM_001298.2 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:98986504 C>A maps to NM_001298.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:99013597 G>A maps to NM_001298.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:99012949 G>T maps to NM_001298.2 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:6260973 G>T maps to NM_001037329.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:6261341 G>T maps to NM_001037329.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:6262814 G>T maps to NM_001037329.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:6265579 G>T maps to NM_001037329.2 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:6260685 C>A maps to NM_001037329.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:6262678 C>A maps to NM_001037329.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:6265498 G>T maps to NM_001037329.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:57949203 G>C maps to NM_001297.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:57957274 C>T maps to NM_001297.4 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr16:57954297 G>T maps to NM_001297.4 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:57935285 G>A maps to NM_001297.4 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:57998442 G>A maps to NM_001297.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:87638258 G>T maps to NM_019098.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:87656857 A>G maps to NM_019098.4 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:87656850 T>A maps to NM_019098.4 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:87755831 G>T maps to NM_019098.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:87645121 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:87591392 G>C maps to NM_019098.4 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:87588160 G>T maps to NM_019098.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:87679266 G>C maps to NM_019098.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:87656905 T>A maps to NM_019098.4 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:87683232 G>A maps to NM_019098.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr8:87679338 G>T maps to NM_019098.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:87641255 G>T maps to NM_019098.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:87638249 A>G maps to NM_019098.4 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:87738862 G>T maps to NM_019098.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:66049782 G>C maps to NM_182553.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:224922381 C>A maps to NM_152495.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:224922276 T>C maps to NM_152495.1 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:224544694 C>T maps to NM_014184.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:26510755 C>A maps to ENST00000374253 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr1:26507363 C>T maps to ENST00000374253 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:26514739 C>G maps to ENST00000374253 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:26513900 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:21609189 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:21627327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:21545095 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:21488898 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:21545046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:21627540 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:21534735 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:21667054 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:21609203 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:21627665 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:21609203 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:21508640 A>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:21627612 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:21444637 T>C did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:21670427 G>C did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:21613103 G>C did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:21545027 C>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:21450828 G>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:21488893 T>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:21534653 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:21627365 C>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:21670455 A>C did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:21450848 C>G did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:21450745 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:21624982 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:21609266 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:21624934 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:21627340 C>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:21627460 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:21444615 T>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:21627196 C>A did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:21627588 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:21534638 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:21608720 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:154763226 C>G maps to NM_173515.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:11657492 C>T maps to NM_001299.4 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:11660567 C>A maps to NM_001299.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr19:1037754 C>T maps to NM_004368.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:95368679 G>A maps to NM_001839.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:101122150 C>T maps to NM_020348.2 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:101136905 C>A maps to NM_020348.2 Y757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:101090478 C>T maps to NM_020348.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:101150159 C>A maps to NM_020348.2 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:101117350 G>A maps to NM_020348.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:104679103 C>T maps to NM_017649.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:104687114 G>A maps to NM_199077.1 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:97427780 G>T maps to NM_020184.3 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:97463257 C>T maps to NM_020184.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:58621299 G>T maps to NM_016284.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:58633193 C>T maps to NM_016284.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:58580243 G>C maps to NM_016284.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:58616807 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:58621688 G>A maps to NM_016284.3 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:58617058 C>A maps to NM_016284.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:58571123 T>C maps to NM_016284.3 G1805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:58615250 G>A maps to NM_016284.3 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:32745454 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:70713109 G>T maps to NM_014515.5 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:70747664 C>T maps to NM_014515.5 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:54647869 G>C maps to NM_014516.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:54647833 C>A maps to NM_014516.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:54652037 A>G maps to NM_014516.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:54649348 G>T maps to NM_014516.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:54659090 G>A maps to NM_014516.3 K736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:135106984 T>A maps to NM_001190850.1 K98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:135080501 G>C maps to NM_001190850.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:135095328 G>A maps to NM_001190850.1 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:135099130 G>C maps to NM_001190850.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr5:179976928 A>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr4:78652604 C>A maps to ENST00000512485 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:78697425 C>A maps to ENST00000512485 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr17:40125653 G>A maps to NM_033133.4 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:155295765 G>C maps to NM_001103176.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:155295763 T>C maps to NM_001103176.1 *93W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:42905836 C>T maps to NM_006586.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:42905453 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:88854042 G>T maps to NM_016083.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:88854123 G>A maps to NM_016083.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:88854581 G>A maps to NM_016083.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:88854095 T>A maps to NM_016083.4 K300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:88853844 A>G maps to NM_016083.4 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:24201555 T>A maps to NM_001841.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:24201957 C>T maps to NM_001841.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:246784845 G>T maps to NM_152609.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:246829095 C>T maps to NM_152609.2 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:246810552 C>T maps to NM_152609.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:246811010 C>G maps to NM_152609.2 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:246784875 A>G maps to NM_152609.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:40959839 T>A maps to NM_173478.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:40958758 C>T maps to NM_173478.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr17:40957870 G>C maps to NM_173478.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:58390329 G>A maps to NM_000614.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr9:34557977 C>T maps to NM_147164.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:34564626 G>A maps to NM_147164.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr9:34557530 G>A maps to NM_147164.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr9:34557623 G>T maps to NM_147164.1 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr9:17409324 G>T maps to NM_017738.2 G884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:17395055 G>T maps to NM_017738.2 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr9:17394936 A>T maps to NM_017738.2 K829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:17388158 G>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:17484327 G>A maps to NM_017738.2 V1297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:41323637 A>G maps to NM_001843.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:41312564 G>A maps to NM_001843.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:41333203 G>C maps to NM_001843.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:41419070 C>A maps to NM_001843.2 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:41316171 T>C maps to NM_001843.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:41422923 C>A maps to NM_001843.2 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:41421698 T>A maps to NM_001843.2 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:41337887 C>A maps to NM_001843.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:41463833 C>T maps to NM_001843.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:41337491 G>T maps to NM_001843.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:41323596 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:41323781 C>A maps to NM_001843.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr12:41337795 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:41463806 C>T maps to NM_001843.2 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr12:41419052 C>A maps to NM_001843.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205034236 C>A maps to NM_005076.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:205042200 G>T maps to NM_005076.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:205030381 C>A maps to NM_005076.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:205038617 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:205036280 C>T maps to NM_005076.3 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:205028299 G>A maps to NM_005076.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:205030522 C>A maps to NM_005076.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:205031665 C>A maps to NM_005076.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205035634 G>A maps to NM_005076.3 W628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:205042859 G>A maps to NM_005076.3 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:205031636 C>T maps to NM_005076.3 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:205033552 C>T maps to NM_005076.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:74413645 A>C maps to NM_020872.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:74334528 C>G maps to NM_020872.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74334492 A>G maps to NM_020872.1 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:74411126 C>G maps to NM_020872.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:74334454 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:74350796 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:74548835 T>G maps to NM_020872.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr3:74347276 C>A maps to NM_020872.1 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr3:74411060 C>T maps to NM_020872.1 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:74315767 T>C maps to NM_020872.1 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:74334465 G>A maps to NM_020872.1 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr3:74350906 T>G maps to NM_020872.1 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr3:74316415 C>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr3:74474017 G>A maps to NM_020872.1 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:74414806 C>A maps to NM_020872.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:74350698 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:74347252 C>A maps to NM_020872.1 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:2944633 T>A maps to NM_175607.1 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:2778004 A>G maps to NM_175607.1 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:3083997 C>T maps to NM_175607.1 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:2908580 G>T maps to NM_175607.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:2924926 G>T maps to NM_175607.1 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:2967316 A>T maps to NM_175607.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr3:3078941 A>T maps to NM_175607.1 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:99715817 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:99715984 C>T maps to NM_014361.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:100226947 G>A maps to NM_014361.2 W1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:99827595 G>T maps to NM_014361.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:100169964 T>A maps to NM_014361.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:100126552 G>C maps to NM_014361.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr11:100169955 T>C maps to NM_014361.2 N816N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:100170105 G>A maps to NM_014361.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:99872826 T>G maps to NM_014361.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:100095500 C>A maps to NM_014361.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:100061935 G>A maps to NM_014361.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99941252 G>T maps to NM_014361.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:99945011 T>C maps to NM_014361.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:99690431 G>C maps to NM_014361.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr11:99872787 G>A maps to NM_014361.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr11:100170003 C>A maps to NM_014361.2 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:100141899 A>T maps to NM_014361.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:99944984 C>A maps to NM_014361.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:99690496 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:99942488 C>A maps to NM_014361.2 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:1445041 C>A maps to NM_014461.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:1415641 A>C maps to NM_014461.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:1415381 C>A maps to NM_014461.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:1424652 G>T maps to NM_014461.2 E732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:1418746 C>A maps to NM_014461.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr3:1369193 A>G maps to NM_014461.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr3:1371542 G>T maps to NM_014461.2 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:40840597 G>C maps to NM_003632.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:40844609 G>A maps to NM_003632.2 W875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr17:40842163 C>T maps to NM_003632.2 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:147183116 G>T maps to NM_014141.5 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:146818110 G>C maps to NM_014141.5 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:147336342 C>A maps to NM_014141.5 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:147600732 C>A maps to NM_014141.5 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:146805425 C>A maps to NM_014141.5 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:147914551 C>G maps to NM_014141.5 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr7:147336252 C>T maps to NM_014141.5 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:146471384 C>A maps to NM_014141.5 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:148112509 C>G maps to NM_014141.5 G1266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:147914434 A>G maps to NM_014141.5 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:146536800 A>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr7:146536867 C>A maps to NM_014141.5 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr7:146818107 A>T maps to NM_014141.5 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:147259349 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:148080825 C>A maps to NM_014141.5 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:147869450 C>A maps to NM_014141.5 S964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:146829575 G>A maps to NM_014141.5 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:147869547 T>C maps to NM_014141.5 Y996Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr7:146997299 C>T maps to NM_014141.5 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr7:146997362 C>T maps to NM_014141.5 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:147926771 C>A maps to NM_014141.5 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:147926772 C>T maps to NM_014141.5 R1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr7:147336366 C>T maps to NM_014141.5 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr7:146536992 C>T maps to NM_014141.5 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:147675036 C>A maps to NM_014141.5 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:146829374 G>C maps to NM_014141.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:146829413 C>A maps to NM_014141.5 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr7:147183025 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr7:147259228 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:39171477 C>T maps to NM_033655.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:76555171 T>A maps to NM_033401.3 L833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:76482811 A>G maps to NM_033401.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:76569482 C>A maps to NM_033401.3 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:76573653 G>T maps to NM_033401.3 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:76528858 C>A maps to NM_033401.3 Y710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:76513433 C>G maps to NM_033401.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76486439 T>A maps to NM_033401.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:76513433 C>A maps to NM_033401.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr16:76350352 C>T maps to NM_033401.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:76556002 C>A maps to NM_033401.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:76482784 G>A maps to NM_033401.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:76495943 T>A maps to NM_033401.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:76495953 C>T maps to NM_033401.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:76513434 G>T maps to NM_033401.3 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:76569440 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:76481990 T>A maps to NM_033401.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:76555039 C>A maps to NM_033401.3 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:76523734 G>T maps to NM_033401.3 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:76486649 C>A maps to NM_033401.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:76532466 C>A maps to NM_033401.3 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:76513353 G>T maps to NM_033401.3 G600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:76486532 T>A maps to NM_033401.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:76569472 G>T maps to NM_033401.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr16:76528936 C>A maps to NM_033401.3 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:125660660 G>C maps to NM_130773.2 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:125261888 C>A maps to NM_130773.2 C360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:125555739 C>A maps to NM_130773.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:125367480 G>T maps to NM_130773.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:125671720 C>A maps to NM_130773.2 T1259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr2:125555844 C>A maps to NM_130773.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:124979372 C>A maps to NM_130773.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:125660603 C>A maps to NM_130773.2 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:125281973 G>A maps to NM_130773.2 P473P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:125671705 C>T maps to NM_130773.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:125547668 C>T maps to NM_130773.2 Y980Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:125232345 A>T maps to NM_130773.2 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:125521641 C>T maps to NM_130773.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:125671742 C>T maps to NM_130773.2 Q1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:124783244 G>T maps to NM_130773.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:125192148 C>A maps to NM_130773.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:125261972 G>C maps to NM_130773.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:125504839 C>A maps to NM_130773.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:125405431 C>T maps to NM_130773.2 Y657Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:125204378 C>A maps to NM_130773.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:125204375 G>T maps to NM_130773.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:125660516 C>A maps to NM_130773.2 C1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:125262074 T>A maps to NM_130773.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:125530376 T>C maps to NM_130773.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:125547602 C>A maps to NM_130773.2 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:125192149 C>T maps to NM_130773.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:125192170 G>T maps to NM_130773.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:125671837 C>T maps to NM_130773.2 S1298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:125281943 G>T maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:125284886 C>A maps to NM_130773.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:125261951 C>T maps to NM_130773.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:125547510 G>T maps to NM_130773.2 G928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:125671708 C>T maps to NM_130773.2 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:125504878 G>T maps to NM_130773.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:125530388 C>A maps to NM_130773.2 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:125530592 A>T maps to NM_130773.2 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:125284955 G>A maps to NM_130773.2 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:125192088 A>T maps to NM_130773.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:7838316 C>T maps to NM_001037144.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:7838352 C>T maps to NM_001037144.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:7849269 C>T maps to NM_001037144.4 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:40716075 C>T maps to NM_001042532.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:40717804 G>C maps to NM_001042532.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:51097084 C>A maps to ENST00000395542 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:51111276 C>A maps to ENST00000395542 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:51111320 C>A maps to ENST00000395542 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:51251815 T>A maps to ENST00000395542 K256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr7:51261078 A>G maps to ENST00000395542 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:51096452 C>G maps to ENST00000395542 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr7:51095432 C>T maps to ENST00000395542 A1202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:51095654 G>A maps to ENST00000395542 H1128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:51258589 G>A maps to ENST00000395542 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr7:51203959 C>A maps to ENST00000395542 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:165561010 C>A maps to ENST00000392717 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:165584559 G>A maps to ENST00000392717 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:165559623 T>C maps to ENST00000392717 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:165551804 A>G maps to ENST00000392717 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr2:165560971 C>A maps to ENST00000392717 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr14:31348047 C>A maps to NM_004086.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:31349862 G>A maps to NM_004086.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr14:31354732 C>T maps to NM_004086.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr14:31346906 C>A maps to NM_004086.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr14:31344260 G>C did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr14:31355423 A>C maps to NM_004086.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:31346776 G>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:71189307 G>T maps to NM_018714.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:230822782 C>T maps to NM_007357.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:230795244 T>C maps to NM_007357.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:230814765 G>A maps to NM_007357.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:230822838 C>G maps to NM_007357.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:46083855 C>T maps to NM_031431.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:46103924 G>T did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr13:46054292 G>A maps to NM_031431.2 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr13:46050483 T>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr13:46060664 C>T maps to NM_031431.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr16:70542343 C>A maps to NM_015386.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:70531929 G>C maps to NM_015386.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:23428348 T>A maps to NM_153603.3 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:23404668 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:55027939 A>C maps to NM_004645.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr17:55027857 C>A maps to NM_004645.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:116446630 G>A maps to NM_000493.3 L9L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-64-5779-01A-01D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-78-7161-01A-11D-2036-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-78-7220-01A-11D-2036-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-8669-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:103444660 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:103379961 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:103487271 C>T maps to NM_080629.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:103471677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:103471864 G>A maps to NM_080629.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103345237 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:103467507 T>C maps to NM_080629.2 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:103496797 C>A maps to NM_080629.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:103544257 T>C maps to NM_080629.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:103449746 C>A maps to NM_080629.2 G847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:103352407 G>T maps to NM_080629.2 R1617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:103540212 C>T maps to NM_080629.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:103364516 G>A maps to NM_080629.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:103468347 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:103462665 T>C maps to NM_080629.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:103352612 C>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr1:103468347 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:103474072 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:103404625 C>A maps to NM_080629.2 G1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:103461465 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:103428211 T>A maps to NM_080629.2 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:103348759 C>A maps to NM_080629.2 E1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:103573698 C>A maps to NM_080629.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:103345256 T>A maps to NM_080629.2 T1764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:103548451 G>T maps to NM_080629.2 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103348789 C>A maps to NM_080629.2 E1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:103444651 A>T maps to NM_080629.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:103364266 T>C maps to NM_080629.2 A1413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:103544305 C>A maps to NM_080629.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:103453263 T>C maps to NM_080629.2 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:103449738 A>T maps to NM_080629.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:103388945 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:103540336 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:103427821 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:103379961 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:103400049 C>T maps to NM_080629.2 E1197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:33133722 G>T maps to NM_080680.2 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33139546 C>T maps to NM_080680.2 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33153522 G>C maps to NM_080680.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:33156807 C>G maps to NM_080680.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:33144975 G>A maps to NM_080680.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:33139528 C>A maps to NM_080680.2 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:33141522 C>G did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr6:33139581 G>A maps to NM_080680.2 R1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr6:33141290 C>A maps to NM_080680.2 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr6:33143434 G>A maps to NM_080680.2 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:33157166 A>G maps to NM_080680.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:33135283 C>A maps to NM_080680.2 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:33151933 G>T maps to NM_080680.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:75843578 C>A maps to ENST00000322507 E1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:75799843 C>A maps to ENST00000322507 G2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:75860866 G>C maps to ENST00000322507 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:75798879 T>A maps to ENST00000322507 G2984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:75801214 T>C maps to ENST00000322507 K2892K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:75839937 C>A maps to ENST00000322507 G2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:75834046 C>A maps to ENST00000322507 G2216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr6:75840694 T>A maps to ENST00000322507 I1980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:75812365 G>A maps to ENST00000322507 Q2788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:75899097 C>A did not map to a codon.
Alternatively spliced codon TCGA-73-4670-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:75813478 C>G maps to ENST00000322507 G2771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:75804894 C>A maps to ENST00000322507 G2860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr6:75898121 G>T maps to ENST00000322507 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr6:75892911 G>C maps to ENST00000322507 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:75893729 T>C maps to ENST00000322507 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:75884985 C>A maps to ENST00000322507 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:75806980 T>C maps to ENST00000322507 P2855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:71707070 T>C maps to ENST00000356340 H666H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr10:71686840 A>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:71707088 G>A maps to ENST00000356340 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:71562454 C>T maps to ENST00000356340 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:71678039 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:71690196 C>A maps to ENST00000356340 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:71692332 C>A maps to ENST00000356340 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:121216050 G>T maps to NM_021110.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:121259924 C>T maps to NM_021110.1 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:121237373 T>A maps to NM_021110.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:121215954 A>G maps to NM_021110.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121224716 G>T maps to NM_021110.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr8:121267560 C>A maps to NM_021110.1 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:121219203 G>A maps to NM_021110.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:121267515 T>G maps to NM_021110.1 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:121301935 C>T maps to NM_021110.1 I1389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:121228645 C>T maps to NM_021110.1 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:121220514 G>A maps to NM_021110.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:121174764 C>T maps to NM_021110.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:121267477 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr8:121354681 C>T maps to NM_021110.1 Q1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:121239002 G>T maps to NM_021110.1 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:121239520 T>C maps to NM_021110.1 Y689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:121357761 C>T maps to NM_021110.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:121309823 C>A maps to NM_021110.1 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:101807015 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:101748342 C>T maps to NM_001855.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:101788229 C>A maps to NM_001855.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:101804357 T>A maps to NM_001855.3 L848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:101806866 G>A maps to NM_001855.3 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:101797642 C>A maps to NM_001855.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:101797629 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:101788184 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:101817382 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:101824293 G>T maps to NM_001855.3 A1148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr9:101832053 A>G maps to NM_001855.3 G1351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:101747955 G>A maps to NM_001855.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:101800986 C>A maps to NM_001855.3 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:101825333 A>G maps to NM_001855.3 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:101806848 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:101749649 G>A maps to NM_001855.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:101802813 G>A maps to NM_001855.3 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:101825333 A>T maps to NM_001855.3 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr9:101787220 T>A maps to NM_001855.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:101817399 A>G maps to NM_001855.3 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:101824376 T>A maps to NM_001855.3 L1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:101797390 C>T maps to NM_001855.3 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:32167740 G>A maps to NM_001856.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:32164182 C>T maps to NM_001856.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:32162566 G>A maps to NM_001856.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:32145268 G>T maps to NM_001856.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32138037 C>T maps to NM_001856.3 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:32157623 C>A maps to NM_001856.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:32154670 G>A maps to NM_001856.3 Q546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:105796298 C>T maps to NM_000494.3 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr10:105800829 G>A maps to NM_000494.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr10:105797469 T>C maps to NM_000494.3 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:105798212 G>A maps to NM_000494.3 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr10:105801267 G>C maps to NM_000494.3 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr10:105792027 G>T maps to NM_000494.3 R1487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:105830295 G>T maps to NM_000494.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:46888411 G>T maps to ENST00000359759 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:46908345 G>T maps to ENST00000359759 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr21:46901926 G>A maps to ENST00000359759 Q969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:46925786 C>A maps to ENST00000359759 G1456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:46875677 C>T maps to ENST00000359759 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:46900711 A>G maps to ENST00000359759 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:70647964 T>A maps to NM_001858.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:70866083 T>A maps to NM_001858.4 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:70916935 C>A maps to NM_001858.4 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:70745794 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:70850844 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:70847590 A>T maps to NM_001858.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:70647992 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:70916659 T>C maps to NM_001858.4 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:70881869 A>C maps to NM_001858.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:70909315 G>A maps to NM_001858.4 R1033R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:70894798 G>T maps to NM_001858.4 G950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:70900065 G>A maps to NM_001858.4 E1025E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:70877915 G>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr6:70608846 A>T maps to NM_001858.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:70639420 T>C maps to NM_001858.4 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:70847627 A>T maps to NM_001858.4 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr6:70847633 G>T maps to NM_001858.4 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:48271987 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:48272648 G>A maps to NM_000088.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:48270399 G>A maps to NM_000088.3 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:94054960 C>T maps to NM_000089.3 Q941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94054500 G>T maps to NM_000089.3 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:94057054 C>A maps to NM_000089.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:94041393 C>A maps to NM_000089.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:94024364 C>A maps to NM_000089.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr7:94053706 C>T maps to NM_000089.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:94038732 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:94059611 A>G maps to NM_000089.3 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:94049555 G>T maps to NM_000089.3 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr7:94033912 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:94039099 T>C maps to NM_000089.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:94053647 G>T maps to NM_000089.3 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:61951686 C>A maps to ENST00000326996 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:61945461 C>A maps to ENST00000326996 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:61951698 G>T maps to ENST00000326996 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:61960994 G>A maps to ENST00000326996 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr20:61951527 C>A maps to ENST00000326996 G1025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr20:61937231 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:61937380 G>C maps to ENST00000326996 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:61959817 G>A maps to ENST00000326996 W1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr20:61950473 G>T maps to ENST00000326996 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr20:61950472 C>A maps to ENST00000326996 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:55924960 C>A maps to NM_030820.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:56047341 C>A maps to NM_030820.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55924963 G>T maps to NM_030820.3 C820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:55932125 C>A maps to NM_030820.3 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:55922555 C>A maps to NM_030820.3 G925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:56047367 G>A maps to NM_030820.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:56021687 C>T maps to NM_030820.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:56006636 C>G did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr6:55933887 C>A maps to NM_030820.3 G683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr6:55924819 T>C maps to NM_030820.3 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr6:55925730 C>A maps to NM_030820.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:55925586 C>A maps to NM_030820.3 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:139715563 G>C maps to NM_152888.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:139629198 G>A maps to NM_152888.1 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:139614396 G>A maps to NM_152888.1 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:139668137 A>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:139737680 G>A maps to NM_152888.1 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:139707073 C>A maps to NM_152888.1 E881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:139833474 C>A maps to NM_152888.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139824059 G>T maps to NM_152888.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr8:139611018 C>T maps to NM_152888.1 E1436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:139895397 C>A maps to NM_152888.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:139606338 G>T maps to NM_152888.1 G1512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:139668138 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:139629165 G>T maps to NM_152888.1 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:139815174 T>C maps to NM_152888.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:139890200 G>A maps to NM_152888.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:139733011 T>C maps to NM_152888.1 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:139833459 T>A maps to NM_152888.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr8:139707122 C>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:139642991 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:139609198 G>T maps to NM_152888.1 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:139629191 C>A maps to NM_152888.1 G1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:139788253 C>G did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:139661906 C>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr8:139774679 C>T maps to NM_152888.1 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:139728490 C>A maps to NM_152888.1 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:139705900 T>A maps to NM_152888.1 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:139638486 C>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr8:139697474 G>T maps to NM_152888.1 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:139820031 G>T maps to NM_152888.1 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:177690295 C>A maps to ENST00000390654 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:177683395 C>T maps to ENST00000390654 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr5:177733900 G>T maps to ENST00000390654 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:177690214 G>T maps to ENST00000390654 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:86250027 G>A maps to NM_152890.5 Q1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:86304321 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:86246908 A>C maps to NM_152890.5 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:86308022 C>T maps to NM_152890.5 R1172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:86581034 T>C maps to NM_152890.5 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:86377097 C>A maps to NM_152890.5 G861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:86590638 G>A maps to NM_152890.5 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:86591501 G>A maps to NM_152890.5 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr1:86342843 C>A maps to NM_152890.5 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:86482851 A>C maps to NM_152890.5 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:86590977 G>A maps to NM_152890.5 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:86578264 T>C maps to NM_152890.5 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:86289272 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:86453337 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:86306904 T>A maps to NM_152890.5 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:86591211 G>T maps to NM_152890.5 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:86200647 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:86591274 G>T maps to NM_152890.5 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:109767293 C>A did not map to a codon.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr4:109858995 C>A maps to ENST00000333642 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:109931530 C>A maps to ENST00000333642 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:109805342 C>A maps to ENST00000333642 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:109810879 C>A maps to ENST00000333642 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:110222977 G>C maps to ENST00000333642 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:109839345 T>C maps to ENST00000333642 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr4:109753570 C>A maps to ENST00000333642 G559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr4:109822298 T>C maps to ENST00000333642 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:109767303 A>T maps to ENST00000333642 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr9:116931658 C>A maps to NM_032888.2 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:116930611 C>T maps to NM_032888.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr9:117002712 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:117027202 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:116930158 G>T maps to NM_032888.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:117028853 G>T maps to NM_032888.2 G1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:116930894 C>T maps to NM_032888.2 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:7571509 G>C maps to NM_001037763.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr7:7476095 T>C did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:7415128 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr7:7476024 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:7545643 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:7413109 C>A maps to NM_001037763.2 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:7480458 G>A maps to NM_001037763.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:48391490 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:48375179 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:48369121 G>A maps to NM_001844.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:48367955 C>A maps to NM_001844.4 L1411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:48377887 T>G maps to NM_001844.4 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:48370305 A>T maps to NM_001844.4 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:48378331 C>G maps to NM_001844.4 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:48380959 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr12:48369262 G>T maps to NM_001844.4 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:48386699 C>A maps to NM_001844.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr12:48369226 G>A maps to NM_001844.4 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:48367949 G>T maps to NM_001844.4 I1413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:48371819 C>A maps to NM_001844.4 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:48367916 C>T maps to NM_001844.4 E1424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:48383581 G>T maps to NM_001844.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:189871099 T>A maps to NM_000090.3 G1041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:189868183 T>C maps to NM_000090.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:189862451 A>G maps to NM_000090.3 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189856421 G>T maps to NM_000090.3 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:189866154 A>C maps to NM_000090.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:189871661 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr2:189851865 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189849688 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:189872627 G>A maps to NM_000090.3 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:189850438 C>T maps to NM_000090.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:189870984 G>A maps to NM_000090.3 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr2:189861943 G>A maps to NM_000090.3 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:189859320 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:189849636 A>T maps to NM_000090.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:189875588 C>A maps to NM_000090.3 T1409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189859296 G>T maps to NM_000090.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:189871111 T>G maps to NM_000090.3 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr2:189855030 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:189862436 T>A maps to NM_000090.3 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:189856908 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:189859447 A>T did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr2:189872831 A>T maps to NM_000090.3 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:189871171 A>G maps to NM_000090.3 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:189874946 T>A maps to NM_000090.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr2:189873790 G>T maps to NM_000090.3 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:189875045 G>A maps to NM_000090.3 E1322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:110831279 C>A maps to NM_001845.4 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:110822945 G>C maps to NM_001845.4 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr13:110822017 A>G maps to NM_001845.4 G1278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:110822020 G>T maps to NM_001845.4 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:110819541 C>T maps to NM_001845.4 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:110829280 C>T maps to NM_001845.4 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:110822981 C>T maps to NM_001845.4 Q1218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr13:110859047 G>A maps to NM_001845.4 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:110814613 G>T maps to NM_001845.4 Y1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr13:110827015 T>A maps to NM_001845.4 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr13:110826256 C>T maps to NM_001845.4 K1165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:110830258 G>T maps to NM_001845.4 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:110817206 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr13:110827078 C>G maps to NM_001845.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr13:110857876 G>T maps to NM_001845.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr13:110866344 C>A maps to NM_001845.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr13:110857882 G>T maps to NM_001845.4 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:111121562 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:111009826 G>A maps to NM_001846.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:111082233 G>T maps to NM_001846.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:111158939 C>T maps to NM_001846.2 H1527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:111130464 T>A maps to NM_001846.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:111132682 G>T maps to NM_001846.2 G902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:111092174 C>T maps to NM_001846.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:111130347 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr13:111088677 G>A maps to NM_001846.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr13:111160489 G>T maps to NM_001846.2 A1601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:228173982 T>C maps to NM_000091.4 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:228137669 G>C maps to NM_000091.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:227983372 T>A maps to ENST00000396625 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:227924918 C>T maps to ENST00000396625 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:227973938 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:228009237 T>C maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr2:227896700 T>A maps to ENST00000396625 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:227876936 A>C maps to ENST00000396625 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr2:227915773 T>C maps to ENST00000396625 P1023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:227886842 T>A maps to ENST00000396625 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:227919418 G>A maps to ENST00000396625 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:227924192 C>A maps to ENST00000396625 G771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:227915797 C>A maps to ENST00000396625 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:228004955 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:107814661 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:107807132 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:107935989 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:107814668 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:107911594 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:107821580 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:107938499 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:107811886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:107930821 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107838783 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:107863583 G>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:107911646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:107802317 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:107930916 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:107802371 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:107911659 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:107930772 T>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:107924144 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:107842031 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:107821199 G>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:107841985 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:107840674 T>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:107827714 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:107807110 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:107898560 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:107858175 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:107858176 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:107802323 C>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:107823932 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:107939544 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:107844632 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:107865997 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:107865998 C>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:107938035 G>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:107844670 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:107869444 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:107939560 T>C did not map to a codon.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr23:107834437 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:107920743 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:107821561 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:107821200 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:107840651 G>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:107846234 C>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:107930877 T>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:107909763 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:107842069 G>A did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr23:107838764 T>G did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr23:107840674 T>G did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:107823944 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:107930734 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:107865937 C>G did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr23:107911554 A>G did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:107869497 C>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:107929350 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:107909781 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:107834355 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:107811894 G>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:107938529 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:107923921 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:107865949 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:107823920 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:107402767 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:107457415 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:107418906 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:107422488 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:107422491 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:107419022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107422066 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:107408243 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:107404922 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:107417734 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:107422548 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:107400453 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:107403708 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:107434702 G>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:107431763 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:107433694 G>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:107439761 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:107414122 A>T did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:107418882 C>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:107464478 T>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:107417712 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:107420136 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:107404897 A>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:107414631 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:107430467 A>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:107430449 T>C did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:107464501 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:107464502 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:107437787 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:107554021 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:107554022 C>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:107418906 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:107407908 G>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:107554030 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:107413871 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:107430487 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:107402957 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:107422546 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:107412727 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:107423778 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:137619237 G>T maps to NM_000093.3 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:137664634 G>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:137704348 G>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:137708876 C>T maps to NM_000093.3 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:137716552 G>T maps to NM_000093.3 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:137644491 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr9:137646138 C>A maps to NM_000093.3 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:137701051 A>T maps to NM_000093.3 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr9:137630336 C>T maps to NM_000093.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:137686945 G>T maps to NM_000093.3 G907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:137646163 G>T maps to NM_000093.3 G607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:137727019 C>T maps to NM_000093.3 P1780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:137622311 C>T maps to NM_000093.3 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:137688227 C>T maps to NM_000093.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:137642676 C>T maps to NM_000093.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr9:137726875 G>T maps to NM_000093.3 R1732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr9:137708925 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:137660254 G>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr9:137709647 G>T maps to NM_000093.3 E1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:137645730 G>T maps to NM_000093.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:137703219 C>T maps to NM_000093.3 I1188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:189945769 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:189922114 G>T maps to NM_000393.3 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:189904124 T>A maps to NM_000393.3 P1266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:189929291 T>A maps to NM_000393.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:189904154 C>A maps to NM_000393.3 A1256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:189931187 G>A maps to NM_000393.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr2:189950489 T>C maps to NM_000393.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:189925509 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:189944756 C>A maps to NM_000393.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:189927996 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:189929365 G>T maps to NM_000393.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:189907499 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:189916208 T>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:189899872 A>T maps to NM_000393.3 Y1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:189917696 T>A maps to NM_000393.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:189904154 C>A maps to NM_000393.3 A1256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:189918905 C>T maps to NM_000393.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:189916107 C>A maps to NM_000393.3 G957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:189932739 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:189916051 C>A maps to NM_000393.3 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:10080322 C>T maps to NM_015719.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:10077013 G>A maps to NM_015719.3 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr19:10079105 C>T maps to NM_015719.3 Q1423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:10114755 G>T maps to NM_015719.3 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:10091369 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10108082 G>T maps to NM_015719.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10102466 G>A maps to NM_015719.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:10116470 C>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr19:10102480 C>A maps to NM_015719.3 G644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:10089593 G>T maps to NM_015719.3 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:10099826 C>A maps to NM_015719.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:10088271 G>T maps to NM_015719.3 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:10114728 C>T maps to NM_015719.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:10089888 T>A maps to NM_015719.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr21:47410684 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:47423461 G>T maps to NM_001848.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr21:47423395 C>T maps to NM_001848.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr21:47422259 C>G maps to NM_001848.2 S732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:47410955 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr21:47421171 A>T maps to NM_001848.2 K610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:47542429 C>G maps to NM_001849.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:47542059 C>T maps to NM_001849.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr21:47545883 C>A maps to NM_001849.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr21:47531437 G>T maps to NM_001849.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr21:47552429 C>A maps to NM_001849.3 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr21:47546149 G>A maps to NM_001849.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr21:47552222 C>T maps to NM_001849.3 H939H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr21:47532109 G>T maps to NM_001849.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:238303367 C>A maps to NM_004369.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:238280774 C>A maps to NM_004369.3 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:238274403 G>A maps to NM_004369.3 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:238245033 T>C maps to NM_004369.3 P2903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:238274646 A>G maps to NM_004369.3 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:238253295 G>T maps to NM_004369.3 T2455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:238253292 C>T maps to NM_004369.3 T2456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:238244934 C>A maps to NM_004369.3 V2936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:238296690 C>A maps to NM_004369.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:238277614 G>T maps to NM_004369.3 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:238283181 A>G maps to NM_004369.3 F1184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr2:238267211 A>G maps to NM_004369.3 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:238243416 G>A maps to NM_004369.3 A3027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:238280651 G>T maps to NM_004369.3 V1336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:238277461 C>A maps to NM_004369.3 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:238244985 A>T maps to NM_004369.3 A2919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:238275573 T>A maps to NM_004369.3 G1752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:238277614 G>T maps to NM_004369.3 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:238250708 C>T maps to NM_004369.3 L2588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr2:238268748 C>A maps to NM_004369.3 P2088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:238268031 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:238262031 A>T maps to NM_004369.3 G2214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:238303670 C>A maps to NM_004369.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:238263549 C>A maps to NM_004369.3 G2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:238289822 C>A maps to NM_004369.3 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:238275447 G>C maps to NM_004369.3 A1794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:238287659 G>A maps to NM_004369.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:238275810 G>T maps to NM_004369.3 G1673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:238296687 C>A maps to NM_004369.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr2:238283327 G>A maps to NM_004369.3 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:238296627 G>C maps to NM_004369.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:238275605 G>T maps to NM_004369.3 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:130095203 C>T maps to ENST00000312481 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:130159388 T>A maps to ENST00000312481 L2069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr3:130159052 T>C maps to ENST00000312481 P1957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:130189805 T>A maps to ENST00000312481 T2523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr3:130159235 T>C maps to ENST00000312481 S2018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:130282041 T>C maps to NM_001102608.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:130290237 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:130284241 C>T maps to NM_001102608.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:130284195 C>A maps to NM_001102608.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:130285828 A>C maps to NM_001102608.1 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:130293295 G>T maps to NM_001102608.1 V1158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130290118 C>G maps to NM_001102608.1 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:130284397 C>A maps to NM_001102608.1 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:130284020 C>G maps to NM_001102608.1 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:130293196 G>C maps to NM_001102608.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:130285925 G>T maps to NM_001102608.1 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:130285903 C>A maps to NM_001102608.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:130282480 G>T maps to NM_001102608.1 G212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:130305491 G>T maps to NM_001102608.1 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr3:130329536 G>A maps to NM_001102608.1 V1599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:130282200 T>A maps to NM_001102608.1 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:130305377 G>T maps to NM_001102608.1 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:130368297 C>G maps to NM_001102608.1 S1875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:48603990 C>A maps to NM_000094.3 R2770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:48621049 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:48609588 G>T maps to NM_000094.3 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:48604137 C>A maps to NM_000094.3 V2753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:48620454 C>A maps to NM_000094.3 A1503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:48630048 G>A maps to NM_000094.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr3:48614315 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:48623527 A>T maps to NM_000094.3 C1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:48613830 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:48612108 C>G did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:48604562 G>T maps to NM_000094.3 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr3:48629409 C>A maps to NM_000094.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:48629361 A>T maps to NM_000094.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:48629394 G>A maps to NM_000094.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:48604356 C>A maps to NM_000094.3 G2737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr3:48605321 A>T maps to NM_000094.3 G2626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr3:48629628 C>A maps to NM_000094.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:48618578 T>A maps to NM_000094.3 G1637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:36564488 C>A maps to NM_005202.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:70944627 C>A maps to NM_001851.4 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:71009777 C>T maps to NM_001851.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:71009822 G>T maps to NM_001851.4 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:71004157 G>C maps to NM_001851.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:70964867 C>A maps to NM_001851.4 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:70926770 A>T maps to NM_001851.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:70979356 G>T maps to NM_001851.4 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:71011743 G>A maps to NM_001851.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:70991091 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:70948954 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:70962015 A>G maps to NM_001851.4 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:40776819 T>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:40770188 C>A maps to NM_001852.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:40768851 C>A maps to NM_001852.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:61468486 C>T maps to NM_001853.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:61468463 A>C maps to NM_001853.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:61460981 C>A maps to NM_001853.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr20:61452878 C>A maps to NM_001853.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:61453479 C>T maps to NM_001853.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr20:61460277 G>T maps to NM_001853.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:61453143 C>A maps to NM_001853.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61461737 C>T maps to NM_001853.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:61458591 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr20:61461719 C>T maps to NM_001853.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:120118126 G>A maps to NM_006438.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:120103385 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:3691446 C>T maps to ENST00000418971 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:3691617 C>T maps to ENST00000418971 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:3685138 A>G maps to ENST00000418971 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:3691503 C>T maps to ENST00000418971 G218G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-A490-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:3685150 C>A maps to ENST00000418971 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:3652049 T>A maps to ENST00000418971 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:3691315 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr18:334870 C>A maps to NM_130386.2 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:346493 G>T maps to NM_130386.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr18:346703 G>A maps to NM_130386.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:331744 C>T maps to NM_130386.2 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:335054 A>T maps to NM_130386.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:348116 G>C maps to NM_130386.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr18:347057 G>T maps to NM_130386.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr18:333008 G>A maps to NM_130386.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:331762 T>C maps to NM_130386.2 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:15531039 G>T maps to NM_005677.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:15512053 G>T maps to NM_005677.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:62228014 G>T maps to NM_152516.2 R120R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z052-01A-01W-0747-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr3:149468638 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:149470066 G>A maps to NM_016094.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:31294515 G>A maps to NM_053041.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:31294521 C>T maps to NM_053041.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160268766 C>T maps to NM_001098398.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:14496147 C>A maps to NM_001144061.1 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:14482761 C>T maps to NM_001144061.1 Q842Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:14512185 T>A maps to NM_001144061.1 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:139102205 A>G maps to NM_004766.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:139092570 C>A maps to NM_004766.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:128987440 G>A maps to NM_016128.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:128971503 C>T maps to NM_016128.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:128979529 A>T maps to NM_016128.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:49426537 T>C maps to NM_001143887.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:17174122 T>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:67971597 C>A maps to NM_006837.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:99688550 C>T maps to NM_006833.4 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:6839591 G>T maps to NM_001164093.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:6839881 C>T maps to NM_001164093.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:6838546 T>C maps to NM_001164093.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:238005468 A>T maps to NM_006710.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:56661649 G>C maps to NM_144576.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:198327292 A>G maps to NM_025147.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:198327272 C>T maps to NM_025147.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:84191123 C>A maps to NM_015697.7 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:99825362 T>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:99817543 C>A maps to NM_017421.3 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:131087420 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:120960071 G>C maps to NM_032314.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr12:120966863 G>A maps to NM_032314.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:120966839 C>A maps to NM_032314.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:74428032 T>A maps to NM_182476.1 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr16:19088644 G>A maps to NM_016138.4 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:57493629 C>T maps to NM_020312.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:57490420 G>C maps to NM_020312.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:47663869 T>A maps to NM_006587.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:47746536 C>A maps to NM_006587.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:47808935 G>T maps to NM_006587.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:47667171 C>T maps to NM_006587.2 W489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr4:47765547 C>A maps to NM_006587.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:47685847 G>A maps to NM_006587.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr4:47808992 C>A maps to NM_006587.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:47746497 G>T maps to NM_006587.2 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:47602302 G>T maps to NM_006587.2 Y958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:47625739 G>T maps to NM_006587.2 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:30198004 C>T maps to NM_007074.3 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr12:109052653 C>A maps to ENST00000420959 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:109055931 T>C maps to ENST00000420959 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:100893275 G>A maps to NM_052820.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:69003990 G>T maps to NM_006091.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr15:69003978 G>T maps to NM_006091.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:27943985 G>T maps to ENST00000345068 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:4455509 C>A maps to NM_024535.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr16:4408411 G>A maps to NM_024535.3 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr16:4411440 C>A maps to NM_024535.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:4411087 T>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:10510147 C>T maps to ENST00000377049 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:13980263 A>G maps to NM_001303.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:14110403 C>T maps to NM_001303.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:53045692 G>A maps to NM_004375.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:70793066 T>A maps to NM_016468.5 K102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:1015097 G>A maps to NM_001031617.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:85838697 G>T maps to NM_001861.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr20:30227859 G>A maps to NM_032609.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:30232607 G>C maps to NM_032609.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:36142162 G>A maps to ENST00000392201 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr19:36145512 C>T maps to ENST00000392201 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55865832 G>A maps to NM_144613.4 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:75950954 C>A maps to NM_001865.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:46737032 A>C maps to NM_130902.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93813685 C>G maps to NM_182971.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:148927061 G>T maps to NM_000096.3 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:148904391 T>C maps to NM_000096.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:148928103 C>A maps to NM_000096.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr16:19562547 G>T maps to NM_014711.4 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr16:19557736 T>A maps to NM_014711.4 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:130020971 G>A maps to NM_001868.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:130023601 C>G maps to NM_001868.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr7:130021968 G>T maps to NM_001868.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:130021574 C>T maps to NM_001868.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:130025023 C>G maps to NM_001868.2 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:130023295 G>A maps to NM_001868.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:129914996 C>T maps to NM_001869.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:148586790 C>A maps to NM_001870.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr3:148586700 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr3:148614331 C>T maps to NM_001870.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:129962386 C>T maps to NM_016352.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:129950738 G>A maps to NM_016352.3 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr7:129944316 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:130008320 C>A maps to NM_080385.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:130007796 C>A maps to NM_080385.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:129987643 C>T maps to NM_080385.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:130007239 C>A maps to NM_080385.4 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:129989905 G>T maps to NM_080385.4 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:68334753 T>C maps to NM_020361.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr8:68423859 C>A maps to NM_020361.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:17058019 C>T maps to ENST00000443236 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:17091487 T>C maps to ENST00000443236 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:17056481 G>A maps to ENST00000443236 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr19:17122453 G>A maps to ENST00000443236 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:17081752 G>A maps to ENST00000443236 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:17013616 G>C maps to ENST00000443236 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr19:17091400 C>T maps to ENST00000443236 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:17036174 G>A maps to ENST00000443236 V1183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:148558728 C>T maps to NM_001871.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:148545857 G>A maps to NM_001871.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:46656574 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:46679111 G>T maps to NM_001872.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:46658366 C>A maps to NM_001872.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:28754529 C>T maps to NM_001304.4 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:28791657 C>T maps to NM_001304.4 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:83215262 A>T maps to ENST00000261723 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:83215960 G>A maps to ENST00000261723 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:83240092 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:83226623 T>A maps to ENST00000261723 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:173376572 G>T maps to NM_030627.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:173376509 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:175306001 G>A maps to NM_001008220.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr15:75119190 G>A maps to NM_001030005.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr15:75122473 G>T maps to NM_001030005.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr18:56963965 G>T maps to NM_181654.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr18:56964066 C>A maps to NM_181654.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:69265574 G>T maps to NM_001874.4 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:69326541 C>A maps to NM_001874.4 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:101829548 G>T maps to NM_001308.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:101814131 G>T maps to NM_001308.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:101841175 A>G maps to NM_001308.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:101816843 T>A maps to NM_001308.2 K313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:101825117 C>A maps to NM_001308.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:194062981 G>T maps to NM_001080513.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:194063200 C>T maps to NM_001080513.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr3:194062054 C>T maps to NM_001080513.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:194062714 C>T maps to NM_001080513.2 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:34214258 G>T maps to NM_003915.5 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:57155063 C>G maps to NM_152727.5 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:57147279 G>A maps to NM_152727.5 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:87568355 T>G maps to NM_003909.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:87552537 C>T maps to NM_003909.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr8:87549855 A>T maps to NM_003909.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:87559998 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:131418773 T>G maps to ENST00000502818 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:131388541 C>A maps to ENST00000502818 G238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:131283073 G>T maps to ENST00000502818 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:131261464 G>T maps to ENST00000502818 S510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:36712914 G>T maps to NM_020939.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:36710125 G>T maps to NM_020939.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr6:36712920 T>A maps to NM_020939.1 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:36724072 C>A maps to NM_020939.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:36710131 C>A maps to NM_020939.1 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:24542766 C>A maps to NM_006032.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr14:24546878 C>A maps to NM_006032.2 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr14:24546539 C>A maps to NM_006032.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr14:24542888 T>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:9767701 T>C maps to ENST00000383832 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:9768830 G>T maps to ENST00000383832 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:207827199 A>G maps to NM_173077.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:207827200 G>T maps to NM_173077.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:207814382 G>T maps to NM_173077.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:207824395 C>G maps to NM_173077.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:207814374 A>T maps to NM_173077.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:98307609 C>T maps to NM_000097.5 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:98304295 G>T maps to NM_000097.5 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:12798544 G>A maps to NM_018340.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr16:12798850 C>A maps to NM_018340.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:12798484 G>A maps to NM_018340.2 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:12897561 A>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:211518746 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:211515107 A>T maps to NM_001122633.1 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:211421525 G>T maps to NM_001122633.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:211512693 C>A maps to NM_001122633.1 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:211527851 C>A maps to NM_001122633.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:211527881 T>A maps to NM_001122633.1 A1327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:211476929 C>T maps to NM_001122633.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:211507347 G>T maps to NM_001122633.1 E1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:211523381 C>A maps to NM_001122633.1 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:211532907 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211438023 A>C maps to NM_001122633.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525276 C>T maps to NM_001122633.1 F1281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:211525285 G>T maps to NM_001122633.1 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:211527867 C>A maps to NM_001122633.1 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:211460215 C>G maps to NM_001122633.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr2:211442194 G>T maps to NM_001122633.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:211454855 C>T maps to NM_001122633.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:211504763 C>A maps to NM_001122633.1 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:211447390 G>T maps to NM_001122633.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:211515146 G>T maps to NM_001122633.1 A1161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:211503872 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:211467007 C>A maps to NM_001122633.1 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:211456689 T>C maps to NM_001122633.1 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr2:211532995 G>C maps to NM_001122633.1 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:211541814 G>T maps to NM_001122633.1 R1459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:211455574 T>C maps to NM_001122633.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr14:92627505 C>T maps to NM_017437.1 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:92609388 C>T maps to NM_017437.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr14:92625581 G>T maps to NM_017437.1 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:9593039 A>G did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:9572792 C>T maps to NM_016207.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:9571000 C>A maps to NM_016207.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:9572813 G>A maps to NM_016207.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:1248218 A>G maps to NM_017871.4 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:1255873 G>A maps to NM_017871.4 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:1256374 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:99047932 C>T maps to NM_006693.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:99051638 G>A maps to NM_006693.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:69653890 T>C maps to ENST00000266679 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr12:69652538 A>G maps to ENST00000266679 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:61187393 C>A maps to NM_024811.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:61179383 C>A maps to NM_024811.3 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:68549255 G>A maps to NM_001876.3 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:68540864 G>A maps to NM_001876.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:68564362 T>A maps to NM_001876.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:51012809 C>T maps to NM_152245.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr22:51015405 G>A maps to NM_152245.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:50204051 C>G maps to NM_152359.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:50212074 G>A maps to NM_152359.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:50214065 G>T maps to NM_152359.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:53676596 C>T maps to NM_000098.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:29111967 C>T maps to NM_031311.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr7:29070207 C>A maps to NM_031311.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:29160637 G>A maps to NM_031311.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:29103812 G>C maps to NM_031311.3 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr7:29132282 G>A maps to NM_031311.3 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:88008655 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:88008722 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:88008696 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:88008703 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:88009302 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:88008424 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:88009277 A>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:88009006 A>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:88009016 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:88009013 C>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:88008984 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:88008863 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:88009036 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:88008835 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:88008693 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:88008904 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:88008500 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:88008500 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:88009102 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:88009254 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:88009035 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr20:2776023 C>A maps to NM_019609.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr20:2774856 C>A maps to NM_019609.4 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:2777741 T>C did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:2776527 C>T maps to NM_019609.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:2776937 C>A maps to NM_019609.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:2775006 G>T maps to NM_019609.4 Y678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:2778928 C>A maps to NM_019609.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:2778832 C>A maps to NM_019609.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr20:2775048 C>G maps to NM_019609.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr20:2779518 G>T maps to NM_019609.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:125526640 C>A maps to NM_198148.2 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:125528161 C>A maps to NM_198148.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:125526524 A>G maps to NM_198148.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:125521448 C>T maps to NM_198148.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:125521573 G>T maps to NM_198148.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:125521563 C>T maps to NM_198148.2 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:8609142 C>A maps to NM_001014447.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:8621241 C>T maps to NM_001014447.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:8616158 C>T maps to NM_001014447.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:8608531 C>T maps to NM_001014447.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr4:8621184 C>A maps to NM_001014447.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr4:8621067 C>A maps to NM_001014447.2 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:8605877 C>A maps to NM_001014447.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:207679246 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:207680056 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:207739212 T>C maps to NM_000651.4 Y1299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:207789974 C>A maps to NM_000651.4 P2239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:207785157 G>A maps to NM_000651.4 T2144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:207790118 C>A maps to NM_000651.4 A2287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:207696983 C>T maps to NM_000651.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:207748948 C>G maps to NM_000651.4 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:207669647 C>T maps to NM_000651.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:207782701 T>C maps to NM_000651.4 F1988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:207851642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:207868058 G>C maps to NM_175710.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:207867944 T>C maps to NM_175710.1 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:207881564 G>C maps to NM_175710.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207867884 G>A maps to NM_175710.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:207890989 G>C maps to NM_175710.1 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:207868040 T>C maps to NM_175710.1 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:207871170 A>T maps to NM_175710.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:207850818 G>A maps to NM_175710.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:207642061 T>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:207648400 C>T maps to NM_001006658.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:207646411 C>A maps to NM_001006658.2 Y622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:207658874 T>A maps to NM_001006658.2 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:207647209 T>C maps to NM_001006658.2 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:207644133 C>T maps to NM_001006658.2 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:207640000 A>G maps to NM_001006658.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:94243995 G>C maps to NM_003805.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:94243992 C>T maps to NM_003805.3 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:1706002 G>T maps to NM_020825.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:1709951 G>C maps to NM_020825.3 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr9:131860345 C>T maps to NM_000755.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:197396582 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197446915 G>A maps to NM_201253.2 Q1376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:197446846 C>T maps to NM_201253.2 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:197404112 C>A maps to NM_201253.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:197404271 G>T maps to NM_201253.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:197404098 G>T maps to NM_201253.2 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:197404356 G>T maps to NM_201253.2 E1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr1:197316537 G>A maps to NM_201253.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:197404109 T>A maps to NM_201253.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:197398724 G>T maps to NM_201253.2 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:197398712 C>A maps to NM_201253.2 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:197404355 G>A maps to NM_201253.2 Q1121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:197390931 C>A maps to NM_201253.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:197403857 T>C maps to NM_201253.2 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:197390931 C>A maps to NM_201253.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr1:197407737 G>T maps to NM_201253.2 G1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:197396974 G>A maps to NM_201253.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:126125171 C>T maps to NM_173689.5 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:126125300 C>A maps to NM_173689.5 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr9:126129601 G>T maps to NM_173689.5 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:126136902 C>A maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:126129485 G>T maps to NM_173689.5 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr9:126132528 C>A maps to NM_173689.5 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:126125303 G>A maps to NM_173689.5 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr9:126132894 G>A maps to NM_173689.5 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:152487954 G>T maps to NM_019060.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:46332679 C>G maps to ENST00000288400 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137612986 G>A maps to NM_194071.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:137586169 T>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:4171671 C>T maps to NM_032607.1 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:4154900 T>G maps to NM_032607.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:4171660 A>T maps to NM_032607.1 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:28843964 G>A maps to NM_182898.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr7:28848986 G>T maps to NM_182898.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:28848928 G>A maps to NM_182898.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:28848854 C>T maps to NM_182898.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:28610084 C>T maps to NM_182898.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr16:3779781 G>A maps to NM_004380.2 Q1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:3778777 G>C maps to NM_004380.2 L2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:3843557 C>A maps to NM_004380.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:3778084 G>C maps to NM_004380.2 L2321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr16:3801725 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:85375676 C>T maps to NM_001039618.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:102000098 C>G maps to NM_153836.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:50315237 C>T maps to NM_001135101.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr22:50316927 G>A maps to NM_001135101.1 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr10:35495853 C>T maps to ENST00000429130 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:67089173 A>T maps to NM_000756.2 L180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:76259265 C>T maps to NM_001882.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr5:76249021 G>A maps to NM_001882.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:43910879 C>A maps to NM_001145146.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:43907549 C>A maps to NM_001145146.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:43907805 C>A maps to NM_001145146.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr17:43906654 C>G maps to NM_001145146.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:43906639 C>T maps to NM_001145146.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:43908258 C>T maps to NM_001145146.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:30693186 G>A maps to ENST00000348438 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:36737267 T>A maps to NM_016441.2 C548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:36739427 C>T maps to NM_016441.2 H557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:36775744 A>G maps to NM_016441.2 R1004R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:36583747 G>T maps to NM_016441.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:105945825 C>A maps to ENST00000483017 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr14:105945513 C>T maps to ENST00000483017 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:43274006 G>A maps to ENST00000449267 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:43274040 C>A maps to ENST00000449267 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:43275481 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1389174 C>T maps to NM_175918.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr4:1389480 C>T maps to NM_175918.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:1389285 G>C maps to NM_175918.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:1389357 G>T maps to NM_175918.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:1389250 G>T maps to NM_175918.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:1388538 C>A maps to NM_175918.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:1389499 C>T maps to NM_175918.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:49803148 G>T maps to NM_001131.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49660566 C>T maps to ENST00000211238 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:49666176 A>T maps to ENST00000211238 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:49660541 C>A maps to ENST00000211238 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr6:49663606 C>T maps to ENST00000211238 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr6:49665655 C>A maps to ENST00000211238 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr6:49696490 G>T maps to NM_001190986.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49696538 A>G maps to NM_001190986.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:49704214 G>T maps to NM_001190986.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:49704163 C>A maps to NM_001190986.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr6:49696553 G>A maps to NM_001190986.1 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:75944443 A>T maps to NM_031461.5 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:75932314 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:75927085 G>T maps to NM_031461.5 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:75924671 G>A maps to NM_031461.5 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:75898354 G>T maps to NM_031461.5 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:75898315 T>C maps to NM_031461.5 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:75927083 C>A maps to NM_031461.5 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr16:84884259 G>T maps to NM_031476.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:84940226 G>T maps to NM_031476.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr17:1359351 C>A maps to NM_016823.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr22:21288426 G>T maps to NM_005207.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:18709362 G>T maps to NM_004750.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:18710442 G>T maps to NM_004750.4 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:1315011 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:1321325 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:1321327 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:1325340 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:1325459 G>C did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:1317533 G>T did not map to a codon.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr23:1317533 G>T did not map to a codon.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr23:1317534 G>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:1331518 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:1321355 T>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:1321381 C>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:1321390 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:5862926 C>A maps to NM_001014809.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:5844825 A>T maps to NM_001014809.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5837731 C>T maps to NM_001014809.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:5837716 G>T maps to NM_001014809.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:5862765 C>A maps to NM_001014809.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr20:20031145 C>A maps to NM_016652.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:20018209 C>T maps to NM_016652.4 W712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:20023160 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:152382720 G>A maps to NM_016190.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:152382570 C>T maps to NM_016190.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:17266429 C>A maps to NM_014675.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:17280754 C>G maps to NM_014675.3 S1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:17249186 G>A maps to NM_014675.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:17266477 A>T maps to NM_014675.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:17292344 C>T maps to NM_014675.3 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:17266417 G>A maps to NM_014675.3 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:17265549 C>A maps to NM_014675.3 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:17249171 C>T maps to NM_014675.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:17256513 G>T maps to NM_014675.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:17295726 G>T maps to NM_014675.3 L1731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:17250964 C>T maps to NM_014675.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:17265570 C>A maps to NM_014675.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:17298932 G>T maps to NM_014675.3 E2016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:17296380 G>T maps to NM_014675.3 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:86991145 C>T maps to NM_001143935.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:87021879 A>T did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr7:87022299 G>T maps to NM_001143935.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:159683533 G>A maps to NM_000567.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:99625319 G>A maps to NM_018058.4 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr10:99667821 G>A maps to NM_018058.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:122722483 G>T maps to NM_019604.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:122720872 C>A maps to NM_019604.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:122738174 G>T maps to NM_019604.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:122726460 C>T maps to NM_019604.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:33155721 G>C maps to NM_006371.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:153924737 G>A maps to NM_181715.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:153925802 G>A maps to NM_181715.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:48342692 G>A maps to NM_000554.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:48343049 G>T maps to NM_000554.4 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr19:48339552 G>T maps to NM_000554.4 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:48342704 C>A maps to NM_000554.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:48342785 C>G maps to NM_000554.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:107395550 C>A maps to NM_004075.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:107486640 G>A maps to NM_004075.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:45891163 G>T maps to NM_021117.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr21:44592263 C>A maps to NM_000394.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:111782352 C>A maps to NM_001885.1 L32L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:111782352 C>A maps to NM_001885.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:219856955 G>A maps to NM_057094.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:219855629 C>A maps to NM_057094.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:219857786 C>A maps to NM_057094.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:27024277 C>A maps to NM_001886.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr22:27021528 C>A maps to NM_001886.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:26995454 C>T maps to NM_001887.3 *253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:27008145 G>A maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr22:26995495 G>A maps to NM_001887.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr22:27003933 C>T maps to NM_001887.3 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:27003954 G>T maps to NM_001887.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr22:26997913 C>A maps to NM_001887.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr22:27012229 C>T maps to NM_001887.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr22:25625530 G>T maps to NM_000496.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr22:25601329 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:25603130 C>T maps to NM_004076.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:25598759 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97596394 G>A maps to ENST00000182096 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr3:97634555 C>G maps to ENST00000182096 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:209007436 C>T maps to NM_005210.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:209007451 C>A maps to NM_005210.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:209007475 G>A maps to NM_005210.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:208994374 G>T maps to NM_020989.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:208992947 C>A maps to NM_020989.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:208994224 G>T maps to NM_020989.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:208994247 A>G maps to NM_020989.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:208988976 G>T maps to NM_006891.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:208986483 C>A maps to NM_006891.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:208986411 G>T maps to NM_006891.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:151135180 G>A maps to NM_144727.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:151135212 C>A maps to NM_144727.1 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:186256670 G>A maps to NM_017541.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:186257350 A>T maps to NM_017541.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:186257179 G>C maps to NM_017541.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:75175923 A>T maps to NM_001889.3 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:75175817 G>A maps to NM_001889.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr21:34974652 T>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:53564228 G>A maps to NM_015989.4 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:151908929 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:151908823 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:151908859 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:151908882 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:10856657 C>T maps to NM_003651.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:115273173 C>T maps to NM_001130523.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:115262198 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:47682794 T>C maps to NM_001316.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:47688839 C>A maps to NM_001316.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:47711370 T>A maps to NM_001316.2 Y899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:110466589 G>C maps to NM_000757.4 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:149449493 C>T maps to NM_005211.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149433715 C>T maps to NM_005211.3 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:149449435 C>A maps to NM_005211.3 G504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:149460351 G>T maps to NM_005211.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr5:149457737 G>T maps to NM_005211.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:149452877 G>A maps to NM_005211.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr5:149441325 G>T maps to NM_005211.3 Y571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149433913 C>A maps to NM_005211.3 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr5:149447882 C>A maps to NM_005211.3 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:149460555 G>T maps to NM_005211.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:131409602 C>A maps to NM_000758.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:131409790 C>T maps to NM_000758.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:1413326 T>C did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:1428411 C>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:1407433 G>C did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:1413266 G>C did not map to a codon.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr23:1407691 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:1419440 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:1407712 C>T did not map to a codon.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr23:1419395 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:1428321 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:1409277 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:1413303 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:1413303 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr23:1413248 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:1428393 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:37334172 C>A maps to ENST00000262825 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:37334109 G>T maps to ENST00000262825 G760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:37334021 G>T maps to ENST00000262825 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:37326759 C>T maps to ENST00000262825 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr22:37326822 C>A maps to ENST00000262825 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:37333577 C>A maps to ENST00000262825 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr22:37332658 G>A maps to ENST00000262825 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:38171995 C>G maps to NM_000759.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:36932410 G>T maps to NM_156039.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:36932017 G>T maps to NM_156039.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:36932023 T>A maps to NM_156039.3 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:36934858 C>T did not map to a codon.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr1:36934778 G>C maps to NM_156039.3 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:19297442 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:43678848 C>G maps to NM_018590.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:43650779 A>T maps to NM_018590.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:43651074 G>T maps to NM_018590.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:43650905 G>C maps to NM_018590.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr17:61972492 T>A maps to NM_001317.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:61972387 G>A maps to NM_001317.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:61949662 G>T maps to NM_020991.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr17:61950685 G>A maps to NM_020991.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:61949936 C>A maps to NM_020991.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:61988147 C>T maps to NM_022579.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:61987229 G>T maps to NM_022579.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:61987076 G>A maps to NM_022579.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:61988156 T>A maps to NM_022579.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr15:75093897 G>A maps to NM_004383.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:2830667 G>T maps to NM_033225.5 S2965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:3087560 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:2857501 A>G maps to NM_033225.5 S2727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:3081279 C>A maps to NM_033225.5 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr8:3245076 G>A maps to NM_033225.5 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:2966134 G>A maps to NM_033225.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3045484 G>T maps to NM_033225.5 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046425 C>A maps to NM_033225.5 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:3046429 A>T maps to NM_033225.5 V1834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:3205672 T>A maps to NM_033225.5 G1105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:3263597 T>A maps to NM_033225.5 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:2855611 C>A maps to NM_033225.5 T2766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:2820156 C>A maps to NM_033225.5 V3153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3443691 G>C maps to NM_033225.5 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:3565936 G>T maps to NM_033225.5 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:2949080 A>T maps to NM_033225.5 T2414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:2967786 C>A maps to NM_033225.5 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:3000071 G>A maps to NM_033225.5 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:2944742 C>T maps to NM_033225.5 A2450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr8:3263579 C>A maps to NM_033225.5 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr8:2967819 G>T maps to NM_033225.5 T2156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:3474239 G>A maps to NM_033225.5 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:3474269 C>A maps to NM_033225.5 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:3265421 G>T maps to NM_033225.5 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:2818701 C>A maps to NM_033225.5 T3221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:2886839 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:3245094 C>A maps to NM_033225.5 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:3000194 A>T maps to NM_033225.5 G2011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr8:2830735 G>C maps to NM_033225.5 L2942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:2910158 A>T maps to NM_033225.5 C2495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr8:2796232 A>T maps to NM_033225.5 A3523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:3216749 A>G maps to NM_033225.5 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:3076776 C>A maps to NM_033225.5 E1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:3265712 C>T maps to NM_033225.5 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:3000044 G>T maps to NM_033225.5 L2061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr8:2944625 G>T maps to NM_033225.5 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr8:3245154 G>A maps to NM_033225.5 N881N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr8:4851911 C>A maps to NM_033225.5 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:3045445 G>T maps to NM_033225.5 S1855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:3072115 A>T maps to NM_033225.5 C1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:3059238 C>A maps to NM_033225.5 G1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr8:3000122 G>T maps to NM_033225.5 Y2035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:3565956 C>A maps to NM_033225.5 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8648-01A-11D-2393-08 chr8:3165841 G>T maps to NM_033225.5 S1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:3000068 C>G maps to NM_033225.5 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:4494937 G>T maps to NM_033225.5 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:3087682 C>T maps to NM_033225.5 E1408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:3889490 G>T maps to NM_033225.5 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr8:2855611 C>A maps to NM_033225.5 T2766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:2832047 C>A maps to NM_033225.5 E2889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:2875997 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:2857500 C>A maps to NM_033225.5 G2728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:3046417 C>T maps to NM_033225.5 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr8:2832024 C>G maps to NM_033225.5 T2896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr8:3000070 G>A maps to NM_033225.5 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr8:2820009 G>A maps to NM_033225.5 S3202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:3000056 C>A maps to NM_033225.5 T2057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:2855611 C>A maps to NM_033225.5 T2766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:3000086 C>G maps to NM_033225.5 T2047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:2818668 G>C maps to NM_033225.5 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr8:2910134 G>A maps to NM_033225.5 N2503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:34006260 C>T maps to ENST00000373381 G3125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:34049278 G>A maps to ENST00000373381 L2361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:34082548 G>A maps to ENST00000373381 P1951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:33985219 C>A maps to ENST00000373381 R3558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:34383798 G>T maps to ENST00000373381 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:34088982 C>T maps to ENST00000373381 L1863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:34046431 G>T maps to ENST00000373381 T2396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34174808 G>T maps to ENST00000373381 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:34190164 C>A maps to ENST00000373381 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:34006739 G>T maps to ENST00000373381 P3109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:34083157 C>A maps to ENST00000373381 E1923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr1:34071023 G>A maps to ENST00000373381 G2090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:34192227 A>T maps to ENST00000373381 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:34209108 G>A maps to ENST00000373381 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:34276466 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:34286078 G>T maps to ENST00000373381 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:34049272 C>T maps to ENST00000373381 E2363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:34401427 G>T maps to ENST00000373381 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:34052733 G>A maps to ENST00000373381 I2257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:34498243 G>T maps to ENST00000373381 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:34011692 G>T maps to ENST00000373381 S2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:34383834 C>A maps to ENST00000373381 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:34192209 G>T maps to ENST00000373381 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:34204792 G>T maps to ENST00000373381 C732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:34182012 C>G maps to ENST00000373381 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:34554599 G>A maps to ENST00000373381 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:34049353 G>A maps to ENST00000373381 P2336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:34035016 G>A maps to ENST00000373381 C2656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr1:34204867 G>A maps to ENST00000373381 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:34002678 C>A maps to ENST00000373381 T3234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:34090211 C>T maps to ENST00000373381 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr1:34003150 G>A maps to ENST00000373381 F3190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:34238302 C>G maps to ENST00000373381 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:34190195 C>G maps to ENST00000373381 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:34208986 T>A maps to ENST00000373381 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:34037282 G>T maps to ENST00000373381 G2562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:34117963 C>G maps to ENST00000373381 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:113308146 A>T maps to NM_198123.1 C2843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:113293553 G>A maps to NM_198123.1 T3119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:113253964 G>C maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:113332154 C>T maps to NM_198123.1 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:113668559 C>A maps to NM_198123.1 E943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:113668413 A>T maps to NM_198123.1 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113323243 C>A maps to NM_198123.1 G2616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:113516124 T>C maps to NM_198123.1 Q1659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:113349925 C>A maps to NM_198123.1 P2229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:114110983 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:113364658 C>A maps to NM_198123.1 G2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:113249506 G>T maps to NM_198123.1 P3513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:113392685 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:114111192 C>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:113358404 C>A maps to NM_198123.1 V2121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:113421256 C>A maps to NM_198123.1 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:114186082 T>A maps to NM_198123.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:113668425 T>C maps to NM_198123.1 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:113421175 C>A maps to NM_198123.1 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:113253964 G>A maps to NM_198123.1 P3484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr8:113304808 G>A maps to NM_198123.1 C2915C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:113668509 T>A maps to NM_198123.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr8:113657408 G>T maps to NM_198123.1 S1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:113599347 C>A maps to NM_198123.1 G1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:113323387 G>T maps to NM_198123.1 Y2568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:113694835 C>A maps to NM_198123.1 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr8:113358371 G>T maps to NM_198123.1 P2132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:113650924 C>A maps to NM_198123.1 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:113249467 C>A maps to NM_198123.1 G3526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:113484861 C>A maps to NM_198123.1 G1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:113484862 C>T maps to NM_198123.1 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:113304805 C>T maps to NM_198123.1 Q2916Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:113303847 G>A maps to NM_198123.1 Y2955Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:113395868 T>C maps to NM_198123.1 T1986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:113649130 C>T maps to NM_198123.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:113960089 A>G maps to NM_198123.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr8:113812475 C>T maps to NM_198123.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:113484936 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr8:113237149 A>T maps to NM_198123.1 P3658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr8:114326897 A>G maps to NM_198123.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:113668536 T>C maps to NM_198123.1 E950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:114326846 G>T maps to NM_198123.1 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:114186068 C>A maps to NM_198123.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:114326963 A>T maps to NM_198123.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:113326135 T>A maps to NM_198123.1 I2565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:113421186 G>A maps to NM_198123.1 Q1824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr8:113237133 C>A maps to NM_198123.1 G3664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113275988 T>A maps to NM_198123.1 T3247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:113651000 A>G maps to NM_198123.1 Y1150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:113246619 C>A maps to NM_198123.1 E3572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:113249557 G>T maps to NM_198123.1 A3496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:114388965 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr8:113418828 A>G maps to NM_198123.1 H1911H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr8:114326874 G>C maps to NM_198123.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:113402891 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:113966911 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:113516135 C>A maps to NM_198123.1 G1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:113933928 G>T maps to NM_198123.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:113960055 C>A maps to NM_198123.1 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:113266555 C>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr8:113318299 G>A maps to NM_198123.1 L2669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:113363470 A>T maps to NM_198123.1 G2086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:113662467 C>A maps to NM_198123.1 G1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:113326249 G>T maps to NM_198123.1 S2527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:113347558 G>A maps to NM_198123.1 H2388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:113562933 A>T maps to NM_198123.1 Y1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:113563041 A>T maps to NM_198123.1 G1474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:113276006 A>G maps to NM_198123.1 N3241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:113585859 A>T maps to NM_198123.1 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:113662578 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:113988230 C>A maps to NM_198123.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:113323374 C>A maps to NM_198123.1 E2573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:113353817 C>A maps to NM_198123.1 R2180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:113241098 G>T maps to NM_198123.1 S3617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:114185957 G>A maps to NM_198123.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:114186077 G>A maps to NM_198123.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:113349770 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:113564842 T>A maps to NM_198123.1 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:114448904 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr8:113651093 G>A maps to NM_198123.1 D1119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:113293531 G>T maps to NM_198123.1 R3127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr8:113304781 A>C maps to NM_198123.1 P2924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:113299452 G>A maps to NM_198123.1 G3057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:113318319 G>T maps to NM_198123.1 R2663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr8:113697848 C>A maps to NM_198123.1 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr8:114326874 G>T maps to NM_198123.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr8:113402961 G>C maps to NM_198123.1 Y1955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:113256650 G>C maps to NM_198123.1 T3458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:113331069 A>T maps to NM_198123.1 C2452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr8:113316983 A>G maps to NM_198123.1 T2744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr8:113988159 A>G maps to NM_198123.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:113299446 T>A maps to NM_198123.1 P3059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:113363402 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:113293558 C>A maps to NM_198123.1 G3118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:114185949 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:113304919 A>T maps to NM_198123.1 P2878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:113678553 C>T maps to NM_198123.1 W923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr8:113314022 T>C maps to NM_198123.1 L2813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr8:113259300 T>C maps to NM_198123.1 T3390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:113249520 C>A maps to NM_198123.1 G3509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr8:113293412 A>T maps to NM_198123.1 P3166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:113303861 C>A maps to NM_198123.1 G2951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:113347693 T>A maps to NM_198123.1 P2343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:113484886 T>A maps to NM_198123.1 P1776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:113702181 G>T maps to NM_198123.1 C690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:113303892 G>T maps to NM_198123.1 A2940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:113267541 G>T maps to NM_198123.1 S3326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:70804919 G>A maps to NM_001890.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:70823393 C>A maps to NM_001891.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:70823090 A>T maps to NM_001891.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:71115133 C>G maps to NM_005212.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:148930455 C>G maps to NM_001025105.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr13:37679150 C>T maps to NM_145203.5 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr13:37678511 G>T maps to NM_145203.5 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:37679015 G>T maps to NM_145203.5 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:80231248 C>T maps to NM_001893.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:64499793 C>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr19:1979752 G>A maps to NM_001319.6 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr20:472912 T>C maps to NM_177559.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:476446 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:480523 C>A maps to NM_177559.2 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:58220673 A>C maps to NM_001896.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr16:58220682 C>A maps to NM_001896.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968001 G>T maps to NM_001897.4 L2286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:75968733 A>T maps to NM_001897.4 T2042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75975008 C>G maps to NM_001897.4 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75983078 G>A maps to NM_001897.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:75981641 C>T maps to NM_001897.4 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:75968835 G>T maps to NM_001897.4 G2008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:75981536 G>A maps to NM_001897.4 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:75979976 G>T maps to NM_001897.4 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr15:75981599 G>T maps to NM_001897.4 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:75982103 G>T maps to NM_001897.4 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:75974657 G>T maps to NM_001897.4 A1642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr15:75982727 T>C maps to NM_001897.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr15:75968961 G>T maps to NM_001897.4 L1966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr15:75977205 C>T maps to NM_001897.4 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:47604137 A>C maps to ENST00000383738 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:68092153 T>C maps to ENST00000389042 A1101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:68024300 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:68107671 C>T maps to ENST00000389042 D1205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:68007595 A>T maps to ENST00000389042 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:68049689 G>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:68049812 C>G maps to ENST00000389042 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:67998345 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr8:68074104 C>T maps to ENST00000389042 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:51458020 G>A maps to NM_030809.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:166536136 C>T maps to ENST00000409420 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:166533118 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166535348 G>T maps to ENST00000409420 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:166535351 C>T maps to ENST00000409420 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:201453891 G>A maps to NM_001193572.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:18123563 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:18168093 C>A maps to NM_020536.4 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr20:18123430 G>T maps to NM_020536.4 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr20:18143375 G>A maps to NM_020536.4 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:23731386 G>T maps to NM_001898.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:23729727 C>A maps to NM_001898.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr20:23731379 C>A maps to NM_001898.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:23729676 G>A maps to NM_001898.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:23431199 A>G maps to NM_130794.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:23432473 G>T maps to NM_130794.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:23433352 T>A maps to NM_130794.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:23433364 C>T maps to NM_130794.1 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:65780861 G>T maps to NM_001323.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:23476502 C>T maps to NM_005492.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:23473695 C>A maps to NM_005492.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:23584170 G>A maps to NM_001008693.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr20:23584334 G>A maps to NM_001008693.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:23546693 G>A maps to NM_080610.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:122060407 C>T maps to NM_005213.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr20:54972261 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:54978522 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:100086549 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:100078975 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:100075408 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:100087794 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:100078901 G>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:100093250 A>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:100087744 C>G did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:33112196 G>T maps to NM_001326.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:33108569 G>A maps to NM_001326.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr11:33127178 T>C maps to NM_001326.2 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:23425463 C>A maps to NM_138283.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:23420936 G>T maps to NM_138283.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:134947983 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:134947927 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:134948091 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:134948042 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:134947916 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:120009184 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:120009283 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:120008750 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr23:120008903 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:120009187 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:120009173 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:120008939 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:120009126 C>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:120008928 G>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:120009287 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:120009288 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:120009269 T>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr23:120009411 G>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:120008849 C>G did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:120009313 C>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:120008978 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:120008814 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:120008754 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:120008755 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:120009065 C>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:120008812 C>G did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:120007833 G>A did not map to a codon.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr23:120008978 T>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:120009216 G>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:120008947 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:120009177 G>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:120007836 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:120008978 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:120009351 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:153880486 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:153880407 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:153880824 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:153880632 C>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:153880626 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153881653 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:153880595 T>C did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:153881555 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:19996718 A>T maps to NM_172241.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:19995629 A>T maps to NM_172241.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:19997744 A>G maps to NM_172241.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr18:19995860 A>G maps to NM_172241.2 N638N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr18:19996169 C>T maps to NM_172241.2 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:19996924 T>A maps to NM_172241.2 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr18:19996601 G>A maps to NM_172241.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19997689 A>G maps to NM_172241.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:39815111 A>G maps to ENST00000396158 Q617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:39762579 G>T maps to ENST00000396158 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:39819421 C>G maps to ENST00000396158 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr14:39763268 A>T maps to ENST00000396158 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:143453487 T>A maps to NM_178561.4 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:143453539 C>T maps to NM_178561.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:143453686 A>G maps to NM_178561.4 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr7:143453482 G>C maps to NM_178561.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr4:1206183 G>C maps to NM_001328.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr4:1206786 G>A maps to NM_001328.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:1206750 G>A maps to NM_001328.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr4:1206123 G>A maps to NM_001328.2 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:1231988 C>A maps to NM_001328.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:126714717 C>G maps to NM_022802.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:126715737 C>T maps to NM_022802.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr10:126716013 C>A maps to NM_022802.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67645893 G>C maps to NM_006565.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:56087659 A>T maps to ENST00000423479 Y493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:56099045 C>G maps to ENST00000423479 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr20:56089660 C>G maps to ENST00000423479 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:56098883 G>T maps to ENST00000423479 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr20:56073695 A>C maps to ENST00000423479 P634P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr18:77455260 G>T maps to NM_004715.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:77455236 G>C maps to NM_004715.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:77474521 G>A maps to NM_004715.3 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:44789290 G>T maps to NM_016396.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:44811446 C>G maps to NM_016396.2 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr15:44751318 C>G maps to NM_016396.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr15:44789291 T>C maps to NM_016396.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70904436 G>T maps to NM_001902.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:70904451 G>T maps to NM_001902.5 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:70877130 C>T maps to NM_001902.5 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:104390388 T>A maps to NM_138455.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:104388027 C>T maps to NM_138455.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:204735474 G>T maps to NM_005214.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:138260224 A>T maps to ENST00000355078 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:138160262 A>G maps to ENST00000355078 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:138147982 A>T maps to ENST00000355078 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr5:138163364 C>T maps to ENST00000355078 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:138269492 G>A maps to ENST00000355078 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:138266205 G>A maps to ENST00000355078 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:79878762 G>T maps to ENST00000402739 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80874768 C>A maps to ENST00000402739 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:79878744 G>C maps to ENST00000402739 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:80085186 C>A maps to ENST00000402739 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:80101224 G>T maps to ENST00000402739 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:80816439 G>T maps to ENST00000402739 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:80646671 G>A maps to ENST00000402739 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:80646672 G>T maps to ENST00000402739 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:79878680 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:80773161 C>A maps to ENST00000402739 S505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:80874708 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:80101281 G>T maps to ENST00000402739 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:80773162 A>G maps to ENST00000402739 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:80808890 A>C maps to ENST00000402739 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:80096940 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:80874840 T>A maps to ENST00000402739 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:80831225 T>A maps to ENST00000402739 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:80620353 G>T maps to ENST00000402739 G359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr2:80773042 C>A maps to ENST00000402739 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:80835319 A>T maps to ENST00000402739 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:80874885 G>T maps to ENST00000402739 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:80808943 G>T maps to ENST00000402739 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:80874879 C>A maps to ENST00000402739 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:80772104 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:69281659 G>A maps to NM_013266.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:67829201 C>A maps to NM_013266.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr10:68940122 G>A maps to NM_013266.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr10:68138982 A>T maps to NM_013266.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:67680291 G>A maps to NM_013266.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:68979559 G>T maps to NM_013266.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:111706258 G>A maps to NM_003798.2 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:111735092 C>T maps to NM_003798.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:36361318 G>A maps to NM_030877.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:57564428 G>T maps to NM_001085458.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:11117570 G>T maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:11082865 G>T maps to NM_001332.2 C910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:11236871 G>A maps to NM_001332.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:11384963 G>T maps to NM_001332.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:11411695 G>A maps to NM_001332.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:11111031 T>A maps to NM_001332.2 K801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:11384978 G>C maps to NM_001332.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:11411689 C>A maps to NM_001332.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:11364841 C>T maps to NM_001332.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:11159691 G>A maps to NM_001332.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:11364913 G>C maps to NM_001332.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:11199608 C>A maps to NM_001332.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:11565144 G>A maps to NM_001332.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:11098737 C>A maps to NM_001332.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:11082808 G>T maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:11346710 G>T maps to NM_001332.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:11159797 G>T maps to NM_001332.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:11364946 C>G maps to NM_001332.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:11023091 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:11159691 G>A maps to NM_001332.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:11023017 G>C maps to NM_001332.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:11732328 C>A maps to NM_001332.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:11111043 C>A maps to NM_001332.2 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:11082811 G>C maps to NM_001332.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:11117651 G>T maps to NM_001332.2 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:10973684 G>C maps to NM_001332.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:11397315 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:10988343 T>A maps to NM_001332.2 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:41450571 C>G maps to NM_001905.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr1:41475252 C>T maps to NM_001905.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:16696554 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:16717204 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:16707657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:16711540 C>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:16717202 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:16635338 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:16635351 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:16707679 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:10781720 G>A maps to NM_014633.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:15768969 G>T maps to NM_007272.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:15770035 G>A maps to NM_007272.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr16:67965048 G>A maps to NM_001907.2 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:67965099 G>T maps to NM_001907.2 C19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:44527061 C>T maps to NM_000308.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr20:44522626 G>A maps to NM_000308.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:44523506 C>T maps to NM_000308.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:11703194 G>C maps to NM_147783.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:88042329 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:88027449 A>G maps to NM_001814.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:1778747 G>A maps to NM_001909.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:1775104 G>A maps to NM_001909.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:206325296 G>A maps to ENST00000361052 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:206331182 T>G maps to ENST00000361052 *402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:206317608 C>T maps to ENST00000361052 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:206317609 C>T maps to ENST00000361052 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:206328752 G>T maps to ENST00000361052 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:66335022 G>A maps to NM_003793.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:66333374 G>C maps to NM_003793.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:66333335 G>A maps to NM_003793.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:25044574 G>T maps to NM_001911.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:25042902 G>T maps to NM_001911.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:25044511 C>A maps to NM_001911.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:25042851 G>T maps to NM_001911.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:79229741 C>T maps to NM_004390.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:150769292 G>A maps to NM_000396.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:150772098 C>T maps to NM_000396.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:150776577 C>A maps to NM_000396.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:99799532 C>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:99795257 G>A maps to NM_001333.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr4:156847222 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:150727500 C>A maps to NM_004079.4 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr11:70279298 C>T maps to NM_001184740.1 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:70281796 C>T maps to NM_001184740.1 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:70279259 G>A maps to NM_001184740.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:70253622 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:70279239 A>T maps to NM_001184740.1 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:117365196 G>A maps to NM_033427.2 H1390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:117431239 G>A maps to NM_033427.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:117375440 C>T maps to NM_033427.2 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr7:117431680 T>A maps to NM_033427.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:117432096 C>A maps to NM_033427.2 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:117424407 G>A maps to NM_033427.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:117424333 A>T maps to NM_033427.2 L748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:117432193 G>T maps to NM_033427.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:117424404 A>G maps to NM_033427.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:117407143 A>T maps to NM_033427.2 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr7:117431742 G>A maps to NM_033427.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:117398004 C>A maps to NM_033427.2 V1064V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr7:117420572 G>A maps to NM_033427.2 Y815Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:117432136 G>T maps to NM_033427.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:112999883 C>A maps to NM_018704.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:16878336 C>A maps to NM_001081.3 S3359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:16942701 G>A maps to NM_001081.3 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:17142109 G>A maps to NM_001081.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:17157574 C>A maps to NM_001081.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16960651 T>A maps to NM_001081.3 T2323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:16957928 G>C maps to NM_001081.3 L2367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17152916 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:17169919 G>A maps to NM_001081.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:17169920 G>A maps to NM_001081.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:16975227 C>A maps to NM_001081.3 P1994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr10:17156056 T>C maps to NM_001081.3 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:16989298 G>A maps to NM_001081.3 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr10:16975227 C>A maps to NM_001081.3 P1994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:16996412 T>C maps to NM_001081.3 R1610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr10:17126431 C>A maps to NM_001081.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr10:16918968 C>G maps to NM_001081.3 G3011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:16975089 T>A maps to NM_001081.3 R2040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:16942696 C>A maps to NM_001081.3 L2779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr10:17087119 G>T maps to NM_001081.3 Y1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:16930565 C>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr10:17157486 G>A maps to NM_001081.3 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:16989352 C>A maps to NM_001081.3 T1741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:16982166 C>A maps to NM_001081.3 T1804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:16948340 C>T maps to NM_001081.3 R2591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:16975227 C>A maps to NM_001081.3 P1994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr10:17153049 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:16893277 C>A maps to NM_001081.3 E3207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:17110258 C>A maps to NM_001081.3 E938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:16980991 T>C maps to NM_001081.3 E1901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:16930443 G>A maps to NM_001081.3 L2959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr10:16979637 C>T maps to NM_001081.3 W1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:16918959 C>A maps to NM_001081.3 L3014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:16979675 G>T maps to NM_001081.3 S1947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:55945510 G>T maps to NM_017949.1 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr17:55951068 C>T maps to NM_017949.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:55950054 C>G maps to NM_017949.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:148427225 C>G maps to NM_003592.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:35333796 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:35327985 C>A maps to NM_001198778.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:35318520 T>C maps to NM_001198778.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:35333507 G>A maps to NM_001198778.1 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:225376299 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:225346794 C>A maps to NM_003590.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr2:225339002 G>A maps to NM_003590.3 R756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr13:113887577 C>T maps to NM_001008895.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr13:113907458 C>T maps to NM_001008895.1 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113883758 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr13:113897451 C>T maps to NM_001008895.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:119694175 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:119660693 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:119678059 T>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:119666390 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:119673216 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:119668354 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr23:119664013 T>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:119694233 A>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:119694152 G>C did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:119664097 T>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:119666434 T>A did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr23:119678407 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr23:119680992 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:119672060 C>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:107904542 C>T maps to NM_003478.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:107969144 G>A maps to NM_003478.3 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:43019122 C>T maps to NM_001168370.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr6:43014809 C>A maps to NM_001168370.1 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:43019472 C>G maps to NM_001168370.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr6:43019056 C>T maps to NM_001168370.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:43014776 C>T maps to NM_001168370.1 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:43020328 C>A maps to NM_001168370.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:43152182 G>A maps to ENST00000354495 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:43167689 C>T maps to ENST00000354495 F1060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr6:43155662 C>G maps to ENST00000354495 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr6:43171717 C>T maps to ENST00000354495 T1384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr6:43181475 G>A maps to ENST00000354495 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:33384896 C>A maps to NM_001014433.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:101514310 A>T maps to NM_015960.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:101514355 T>C maps to NM_015960.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:101882786 A>T maps to ENST00000360264 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:101925178 C>T maps to NM_001913.2 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:101844856 C>A maps to ENST00000360264 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101892231 G>T maps to ENST00000360264 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:101671404 C>T maps to ENST00000360264 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr7:101833098 G>T maps to ENST00000360264 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:101459330 G>C maps to ENST00000360264 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:101843430 G>T maps to ENST00000360264 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:101877435 G>T maps to ENST00000360264 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:101845297 G>A maps to ENST00000360264 Q918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:111729243 G>A maps to NM_015267.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:111786099 C>A maps to NM_015267.3 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:111746127 C>T maps to NM_015267.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:111742069 C>A maps to NM_015267.3 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr12:111758467 C>T maps to NM_015267.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:111772464 G>A maps to NM_015267.3 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:111748403 G>A maps to NM_015267.3 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:111779638 G>T maps to NM_015267.3 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr12:111733213 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:111758260 T>C maps to NM_015267.3 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:111785648 C>A maps to NM_015267.3 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:111785441 G>T maps to NM_015267.3 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:111776135 C>A maps to NM_015267.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:111779638 G>T maps to NM_015267.3 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:111748230 G>T maps to NM_015267.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:111758182 C>G maps to NM_015267.3 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:111745013 G>A maps to NM_015267.3 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:111729345 C>A maps to NM_015267.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:111731316 C>A maps to NM_015267.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:111785480 C>A maps to NM_015267.3 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:111749979 G>A maps to NM_015267.3 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:111748358 C>A maps to NM_015267.3 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr10:124596449 C>A maps to NM_022034.4 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:124593397 G>A maps to NM_022034.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:124595809 C>A maps to NM_022034.4 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:94704545 T>G maps to NM_016403.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:180830694 C>A maps to NM_020943.2 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr2:180818937 T>C maps to NM_020943.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:180818937 T>C maps to NM_020943.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:180810027 G>C maps to NM_020943.2 S852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:36971176 G>C maps to NM_017748.3 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:64314066 C>A maps to NM_005869.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:64070588 A>G maps to NM_005869.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:102003469 G>A maps to NM_018294.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:107197779 C>A did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr11:107299925 T>C maps to NM_152434.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr11:107299701 C>T maps to NM_152434.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:49032884 C>A maps to NM_025087.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:48996750 C>A maps to NM_025087.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48994051 C>T maps to NM_025087.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:48996697 A>T maps to NM_025087.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:49005779 C>T maps to NM_025087.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:39307727 C>T maps to NM_001171174.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:39307160 C>T maps to NM_001171174.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:39307745 G>A maps to NM_001171174.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr3:39307922 G>T maps to NM_001171174.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:39307286 G>A maps to NM_001171174.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:39307067 G>T maps to NM_001171174.1 C343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr21:18919472 C>T maps to NM_001338.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr21:18919366 C>T maps to NM_001338.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr4:74735446 C>T maps to NM_001511.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:76957125 G>A maps to NM_005409.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:44874112 G>A maps to NM_001178134.1 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:44873301 G>C maps to NM_001178134.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr10:44871480 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:134914176 C>A maps to NM_004887.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr4:74964333 C>A maps to NM_002089.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:74902979 C>T maps to NM_002090.2 *108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:74864244 C>T maps to NM_002994.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:74702789 G>A maps to NM_002993.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:74702982 C>A maps to NM_002993.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr4:76924828 C>T maps to NM_002416.1 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:76927398 A>T maps to NM_002416.1 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:76928569 G>A maps to NM_002416.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr4:76927299 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:219029205 G>T maps to NM_000634.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:219000009 C>T maps to NM_001168298.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:218999802 C>A maps to NM_001168298.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:219000216 C>A maps to NM_001168298.1 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr2:219000465 C>A maps to NM_001168298.1 Y314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr23:70836738 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:70837091 A>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:70836378 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:136872636 G>T maps to NM_001008540.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:118764810 C>A maps to NM_001716.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:118765014 G>A maps to NM_001716.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:45988827 T>A maps to NM_006564.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:237489986 C>G maps to NM_020311.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr18:47809013 C>T maps to NM_001101654.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr18:47811485 G>C maps to NM_001101654.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:139060296 T>C maps to NM_016463.7 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:144909438 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:144909467 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:144909467 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:144909296 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:30577697 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:30577700 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:30578174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:30577879 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:30577750 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:30578216 T>C did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:30578091 T>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:30578035 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:30577854 A>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:35974186 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:35993265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:35944188 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:35990040 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:35966553 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:35969250 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:35974240 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:35989774 C>T did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:35985840 G>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:35988981 T>C did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:35993958 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:35971800 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:35993864 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:35969363 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:35988933 G>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:35989004 A>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:35969946 A>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:35985932 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:35989827 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:35993837 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:35989824 G>C did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:35993823 G>C did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:35966463 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:35944172 T>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:35993818 C>A did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr23:35970045 C>T did not map to a codon.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr23:35966467 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:35974293 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:35974305 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:35971760 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:35971831 C>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:36007541 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:35966464 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:35970074 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:36007509 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:19968953 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:19971150 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:19983546 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:19984301 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:19973540 T>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:19983754 A>C did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:19983617 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:75397739 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:75396787 G>T did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:75397470 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:75396724 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:75395336 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:37850382 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:37850386 G>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:37850252 T>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:37850305 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:37850307 C>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:37850409 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:37850306 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:37850307 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:45013395 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:45013396 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:45051244 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:45051167 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:45013319 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:45010942 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:45059912 A>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:45013317 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:45051015 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:40496312 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:40495906 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:40498350 T>C did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:40506711 C>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:40489997 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:148627287 A>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr23:148628442 G>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:148628334 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:148628314 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:149101927 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:149100951 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:149101925 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:149100785 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:106459948 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:106462127 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:106459968 C>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:106466058 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:106486459 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:106456219 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:134303588 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:134292126 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:134294448 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:134303517 C>G did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr23:134303633 C>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:134305008 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:134303518 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:118673719 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:118675325 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:118676545 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:118699216 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:118678318 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:118678384 T>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:118699204 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:105868403 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:105868455 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:105855777 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:105905388 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:105905389 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:105905438 C>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:105891593 G>C did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:105855610 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:105882816 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:105876406 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:23956663 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:36122804 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:36122682 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr23:36103614 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr23:36091389 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr23:36091418 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:36103456 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:36156082 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:36122631 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:36162710 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:36091255 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:36103604 A>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:36162922 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:36103527 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:36091369 C>A did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:36156569 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:36156526 T>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:36162679 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:36117907 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:36091256 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:36091443 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:36122644 C>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:36162688 G>T did not map to a codon.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr23:36117960 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:36122701 T>C did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:36091355 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:36091480 G>C did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:115593078 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:115593112 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:115592959 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:115593005 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:70326387 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:70325861 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:139038424 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:139038643 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:139038137 C>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:139040233 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:139038575 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:139038298 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:139038878 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:139047581 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:139038670 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:139038280 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:139038281 A>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:139038301 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:139038324 T>C did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:139047601 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:139038470 C>G did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:139038482 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:139038791 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr23:139038637 G>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:61511885 G>A maps to NM_001915.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:110038803 C>T maps to NM_001134400.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr1:202931771 G>A maps to NM_016243.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr6:84630847 T>C maps to NM_016230.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:84649817 A>T maps to NM_016230.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:84645952 A>T maps to NM_016230.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:84618741 C>G maps to NM_016230.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:61121426 C>G maps to NM_001161454.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr11:61124139 G>A maps to NM_001161454.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:61120464 G>A maps to NM_001161454.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:37664300 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:37658246 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:37663179 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:37668872 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:37651311 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:37653015 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:37670071 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:37655267 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:37663314 G>T did not map to a codon.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr23:37663303 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:37658309 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37670134 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:37653053 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:37655390 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:37663303 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:37642837 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:172411084 G>T maps to NM_024843.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:145150776 G>A maps to NM_001916.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr7:25163618 C>T maps to NM_018947.5 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:22933575 A>G maps to NM_014608.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:22945110 G>T maps to NM_014608.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:22980099 G>T maps to NM_014608.2 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr15:22958261 G>A maps to NM_014608.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:156787322 C>T maps to ENST00000442283 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr5:156766099 G>T maps to ENST00000442283 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:156746825 C>T maps to ENST00000442283 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:156768108 G>T maps to ENST00000442283 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:74533540 C>T maps to NM_134268.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:74533528 G>T maps to NM_134268.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr17:74533525 C>A maps to NM_134268.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:145689626 C>A maps to NM_001129888.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:83127977 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:83128937 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:83128562 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:83128908 A>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:83129164 T>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:83129329 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:83128658 A>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:83128652 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:83129209 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:83129210 T>C did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:83129463 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:83126523 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:83128432 A>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:83129555 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:83129399 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:83116204 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:83127970 G>C did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:83129173 G>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:83128147 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:83129029 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:83129058 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:83128555 T>A did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:83128347 C>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:83129063 C>A did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:83128706 G>C did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:83127988 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:83128862 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:83128431 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:83129602 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:83128821 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:83129039 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:105767800 C>A maps to NM_001340.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:105767377 A>T maps to NM_001340.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:50813642 C>G maps to ENST00000311559 L402L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-1676-01A-01D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:50818356 G>C maps to ENST00000311559 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:50813604 G>T maps to ENST00000311559 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr16:50830352 A>G maps to ENST00000311559 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:50783813 C>T maps to ENST00000311559 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:74659770 G>T maps to NM_000781.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr8:143958263 C>G maps to ENST00000377675 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143960554 G>A maps to ENST00000377675 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:143958140 C>T maps to ENST00000377675 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:143958290 C>T maps to ENST00000377675 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:143957749 G>T maps to ENST00000377675 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:143955803 G>A maps to ENST00000377675 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr8:143957736 C>A maps to ENST00000377675 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:143958502 C>A maps to ENST00000377675 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:143958504 G>A maps to ENST00000377675 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143955875 T>A maps to ENST00000377675 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:143957126 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:143956676 C>A maps to ENST00000377675 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:143957788 G>T maps to ENST00000377675 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143994819 G>T maps to NM_000498.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:143995724 G>T maps to NM_000498.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:143994038 G>T maps to NM_000498.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:143999130 G>T maps to NM_000498.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143996513 C>A maps to NM_000498.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:143996265 A>C maps to NM_000498.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr8:143993990 G>A maps to NM_000498.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:143993974 C>A maps to NM_000498.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:143999043 G>T maps to NM_000498.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143995832 A>G maps to NM_000498.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:143999136 G>T maps to NM_000498.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:143996510 C>T maps to NM_000498.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:143999172 G>T maps to NM_000498.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr8:143999130 G>T maps to NM_000498.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:143993948 G>A maps to NM_000498.3 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:143994222 C>T maps to NM_000498.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:143994786 C>G maps to NM_000498.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:143998476 C>T maps to NM_000498.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:104593790 A>G did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr10:104597000 G>A maps to NM_000102.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:51514612 C>G maps to NM_031226.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr15:51535049 G>A maps to NM_031226.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:75013387 T>G maps to NM_000499.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:75014928 C>G maps to NM_000499.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr15:75047188 C>A maps to NM_000761.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:38301581 A>T maps to NM_000104.3 L317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:204116832 G>C did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:204150333 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:32006973 C>T maps to NM_000500.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:32007877 G>T maps to NM_000500.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:32008280 C>T maps to NM_000500.5 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:52781003 G>T maps to NM_000782.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:52782352 A>T maps to NM_000782.4 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:52786158 G>T maps to NM_000782.4 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:94834544 C>A maps to NM_000783.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:94834798 C>A maps to NM_000783.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:94835009 G>T maps to NM_000783.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:94836937 G>T maps to NM_000783.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:72360360 G>A maps to NM_019885.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:72359592 G>A maps to NM_019885.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:72374758 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:72362449 G>C maps to NM_019885.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:72361996 G>T maps to NM_019885.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr2:72360361 C>A maps to NM_019885.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr2:72360349 G>T maps to NM_019885.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr2:72362005 T>A maps to NM_019885.2 K249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr2:72360160 G>A maps to NM_019885.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:94828348 C>T maps to NM_183374.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr10:94828196 G>T maps to NM_183374.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:219674424 G>T maps to NM_000784.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr2:219677416 C>T maps to NM_000784.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:58156978 G>T maps to NM_000785.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:58160729 G>C maps to NM_000785.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:127950840 C>A maps to NM_001001665.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:127944891 C>T maps to NM_001001665.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:127958833 G>A maps to NM_001001665.3 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:41601806 G>T maps to NM_000766.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr19:41601770 T>C maps to NM_000766.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:41596336 G>A maps to NM_000766.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:41597722 C>T maps to NM_000766.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:41355873 G>T maps to NM_000762.5 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:41386405 G>A maps to NM_000764.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:41387974 G>T maps to NM_000764.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr19:41386438 C>T maps to NM_000764.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:41512963 C>T maps to NM_000767.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41512852 C>T maps to NM_000767.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:41522587 G>T maps to NM_000767.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:41518390 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:96443608 C>A maps to NM_000772.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:96484143 C>A maps to NM_000772.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:96534880 G>T maps to NM_000769.1 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:96535208 C>A maps to NM_000769.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr10:96580311 C>T maps to NM_000769.1 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr10:96522525 C>T maps to NM_000769.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr10:96609702 T>A maps to NM_000769.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:96609672 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:96802715 G>A maps to NM_000770.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:96802751 A>T maps to NM_000770.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:96805588 C>A maps to NM_000770.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:96805585 C>A maps to NM_000770.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:96748683 C>T maps to NM_000771.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:96748757 C>T maps to NM_000771.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr10:96745822 C>T maps to NM_000771.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr10:96698552 G>C maps to NM_000771.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr22:42524884 G>A maps to NM_000106.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:135346287 T>C maps to NM_000773.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:135341024 C>T maps to NM_000773.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:135351253 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:135346332 C>T maps to NM_000773.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:41622110 A>T maps to NM_000774.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:41622227 G>A maps to NM_000774.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr19:41630660 C>A maps to NM_000774.3 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:60377302 A>G maps to NM_000775.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41712284 G>A maps to ENST00000301173 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:41703807 G>T maps to ENST00000301173 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:41704793 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:108866741 G>T maps to NM_183075.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:1024665 C>A maps to NM_017781.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:1027058 C>A maps to NM_017781.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:46555803 T>C maps to NM_016593.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:99377623 G>A maps to NM_017460.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:99358456 A>C maps to NM_017460.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99447309 C>T maps to NM_022820.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:99463536 G>T maps to NM_022820.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:99457478 C>T maps to NM_022820.3 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:99454460 A>T maps to NM_022820.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:99262906 A>G maps to NM_000777.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:99261602 G>A maps to NM_000777.3 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:99277498 C>T maps to NM_000777.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:99258181 G>T maps to NM_000777.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:99332707 G>A maps to ENST00000292414 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:99311121 G>A maps to ENST00000292414 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:99319929 T>C maps to ENST00000292414 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:100182492 C>T maps to NM_006668.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:100165800 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:100182220 C>T maps to NM_006668.1 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:47400231 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:47395891 G>C maps to ENST00000371904 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:47395936 G>T maps to ENST00000371904 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:47400756 G>T maps to ENST00000371904 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:47282728 G>T maps to NM_001099772.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:47284380 T>C maps to NM_001099772.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:47283691 C>G maps to NM_001099772.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:47276490 G>A maps to NM_001099772.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:47278264 C>T maps to NM_001099772.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:16034627 C>T maps to NM_021187.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16025116 G>A maps to NM_021187.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:16025584 G>T maps to NM_021187.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:16033241 T>C did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:16040369 C>A maps to NM_021187.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:16035674 C>T maps to NM_021187.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:16045056 G>T maps to NM_021187.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:16038019 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15784337 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:15807816 C>G maps to NM_023944.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15789215 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr19:15789144 G>A maps to NM_023944.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:15794431 C>T maps to NM_023944.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:15784347 G>T maps to NM_023944.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:16008415 G>T maps to NM_001082.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:16008394 C>A maps to NM_001082.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:15990586 C>A maps to NM_001082.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:15651461 C>G maps to NM_173483.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:15648394 C>A maps to NM_173483.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:15636269 G>T maps to NM_173483.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:15651521 G>T maps to NM_173483.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:15769364 G>A maps to NM_000896.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:15769109 C>A maps to NM_000896.2 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:15760836 G>A maps to NM_000896.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr19:15760977 A>G maps to NM_000896.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:15756551 C>G maps to NM_000896.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr19:15769109 C>T maps to NM_000896.2 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:15734866 G>T maps to NM_007253.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:15739234 C>A maps to NM_007253.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:15734083 G>T maps to NM_007253.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:15733987 C>A maps to NM_007253.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:15734145 C>A maps to NM_007253.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:187122496 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:47489620 C>A maps to NM_178033.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:47582405 T>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:47548003 A>C did not map to a codon.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr7:91752551 G>C maps to NM_000786.3 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:91763537 G>A maps to NM_000786.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:59404998 G>A maps to NM_000780.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:59410853 G>T maps to NM_000780.3 Y85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:59410880 G>A maps to NM_000780.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr8:59409715 C>A maps to NM_000780.3 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:59409191 C>A maps to NM_000780.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:59409536 C>G maps to NM_000780.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr8:59405016 G>A maps to NM_000780.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:65537044 C>A maps to NM_004820.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr8:65528461 T>G maps to NM_004820.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:65517322 C>T maps to NM_004820.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:65509419 T>A maps to NM_004820.3 K434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:65517309 G>A maps to NM_004820.3 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:65528838 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:65528404 G>C maps to NM_004820.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:42916063 C>G maps to NM_004391.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:42917134 C>T maps to NM_004391.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:42917185 G>C maps to NM_004391.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:86048466 C>G maps to NM_001554.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:77529229 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:77528649 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:77528733 A>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:77528785 A>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:77528532 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:77528878 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:77528433 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:77528598 G>C did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:77529057 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:49281192 G>T maps to NM_020377.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:76695000 C>A maps to NM_004762.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:6210908 C>T maps to ENST00000396741 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:6213365 T>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:6217527 T>A maps to ENST00000396741 P98P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37695347 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:37690735 A>G maps to NM_013385.3 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr22:37707027 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr22:37699443 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr22:37707038 G>A maps to NM_013385.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:158272581 C>A maps to NM_004288.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr22:24718717 G>A maps to NM_015330.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr22:24718429 T>A maps to NM_015330.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:20000014 C>T maps to NM_001033553.1 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:20108580 G>T maps to NM_001033553.1 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:20013765 G>A maps to NM_001033553.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr21:27945253 G>A maps to ENST00000435845 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr21:27938636 C>A maps to ENST00000435845 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:27840858 A>G maps to ENST00000435845 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:242707189 G>T maps to NM_152783.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:242695428 G>T maps to NM_152783.3 G436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242689674 C>G maps to NM_152783.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:242690736 G>A maps to NM_152783.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:242707233 C>T maps to NM_152783.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:242690763 G>C maps to NM_152783.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:242683208 G>T maps to NM_152783.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:4393281 C>G maps to NM_001040101.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr4:4411340 C>A maps to NM_001040101.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59757933 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:39851748 T>A maps to ENST00000398904 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:39841120 G>C maps to ENST00000398904 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr6:39832222 C>T maps to ENST00000398904 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr6:39869750 C>T maps to ENST00000398904 R1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:57476946 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:57756645 G>T maps to ENST00000371231 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:57480982 G>T maps to ENST00000371231 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:57476937 G>T maps to ENST00000371231 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:57476877 G>T maps to ENST00000371231 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:57602314 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:57537953 A>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:57537197 G>T maps to ENST00000371231 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:57528577 C>A maps to ENST00000371231 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:57537272 G>T maps to ENST00000371231 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:57480985 G>A maps to ENST00000371231 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:57481087 G>T maps to ENST00000371231 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:39377208 G>A maps to NM_001343.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:39382953 C>A maps to NM_001343.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:39383130 C>A maps to NM_001343.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:39388915 A>T maps to NM_001343.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr5:39376764 C>T maps to NM_001343.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr5:39382718 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:39383358 G>T maps to NM_001343.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:39393457 G>A maps to NM_001343.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:39390614 G>A maps to NM_001343.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:39394406 C>A maps to NM_001343.2 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr5:39376764 C>T maps to NM_001343.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:39382779 G>A maps to NM_001343.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr5:39392556 C>A maps to NM_001343.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:124544668 G>A maps to ENST00000408936 Q1154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:124534909 G>A maps to ENST00000408936 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:124534888 G>T maps to ENST00000408936 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:124534996 G>A maps to ENST00000408936 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr13:72134054 G>A maps to ENST00000359684 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr13:72063269 C>A maps to ENST00000359684 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:72440370 G>T maps to ENST00000359684 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:72049303 G>A maps to ENST00000359684 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:72255996 G>T maps to ENST00000359684 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:85404022 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:86071077 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:85769354 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:85950085 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:86068171 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:85404013 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:86071098 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:85906143 A>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:86067925 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:86067969 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:86068164 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:86067911 C>A did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:86069768 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:85403694 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:86069787 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:85769387 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:86067904 G>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:85769307 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:85403693 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:85403941 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:85950161 A>G did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:86069768 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:86067860 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:85950088 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:85950112 G>C did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:85969641 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:85994884 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:85906101 A>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:85769352 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:85403694 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:85906053 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:85969642 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:86069727 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:86067911 C>G did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:85769324 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:85950039 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:85994857 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:86087117 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:59112600 G>A maps to NM_016651.5 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:59112837 G>A maps to NM_016651.5 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:59112432 T>A maps to NM_016651.5 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:59112609 A>G maps to NM_016651.5 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:59112633 G>A maps to NM_016651.5 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:59112624 C>T maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr14:59113479 C>T maps to NM_016651.5 Y713Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:47151759 G>A maps to NM_145056.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr14:23057907 G>C maps to NM_001344.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:49568630 G>A maps to NM_004393.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr3:49568390 C>T maps to NM_004393.4 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:49569740 C>T maps to NM_004393.4 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:61502410 G>A maps to NM_006133.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:61508791 G>A maps to NM_006133.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:61490343 C>T maps to NM_006133.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:61511534 C>G maps to NM_006133.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:61495622 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:61511783 G>T maps to NM_006133.2 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr7:6485623 G>A maps to NM_139179.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:61106795 C>A maps to NM_015533.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr11:61105498 C>T maps to NM_015533.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:61112950 G>C maps to NM_015533.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:61106637 G>A maps to NM_015533.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:61110122 G>A maps to NM_015533.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:13080561 C>T maps to NM_152654.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr19:13080791 C>T maps to NM_152654.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:109294181 C>A maps to NM_001917.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:109292562 C>A maps to NM_001917.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:109294178 G>C did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:109278817 G>A maps to NM_001917.4 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr13:106118651 G>T maps to NM_172370.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr13:106119490 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:10681214 T>A maps to ENST00000432074 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:155699057 G>A maps to NM_004632.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155701745 C>G maps to NM_004632.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:90263693 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:90321153 G>A maps to NM_004938.2 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:90312087 G>T maps to NM_004938.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr9:90220045 C>T maps to NM_004938.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3960089 G>C maps to NM_001348.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:3959299 G>A maps to NM_001348.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:3960102 C>G did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:159672218 C>T maps to NM_001017920.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:100774381 G>A maps to NM_014395.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:159175729 G>T maps to NM_001122951.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159176164 C>T maps to NM_001122951.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:159175966 G>T maps to NM_001122951.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:159175441 G>T maps to NM_001122951.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:159175264 C>G maps to NM_001122951.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:159175666 G>T maps to NM_001122951.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:159175305 G>A maps to NM_001122951.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:159175417 C>A maps to NM_001122951.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:159176074 G>T maps to NM_001122951.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:173822599 C>G maps to NM_018122.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33287596 T>C maps to NM_001350.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr6:33289182 G>C maps to NM_001350.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr6:33286534 G>A maps to NM_001350.4 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:1433736 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:1433756 A>G maps to NM_170711.1 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:121971073 G>T maps to NM_014618.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:122075576 T>A maps to NM_014618.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr9:122011271 G>T maps to NM_014618.2 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:122004411 C>G maps to NM_014618.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:121930354 G>A maps to NM_014618.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr9:121929697 G>A maps to NM_014618.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr9:121929769 A>T maps to NM_014618.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr9:121929565 G>C maps to NM_014618.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:87530129 G>A maps to NM_006716.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr7:87533695 T>C maps to NM_006716.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr17:42800312 G>T maps to NM_145663.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:42815765 G>T maps to NM_145663.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:42786720 G>T maps to NM_145663.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:42825783 C>T maps to NM_145663.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:136501726 G>T maps to NM_000787.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:136501611 C>A maps to NM_000787.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr9:136508551 C>T maps to NM_000787.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:136523514 G>A maps to NM_000787.3 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr9:136501720 C>A maps to NM_000787.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:136508656 C>T maps to NM_000787.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:176885525 C>A maps to ENST00000393565 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:176887644 C>T maps to ENST00000393565 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:176885478 G>A maps to ENST00000393565 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:44097388 G>A maps to NM_001122956.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:44097820 G>T maps to NM_001122956.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:49136877 G>A maps to NM_001352.3 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr3:137886024 T>A maps to NM_016216.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:137880799 T>C maps to NM_016216.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:100681575 C>T maps to NM_001918.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:100672087 C>T maps to NM_001918.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:100661969 G>A maps to NM_001918.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100672122 G>A maps to NM_001918.2 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr11:20177909 G>A maps to ENST00000227256 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr12:45410211 C>A maps to NM_001004329.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:24588397 C>G maps to NM_025230.4 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr9:34093434 G>T maps to NM_015397.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr9:34089568 G>A maps to NM_015397.3 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:125685885 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:125685830 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:125686304 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr23:125686547 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:125686200 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:125686416 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:125686542 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:125685682 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:125686464 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:125685302 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:125685252 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:125685235 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:125685986 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:125686175 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr23:125686523 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:125686585 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:125685252 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:125685682 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:125686242 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:125685888 T>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:125685378 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:125686030 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:125686503 C>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:125685649 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:125685463 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:125686413 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:125686197 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:125686487 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:125685550 T>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:125686023 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:125685508 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:125685397 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:125685958 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr23:125685796 C>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:125685454 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:125685658 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:125685861 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:125685539 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:125685291 G>T did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:125685330 A>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:125686014 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:125686108 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:125686259 A>G did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:125686234 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:125686012 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:125686365 G>C did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:125685269 A>T did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:125685340 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:125685607 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:125685301 C>G did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:125686317 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:125686552 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:125685527 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:125686543 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:125298631 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:125298846 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:125298567 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:125298618 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:125299289 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:125298775 G>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:125298904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:125299580 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:125298617 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:125298933 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:125299719 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:125298867 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:125299402 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:125299512 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:125299020 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:125299046 G>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:125298987 C>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:125298800 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:125299760 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:125298593 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:125299864 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:125298781 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:125299577 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:125299862 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:125298988 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:125298752 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:125298866 T>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:125299814 C>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:125299370 C>G did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:125298848 C>G did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:125298975 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:125299716 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:125298758 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:125298587 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:125299246 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:125299758 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:125299258 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:125298589 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:125298729 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:125299019 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:125298529 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:125298988 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:125299100 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:125298676 G>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:125298851 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:125299248 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:125299275 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:125299276 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:125298875 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:125298773 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:125299884 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:125299601 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:125299067 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:125299272 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:125298901 G>T did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:125299866 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:125299008 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:104447973 C>T maps to NM_015420.6 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:104427487 C>T maps to NM_015420.6 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:104427283 G>A maps to NM_015420.6 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:14070232 C>G maps to NM_138353.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:17805365 C>A maps to NM_017741.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:172337512 A>G maps to NM_025000.3 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:73408451 G>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr14:73420893 C>T maps to NM_015604.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:41984937 G>T maps to NM_001029955.3 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:88885767 C>G maps to NM_152418.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:88885798 G>T maps to NM_152418.3 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:88885653 G>A maps to NM_152418.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:88885128 G>C maps to NM_152418.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:88885434 A>T maps to NM_152418.3 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:88885965 C>A maps to NM_152418.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:88885554 C>A maps to NM_152418.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:88885713 C>A maps to NM_152418.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr8:88885872 G>C maps to NM_152418.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:88885884 T>A maps to NM_152418.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:88885962 C>A maps to NM_152418.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:88885083 G>C maps to NM_152418.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:88885854 G>T maps to NM_152418.3 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:88885886 G>T maps to NM_152418.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:88885101 C>A maps to NM_152418.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr8:88885128 G>A maps to NM_152418.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:88886058 G>T maps to NM_152418.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:88885554 C>T maps to NM_152418.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:88885821 C>T maps to NM_152418.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:88886136 C>A maps to NM_152418.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:88885611 C>T maps to NM_152418.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr8:88885414 C>T maps to NM_152418.3 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:88885200 G>T maps to NM_152418.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr8:88885344 C>G maps to NM_152418.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr8:88885611 C>A maps to NM_152418.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:88885344 C>G maps to NM_152418.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr8:88885794 C>A maps to NM_152418.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:88885794 C>A maps to NM_152418.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:88885053 G>T maps to NM_152418.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:88886135 C>A maps to NM_152418.3 G22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:69529103 G>A maps to NM_003861.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69520615 T>A maps to NM_003861.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr14:69520960 C>T maps to NM_003861.2 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:69522222 G>A maps to NM_003861.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:167973204 A>T maps to ENST00000367840 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:168034949 G>T maps to ENST00000367840 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr17:61657204 G>T maps to NM_005828.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:160201109 C>G maps to NM_015726.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:160209656 G>A maps to NM_015726.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:160209913 G>C maps to NM_015726.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:160210061 A>G maps to NM_015726.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:27998807 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:27997830 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:27997758 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:27998071 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:27998440 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:27998042 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:27998106 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:27998020 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:27998544 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:27998545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:27999003 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:27998032 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:27999350 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:27998523 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:27999417 G>C did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:27999364 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:27998578 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:27997755 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:27998828 C>G did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:27998991 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:27998160 A>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:27998836 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:27999045 C>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:27997944 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:27999394 C>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:27999034 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:27998428 A>G did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:27998407 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:27999165 C>A did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:27999371 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:27998775 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:27999257 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:27766659 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:27766464 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:27766652 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:27765054 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:27766227 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:27766228 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:27765782 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:27765837 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:27766165 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:27766500 T>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:27766140 G>T did not map to a codon.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr23:27766804 G>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:27766389 A>G did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:27765718 T>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:27765739 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:27766003 C>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:27766033 C>A did not map to a codon.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr23:27765085 A>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:27765097 C>A did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:27766229 C>G did not map to a codon.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr23:27766044 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:117864320 G>T maps to ENST00000338728 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117841006 C>T maps to ENST00000338728 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:117864335 G>T maps to ENST00000338728 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:117861836 C>T maps to ENST00000338728 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:98518497 G>A maps to ENST00000326857 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:50936981 A>C maps to NM_005215.3 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734107 T>A maps to NM_005215.3 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:50734143 G>C maps to NM_005215.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:50683753 G>T maps to NM_005215.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:50734080 G>T maps to NM_005215.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51025875 G>A maps to NM_005215.3 Q1369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:51025665 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:50923678 C>A maps to NM_005215.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr18:50961541 A>T maps to NM_005215.3 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr18:51057012 C>A maps to NM_005215.3 S1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr18:50985712 A>T maps to NM_005215.3 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr18:50589768 C>A maps to NM_005215.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:50866233 G>A maps to NM_005215.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr18:50450201 C>A maps to NM_005215.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr18:50705364 C>A maps to NM_005215.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:50918211 C>A maps to NM_005215.3 Y881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:31327811 G>T maps to NM_181807.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:31327936 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:31312213 C>A maps to NM_181807.2 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:31349725 T>C maps to NM_181807.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:31312343 A>T maps to NM_181807.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:31327897 G>T maps to NM_181807.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:24178854 T>A maps to NM_016356.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:32678381 C>G maps to NM_001099434.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:6662547 C>A maps to NM_003737.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:6647185 T>A maps to NM_003737.2 T2232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:6647527 C>A maps to NM_003737.2 G2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6653760 A>T maps to NM_003737.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:6646565 G>A maps to NM_003737.2 L2337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6651356 C>T maps to NM_003737.2 E1556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:6650722 C>A maps to NM_003737.2 R1707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr11:6661628 C>A maps to NM_003737.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:6643582 T>C maps to NM_003737.2 R3108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:6653769 C>A maps to NM_003737.2 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:6661320 G>A maps to NM_003737.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:6646948 C>T maps to NM_003737.2 L2247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:6662463 T>C maps to NM_003737.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:6652388 A>T maps to NM_003737.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:6661761 G>T maps to NM_003737.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr11:6648020 T>G maps to NM_003737.2 P2083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:6648656 C>A maps to NM_003737.2 G1871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr11:6661974 C>A maps to NM_003737.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr11:6651237 G>C maps to NM_003737.2 S1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:6662270 G>T maps to NM_003737.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:6646660 G>C maps to NM_003737.2 S2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:6648428 G>A maps to NM_003737.2 T1947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:155241864 G>T maps to NM_017639.3 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:155161690 G>A maps to NM_017639.3 Q1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr4:155226291 G>T maps to NM_017639.3 T1329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:155287360 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:155298497 G>T maps to NM_017639.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:155226378 G>T maps to NM_017639.3 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:155157031 A>T maps to NM_017639.3 P2469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:155250851 G>T maps to NM_017639.3 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr4:155219857 C>A maps to NM_017639.3 G1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:155191130 A>G maps to NM_017639.3 P1711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr4:155156785 C>T maps to NM_017639.3 L2551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr4:155158150 G>A maps to NM_017639.3 V2096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:155219642 A>G maps to NM_017639.3 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:155256212 G>T maps to NM_017639.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr4:155155735 G>A maps to NM_017639.3 I2901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:155241957 G>C maps to NM_017639.3 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr4:155219117 G>T maps to NM_017639.3 G1661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr4:155253831 T>A maps to NM_017639.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr4:155287386 G>T maps to NM_017639.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:155157459 G>A maps to NM_017639.3 L2327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:2296867 G>A maps to NM_001919.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:71863874 T>A maps to ENST00000504952 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:71889416 T>G maps to ENST00000504952 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:36428695 C>A maps to NM_004734.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr13:36362407 A>G maps to NM_004734.4 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:36699914 C>G maps to NM_004734.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:36700172 C>T maps to NM_004734.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr13:36348798 C>A maps to NM_004734.4 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:36401821 C>A maps to NM_004734.4 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr13:36700231 G>T maps to NM_004734.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:151023954 T>C maps to NM_001040261.4 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:36779985 C>T maps to NM_033403.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:36779849 C>A maps to NM_033403.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:36756821 T>C maps to NM_033403.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:36756824 T>C maps to NM_033403.1 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:36780003 T>C maps to NM_033403.1 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:36779823 G>T maps to NM_033403.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:36778974 G>C maps to NM_033403.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:36763035 C>A maps to NM_033403.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:36763036 G>A maps to NM_033403.1 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr10:115602233 C>A maps to NM_014881.3 E845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr10:115603978 G>A maps to NM_014881.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:114450662 G>T maps to NM_022836.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:114453879 G>T maps to NM_022836.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr10:14987183 T>A maps to NM_001033855.1 K56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:14976701 C>A maps to NM_001033855.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:14974897 G>A maps to NM_001033855.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:91572167 G>A maps to NM_133503.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:53326446 C>T maps to ENST00000480258 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:112337368 G>A maps to NM_152624.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:126201303 A>G maps to NM_014026.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:126201330 A>T maps to NM_014026.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:126215447 C>G maps to NM_014026.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:155011885 G>T maps to NM_152494.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:155006926 G>T maps to NM_152494.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:155011918 C>A maps to NM_152494.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:155006532 G>A maps to NM_152494.3 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:155018632 T>A maps to NM_152494.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:155015856 C>G maps to NM_152494.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155001739 C>T maps to NM_144622.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:95095717 A>G maps to NM_001129889.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:95092210 C>A maps to NM_001129889.1 G534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:95131259 C>A maps to NM_001129889.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr13:95121090 C>G maps to NM_001129889.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:95121240 G>A maps to NM_001129889.1 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr13:95121219 C>A maps to NM_001129889.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:95121297 T>C maps to NM_001129889.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:183836691 G>A maps to NM_001012732.1 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:183814233 G>A maps to NM_001012732.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:74593019 C>T maps to NM_004082.4 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:74604791 G>C maps to NM_004082.4 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:74593142 A>C maps to NM_004082.4 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:34614162 T>C maps to NM_024348.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:150138537 C>T maps to NM_001135643.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:150121677 G>T maps to NM_001135643.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:150111015 T>A maps to NM_001135643.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:150102500 C>T maps to NM_001135643.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr5:150138542 G>A maps to NM_001135643.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:23677035 C>T maps to NM_032486.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:23678455 G>T maps to NM_032486.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:30435739 G>A maps to NM_024096.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:182665024 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:182662961 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr13:114128537 G>A maps to NM_001014283.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr13:114138334 G>A maps to NM_001014283.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:52740524 A>G maps to ENST00000451288 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr4:52779532 C>T maps to ENST00000451288 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr4:52729837 C>T maps to ENST00000451288 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr4:52779737 A>G maps to ENST00000451288 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:102933090 T>C maps to NM_032299.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:110574131 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:110644335 C>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:110574145 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:110574146 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:110653442 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:110574145 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr23:110654182 T>C did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:110654192 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:110653990 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:110653414 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:110574137 G>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:110654012 G>A did not map to a codon.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr23:110654183 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:110654144 G>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:110653617 A>G did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:110574253 T>C did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:110644529 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:110653472 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:79994491 C>A maps to NM_016286.3 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:61091480 G>C maps to NM_001923.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:61081949 T>C maps to NM_001923.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:61079459 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:61077400 T>C maps to NM_001923.3 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:61084006 C>A maps to NM_001923.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:61097029 G>A maps to NM_001923.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:47256827 C>T maps to NM_000107.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:50531021 G>A maps to NM_000790.3 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:38110568 A>G maps to NM_001164232.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:38095614 G>C maps to NM_001164232.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr8:38090548 C>T maps to NM_001164232.1 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:103908002 C>A maps to NM_001001711.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:103908281 C>G maps to NM_001001711.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr11:103908470 T>A maps to NM_001001711.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:103907618 C>A maps to NM_001001711.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103908254 C>A maps to NM_001001711.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:103908368 C>A maps to NM_001001711.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:103907703 C>A maps to NM_001001711.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:103908011 C>A maps to NM_001001711.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:103907789 G>T maps to NM_001001711.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:15956965 C>T maps to NM_032341.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:15953186 C>T maps to NM_032341.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:57910624 C>G maps to NM_001195056.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:49391857 C>T maps to NM_015086.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:49391599 C>A maps to NM_015086.1 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr12:49391545 C>G maps to NM_015086.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:110714268 G>T maps to NM_003649.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:110714106 A>T maps to NM_003649.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:110714463 G>T maps to NM_003649.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:110714246 C>A maps to NM_003649.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:110714064 C>A maps to NM_003649.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:110714394 G>C maps to NM_003649.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:110714367 C>T maps to NM_003649.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:20987828 G>A maps to NM_005216.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:30862314 G>A maps to NM_013994.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr6:30865939 G>A maps to NM_013994.2 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:30865368 C>T maps to NM_013994.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr6:30866675 G>T maps to NM_013994.2 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:162745597 C>A maps to NM_006182.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:162741928 G>T maps to NM_006182.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:162745570 C>A maps to NM_006182.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:162748380 T>A maps to NM_006182.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:162729652 G>T maps to NM_006182.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr1:162740300 A>G maps to NM_006182.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:162745480 C>A maps to NM_006182.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:162688891 G>T maps to NM_006182.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:162731242 A>G maps to NM_006182.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:162740291 G>A maps to NM_006182.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:162748458 G>A maps to NM_006182.2 Q791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:162745579 T>C maps to NM_006182.2 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr20:3175939 C>T maps to NM_023935.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr20:3171460 C>A maps to NM_023935.1 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:15742715 G>T maps to NM_004939.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:108709289 G>T maps to NM_004398.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:108593862 G>T maps to NM_004398.2 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:108594086 A>T maps to NM_004398.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:108562631 G>A maps to NM_004398.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:108550196 C>A maps to NM_004398.2 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:108535975 C>T maps to NM_004398.2 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:108594024 G>T maps to NM_004398.2 G601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:108547964 G>T maps to NM_004398.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr12:31249590 G>T maps to NM_030653.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr12:31236919 G>A maps to NM_030653.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:31249671 G>A maps to NM_030653.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:31256873 G>A maps to NM_152438.1 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr22:38891936 T>A maps to NM_001098504.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:118579624 G>T maps to NM_006773.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:118577318 T>C maps to NM_006773.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:118577358 G>T maps to NM_006773.3 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:118579436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:118572406 C>G maps to NM_006773.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:118582658 G>A maps to NM_006773.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:118579309 G>A maps to NM_006773.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:70363366 C>A maps to NM_007242.4 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr16:70363205 C>T maps to NM_007242.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:112309028 A>T maps to NM_007204.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr10:70728877 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:70733332 G>T maps to NM_004728.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:49239370 G>A maps to NM_004818.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:49231354 C>T maps to NM_004818.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49231389 C>A maps to NM_004818.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:49233638 T>C maps to NM_004818.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:49231324 C>T maps to NM_004818.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr12:49225084 T>C maps to NM_004818.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94545841 C>A maps to NM_020414.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:94526847 C>A maps to NM_020414.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr14:94545587 C>T maps to NM_020414.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr14:94527355 G>A maps to NM_020414.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr14:94527332 C>A maps to NM_020414.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr14:94526679 C>A maps to NM_020414.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr11:125778352 G>A maps to NM_013264.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:134703356 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:134681098 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:134690114 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:134680394 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:134713797 A>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:134680667 A>T did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:134681099 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:134680704 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:134681064 G>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:134713925 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:134655005 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:134709150 G>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:134681153 G>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:134679427 G>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:134680704 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:134715513 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr23:134680695 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:134679346 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:134715459 A>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:134654921 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:134680695 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:134683589 C>A did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr20:47838009 C>T maps to NM_017895.7 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr20:47835999 C>G maps to NM_017895.7 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr20:47851568 G>T maps to NM_017895.7 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:68055793 C>A maps to NM_018380.3 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:135470483 C>T maps to NM_022779.7 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr9:135522350 C>A maps to NM_022779.7 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:135523916 G>T maps to NM_022779.7 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:41196687 G>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:41203340 C>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:41203610 G>A did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:41206646 G>A did not map to a codon.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr24:15026554 T>C did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr24:15021273 G>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr5:55082456 C>T maps to NM_024415.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:55083795 G>A maps to NM_024415.2 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:55086460 A>G maps to NM_024415.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr5:55110998 T>C maps to NM_024415.2 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:55094337 C>T maps to NM_024415.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:61890702 G>T maps to NM_203499.1 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:61877961 C>T maps to NM_203499.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:74116136 C>A maps to NM_018665.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:74123508 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:74117808 G>A maps to NM_018665.2 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:134147432 C>T maps to ENST00000452510 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:134102699 G>T maps to ENST00000452510 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr5:134147432 C>T maps to ENST00000452510 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:12966354 G>T maps to NM_016355.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr12:12976217 C>T maps to NM_016355.3 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:19031458 G>A maps to NM_019070.4 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:70666760 G>T maps to NM_024045.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:70672915 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr10:70673213 G>A maps to NM_024045.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:132624411 T>C maps to NM_175066.3 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:35980933 T>A maps to NM_007010.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr17:36002304 C>T maps to NM_007010.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:23020011 G>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:23019759 G>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:23018322 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:23018307 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:23018527 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:23019472 G>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:23018535 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:23019063 C>A did not map to a codon.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr23:23019709 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:23018371 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113599743 T>A maps to NM_001111322.1 K752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:113603730 G>A maps to NM_001111322.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:113614681 G>A maps to NM_001111322.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:113614690 G>A maps to NM_001111322.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:124104072 C>G maps to NM_020936.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:124097727 A>T maps to NM_020936.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:124091976 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:32488877 T>A maps to NM_014314.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:32487950 G>A maps to NM_014314.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:32480280 G>A maps to NM_014314.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:32492479 G>A maps to NM_014314.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:200613582 T>A maps to NM_001031725.4 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:200635198 C>A maps to NM_001031725.4 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:118650397 T>C maps to NM_004397.4 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:169158900 T>A maps to NM_017631.5 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:169204671 G>C maps to NM_017631.5 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:169158467 G>C maps to NM_017631.5 L1460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:169196579 C>G maps to NM_017631.5 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:169227604 C>A maps to NM_017631.5 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:169213029 C>A maps to NM_017631.5 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:169146827 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:169205969 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr4:169183234 G>A maps to NM_017631.5 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:169208280 G>C maps to NM_017631.5 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:169337906 C>T maps to NM_001012967.1 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:169348278 A>T maps to NM_001012967.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr4:169377303 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:169341504 A>T maps to NM_001012967.1 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:674760 C>A maps to NM_021008.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:118164402 G>A maps to NM_017418.2 *71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:91063967 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:455025 T>G maps to ENST00000382934 *51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:35277469 G>T maps to NM_022047.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr6:35289066 C>A maps to NM_022047.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:35278300 G>A maps to NM_022047.3 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr8:6793541 T>A maps to NM_001925.1 *98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:6914087 G>T maps to NM_021010.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr8:6783428 C>T maps to NM_001926.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:6782403 G>T maps to NM_001926.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:49976888 C>A maps to NM_001037728.2 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:50011297 G>T maps to NM_001037498.1 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:50016256 G>T maps to NM_001037498.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:50011326 T>A maps to NM_001037498.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:50016295 G>A maps to NM_001037498.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:49936500 G>A maps to NM_001037729.1 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:29847347 G>T maps to NM_001037730.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr20:29956497 C>A maps to NM_054112.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:29960909 T>G maps to NM_054112.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr20:29965048 T>C maps to NM_153289.2 *85W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:29978252 G>A maps to NM_153323.3 L12L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4514-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:30037859 T>C maps to NM_153324.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr20:30053416 A>C maps to NM_001037500.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr20:76730 T>C maps to NM_153325.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:139529 C>T maps to NM_139074.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr4:9452084 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:9452125 T>C maps to NM_001040448.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:100613145 G>C maps to NM_206918.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:18250028 T>C maps to NM_003472.3 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40980947 G>A maps to NM_022774.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:126214566 A>C maps to NM_020946.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr9:126214605 C>T maps to NM_020946.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:197643290 T>C maps to NM_001195215.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:197643272 G>A maps to NM_001195215.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:6468427 A>G maps to NM_024898.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:6472947 A>T maps to NM_024898.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:140301876 C>T maps to NM_015689.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:140223131 G>A maps to NM_015689.3 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:140287450 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:140246655 G>A maps to NM_015689.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:140302056 C>T maps to NM_015689.3 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr7:140221721 G>A maps to NM_015689.3 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:140285454 C>A maps to NM_015689.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:140246697 G>T maps to NM_015689.3 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:140301464 G>T maps to NM_015689.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:115144126 A>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:111743051 G>A maps to NM_024901.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:142161884 C>T maps to NM_014957.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr8:142202482 T>C maps to NM_014957.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:142190927 G>T maps to NM_014957.2 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:142178211 G>A maps to NM_014957.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:142160994 C>A maps to NM_014957.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:65989641 T>C maps to ENST00000443035 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr15:66034065 T>C maps to ENST00000443035 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr15:65959864 C>T maps to ENST00000443035 W1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:153911513 G>C maps to NM_014856.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:153907269 C>T maps to NM_014856.2 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:153913379 C>A maps to NM_014856.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:153916757 A>T maps to NM_014856.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19352177 G>T maps to NM_017925.4 E1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:19296153 C>G maps to NM_017925.4 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:19332139 A>C maps to NM_017925.4 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr9:19372101 G>A maps to NM_017925.4 Q1651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr9:19316465 C>T maps to NM_017925.4 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:9200581 G>C maps to NM_015213.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:9228270 T>A maps to NM_015213.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr11:9215172 G>A maps to NM_015213.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:31566470 C>T maps to NM_144973.3 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:31576609 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:31566439 T>G maps to NM_144973.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:31566440 T>A maps to NM_144973.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:31577522 G>T maps to NM_144973.3 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:31633190 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:31568371 T>C maps to NM_144973.3 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr12:31566416 G>T maps to NM_144973.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:31540671 G>T maps to NM_144973.3 A1230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:68944886 T>C maps to NM_001114120.1 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:68943529 T>C maps to NM_001114120.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:59943223 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:59899304 C>T maps to NM_018369.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:100660778 G>A maps to ENST00000422147 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:100660848 C>G maps to ENST00000422147 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:32270282 A>G maps to NM_001136029.1 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:32217560 G>A maps to NM_001136029.1 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr22:32239156 G>T maps to NM_001136029.1 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr8:121021281 G>T maps to NM_022783.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:33054338 G>A maps to NM_001077242.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr12:16109964 C>T maps to NM_015954.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:124034968 C>T maps to NM_024295.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:124031532 C>T maps to NM_024295.4 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:220290415 C>A maps to NM_001927.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:220284871 C>A maps to NM_001927.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr2:220285260 G>A maps to NM_001927.3 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:89056256 C>T maps to NM_017996.3 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:3775364 C>T maps to ENST00000430539 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:3789063 C>G maps to ENST00000430539 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:3786207 G>T maps to ENST00000430539 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:24738645 C>T maps to NM_001127453.1 *497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:24758725 C>T maps to NM_001127453.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:24738724 G>A maps to NM_001127453.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:117241033 C>T maps to NM_015404.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr9:117266555 G>A maps to NM_015404.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:117185644 C>A maps to NM_015404.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:117240844 C>A maps to NM_015404.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:179319182 G>A maps to NM_001042702.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:145541078 G>A maps to NM_012079.4 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:69424216 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:69421828 G>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:69421845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:19132105 C>A maps to NM_022719.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr22:19044597 G>A maps to NM_005137.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:20093786 G>T maps to NM_022720.6 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:20074812 G>A maps to NM_022720.6 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:56330337 A>G maps to NM_201554.1 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr12:56346579 C>T maps to NM_201554.1 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:14188794 G>T maps to NM_004080.2 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:14216475 C>T maps to NM_004080.2 Q765Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:14722410 G>A maps to NM_004080.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:14216489 C>A maps to NM_004080.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:14613845 G>A maps to NM_004080.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:14620576 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:14378205 C>A maps to NM_004080.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:14661112 G>A maps to NM_004080.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:14613926 C>T maps to NM_004080.2 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:14741332 C>A maps to NM_004080.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:14775747 A>T maps to NM_004080.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:14620559 G>C maps to NM_004080.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:14797348 T>A maps to NM_004080.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:14378176 G>C maps to NM_004080.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:14724897 G>T maps to NM_004080.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr7:14722177 T>G maps to NM_004080.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:14775720 G>A maps to NM_004080.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:234370996 C>A maps to NM_152879.2 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:234365974 G>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:234343524 G>C maps to NM_152879.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:234343476 G>A maps to NM_152879.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:54921472 C>A maps to NM_003647.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:54912248 G>T maps to NM_003647.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:186006669 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:186038185 T>A maps to NM_001346.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:185906045 G>T maps to NM_001346.2 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr3:185969565 G>A maps to NM_001346.2 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:42784848 G>T maps to NM_178009.2 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:42780200 C>T maps to NM_178009.2 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:137080402 G>T maps to NM_004717.2 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:137075974 A>G maps to NM_004717.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:137341259 T>G maps to NM_004717.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:137330262 C>T maps to NM_004717.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:137308270 A>G maps to NM_004717.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:137363341 G>T maps to NM_004717.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:137308240 C>T maps to NM_004717.2 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr7:137170140 G>C maps to NM_004717.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:137150700 C>T maps to NM_004717.2 A863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:137266617 T>A maps to NM_004717.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:137170119 C>T maps to NM_004717.2 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:137172360 G>A maps to NM_004717.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr7:137341229 G>A maps to NM_004717.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:137076037 G>A maps to NM_004717.2 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:50119911 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:50133403 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:50133404 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:50121186 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:50213371 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:50167245 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:50134574 C>G did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:50133387 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:50135413 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:50213147 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:50136183 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:50135447 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:50213190 G>A did not map to a codon.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr23:50119765 A>C did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:50213475 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:50122675 A>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:50111964 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:50213229 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:50136331 G>T did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:50113549 T>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:50136177 C>A did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:50129404 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:50213334 G>T did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:50146579 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:50112014 T>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:50213527 C>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:50213489 G>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:50213490 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:50127766 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:50111948 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:50121610 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:50163468 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:50118031 C>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:957012 G>C maps to NM_001347.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:954878 G>T maps to NM_001347.2 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:46398735 C>T maps to NM_001105540.1 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr2:74166085 A>G maps to NM_080916.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:55331014 G>A maps to NM_014762.3 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:71146588 C>A maps to NM_001360.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:71146759 G>A maps to NM_001360.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:71146435 C>A maps to NM_001360.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:71146663 C>A maps to NM_001360.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:26795510 A>T maps to NM_024887.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr19:49445799 C>T maps to NM_014475.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:99371313 G>A maps to NM_138413.3 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:12788167 G>A maps to NM_001930.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:12790351 T>C maps to NM_001930.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:34956173 C>G maps to NM_024308.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr13:52345611 C>T maps to NM_001031719.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr13:52351195 C>T maps to NM_001031719.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:24113331 C>T maps to NM_182908.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:12677257 C>T maps to NM_004753.4 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:24424306 G>A maps to NM_021004.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:24435559 G>C maps to NM_021004.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr14:24511937 G>A maps to NM_001082488.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:24464290 C>T maps to NM_198083.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:60620772 A>G maps to NM_016029.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:60611731 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:21075494 C>G maps to NM_015510.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:9684873 C>T maps to ENST00000330255 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:9676189 G>T maps to ENST00000330255 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:9683331 G>C maps to ENST00000330255 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr17:9694561 G>A maps to ENST00000330255 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:169938309 C>A maps to NM_001142271.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr2:169938261 C>T maps to NM_001142271.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:2184983 C>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:2161227 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:2161156 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:2139105 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:2209549 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:2161186 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:2184952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr10:12136102 C>T maps to NM_018706.5 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:12136081 G>T maps to NM_018706.5 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:12159748 A>C maps to NM_018706.5 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:12131254 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:12143170 G>T maps to NM_018706.5 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:24531294 C>T maps to NM_001358.2 W733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:24542523 C>A maps to NM_001358.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:24585974 G>C maps to NM_001358.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:30630699 C>T maps to NM_003587.4 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:30633332 C>A maps to NM_003587.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr6:30622596 T>C maps to NM_003587.4 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:30640596 C>A maps to NM_003587.4 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:30633458 G>A maps to NM_003587.4 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:30639017 G>T maps to NM_003587.4 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:30633345 C>A maps to NM_003587.4 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:54567930 T>A maps to NM_019030.2 R950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:54573087 G>C maps to NM_019030.2 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:54557318 A>G maps to NM_019030.2 Y1279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:47882656 C>T maps to NM_138615.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:47890011 C>T maps to NM_138615.2 D849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:127540982 G>C maps to NM_018180.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:127569374 C>A maps to NM_018180.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:5364390 G>A maps to ENST00000457531 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:47876923 G>T maps to NM_014681.5 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:47865872 G>T maps to NM_014681.5 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:47876149 G>C maps to NM_014681.5 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr19:47883025 C>T maps to NM_014681.5 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:37647445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:154011602 T>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:154042079 G>A maps to NM_020865.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr3:154042091 T>A maps to NM_020865.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:125449040 G>A maps to NM_032656.3 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:125441675 G>A maps to NM_032656.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr12:125434578 C>G maps to NM_032656.3 R1081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:125455931 C>T maps to NM_032656.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:125438723 C>T maps to NM_032656.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:72142724 C>T maps to NM_014003.3 R1094R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:72141382 C>T maps to NM_014003.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:72146374 G>T maps to NM_014003.3 T1221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr16:72133734 G>T maps to NM_014003.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:72137098 C>G maps to NM_014003.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr16:72132852 C>T maps to NM_014003.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:72130816 G>T maps to NM_014003.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr17:57684529 C>G maps to NM_024612.4 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:57682540 C>G maps to NM_024612.4 S656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:39050218 G>T maps to NM_198963.1 G1069G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:39050299 G>A maps to NM_198963.1 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:39089318 T>A maps to NM_198963.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:39088948 C>T maps to NM_198963.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:39088708 C>G maps to NM_198963.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr2:39082375 T>C maps to NM_198963.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:39088701 T>A maps to NM_198963.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:39029994 G>A maps to NM_198963.1 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:39075408 A>T did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr17:40257095 G>A maps to NM_024119.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:40255780 C>A maps to NM_024119.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:40255735 T>A maps to NM_024119.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:40257125 G>T maps to NM_024119.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:41567781 G>C maps to NM_004941.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:41597598 G>T maps to NM_004941.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:41573547 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:41590791 G>T maps to NM_004941.1 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:182822531 G>A maps to NM_001357.4 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:182823167 C>T maps to NM_001357.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:182845246 A>G maps to NM_001357.4 Q626Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:182836115 G>T maps to NM_001357.4 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:122693020 T>A maps to NM_019887.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:140905719 C>T maps to ENST00000398557 Q1153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:140953298 G>A maps to ENST00000398557 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr5:140958701 G>A maps to ENST00000398557 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:96328000 A>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:96213114 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:96212913 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:95993693 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:96220180 A>G did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:96203954 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:96213015 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:96200547 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:96194342 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:96167532 A>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:96167534 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:96220165 C>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:96369869 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:96200586 G>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:96212928 G>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:96369925 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:96603138 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:96354716 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:96197083 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:96354698 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:96354700 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:60582752 T>A maps to NM_001042517.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:60384949 C>T maps to NM_001042517.1 K1045K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:60616825 C>A maps to NM_001042517.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr13:60616905 C>A maps to NM_001042517.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr13:60686167 G>A maps to NM_001042517.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr14:95592940 T>C maps to NM_177438.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr14:95556996 C>A maps to NM_177438.2 P1869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr14:95574289 C>A maps to NM_177438.2 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:95578530 G>A maps to NM_177438.2 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:95596457 G>A maps to NM_177438.2 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr14:95562558 C>A maps to NM_177438.2 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:61537158 C>T maps to NM_022105.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:61542642 C>A maps to NM_033081.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:61513082 C>A maps to NM_033081.2 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr20:61513365 C>A maps to NM_033081.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:61528109 T>A maps to NM_033081.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:61542655 G>A maps to NM_033081.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:61541329 G>A maps to NM_033081.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr20:61511163 G>A maps to NM_033081.2 S2048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr20:61528307 G>A maps to NM_033081.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:61512237 C>A maps to NM_033081.2 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:61512249 C>T maps to NM_033081.2 P1686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr20:61513140 C>T maps to NM_033081.2 E1389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:61511226 C>A maps to NM_033081.2 L2027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr20:61537320 C>A maps to NM_033081.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:61510950 G>A maps to NM_033081.2 R2119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:61510872 C>A maps to NM_033081.2 R2145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr20:61513242 C>A maps to NM_033081.2 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:61511550 G>T maps to NM_033081.2 P1919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:61538497 C>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:54360011 C>A maps to NM_000792.5 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:80677806 G>T maps to NM_001007023.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr14:80669420 T>A maps to NM_001007023.2 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:80669078 C>A maps to NM_001007023.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:102028156 G>T maps to NM_001362.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:102027868 A>G maps to NM_001362.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr14:102028666 C>T maps to NM_001362.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:102027880 G>A maps to NM_001362.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:47987385 G>T maps to ENST00000318711 E1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:47954023 G>T maps to ENST00000318711 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr21:47916916 C>T maps to ENST00000318711 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr21:47971574 G>A maps to ENST00000318711 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr21:47987423 G>T maps to ENST00000318711 V1536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:51108374 A>G maps to NM_173602.2 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:51090958 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:51074452 A>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:51072621 G>A maps to NM_173602.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr12:51097972 C>T maps to NM_173602.2 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:532471 T>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:468955 C>A maps to NM_014974.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:373023 C>G maps to NM_014974.2 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:436003 C>A maps to NM_014974.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:387245 G>C maps to NM_014974.2 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:468767 G>A maps to NM_014974.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:459874 C>T maps to NM_014974.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:403802 G>A maps to NM_014974.2 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:410318 C>A maps to NM_014974.2 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:395292 G>A maps to NM_014974.2 H1029H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr10:403796 G>A maps to NM_014974.2 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:2717372 G>A maps to NM_145173.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:93376016 T>C maps to NM_017594.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr9:93375521 G>T maps to NM_017594.3 C196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:93375826 C>A maps to NM_017594.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:68512911 C>G maps to NM_004675.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:68512794 G>A maps to NM_004675.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:68512326 G>A maps to NM_004675.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:68512814 T>A maps to NM_004675.2 K56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:68512911 C>A maps to NM_004675.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:189599404 C>T maps to NM_052952.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:189599586 C>A maps to NM_052952.2 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:122591346 C>G maps to NM_032839.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr13:73352424 C>T maps to NM_014953.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr13:73346414 T>C did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr13:73345119 T>C maps to NM_014953.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr13:73355907 G>C maps to NM_014953.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr13:73345238 G>A maps to NM_014953.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr15:66618429 A>T maps to NM_001143688.1 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:66604124 C>T maps to NM_001143688.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:233001237 C>G maps to NM_152383.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:233194684 C>T maps to NM_152383.4 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr2:233164817 C>G maps to NM_152383.4 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:231829611 G>A maps to NM_001164537.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:231954126 A>T maps to NM_001164537.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:231829653 A>G maps to NM_001164537.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:232172459 G>A maps to NM_001164537.1 Q848Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:223178674 G>T maps to NM_032890.2 V1312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:223178056 C>T maps to NM_032890.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:223178683 G>A maps to NM_032890.2 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:223156420 G>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:223178803 T>C maps to NM_032890.2 F1355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr1:223177282 C>T maps to NM_032890.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:223179145 G>C maps to NM_032890.2 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:223177006 G>A maps to NM_032890.2 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr15:40660664 C>A maps to NM_033510.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr15:40659392 C>T maps to NM_033510.1 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr15:40661360 T>A maps to NM_033510.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr15:40655996 G>A maps to NM_033510.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr15:40661171 G>T maps to NM_033510.1 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:111844947 C>A maps to NM_001037954.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:153999153 G>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:153996697 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:153993754 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:153994511 C>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:153994219 A>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:154001505 G>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:153997526 T>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:153993239 C>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:54074343 C>A maps to NM_012242.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:54074433 C>T maps to NM_012242.2 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:107846994 G>A maps to NM_014421.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:107956732 G>T maps to NM_014421.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:107847034 C>A maps to NM_014421.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:107845813 G>T maps to NM_014421.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:107845747 T>A maps to NM_014421.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:107846965 G>T maps to NM_014421.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:49868843 G>T maps to NM_014419.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:49878263 C>T maps to NM_014419.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:111908006 A>T maps to NM_001931.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr8:12943414 T>A maps to NM_182643.2 K1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:13259056 A>T maps to NM_182643.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:12957379 G>T maps to NM_182643.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:12957340 A>T maps to NM_182643.2 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:12957115 G>C maps to NM_182643.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr8:12958069 A>T maps to NM_182643.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr8:13251147 G>A maps to NM_182643.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:107557756 G>A maps to NM_000108.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:38151718 C>G maps to NM_007335.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:38126765 G>T maps to NM_007335.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38136441 C>T maps to NM_007335.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:38103699 T>A maps to NM_007335.2 C238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:38151017 G>T maps to NM_007335.2 V1075V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr3:38104069 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:38081081 C>A maps to NM_007335.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr13:51417434 C>T maps to ENST00000504404 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:196812494 T>A maps to NM_004087.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:196842895 C>A maps to NM_004087.2 G482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:196792248 C>T maps to NM_004087.2 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:196867096 C>A maps to NM_004087.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:84245775 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:83585467 C>A maps to NM_001142699.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:83544764 G>A maps to NM_001142699.1 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:83691637 C>A maps to NM_001142699.1 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:84245717 G>T maps to NM_001142699.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:83183790 C>A maps to NM_001142699.1 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:84634150 T>A maps to NM_001364.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:83170878 G>T maps to NM_001142699.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:83544791 C>G maps to NM_001142699.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr11:84245693 G>T maps to NM_001142699.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:69670522 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:69717028 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:69720817 G>A did not map to a codon.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr23:69719799 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:69669598 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:69717038 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:69699099 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095231 G>A maps to NM_001365.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:7095234 G>C maps to NM_001365.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:7107547 G>A maps to NM_001365.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:7094029 G>C maps to NM_001365.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:79571773 C>T maps to NM_004747.3 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:79603413 C>A maps to NM_004747.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:79590498 C>A maps to NM_004747.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:79601668 C>A maps to NM_004747.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:79584143 T>A maps to NM_004747.3 K794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:79556326 C>A maps to NM_004747.3 R1730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr10:79590036 C>A maps to NM_004747.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:3729255 C>A maps to NM_004746.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:3729133 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:3534573 T>A maps to NM_004746.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:3534267 C>T maps to NM_004746.2 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr18:3742494 G>C maps to NM_004746.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr18:3879303 G>A maps to NM_004746.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr18:3567516 G>A maps to NM_004746.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:1624760 G>T maps to ENST00000357934 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:1497608 G>T maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr8:1497623 C>T maps to ENST00000357934 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:1626463 C>A maps to ENST00000357934 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr8:1497410 C>T maps to ENST00000357934 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr8:1624782 C>T maps to ENST00000357934 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:1497407 G>A maps to ENST00000357934 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:1497386 C>A maps to ENST00000357934 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr8:1645344 G>A maps to ENST00000357934 Q885Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr8:1497704 C>T maps to ENST00000357934 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:1574942 G>T maps to ENST00000357934 G436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr8:1575025 C>A maps to ENST00000357934 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:1497161 G>T maps to ENST00000357934 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:1514006 A>T maps to ENST00000357934 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:35365841 G>T maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:35370503 C>A maps to NM_001080418.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:35370453 C>T maps to NM_001080418.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:35365841 G>T maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35060906 G>T maps to ENST00000339266 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:35060386 C>A maps to ENST00000339266 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35128632 C>T maps to ENST00000339266 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr20:35060431 C>A maps to ENST00000339266 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:35060938 C>A maps to ENST00000339266 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:35060446 G>A maps to ENST00000339266 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr20:35060500 C>T maps to ENST00000339266 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:35060506 C>T maps to ENST00000339266 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:35060953 C>A maps to ENST00000339266 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:35128031 C>T maps to ENST00000339266 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr20:35060542 C>T maps to ENST00000339266 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr14:55643877 C>T maps to NM_014750.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:101200977 C>A maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:101195326 C>A maps to NM_003836.5 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr14:101201085 C>A maps to NM_003836.5 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:101201211 G>A maps to NM_003836.5 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:101201078 G>A maps to NM_003836.5 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr14:101200827 G>T maps to NM_003836.5 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:101200981 G>T maps to NM_003836.5 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170592563 G>A maps to NM_005618.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:170592509 C>A maps to NM_005618.3 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr6:170592398 G>A maps to NM_005618.3 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:39998105 C>A maps to NM_016941.3 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:39989983 G>A maps to NM_016941.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr15:41222833 G>T maps to NM_019074.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:75360057 A>T maps to NM_001933.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:172952819 C>T maps to NM_178120.4 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:172952918 C>A maps to NM_178120.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr2:172951499 C>T maps to NM_178120.4 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:172965285 C>T maps to NM_004405.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:48051291 G>T maps to NM_138281.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:96651594 G>A maps to NM_005221.5 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr7:96651594 G>A maps to NM_005221.5 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:96637037 C>G maps to NM_005222.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:96637043 G>A maps to NM_005222.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr7:96639142 T>C maps to NM_005222.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:96637091 C>A maps to NM_005222.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:124399743 C>A maps to ENST00000368915 V2377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:124378842 G>T maps to ENST00000368915 T1745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:124350193 G>T maps to ENST00000368915 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:124361493 C>A maps to ENST00000368915 A1175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:124358326 A>C maps to ENST00000368915 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:124377605 C>A maps to ENST00000368915 Y1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr10:124339220 T>C maps to ENST00000368915 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr10:124339283 C>T maps to ENST00000368915 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr10:124333278 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:124344817 G>A maps to ENST00000368915 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr10:124377623 C>A maps to ENST00000368915 T1661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:124378828 C>T maps to ENST00000368915 Q1741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:124377705 G>T maps to ENST00000368915 G1689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr10:124399749 T>C maps to ENST00000368915 Y2379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr10:124348478 C>G maps to ENST00000368915 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:124331854 C>A maps to ENST00000368915 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:46972732 C>T maps to NM_147192.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:46978111 G>T maps to NM_147192.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:46976806 G>T maps to NM_147192.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:46976690 G>T maps to NM_147192.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:32398632 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:32563306 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:31462616 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:32867854 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:32662373 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:32466685 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:32834588 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:32235068 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:32305788 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:32632454 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:32663189 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:31279100 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr23:32509547 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:31165491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:31496455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:32486716 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:32715993 G>C did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:31224707 T>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:31947759 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:31497207 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:32632477 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:31224698 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:32466603 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:32591899 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:31854904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:32382751 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:32583857 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:32382757 C>T did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr23:31496380 T>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:32827694 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:32591655 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:32591897 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:32430020 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:31514906 T>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:31838175 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:32503070 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:31645940 C>G did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:32717328 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:31279118 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:32366640 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:32632419 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:32717311 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:31165575 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:31200874 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:32382812 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:32404496 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:31462672 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:32862917 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:32398633 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr23:32361372 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:32380906 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:32509488 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:32663082 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:31676130 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:32407679 G>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:32328363 C>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:31947797 G>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:32662423 T>C did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:32841410 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:31462742 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:32407752 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:32429870 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:32482767 G>A did not map to a codon.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr23:32430028 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:32328261 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:32662397 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:32235118 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:31747767 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:32305745 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:32662311 T>C did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:32662312 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:32662315 C>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:32407665 T>C did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:32407767 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:32430027 A>T did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr23:32466630 A>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:32867933 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:32328356 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:32328369 C>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:32429946 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:31196063 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:31496469 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:32490296 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:32591660 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:31227649 A>G did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:33038314 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:32305814 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:32503157 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:32613909 T>C did not map to a codon.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr23:32382728 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:31200971 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:32305734 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:32407764 C>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:32490368 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:31792207 C>G did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:31496491 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:32717411 T>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:32536159 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:32380966 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:32486648 A>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:31341763 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:31676143 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:32717248 G>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:31496474 C>G did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:32503110 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:31986630 C>G did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:33038317 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:31341771 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:31676240 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:32591744 T>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:32663165 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:32632525 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:32472825 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:32827655 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:32834668 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:32380911 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:32481652 C>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:32466620 G>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:32398777 T>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:31222182 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:32305723 C>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:31697667 C>G did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:32486790 G>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:31838118 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:31893484 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:32536135 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:31496434 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:32841471 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:32841503 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr23:32662373 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:32305709 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:32305710 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:32459412 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:31986605 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:31187671 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:78328592 C>A maps to NM_013391.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:78350087 C>A maps to NM_013391.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:78347200 T>A maps to NM_013391.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:78340325 G>A maps to NM_013391.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:78340145 G>A maps to NM_013391.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:78351668 G>A maps to NM_013391.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:35996846 G>A maps to NM_033317.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:88584102 A>T maps to NM_004407.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:88583610 G>A maps to NM_004407.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:88583969 C>G maps to NM_004407.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:88584288 C>T maps to NM_004407.3 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:88584414 C>G maps to NM_004407.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:88584384 G>A maps to NM_004407.3 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:46280927 G>A maps to NM_004409.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:46275985 T>A maps to NM_004409.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:847034 G>T maps to NM_021951.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:968123 C>A maps to NM_021951.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:1057239 G>A maps to NM_181872.4 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:990206 C>T maps to NM_021240.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:990260 G>A maps to NM_021240.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:990261 G>T maps to NM_021240.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:977285 A>G maps to NM_021240.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:990851 G>A maps to NM_021240.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr9:22447345 G>A maps to NM_022160.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:50885149 G>T maps to NM_032110.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:50885182 G>A maps to NM_032110.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr1:50885338 C>A maps to NM_032110.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:53930347 C>A maps to NM_033067.1 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:42351803 G>T maps to ENST00000427618 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:42351721 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:42354679 G>T maps to ENST00000427618 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:86795913 A>G maps to NM_021145.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:86824376 C>A maps to NM_021145.3 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr19:46289892 G>C maps to NM_004943.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:46295690 C>A maps to NM_004943.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:118525451 G>A maps to NM_005509.4 P2395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:118468904 C>G maps to NM_005509.4 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:118502309 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:118485649 C>T maps to NM_005509.4 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:51830520 G>A maps to NM_001174116.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:51743894 C>G did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr15:51791154 C>T maps to NM_001174116.1 E1422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr10:70227878 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:70202765 G>A maps to NM_001080449.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:52433736 C>T maps to ENST00000273600 R4270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:52392593 G>T maps to ENST00000273600 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52392659 C>T maps to ENST00000273600 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:52416446 C>T maps to ENST00000273600 I2639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:52428647 G>T maps to ENST00000273600 R3662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:52398910 C>G maps to ENST00000273600 L1798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:52402840 G>T maps to ENST00000273600 P1950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:52416425 G>A maps to ENST00000273600 A2632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:124360010 T>C maps to NM_207437.3 Y2606Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:124341757 C>A maps to NM_207437.3 V2080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:124268651 C>A maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:124362332 G>T maps to NM_207437.3 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:124274574 C>T maps to NM_207437.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124393957 G>T maps to NM_207437.3 S3204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:124409643 C>T maps to NM_207437.3 Y3820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:124298117 G>A maps to NM_207437.3 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:124403314 C>A maps to NM_207437.3 I3657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:124416649 T>C maps to NM_207437.3 L4313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:124364245 G>A maps to NM_207437.3 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:124330218 G>T maps to NM_207437.3 V1693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:124311322 C>G maps to NM_207437.3 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:124272401 C>T maps to NM_207437.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr12:124265835 G>A maps to NM_207437.3 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:124420006 C>T maps to NM_207437.3 C4465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:124268591 C>G maps to NM_207437.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:124272446 G>A maps to NM_207437.3 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:124417996 C>T maps to NM_207437.3 T4354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:124382515 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:21603921 C>G maps to NM_003777.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:21628229 C>A maps to NM_003777.3 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:21726800 C>T maps to NM_003777.3 T1909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:21788209 C>T maps to NM_003777.3 S2848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:21750233 G>A maps to NM_003777.3 K2256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr7:21723541 G>T maps to NM_003777.3 V1874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:21655912 G>A maps to NM_003777.3 A1366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21698649 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21760404 A>G maps to NM_003777.3 K2406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:21813388 G>T maps to NM_003777.3 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:21640542 G>T maps to NM_003777.3 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:21603894 C>A maps to NM_003777.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:21775401 G>T maps to NM_003777.3 E2536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:21747330 G>A maps to NM_003777.3 L2194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:21856245 C>A maps to NM_003777.3 P3505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:21901538 C>A maps to NM_003777.3 I3764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:21923946 C>T maps to NM_003777.3 I4149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:21646323 A>C maps to NM_003777.3 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:21789411 G>T maps to NM_003777.3 L2937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:21730499 G>T did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:21630879 G>C maps to NM_003777.3 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:21630915 G>T maps to NM_003777.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:21641220 C>G maps to NM_003777.3 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:21730381 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:21639421 C>T maps to NM_003777.3 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr7:21730400 A>G maps to NM_003777.3 E1988E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:21784588 G>A maps to NM_003777.3 V2813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:21784173 T>A maps to NM_003777.3 L2765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:21901562 C>G maps to NM_003777.3 T3772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr7:21847633 G>T maps to NM_003777.3 V3440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:21630858 C>A maps to NM_003777.3 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:21779260 G>T maps to NM_003777.3 V2635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:21805078 C>T maps to NM_003777.3 L2999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:21727127 C>T maps to NM_003777.3 I1976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:21629021 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:57487119 G>A maps to NM_178504.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:76567764 G>T maps to ENST00000389840 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:76498744 G>C maps to ENST00000389840 T1695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:76475160 C>T maps to ENST00000389840 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:76565322 G>C maps to ENST00000389840 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:76433797 G>A maps to ENST00000389840 N3980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:76548887 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:76471464 C>A maps to ENST00000389840 V2788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr17:76570974 C>A maps to ENST00000389840 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr17:76566358 C>A maps to ENST00000389840 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:76501440 G>C maps to ENST00000389840 G1626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:76420028 C>T maps to ENST00000389840 A4472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr17:76525741 T>G maps to ENST00000389840 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:76503839 G>A maps to ENST00000389840 H1424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:76486887 G>T maps to ENST00000389840 R2223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:76557933 C>T maps to ENST00000389840 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:76568964 A>G maps to ENST00000389840 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:76503451 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:76570800 C>T maps to ENST00000389840 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr17:76547655 C>T maps to ENST00000389840 K784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr17:76547657 T>A maps to ENST00000389840 K784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:76450733 G>A maps to ENST00000389840 D3394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7640476 C>T maps to NM_020877.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:7644210 G>A maps to NM_020877.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:7638001 T>C maps to NM_020877.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:7708676 C>T maps to NM_020877.2 N3136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:7667440 C>T maps to NM_020877.2 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:7667524 T>C maps to NM_020877.2 T1090T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7636532 T>C maps to NM_020877.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:7719911 A>G maps to NM_020877.2 L3251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:7705028 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:7736528 G>A maps to NM_020877.2 K4373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:7689629 C>T maps to NM_020877.2 R2106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:7660477 G>T maps to NM_020877.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr17:7695290 C>T maps to NM_020877.2 F2319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:7701121 G>T maps to NM_020877.2 V2735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr17:7663254 G>A maps to NM_020877.2 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr17:7721352 C>T maps to NM_020877.2 N3442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:20944577 G>A maps to NM_017539.1 G4083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:21133418 G>T maps to NM_017539.1 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21042460 G>T maps to NM_017539.1 S1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:21063027 G>T maps to NM_017539.1 R1401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr16:21062988 A>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr16:21078604 T>G maps to NM_017539.1 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:21033321 G>C maps to NM_017539.1 S1916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr16:21109999 C>T maps to NM_017539.1 K819K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr16:21073853 C>A maps to NM_017539.1 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr16:20996848 G>A maps to NM_017539.1 S2405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr16:20975683 G>A maps to NM_017539.1 T3174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr16:20952736 G>A maps to NM_017539.1 L3880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:20966285 C>A maps to NM_017539.1 R3640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:20996455 G>T maps to NM_017539.1 T2536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:21045311 G>T maps to NM_017539.1 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:20948105 G>A maps to NM_017539.1 S3908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:20976220 C>A maps to NM_017539.1 L2995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:20976259 G>T maps to NM_017539.1 T2982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr16:20999166 C>A maps to NM_017539.1 G2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:21031081 G>C maps to NM_017539.1 T1962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr16:20996593 G>A maps to NM_017539.1 L2490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:20996668 T>C maps to NM_017539.1 A2465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:21086872 G>T maps to NM_017539.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:13823413 G>A maps to NM_001369.2 D2215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:13820509 C>G maps to NM_001369.2 G2262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:13841842 T>G maps to NM_001369.2 T1814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:13866015 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:13735345 T>A maps to NM_001369.2 R3885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:13729634 T>C maps to NM_001369.2 P3932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:13759047 C>T maps to NM_001369.2 Q3442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:13868089 G>A maps to NM_001369.2 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:13894779 C>A maps to NM_001369.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:13830205 T>A maps to NM_001369.2 K2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:13820608 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:13737490 C>A maps to NM_001369.2 L3775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:13824388 T>C maps to NM_001369.2 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:13923424 G>A maps to NM_001369.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:13766117 C>T maps to NM_001369.2 L3356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr5:13786443 C>T maps to NM_001369.2 E2888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr5:13701494 T>C maps to NM_001369.2 E4463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr5:13917344 A>G maps to NM_001369.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:13753545 T>C maps to NM_001369.2 P3556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:13922347 G>A maps to NM_001369.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:13883075 G>C maps to NM_001369.2 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:13913874 C>A maps to NM_001369.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:13913875 C>A maps to NM_001369.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:13717422 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:13811775 G>A maps to NM_001369.2 Q2463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:13735297 T>A maps to NM_001369.2 L3901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:13758969 G>C maps to NM_001369.2 A3468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:13766108 T>A maps to NM_001369.2 A3359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr5:13830322 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr5:13735952 C>A maps to NM_001369.2 L3848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr5:13823395 T>C maps to NM_001369.2 E2221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr5:13759022 A>G maps to NM_001369.2 L3451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:13867921 G>A maps to NM_001369.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:13917251 G>A maps to NM_001369.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:84784941 T>G maps to NM_001370.1 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:84784944 C>T maps to NM_001370.1 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:196913023 G>A maps to NM_018897.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:196821990 G>A maps to NM_018897.2 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:196834819 T>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:196753130 C>A maps to NM_018897.2 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196729162 C>A maps to NM_018897.2 E2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:196788435 C>A maps to NM_018897.2 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:196729268 C>A maps to NM_018897.2 G2370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:196892697 C>A maps to NM_018897.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:196681687 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:196718110 C>A maps to NM_018897.2 G2913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:196681572 A>G maps to NM_018897.2 N3180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:196620907 T>C maps to NM_018897.2 K3845K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:196749413 T>A maps to NM_018897.2 R1886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:196737072 G>A maps to NM_018897.2 F2178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:196801369 G>A maps to NM_018897.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:196851787 A>T did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:196788456 G>A maps to NM_018897.2 S1229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr2:196673452 C>A maps to NM_018897.2 E3346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:196791161 T>A maps to NM_018897.2 P1200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr2:196737105 G>C maps to NM_018897.2 L2167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:196664136 T>A maps to NM_018897.2 P3412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:196729355 C>A maps to NM_018897.2 G2341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:196750927 A>G maps to NM_018897.2 D1825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:196722177 T>A maps to NM_018897.2 V2779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:196723446 C>T maps to NM_018897.2 Q2606Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:196661410 C>T maps to NM_018897.2 G3468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:196749431 T>A maps to NM_018897.2 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr2:196664085 T>G maps to NM_018897.2 P3429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:196749472 A>G maps to NM_018897.2 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:38980321 T>A maps to ENST00000327475 T4529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:38758182 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:38818064 A>T maps to ENST00000327475 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:38905909 C>G maps to ENST00000327475 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:38747766 C>T maps to ENST00000327475 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:38840726 G>A maps to ENST00000327475 W2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:38885046 G>A maps to ENST00000327475 R3379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:38813460 G>T maps to ENST00000327475 E1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:38942253 C>A maps to ENST00000327475 P4249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr6:38850691 G>A maps to ENST00000327475 W2610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:38704919 A>G maps to ENST00000327475 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:38875883 C>G maps to ENST00000327475 L3155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr6:38897345 C>T maps to ENST00000327475 G3714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:38862638 A>T maps to ENST00000327475 R2904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr6:38885813 T>C maps to ENST00000327475 F3462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:38881667 C>T maps to ENST00000327475 L3289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:38980306 G>T maps to ENST00000327475 L4524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:38758174 A>G maps to ENST00000327475 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr6:38919258 C>A maps to ENST00000327475 T4126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:38738284 G>T maps to ENST00000327475 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:38980312 C>T maps to ENST00000327475 F4526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr6:38858533 T>G maps to ENST00000327475 T2848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:38919280 A>T maps to ENST00000327475 K4134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr6:38818041 C>T maps to ENST00000327475 Q1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr6:38899690 G>A maps to ENST00000327475 T3781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr6:38818076 G>A maps to ENST00000327475 Q1738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:11597207 C>T maps to NM_001372.3 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:11837220 C>T maps to NM_001372.3 L4108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:11725837 C>A maps to NM_001372.3 I2978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:11522935 G>T maps to NM_001372.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:11556076 G>C did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr17:11696839 G>T maps to NM_001372.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:11513787 G>A maps to NM_001372.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:11622752 C>G maps to NM_001372.3 R1885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:11593662 C>G maps to NM_001372.3 V1508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:11550478 A>G maps to NM_001372.3 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:11660890 G>T maps to NM_001372.3 G2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:11584037 A>G did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:11554418 G>T maps to NM_001372.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:11786979 C>A maps to NM_001372.3 S3628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:11592948 C>A maps to NM_001372.3 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr17:11540015 C>A maps to NM_001372.3 Y567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:11757474 C>T maps to NM_001372.3 F3221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:11593506 G>A maps to NM_001372.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:11631219 T>A maps to NM_001372.3 L1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:11757568 G>T maps to NM_001372.3 E3253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr17:11592888 T>C maps to NM_001372.3 D1250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:11648131 C>T maps to NM_001372.3 L2044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:11607521 G>T maps to NM_001372.3 V1718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:11604446 A>T maps to NM_001372.3 I1678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:11607716 T>C maps to NM_001372.3 D1783D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:11806223 T>A maps to NM_001372.3 A3865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:11786922 G>A maps to NM_001372.3 Q3609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:11806088 T>C maps to NM_001372.3 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr17:11651070 G>T maps to NM_001372.3 E2200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:11865410 T>A maps to NM_001372.3 T4357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:11622803 C>A maps to NM_001372.3 Y1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr17:11532804 T>C maps to NM_001372.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:11772570 G>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:11607518 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:11603163 T>C maps to NM_001372.3 Y1663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:11737983 C>T maps to NM_001372.3 A3092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:11795155 G>A maps to NM_001372.3 E3725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:11778438 C>A maps to NM_001372.3 G3472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:11603151 A>G maps to NM_001372.3 K1659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:11687750 C>T maps to NM_001372.3 I2652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:11687857 T>C did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:11631205 C>T maps to NM_001372.3 I1927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:11671767 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:11809055 G>C maps to NM_001372.3 S3893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr17:11520887 G>T maps to NM_001372.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr17:11593216 G>T maps to NM_001372.3 E1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr17:11607713 C>A maps to NM_001372.3 I1782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:34506793 C>T maps to NM_012144.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:34497157 C>A maps to NM_012144.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:34500816 G>T maps to NM_012144.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr9:34514435 C>A maps to NM_012144.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:72285813 C>A maps to NM_023036.4 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:72308203 G>T maps to NM_023036.4 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:72301558 G>T maps to NM_023036.4 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:72308173 C>T maps to NM_023036.4 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr9:33026882 G>T maps to NM_001539.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr16:4484476 C>T maps to NM_005147.4 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:4500478 C>T maps to NM_005147.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr19:14627609 C>A maps to NM_006145.1 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:186299260 A>G maps to NM_016306.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:186299185 G>A maps to NM_016306.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:73670599 G>A maps to NM_153614.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:100867608 C>A maps to NM_001031723.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:220147599 C>T maps to NM_006736.5 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:220147945 C>T maps to NM_006736.5 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:220146674 C>A maps to NM_006736.5 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:34993418 G>T maps to NM_001135005.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:157178291 C>T maps to NM_058246.3 S226S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8089-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:128181683 C>A maps to NM_153330.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:128181689 G>A maps to NM_153330.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:128181650 C>T maps to NM_153330.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:128181584 G>A maps to NM_153330.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:183584885 T>C maps to NM_018981.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183622483 G>A maps to NM_018981.1 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr2:183608323 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:183601113 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:183582878 G>C maps to NM_018981.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:6712897 T>G maps to NM_018198.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:6704655 G>A maps to NM_018198.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:69565368 T>C maps to NM_021800.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:69571257 C>A maps to NM_201262.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr10:69565451 C>A maps to NM_021800.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:132196823 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:56222304 A>C maps to NM_032364.5 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:15888819 G>A maps to NM_015291.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:15892592 C>A maps to NM_015291.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:41066553 C>A maps to NM_018163.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr5:138761963 G>A maps to NM_152686.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:102957422 C>T maps to NM_014377.1 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr7:102956535 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:102960064 C>T maps to NM_014377.1 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:34954656 G>C did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr5:34936259 G>A maps to NM_194283.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:49742870 G>T maps to NM_024902.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:49743389 A>G maps to NM_024902.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:25190084 G>T maps to NM_016544.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:25174423 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:96439305 A>T maps to NM_006260.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr11:63999375 G>A maps to NM_005528.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:66989047 C>A maps to NM_033105.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:66963822 C>A maps to NM_033105.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:66963857 C>T maps to NM_033105.4 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:66992625 C>A maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr8:67012244 A>G maps to NM_033105.4 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:67012256 A>G maps to NM_033105.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:65855118 G>A maps to ENST00000371069 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:65858333 A>C maps to ENST00000371069 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:65851412 T>A maps to ENST00000371069 C273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:65864514 G>A maps to ENST00000371069 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:65858465 T>A maps to ENST00000371069 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:65874375 C>T maps to ENST00000371069 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:40142373 T>C maps to NM_003315.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr17:40134323 C>A maps to NM_003315.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:28541500 G>A maps to NM_014280.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr14:74154041 G>A maps to NM_031427.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:3706126 C>A maps to NM_005223.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr16:3707075 C>T maps to NM_005223.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:153633814 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153631307 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153631332 T>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:58193942 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:84880403 G>A maps to NM_021233.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84864321 G>T maps to NM_021233.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:84867754 C>A maps to NM_021233.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:140051033 G>A maps to NM_194249.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:230253032 A>G maps to NM_139072.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:230456400 C>T maps to NM_139072.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:230456418 C>T maps to NM_139072.3 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:230231655 C>A maps to NM_139072.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr2:230231611 G>A maps to NM_139072.3 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:6592888 G>T maps to NM_144666.2 T4645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:6588994 C>T maps to NM_144666.2 Q4086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr11:6592280 A>C maps to NM_144666.2 A4513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:130985089 G>T maps to ENST00000372923 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:131008719 G>T maps to ENST00000372923 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:130980951 C>A maps to ENST00000372923 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:130965892 C>G maps to ENST00000372923 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:131004602 G>T maps to ENST00000372923 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:10886571 C>T maps to NM_001005361.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr19:10906046 G>C did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:172013593 C>G did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:172011223 C>G maps to ENST00000359070 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:172277945 A>G maps to ENST00000359070 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:101648709 C>A maps to ENST00000342239 E1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:101716377 G>A maps to ENST00000342239 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:101648680 A>G maps to ENST00000342239 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:101646371 C>T maps to ENST00000342239 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:10287990 G>A maps to NM_001130823.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr19:10251547 G>A maps to NM_001130823.1 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:10254443 G>A maps to NM_001130823.1 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:25523105 C>A maps to NM_175629.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:25472573 C>T maps to NM_153759.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:25470919 C>A maps to NM_175629.1 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:25468193 G>A maps to NM_175629.1 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:25469070 C>A maps to NM_175629.1 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:25497956 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:25470965 C>A maps to NM_175629.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:31376691 G>T maps to NM_006892.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr20:31385000 C>T maps to NM_006892.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:220246786 G>A maps to NM_012100.2 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:220239585 G>A maps to NM_012100.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:220246110 C>T maps to NM_012100.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:98084036 A>T maps to NM_004088.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr10:98078222 G>A maps to NM_004088.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:98097905 C>A maps to NM_004088.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:94337786 T>C maps to NM_014597.4 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:94342194 G>A maps to NM_014597.4 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:94343028 C>T maps to NM_014597.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:94341978 G>A maps to NM_014597.4 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:30021411 C>T maps to NM_003586.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:30021429 C>A maps to NM_003586.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:30021432 G>T maps to NM_003586.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129152930 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:128821560 G>T maps to ENST00000398025 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:129224176 A>T maps to ENST00000398025 K1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:128850971 C>T maps to ENST00000398025 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:129172390 G>A maps to ENST00000398025 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:128769017 A>T maps to ENST00000398025 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:129245679 G>A maps to ENST00000398025 T1857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr10:128923777 C>T maps to ENST00000398025 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:128925931 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:225658115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:225637951 C>T maps to NM_014689.2 E2042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:225709557 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:225630470 G>T maps to NM_014689.2 P2176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:225635347 T>A maps to NM_014689.2 P2073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:225695308 T>A maps to NM_014689.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:225688307 G>T maps to NM_014689.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:225652115 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:225710296 G>A maps to NM_014689.2 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:225729343 T>A maps to NM_014689.2 K510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:225657745 C>T maps to NM_014689.2 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:225738795 T>A maps to NM_014689.2 K392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:225672754 A>C maps to NM_014689.2 L1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:225729618 C>T maps to NM_014689.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:225761064 A>G maps to NM_014689.2 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:225781420 C>T maps to NM_014689.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:225706585 C>A maps to NM_014689.2 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:225729642 T>C maps to NM_014689.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:117677515 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:117742199 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:117712557 G>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:117788870 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:117707970 A>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:117749589 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:117810667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:117775174 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:117722181 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:117758563 A>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:117739207 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:117770345 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:117782932 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:117788699 T>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:117676930 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:117786006 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:117773479 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:117676950 G>A did not map to a codon.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr23:117809950 A>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:117783001 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:117733144 A>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:117719075 A>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:117722149 C>A did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr23:117712547 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:117814494 T>C did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:117788637 T>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:117796679 G>C did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:117676697 A>G did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:117707925 C>A did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:117712606 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:117752664 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr23:117739262 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:117676687 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169469015 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:169474590 C>A maps to NM_004946.2 Y1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:169127117 G>T maps to NM_004946.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:169509852 G>A maps to NM_004946.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:169101389 C>A maps to NM_004946.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:169188528 C>G maps to NM_004946.2 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:169122863 C>A maps to NM_004946.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:169509813 G>A maps to NM_004946.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:169111324 C>G maps to NM_004946.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:169141186 G>T maps to NM_004946.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:169423143 A>G maps to NM_004946.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:169144455 C>A maps to NM_004946.2 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:169508966 C>A maps to NM_004946.2 V1803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:169446069 C>T maps to NM_004946.2 D1113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:169446012 G>A maps to NM_004946.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr5:169126452 G>T maps to NM_004946.2 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:169506024 G>T maps to NM_004946.2 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:169116264 C>A maps to NM_004946.2 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:169122937 G>C maps to NM_004946.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:169174498 C>A maps to NM_004946.2 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:169141373 G>T maps to NM_004946.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:169503078 C>A maps to NM_004946.2 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:169503079 C>A maps to NM_004946.2 R1620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:169230096 G>T maps to NM_004946.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:169461444 G>T maps to NM_004946.2 S1170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr5:169412905 C>A maps to NM_004946.2 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:169145712 C>T maps to NM_004946.2 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:169125405 G>T maps to NM_004946.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:169096304 A>T maps to NM_004946.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:169461501 G>T maps to NM_004946.2 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:169141204 C>A maps to NM_004946.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:169461401 G>C did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr5:169472906 C>T maps to NM_004946.2 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:169472839 T>C maps to NM_004946.2 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:169129337 C>T maps to NM_004946.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr5:169141072 C>A maps to NM_004946.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:169472896 C>T maps to NM_004946.2 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:51370645 C>G maps to NM_004947.4 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr3:51418766 C>G maps to NM_004947.4 S1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:51400008 C>T maps to NM_004947.4 L1733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:51395453 T>A maps to NM_004947.4 P1610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:51126672 G>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:51393610 C>T maps to NM_004947.4 R1447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr3:51196724 G>T maps to NM_004947.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:51392311 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:51418788 T>C maps to NM_004947.4 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr3:51418608 C>T maps to NM_004947.4 S1904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:51265437 C>G maps to NM_004947.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:51251550 A>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:51266192 C>T maps to NM_004947.4 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:51317535 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:111634225 T>C maps to ENST00000428084 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111368371 G>T maps to ENST00000428084 G1962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr7:111462513 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:111368559 C>A maps to ENST00000428084 E1900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr7:111368596 C>T maps to ENST00000428084 V1887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:111541735 C>T maps to ENST00000428084 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:111509683 G>T maps to ENST00000428084 Y685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:111379216 G>A maps to ENST00000428084 I1735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:25226114 C>T maps to NM_024940.6 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr8:25220649 C>T maps to NM_024940.6 Q1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:25159839 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:25101271 G>A maps to NM_024940.6 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr8:25226162 C>T maps to NM_024940.6 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:11326603 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:11325285 C>G maps to ENST00000319867 G1382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:11347229 G>A maps to ENST00000319867 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:63128797 C>A maps to ENST00000371140 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:63001285 C>A maps to ENST00000371140 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:63099201 T>G maps to ENST00000371140 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:62941826 C>A maps to ENST00000371140 G1879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:63084480 C>G maps to ENST00000371140 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:62961328 G>A maps to ENST00000371140 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:62923219 G>A maps to ENST00000371140 V2123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr1:62995044 C>T maps to ENST00000371140 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:446548 C>A maps to NM_203447.3 T1920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:420996 A>C maps to NM_203447.3 R1358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:432258 T>C maps to NM_203447.3 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:340165 A>G maps to NM_203447.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:421070 G>T maps to NM_203447.3 R1382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:334313 C>T maps to NM_203447.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr9:340237 C>G maps to NM_203447.3 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr9:379810 C>T maps to NM_203447.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:328020 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:286582 G>C maps to NM_203447.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr13:99534186 G>A maps to ENST00000428223 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr13:99554619 C>T maps to ENST00000428223 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:99481646 T>A maps to ENST00000428223 K1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:74783135 C>T maps to NM_001381.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:21768282 C>A maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:21767436 G>T maps to NM_003974.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:21768282 C>G maps to NM_003974.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:21769796 C>T maps to NM_003974.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:21766920 G>T maps to NM_003974.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:53260095 G>T maps to NM_018431.3 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:53205292 C>A maps to NM_018431.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr20:53259998 C>A maps to NM_018431.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr18:67266633 C>T maps to NM_152721.5 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:67365638 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr18:67365760 G>T maps to NM_152721.5 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:67508564 G>T maps to NM_152721.5 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:3487293 C>G maps to ENST00000389653 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:3478231 C>T maps to ENST00000389653 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:3494876 C>T maps to ENST00000389653 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr9:131708328 G>A maps to NM_014908.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:131847035 G>T maps to NM_020438.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:131847495 A>T maps to NM_020438.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:83838811 C>G maps to NM_015018.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:83846907 C>A maps to NM_015018.2 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:83845478 A>C maps to NM_015018.2 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:83829488 C>T maps to NM_015018.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:83823061 A>T maps to NM_015018.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:83851638 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:83847153 G>A maps to NM_015018.2 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:37617640 C>T maps to NM_005128.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr21:37617529 G>C maps to NM_005128.2 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:37665643 C>T maps to NM_005128.2 T2224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr21:37633009 T>C maps to NM_005128.2 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:37661498 T>C maps to NM_005128.2 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr21:37618414 G>A maps to NM_005128.2 Q1379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:37572691 G>A maps to NM_005128.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr21:37618237 G>C maps to NM_005128.2 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:2222271 C>G maps to ENST00000221482 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:2191239 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:2210434 G>T maps to ENST00000221482 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr19:2216399 G>T maps to ENST00000221482 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:118971517 G>A maps to NM_001382.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118971089 C>A maps to NM_001382.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:118971379 G>A maps to NM_001382.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:103348125 G>T maps to NM_015448.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:30919714 G>A maps to NM_080870.3 K1158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:89704488 G>A maps to NM_004413.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:89702742 C>T maps to NM_004413.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr16:89703637 G>T maps to NM_004413.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr16:68024722 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:68010018 G>T maps to NM_022357.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr16:68011905 C>A maps to NM_022357.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr16:68014138 G>A maps to NM_022357.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:38709568 A>G did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:38709669 A>T maps to NM_001135155.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:38707043 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:65108446 C>T maps to NM_006268.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:65111509 G>T maps to NM_006268.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:65113495 G>T maps to NM_006268.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:65108945 C>T maps to NM_006268.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:73219971 C>A maps to NM_012074.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:73140966 G>A maps to NM_012074.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:73141017 C>A maps to NM_012074.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:73360772 G>T maps to NM_012074.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:1936832 C>T maps to NM_001383.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:44437602 G>C maps to NM_001384.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:44437101 A>G maps to NM_001384.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:44437842 C>T maps to NM_001384.4 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:44437937 C>G maps to NM_001384.4 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:130699748 G>A maps to ENST00000373110 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:116447481 C>G maps to NM_020868.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:116101468 A>G maps to NM_020868.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:115200394 C>T maps to NM_020868.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr2:116534782 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:116535371 G>A maps to NM_020868.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:116497459 G>T maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:116485390 G>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr2:116503717 T>A maps to NM_020868.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:116283548 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:116525922 G>T maps to NM_020868.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:66258797 C>A maps to NM_005700.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66262852 G>T maps to NM_005700.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:66276548 G>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr11:66264795 C>T maps to NM_005700.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:66272138 A>T maps to NM_005700.3 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:66262833 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:66258842 G>T maps to NM_005700.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:162894881 T>A maps to NM_001935.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:162902122 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:162875236 A>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:162877171 G>T maps to NM_001935.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:162891711 G>A maps to NM_001935.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:162891738 C>A maps to NM_001935.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:154237653 G>A maps to NM_130797.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:154561256 C>A maps to NM_130797.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154143393 G>T maps to NM_130797.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:154684100 C>A maps to NM_130797.2 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:154561169 T>C maps to NM_130797.2 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:154143390 C>A maps to NM_130797.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:154667781 G>T maps to NM_130797.2 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:154564583 A>T maps to NM_130797.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:154237701 C>A maps to NM_130797.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:154679440 C>A maps to NM_130797.2 Y767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:154172102 C>T maps to NM_130797.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:154672597 G>T maps to NM_130797.2 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:154585852 C>A maps to NM_130797.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:154585809 G>A maps to NM_130797.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:154585860 G>A maps to NM_130797.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:154585908 G>A maps to NM_130797.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:154172069 T>C maps to NM_130797.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:65744416 G>A maps to NM_197960.2 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:4702063 C>A maps to ENST00000357909 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:4702108 C>T maps to ENST00000357909 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:109027098 A>G maps to NM_138815.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:109027920 G>A maps to NM_138815.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr3:109023335 G>T maps to NM_138815.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr3:109031470 G>A maps to NM_138815.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:7864237 G>T maps to NM_199286.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:109050770 G>T maps to NM_018189.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:109049545 C>A maps to NM_018189.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr3:109049514 G>A maps to NM_018189.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:74063857 G>T maps to NM_001025290.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:74063702 G>T maps to NM_001025290.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:54140235 G>A maps to NM_001012728.1 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:168670288 G>T maps to NM_001937.4 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:168698316 G>A maps to NM_001937.4 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:35009107 G>A maps to NM_015283.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr7:34989429 C>T maps to NM_015283.1 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:34979783 G>A maps to NM_015283.1 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:34971202 T>A maps to NM_015283.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:34981403 A>T maps to NM_015283.1 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr7:35050941 C>A maps to NM_015283.1 G151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:34971310 A>G maps to NM_015283.1 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:63976266 G>T maps to NM_173812.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr12:63974595 G>T maps to NM_173812.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:64062050 G>T maps to NM_173812.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:63963124 G>T maps to NM_173812.4 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr12:63974553 C>A maps to NM_173812.4 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr12:63954443 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:64061837 G>A maps to NM_173812.4 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:32949373 C>T maps to NM_001172774.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:32930059 G>A maps to NM_001172774.1 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:32928176 A>T maps to NM_001172774.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:95773925 A>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:95800280 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr8:95752000 G>T maps to NM_181787.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:97839178 C>A maps to NM_000110.3 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:97544537 C>A maps to NM_000110.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:98060630 G>C maps to NM_000110.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:98144649 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:105405086 C>G maps to NM_001385.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:105456611 C>G maps to NM_001385.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr8:105405053 T>A maps to NM_001385.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:105441929 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:105436551 A>G maps to NM_001385.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:105405219 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105440264 G>T maps to NM_001385.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:105405086 C>G maps to NM_001385.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:105459731 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:105456569 G>T maps to NM_001385.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:26501588 C>T maps to NM_001197293.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:26484795 C>A maps to NM_001197293.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:146780283 G>T maps to NM_001197294.1 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:134013941 C>A maps to NM_006426.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr10:134017424 C>T maps to NM_006426.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:134006239 C>T maps to NM_006426.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:134017363 G>T maps to NM_006426.2 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:134016184 C>A maps to NM_006426.2 C439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27165428 G>T maps to NM_020134.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:27164858 C>T maps to NM_020134.3 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:27156124 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:27121537 G>T maps to NM_020134.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:74752170 G>C maps to NM_133637.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr2:74752245 T>C maps to NM_133637.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:74752245 T>A maps to NM_133637.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:102302091 C>T maps to NM_018370.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr12:102302115 C>T maps to NM_018370.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:111663243 A>G maps to NM_178454.4 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:174870078 G>T maps to NM_000794.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:174869970 G>T maps to NM_000794.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:174869847 C>T maps to NM_000794.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:174869682 G>T maps to NM_000794.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:174869490 G>T maps to NM_000794.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:174869877 G>A maps to NM_000794.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:174870010 G>T maps to NM_000794.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:113286151 A>T maps to ENST00000355319 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:113286295 C>A maps to ENST00000355319 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:113286301 G>T maps to ENST00000355319 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:113281556 G>T maps to ENST00000355319 Y410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113890578 T>A maps to NM_000796.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:113890710 G>A maps to NM_000796.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:113866280 C>G maps to NM_000796.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr3:113850151 T>A maps to NM_000796.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr3:113890704 G>A maps to NM_000796.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:113850214 C>A maps to NM_000796.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9783982 A>T maps to NM_000798.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:9784741 C>A maps to NM_000798.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:9783934 C>G maps to NM_000798.4 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr4:9783790 G>A maps to NM_000798.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:9784921 G>T maps to NM_000798.4 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:9784741 C>T maps to NM_000798.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:9784156 C>A maps to NM_000798.4 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr4:9784943 G>T maps to NM_000798.4 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr4:9784933 C>T maps to NM_000798.4 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:9785071 G>A maps to NM_000798.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr4:9783853 G>T maps to NM_000798.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr22:31823153 C>T maps to NM_004147.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr17:17997125 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:50594757 C>A maps to NM_001080520.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:50574415 C>G maps to NM_001080520.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:50594739 C>A maps to NM_001080520.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:100503542 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:100491010 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:100496797 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:100496811 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:100486679 G>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:100505949 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:100505909 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:100505910 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:100509420 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:100510192 A>G did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:100503151 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:100496766 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:100496818 A>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:100503149 T>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:100509549 C>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:100509868 G>T did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:100509464 T>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:100505498 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:100494031 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:100494016 G>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:100500400 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:100509550 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:100509460 C>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr18:28712646 G>A maps to NM_024421.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:28737516 G>C maps to NM_024421.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:28714067 C>T maps to NM_024421.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28711631 C>T maps to NM_024421.2 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:28734753 T>A maps to NM_024421.2 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:28736035 C>A maps to NM_024421.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:28713982 T>A maps to NM_024421.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr18:28710635 A>G maps to NM_024421.2 H842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr18:28719717 C>A maps to NM_024421.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr18:28714741 G>T maps to NM_024421.2 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:28662235 T>A maps to ENST00000438199 K424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:28650691 C>A maps to ENST00000438199 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr18:28654793 T>A maps to ENST00000438199 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr18:28648024 C>A maps to ENST00000438199 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr18:28662386 A>T maps to ENST00000438199 Y373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:28602409 C>T maps to NM_001941.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr18:28587017 A>T maps to NM_001941.3 Y581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr18:28609477 T>C maps to NM_001941.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:28587011 G>C maps to NM_001941.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:28586987 A>T maps to NM_001941.3 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28586947 C>A maps to NM_001941.3 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:28588281 G>A maps to NM_001941.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr18:28604351 T>G maps to NM_001941.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr18:28576870 C>A maps to NM_001941.3 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr18:28610995 A>T maps to NM_001941.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:28587994 C>A maps to NM_001941.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:41719759 G>T maps to NM_001389.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr21:41711172 C>T maps to NM_001389.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:41667980 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:42080434 G>T maps to NM_001389.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr21:41711139 G>T maps to NM_001389.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr21:41725581 C>G maps to NM_001389.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr21:41385020 G>T maps to NM_001389.3 L1993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:41496169 G>A maps to NM_001389.3 N1216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr21:41711342 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41539174 T>G maps to NM_001389.3 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:41684034 C>A maps to NM_001389.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr21:41496255 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:41550863 C>T maps to NM_001389.3 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr21:41516529 G>T maps to NM_001389.3 Y1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:41457577 G>T maps to NM_001389.3 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr21:41459131 C>A maps to NM_001389.3 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr21:41725390 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr21:41423904 G>C maps to NM_001389.3 S1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr21:41725497 C>T maps to NM_001389.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:117395562 G>A maps to NM_020693.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:117309679 G>C maps to NM_020693.2 R1448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:117647509 G>A maps to NM_020693.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:117395625 T>C maps to NM_020693.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:117310620 G>T maps to NM_020693.2 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr11:117303887 C>G maps to NM_020693.2 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:117375699 A>G maps to NM_020693.2 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:117302316 C>A maps to NM_020693.2 V1829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:117387250 C>A maps to NM_020693.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:117308779 C>A maps to NM_020693.2 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr11:117308125 C>T did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:117376304 G>C maps to NM_020693.2 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:117389379 G>A maps to NM_020693.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:117389214 G>T maps to NM_020693.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:117376295 G>A maps to NM_020693.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr11:117342707 G>T maps to NM_020693.2 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:117335787 C>T maps to NM_020693.2 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:117376265 C>T maps to NM_020693.2 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:117299193 C>A maps to NM_020693.2 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:117302319 G>T maps to NM_020693.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr11:117376376 C>A maps to NM_020693.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:117299328 C>A maps to NM_020693.2 G2019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:117332277 C>A maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:117308725 G>A maps to NM_020693.2 S1499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:117314752 A>T maps to NM_020693.2 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:120865388 C>T maps to NM_024094.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:120859250 G>A maps to NM_024094.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:116752285 C>T maps to NM_013352.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr6:116720445 G>T maps to NM_013352.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr6:116720481 C>G maps to NM_013352.2 Y23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:116757413 G>T maps to NM_013352.2 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr6:116757313 A>T maps to NM_013352.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:65178452 C>A maps to NM_032160.2 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:28914144 G>T maps to NM_001942.2 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28934678 T>G maps to NM_001942.2 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:28908158 C>A maps to NM_001942.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:28934765 C>A maps to NM_001942.2 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:28906835 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr18:28934525 A>T maps to NM_001942.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr18:28934531 C>T maps to NM_001942.2 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr18:28909949 G>C maps to NM_001942.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr18:28934417 T>A maps to NM_001942.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:28934441 C>A maps to NM_001942.2 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr18:28935209 T>C maps to NM_001942.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr18:28935131 G>T maps to NM_001942.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr18:29122616 C>T maps to NM_001943.3 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:29126201 G>T maps to NM_001943.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr18:29126288 T>C maps to NM_001943.3 A980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr18:29104408 A>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:29126543 T>C maps to NM_001943.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr18:29122595 C>T maps to NM_001943.3 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:29036400 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29037051 G>T maps to NM_001944.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr18:29049187 C>T maps to NM_001944.2 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr18:29041258 G>T maps to NM_001944.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:29049077 G>T maps to NM_001944.2 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:29054363 T>A maps to NM_001944.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr18:29044157 C>T maps to NM_001944.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr18:29049193 C>T maps to NM_001944.2 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr18:29039806 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr18:29036438 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr18:29041193 C>A maps to NM_001944.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr18:29041194 A>G maps to NM_001944.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr18:29044072 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr18:29055706 G>T maps to NM_001944.2 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr18:29055883 C>T maps to NM_001944.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:29055682 C>T maps to NM_001944.2 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr18:29056099 G>A maps to NM_001944.2 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:29056036 G>T maps to NM_001944.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr18:29037026 G>A maps to NM_001944.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr18:29056009 T>C maps to NM_001944.2 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:28980939 T>A maps to NM_001134453.1 Y458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr18:28991302 C>T maps to NM_001134453.1 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:28993188 G>A maps to NM_001134453.1 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr18:28989466 C>A maps to NM_001134453.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr18:28993041 T>C maps to NM_001134453.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr18:28993287 T>A maps to NM_001134453.1 C970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:28993525 C>A maps to NM_001134453.1 R1050R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:28983406 C>T maps to NM_001134453.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr18:28991203 C>G maps to NM_001134453.1 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:28991083 C>A maps to NM_001134453.1 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:28986190 G>A maps to NM_001134453.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr18:28968922 C>T maps to NM_001134453.1 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:35390862 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr20:35384134 G>A maps to NM_001145315.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:35386511 C>A maps to NM_001145315.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr20:35386511 C>A maps to NM_001145315.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr6:7581354 G>A maps to NM_004415.2 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:7585771 C>A maps to NM_004415.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:7585489 G>T maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr6:7584232 T>A maps to NM_004415.2 V2246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:7575649 G>A maps to NM_004415.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr6:7572108 C>A maps to NM_004415.2 C646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr6:7571786 C>T maps to NM_004415.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:7575674 C>T maps to NM_004415.2 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr6:7580652 G>A maps to NM_004415.2 K1410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:7580466 G>C maps to NM_004415.2 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:7583578 A>G maps to NM_004415.2 K2028K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr6:7572276 C>A maps to NM_004415.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr6:7569489 C>T maps to NM_004415.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:7576571 T>C maps to NM_004415.2 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:7585051 G>T maps to NM_004415.2 L2519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:88533715 G>T maps to NM_014208.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:88535002 G>T maps to NM_014208.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr4:88535151 T>C maps to NM_014208.3 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:88534105 C>T maps to NM_014208.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:88534394 A>T maps to NM_014208.3 K353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:88532074 A>T maps to NM_014208.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:56371470 T>A maps to ENST00000361203 I6241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:56481616 C>G maps to ENST00000281662 V2780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:56391359 C>T maps to ENST00000361203 L5765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:56328461 C>T maps to ENST00000361203 R7382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:56418453 C>G did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:56362215 A>T maps to ENST00000361203 G6517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:56391313 C>A maps to ENST00000361203 E5781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr6:56480332 G>A maps to ENST00000281662 S3208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:56462572 G>A maps to ENST00000361203 Q3843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:56328452 T>A maps to ENST00000361203 S7385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:56417868 C>A maps to ENST00000361203 E5030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:56399961 C>A maps to ENST00000361203 S5422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr6:56482782 C>A did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr6:56371587 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:56324943 G>A maps to ENST00000361203 R7452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:56417154 G>A maps to ENST00000361203 R5268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:56393637 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:56347479 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:56328458 T>C maps to ENST00000361203 P7383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:56347513 T>G maps to ENST00000361203 S6912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:56496091 T>C maps to ENST00000361203 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr6:56481835 G>T maps to ENST00000281662 Y2707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr6:56484937 A>T maps to ENST00000281662 L1862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:56425221 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:56483242 G>T maps to ENST00000281662 L2427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:56347591 C>A maps to ENST00000361203 R6886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:56504400 G>A maps to ENST00000361203 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:56357080 G>A maps to ENST00000361203 Q6690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:56458991 C>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:205131162 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:205132892 A>G maps to NM_015375.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:205138855 G>A maps to NM_015375.2 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:205156671 C>A maps to NM_015375.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:205156763 C>A maps to NM_015375.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:205132093 G>C maps to NM_015375.2 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:212273759 C>G maps to NM_016448.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:32428316 G>T maps to NM_001390.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:32374205 G>A maps to NM_001390.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr18:32464693 C>T maps to NM_001390.4 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr18:32407562 C>G maps to NM_001390.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr18:32431844 G>A maps to NM_001390.4 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr18:32455294 C>A maps to NM_001390.4 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:32438300 C>T maps to NM_001390.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr18:32335938 G>C did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:25754370 T>C maps to NM_021907.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:15523327 C>A maps to NM_032122.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:49917564 C>T maps to NM_001144955.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr15:49924459 G>T maps to NM_001144955.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:118176763 G>A maps to NM_173666.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:118183793 G>A maps to NM_173666.2 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:118183838 C>A maps to NM_173666.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:113534584 C>G maps to NM_004416.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:113532911 T>A maps to NM_004416.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:113515245 C>A maps to NM_004416.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:113515277 G>T maps to NM_004416.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:113531398 C>T maps to NM_004416.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr7:76112336 C>T maps to NM_020892.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:76112317 G>T maps to NM_020892.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:76111984 G>T maps to NM_020892.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:76111921 T>C maps to NM_020892.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:76112137 C>T maps to NM_020892.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:76112401 C>G maps to NM_020892.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:76112350 C>T maps to NM_020892.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:76111843 G>A maps to NM_020892.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:58001201 G>T maps to NM_178502.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:122287985 T>A maps to NM_138287.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr3:122289336 A>G maps to NM_138287.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:58949674 A>C maps to NM_015177.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:58949494 A>T maps to NM_015177.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:58972339 C>A maps to NM_015177.1 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:242626192 C>A maps to NM_012145.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7150663 T>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:45426447 C>G maps to NM_175940.1 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr15:45444640 C>T maps to NM_175940.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr15:45444086 G>A maps to NM_175940.1 Q1010Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:45433202 C>T maps to NM_175940.1 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:45400284 G>T maps to NM_014080.4 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr15:45387159 T>A maps to NM_014080.4 K1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:45402678 C>A maps to NM_014080.4 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:45402111 G>A maps to NM_014080.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr15:45393005 G>A maps to NM_014080.4 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:45397882 C>G maps to NM_014080.4 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:45402890 C>T maps to NM_014080.4 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:45389483 G>T maps to NM_014080.4 R1267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr15:45411537 C>A maps to NM_144565.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:45412379 G>T maps to NM_144565.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:45409345 C>T maps to NM_207581.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr15:45408445 T>C maps to NM_207581.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:76797740 G>A maps to NM_001003892.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:76803612 G>T maps to NM_001003892.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:76818122 G>C maps to NM_001003892.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:68072015 G>A maps to NM_017803.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:68107934 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:5789412 G>A maps to NM_020175.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:5788168 G>A maps to NM_020175.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107216864 A>T maps to NM_181581.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:172196064 G>A maps to NM_004417.3 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:221879755 G>A maps to NM_007207.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:221879728 C>A maps to NM_007207.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74001051 T>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:73993543 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:74007069 C>T maps to NM_003584.2 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:161723051 G>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:161719818 G>A maps to NM_007240.1 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:76861637 T>A maps to ENST00000356369 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:76861662 C>A maps to ENST00000356369 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr10:76861686 C>T maps to ENST00000356369 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr10:76857552 C>T maps to ENST00000356369 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:30454915 T>A maps to NM_080611.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr20:30451753 G>A maps to NM_080611.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr20:30450487 C>T maps to NM_080611.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr20:30450487 C>A maps to NM_080611.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:12673888 G>A maps to NM_030640.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:183948267 C>T maps to NM_080876.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr2:183943748 A>T maps to NM_080876.3 K30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:44703496 A>G did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:44703539 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:44703491 C>G did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:44703616 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:44703734 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:44703840 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:44703515 T>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:44703527 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr6:348144 C>T maps to ENST00000457386 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:350825 T>G maps to NM_020185.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:345853 G>T maps to ENST00000457386 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr6:311962 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:159752064 C>A maps to NM_017823.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:159752076 G>A maps to NM_017823.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:33451144 C>G maps to NM_024025.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr8:33451114 A>G maps to NM_024025.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:33451049 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:33449644 G>T maps to NM_024025.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:33449608 T>C maps to NM_024025.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:167095142 C>A maps to NM_001080426.1 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:167097619 C>T maps to NM_001080426.1 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167096833 C>T maps to NM_001080426.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:167096068 C>T maps to NM_001080426.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:167096857 T>C maps to NM_001080426.1 N830N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:167095996 C>A maps to NM_001080426.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:167096794 G>T maps to NM_001080426.1 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:167096671 C>A maps to NM_001080426.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:167097505 A>G maps to NM_001080426.1 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:167096051 G>T maps to NM_001080426.1 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:167097383 C>A maps to NM_001080426.1 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:167095238 G>T maps to NM_001080426.1 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:167088686 G>T maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:167096455 G>C maps to NM_001080426.1 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:167096929 C>A maps to NM_001080426.1 Y854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:167097710 G>T maps to NM_001080426.1 G1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:167095996 C>A maps to NM_001080426.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:167096413 G>A maps to NM_001080426.1 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:167088548 G>A maps to NM_001080426.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:167097511 C>T maps to NM_001080426.1 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:167096999 G>T maps to NM_001080426.1 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:167096824 C>A maps to NM_001080426.1 T819T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-67-3771-01A-01D-1040-01. Mapping will be selected arbitrarily.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:241500166 C>G maps to NM_001033575.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr8:29194881 C>A maps to NM_001394.5 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:112258061 G>T maps to NM_004419.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:89745768 G>A maps to NM_001946.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr3:52088310 C>A maps to NM_001947.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr11:1586993 C>A maps to NM_004420.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:152914961 C>A did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr23:152915087 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:152914892 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:152914745 C>T did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:152915632 G>C did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:152914839 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:152915683 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48624495 C>T maps to NM_001025248.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:183885371 A>T maps to NM_004423.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:183885797 C>T maps to NM_004423.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:183888494 C>T maps to NM_004423.3 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:183884763 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:183888413 G>T maps to NM_004423.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr10:82102069 C>T maps to NM_138812.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:82126469 G>A maps to ENST00000372198 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:46783426 C>T maps to NM_017653.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:46812948 G>T maps to NM_017653.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:46889570 G>A maps to NM_017653.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:46956760 C>A maps to NM_017653.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr18:46917984 G>T maps to NM_017653.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:102446175 C>T maps to NM_001376.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:102452389 C>T maps to NM_001376.4 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:102505473 C>T maps to NM_001376.4 T3781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:102498628 C>T maps to NM_001376.4 Q3302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:102510612 C>T maps to NM_001376.4 G4229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:102476787 G>T maps to NM_001376.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:102493717 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:102506695 G>C maps to NM_001376.4 L3938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:102496194 G>T maps to NM_001376.4 E3228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr14:102481659 C>A maps to NM_001376.4 P2411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr14:102483597 T>C maps to NM_001376.4 Y2674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr14:102452666 G>A maps to NM_001376.4 W702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:102493026 C>T maps to NM_001376.4 H2918H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr14:102469194 G>C maps to NM_001376.4 L1592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:102493035 G>A maps to NM_001376.4 R2921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr14:102514196 G>A maps to NM_001376.4 E4350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:102483805 C>T maps to NM_001376.4 P2714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:102486381 C>A maps to NM_001376.4 L2832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:95499230 C>T maps to NM_004411.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:95662046 T>C maps to NM_004411.4 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr7:95457398 G>T maps to NM_004411.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:95668714 C>G maps to NM_004411.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:95442508 G>T maps to NM_004411.4 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:95665043 C>T maps to NM_004411.4 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr7:95726811 T>C maps to NM_004411.4 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr7:95614125 G>T did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr7:95625310 G>T maps to NM_004411.4 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:32571790 T>A maps to NM_016141.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:102992158 A>T maps to NM_001080463.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:103091377 A>T maps to NM_001080463.1 A2991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:103090681 G>A maps to NM_001080463.1 K2957K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:103006490 G>T maps to NM_001080463.1 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:102991710 G>T maps to NM_001080463.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:103128357 C>T maps to NM_001080463.1 L3502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:103106398 A>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:103062244 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:103006601 A>T maps to NM_001080463.1 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:102999640 G>T maps to NM_001080463.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:103057206 A>T maps to NM_001080463.1 V2290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:102980338 C>T maps to NM_001080463.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:103194612 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:103055672 T>C maps to NM_001080463.1 L2176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:103086511 A>G maps to NM_001080463.1 G2919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:103124056 C>A maps to NM_001080463.1 Y3369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr11:102991262 G>T maps to NM_001080463.1 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr11:103052497 A>T maps to NM_001080463.1 T2120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:44028816 C>A maps to NM_001193464.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:44032290 A>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:44032303 G>A maps to NM_001193464.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:44036904 G>T maps to NM_001193464.1 *353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:120934290 G>T maps to NM_003746.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:120935937 T>C maps to NM_003746.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:56164474 C>T maps to NM_080677.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr16:80583391 C>T maps to NM_130897.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr23:37700310 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:38853122 G>T maps to NM_001396.3 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr21:38884272 C>T maps to NM_001396.3 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr21:38884218 T>C maps to NM_001396.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:40317963 C>A maps to NM_004714.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:68043619 G>T maps to NM_006482.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:206821127 G>T maps to NM_003582.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:4708298 G>T maps to NM_003845.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr12:4708298 G>A maps to NM_003845.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:71839868 C>T maps to NM_001130987.1 I1440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:71829925 C>T maps to NM_001130987.1 I1316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:71788953 C>A maps to NM_001130987.1 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:71780982 G>T maps to NM_001130987.1 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:71788995 G>A maps to NM_001130987.1 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:71747321 C>A maps to NM_001130987.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71741005 G>T maps to NM_001130987.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:71795381 G>C maps to NM_001130987.1 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71753444 G>C maps to NM_001130987.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:71838609 C>T maps to NM_001130987.1 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:71766325 C>A maps to NM_001130987.1 Y511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:71839887 C>T maps to NM_001130987.1 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:71827869 G>T maps to NM_001130987.1 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:71891550 C>G maps to NM_001130987.1 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:71827932 G>T maps to NM_001130987.1 G1286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:71709040 G>C maps to NM_001130987.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:71766319 C>T maps to NM_001130987.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:71781055 C>A maps to NM_001130987.1 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:71838722 C>T maps to NM_001130987.1 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:71886085 C>T maps to NM_001130987.1 Q1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:71825791 G>T maps to NM_001130987.1 E1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:71780145 C>A maps to NM_001130987.1 Y604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:71742829 G>A maps to NM_001130987.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:207516600 G>A maps to NM_001093730.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:207527870 G>T maps to NM_001093730.1 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207564940 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:207527705 T>C maps to NM_001093730.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:207516618 G>A maps to NM_001093730.1 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:207564596 G>T maps to NM_001093730.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:207528120 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr2:207527738 C>G maps to NM_001093730.1 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:55724737 T>A maps to NM_130810.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr13:96293707 C>T maps to NM_198968.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr13:96293706 C>A maps to NM_198968.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr13:96237026 G>T maps to NM_198968.2 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:137799407 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:137783471 G>A maps to NM_173543.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr3:137822392 C>A maps to NM_173543.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108344738 C>A maps to NM_014648.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:108353816 C>T maps to NM_014648.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:108392969 G>T maps to NM_014648.3 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:108394643 C>G maps to NM_014648.3 S902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr20:32267679 G>A maps to NM_005225.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:23857033 C>T maps to NM_004091.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:23842998 G>T maps to NM_004091.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr1:23848399 G>A maps to NM_004091.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:23845602 G>A maps to NM_004091.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr6:20402609 C>T maps to NM_001949.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:86124413 C>T maps to ENST00000256117 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:77438542 T>A maps to NM_203394.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:77423928 C>T maps to NM_203394.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:77424023 C>A maps to NM_203394.2 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:77417887 T>C maps to NM_203394.2 G881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:77436979 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:77444525 T>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:77426849 C>T maps to NM_203394.2 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:19259526 C>G maps to NM_024680.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:19251861 C>T maps to NM_024680.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:2285347 C>T maps to NM_004424.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:121591539 C>A maps to NM_018456.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:23555866 C>T maps to NM_001083614.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:158267099 G>A maps to NM_024007.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:158223454 C>T maps to NM_024007.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:158139336 G>A maps to NM_024007.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:158522671 C>A maps to NM_024007.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:158523360 G>C maps to NM_024007.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:25899679 G>T maps to NM_022659.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:25708267 G>T maps to NM_022659.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:25708200 A>T maps to NM_022659.2 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:131755542 G>C maps to ENST00000355311 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:131761675 C>A maps to ENST00000355311 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:131671815 G>T maps to ENST00000355311 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:131676091 G>C maps to ENST00000355311 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:131666054 C>T maps to ENST00000355311 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr10:131639126 G>T maps to ENST00000355311 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr10:131639111 G>A maps to ENST00000355311 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:131639171 G>T maps to ENST00000355311 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr19:4234670 C>T maps to NM_005755.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:73111552 C>G maps to NM_018029.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:43637202 G>A maps to NM_001159936.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:43632903 C>A maps to NM_001159936.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:43637771 G>A maps to NM_001159936.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:43630367 C>A maps to NM_001159936.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:48386708 G>A did not map to a codon.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr23:48382377 G>A did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:48382175 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:21560097 T>C maps to NM_001397.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:21585236 G>A maps to NM_001397.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr3:183994342 G>A maps to NM_001100120.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr3:184001715 C>T maps to NM_014693.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:233344907 G>T maps to NM_004826.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:233348872 C>A maps to NM_004826.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:233351039 G>T maps to NM_004826.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:127611310 G>C maps to NM_001139510.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:127611328 G>T maps to NM_001139510.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr10:135180497 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:150483445 G>A maps to ENST00000369049 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:150484989 C>A maps to ENST00000369049 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr1:150485218 G>C maps to ENST00000369049 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:150483556 G>A maps to ENST00000369049 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:150484273 C>T maps to ENST00000369049 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:150485939 A>G maps to ENST00000369049 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:95285067 C>T maps to NM_001393.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr9:95284980 C>T maps to NM_001393.3 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr9:95264874 G>A maps to NM_001393.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:172480283 G>T maps to ENST00000392692 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:172482079 G>T maps to ENST00000392692 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:139135692 A>G maps to NM_001195037.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:139167714 A>G maps to NM_001195037.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:139222087 C>G maps to NM_001195037.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:139164322 A>T maps to NM_001195037.2 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:68836383 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:69255352 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:69255359 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:68836337 A>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:69176903 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:68836454 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:65824316 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:65824891 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:65822555 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:65824987 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:65824997 C>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:65819692 A>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:65819508 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:65822525 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:65819380 T>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:65819691 C>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:65835826 C>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:65835827 C>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:109547431 G>T maps to ENST00000376651 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:109513386 G>A maps to ENST00000376651 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr2:109547446 C>G maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:109527496 G>A maps to ENST00000376651 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:109545727 C>T maps to ENST00000376651 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:236631556 C>T maps to NM_145861.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:236645849 C>A maps to NM_145861.2 C183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:236645936 C>T maps to NM_145861.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:236631535 A>G maps to NM_145861.2 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:236645687 G>T maps to NM_145861.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:236645741 G>A maps to NM_145861.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:236590747 C>T maps to NM_145861.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:236645781 C>T maps to NM_145861.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:67911273 C>T maps to NM_014329.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:67914656 G>A maps to NM_014329.3 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:67917909 G>T maps to NM_014329.3 R1355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr16:67911712 A>T maps to NM_014329.3 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:67917625 C>G maps to NM_014329.3 L1335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:21216182 G>C maps to NM_006683.4 *148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:5251930 C>G maps to NM_014674.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:5229960 C>T maps to NM_014674.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr3:5251930 C>A maps to NM_014674.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:33703448 G>C maps to NM_018217.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:33703721 T>A maps to NM_018217.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:184681005 C>A maps to NM_025191.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:184663204 C>A maps to NM_025191.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:184672035 G>A maps to NM_025191.3 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:184706190 G>A maps to NM_025191.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:83402631 C>A maps to NM_005711.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:83362383 G>C maps to NM_005711.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:83362355 C>A maps to NM_005711.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:83356223 G>T maps to NM_005711.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:83476316 G>T maps to NM_005711.3 C83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:83433173 T>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:83402608 G>C maps to NM_005711.3 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:83433158 G>A maps to NM_005711.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:83362355 C>A maps to NM_005711.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:41948216 C>T maps to NM_001956.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr20:57876711 C>T maps to NM_207034.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:148457075 T>A maps to NM_001957.3 C265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:78474774 G>T maps to ENST00000377211 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr13:78477730 C>T maps to ENST00000377211 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:93210068 T>C maps to NM_003566.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr6:74228478 T>C maps to NM_001402.5 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:74228505 A>G maps to NM_001402.5 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:62126414 C>A maps to NM_001958.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr20:62122062 C>A maps to NM_001958.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:62122068 C>A maps to NM_001958.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:62120436 G>T maps to NM_001958.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:207026076 G>T maps to NM_021121.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:207027211 G>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:144663465 G>A maps to NM_032378.4 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:144662226 C>A maps to NM_032378.4 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:144669021 G>A maps to NM_032378.4 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:8080124 A>G maps to NM_004280.4 *175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:8097505 C>G maps to NM_004280.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:62339101 C>T maps to ENST00000378019 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:3979398 C>A maps to NM_001961.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:3982007 G>T maps to NM_001961.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr19:3976626 C>A maps to NM_001961.3 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:3983167 C>A maps to NM_001961.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr19:3984258 G>A maps to NM_001961.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:3979428 G>A maps to NM_001961.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:22237268 G>T maps to NM_013302.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:22269909 C>T maps to NM_013302.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr16:22262544 G>T maps to NM_013302.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr16:22274453 C>T maps to NM_013302.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:22277708 A>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:22269091 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:128127044 C>T maps to NM_021937.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:128127090 C>T maps to NM_021937.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:128060611 G>A maps to NM_021937.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:128060644 C>T maps to NM_021937.3 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:36327310 G>T maps to NM_030636.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:36194547 C>A maps to NM_030636.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:36194772 G>T maps to NM_030636.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:36194112 G>C maps to NM_030636.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:36194190 A>G maps to NM_030636.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:49637301 C>T maps to NM_024593.3 *212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr8:49647698 C>T maps to NM_024593.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:49644011 C>A maps to NM_024593.3 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:245250577 A>G maps to ENST00000421886 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:60484418 C>A maps to NM_001144933.1 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:60484500 G>A maps to NM_001144933.1 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:60483880 T>C maps to NM_001144933.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:60483850 A>T maps to NM_001144933.1 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr17:60469301 G>T maps to NM_001144933.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:3763465 C>A maps to NM_001144958.1 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:3788163 C>T maps to NM_001144958.1 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:3806018 T>A maps to NM_001144958.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:3757646 T>G maps to NM_032680.3 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:28380843 A>T maps to NM_198529.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28380823 C>A maps to NM_198529.3 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:28405332 C>T maps to NM_198529.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:28384844 C>T maps to NM_198529.3 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:28405429 C>A maps to NM_198529.3 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr17:28435020 G>A maps to NM_198529.3 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr17:28410033 G>A maps to NM_198529.3 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr17:28405522 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:43933317 C>G maps to NM_022785.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr22:43950874 C>T maps to NM_022785.3 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:44073893 C>G maps to NM_022785.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr22:44178096 T>A maps to NM_022785.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr22:44178130 G>C maps to NM_022785.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr22:44131812 C>A maps to NM_022785.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr22:44161270 G>T maps to NM_022785.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr22:43996139 G>A maps to NM_022785.3 Y895Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:63999764 G>C did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:64021096 G>A maps to NM_032437.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:56104956 G>A maps to NM_001039349.1 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:65635361 A>T maps to NM_016938.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:65638661 T>A maps to NM_016938.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:19975087 C>A maps to NM_144715.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:19921296 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:19961393 G>T maps to NM_144715.3 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr3:19975198 C>G maps to NM_144715.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:52344531 G>T maps to NM_018100.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:52303262 A>T maps to NM_018100.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:52288817 G>C maps to NM_018100.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:44109565 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:44094636 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:44101395 C>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:44109459 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:44091757 G>T did not map to a codon.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr23:44088988 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:44107588 C>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:44120529 G>T did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:15755204 G>A maps to NM_024329.5 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:155106461 C>A maps to NM_004428.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:155104003 G>T maps to NM_004428.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:1295573 G>T maps to NM_001405.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:106723416 C>A maps to NM_001962.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:106762990 A>G maps to NM_001962.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:68060319 C>T did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:68060217 C>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:68060198 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:68060340 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:68059565 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:68059869 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:132958798 A>G maps to NM_015137.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:132957093 A>C maps to NM_015137.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:132958768 C>T maps to NM_015137.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:132996390 G>A maps to NM_015137.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:132982804 G>C maps to NM_015137.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr8:132998475 T>C maps to NM_015137.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:132997195 G>A maps to NM_015137.3 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:23828663 T>A maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:23826584 G>A maps to NM_005864.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:23829248 C>A did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr15:82533608 A>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr15:82444679 G>A maps to NM_024580.5 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:82533697 C>A maps to NM_024580.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr15:82533631 A>T maps to NM_024580.5 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:82533673 G>A maps to NM_024580.5 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:82422770 C>A maps to NM_024580.5 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr17:42964019 T>A maps to NM_004247.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:110920852 C>T maps to NM_001963.4 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:110884341 C>T maps to NM_001963.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:110864570 A>T maps to NM_001963.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:13636139 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:13645249 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:13645149 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:13624573 C>A did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:13588023 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr23:13636017 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:13641991 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:13607687 G>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:13636053 T>C did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:13607712 C>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:13624534 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:13635948 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:13635971 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:32134871 G>T maps to NM_030652.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:38427130 C>T maps to ENST00000354891 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38464006 C>T maps to ENST00000354891 F991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:38370469 C>G maps to ENST00000354891 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:38451500 C>A maps to ENST00000354891 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:38451482 G>A maps to ENST00000354891 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:38448409 A>T maps to ENST00000354891 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr5:38406982 C>T maps to ENST00000354891 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:38407138 T>A maps to ENST00000354891 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:38407102 T>C maps to ENST00000354891 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:55240711 G>T maps to NM_005228.3 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr7:55220239 G>T maps to NM_005228.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:55242488 G>T maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:55259500 C>T maps to NM_005228.3 I853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:55227988 C>T maps to NM_005228.3 Q486*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-97-8172-01A-11D-2284-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:231509812 C>A maps to NM_022051.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:231557538 G>A maps to NM_022051.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41313711 A>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:34400393 C>A maps to NM_022073.3 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:34419799 G>A maps to NM_022073.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr14:34419910 C>A maps to NM_022073.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:34396239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:137803055 C>G maps to NM_001964.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:64573953 G>A maps to NM_001136178.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr10:64572999 G>A maps to NM_001136178.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr8:22548753 T>C maps to NM_004430.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:73520448 G>A maps to NM_001965.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:63175835 C>T maps to NM_015252.3 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:63053403 G>C did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:63223866 G>A maps to NM_015252.3 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:63101630 A>T maps to NM_015252.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:62974574 G>A maps to NM_015252.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:63101478 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:65358064 T>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:65358033 C>T maps to NM_001099409.1 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr11:65349330 A>G maps to NM_001099409.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:64645663 C>T maps to NM_006795.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr19:48244175 G>T maps to NM_014601.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:31472332 G>T maps to NM_014600.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:31489305 C>T maps to NM_014600.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:31484530 G>T maps to NM_014600.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:31484545 A>T maps to NM_014600.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:31489369 G>T maps to NM_014600.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:31489254 A>T maps to NM_014600.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr3:184922342 T>A maps to NM_001966.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr9:140611348 C>G maps to NM_024757.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:140708893 C>T maps to NM_024757.4 C1064C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr9:140672342 G>T maps to NM_024757.4 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:140671224 G>A maps to NM_024757.4 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:31855432 C>T maps to ENST00000395728 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:31850744 C>T maps to ENST00000395728 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:31852715 C>T maps to ENST00000395728 R864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:31856761 G>C maps to ENST00000395728 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:125448119 G>T maps to ENST00000278903 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:40023400 G>A maps to NM_152361.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:104698155 T>G maps to NM_001008394.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:104697913 G>T maps to NM_001008394.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:65766819 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:20156716 T>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:20148715 T>C did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:20153878 T>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:40352528 T>A maps to NM_005875.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:6085728 C>T maps to NM_014413.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:6089619 C>A maps to NM_014413.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr7:6082606 C>A maps to NM_014413.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:37349651 G>C maps to NM_001135651.1 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr2:37349799 C>A maps to NM_001135651.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr2:37349800 C>A maps to NM_001135651.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:37365451 A>G maps to NM_001135651.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:88890506 T>C maps to NM_004836.5 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:88857451 G>A maps to NM_004836.5 Y1051Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr15:40284373 A>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:40226471 G>T maps to NM_001013703.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr15:40269027 C>G maps to NM_001013703.2 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:40268811 C>T maps to NM_001013703.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr15:40295448 G>A maps to NM_001013703.2 E1097E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:40284430 G>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr15:40293421 G>A maps to NM_001013703.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:75469818 G>C maps to NM_014239.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:75469830 C>T maps to NM_014239.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:45347296 C>T maps to NM_020365.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:45316676 T>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:45407277 C>A maps to NM_020365.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:183858261 C>G maps to NM_003907.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:36380998 G>T maps to NM_012199.2 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:36354196 C>T maps to NM_012199.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:36358879 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:36381062 C>T maps to NM_012199.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:36349033 A>T maps to NM_012199.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:141567244 G>A maps to NM_012154.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:141542187 C>A maps to NM_012154.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:141542157 G>A maps to NM_012154.3 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:36505905 A>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr20:32684605 C>T maps to NM_003908.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:24094890 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr23:24094880 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:24075596 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:120830457 G>A maps to NM_003750.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:2402300 G>A maps to ENST00000314800 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:2409265 G>A maps to ENST00000314800 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:2406158 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:109240539 G>A maps to NM_001568.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:109240592 G>A maps to NM_001568.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:8008913 G>C maps to ENST00000449102 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:8008940 G>A maps to ENST00000449102 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:8013693 G>T maps to ENST00000449102 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:8008910 G>T maps to ENST00000449102 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:117768020 C>A maps to ENST00000411422 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:117768021 C>T maps to ENST00000411422 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:117658740 C>A maps to ENST00000411422 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:32694335 C>T maps to NM_003757.2 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr11:32610278 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:7479966 T>C maps to NM_001416.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr3:186506919 C>T maps to ENST00000440191 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:186503787 T>C maps to ENST00000440191 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:78112899 G>A maps to NM_014740.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr12:53421874 C>T maps to ENST00000438209 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr12:53427590 T>C maps to ENST00000438209 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:176072391 C>T maps to NM_001099408.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:176070228 C>A maps to NM_001099408.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr5:176070153 G>A maps to NM_001099408.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:176070153 G>T maps to NM_001099408.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:233421189 G>T maps to NM_004846.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:233431633 G>T maps to NM_004846.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233431655 G>T maps to NM_004846.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr22:31850285 C>T maps to NM_019843.3 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184045207 G>T maps to NM_001194947.1 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:184046478 C>T maps to NM_001194947.1 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:184045479 C>G maps to NM_001194947.1 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:184042134 G>A maps to NM_001194947.1 T880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:184049276 G>C maps to NM_001194947.1 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr3:184040361 C>T maps to NM_001194947.1 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:184039091 C>T maps to NM_001194947.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:184044713 C>G maps to NM_001194947.1 S1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:184045039 A>T maps to NM_001194947.1 G1162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr3:184049747 C>T maps to NM_001194947.1 R1505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:184040238 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:10821640 G>C maps to ENST00000429377 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:10822110 G>A maps to ENST00000429377 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:10820817 T>C maps to ENST00000429377 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:10821696 G>A maps to ENST00000429377 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:21183972 C>A maps to NM_001198801.1 E1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:21137267 T>C maps to NM_001198801.1 A1549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:21205815 C>A maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:21167520 C>A maps to NM_001198801.1 E1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:21276583 G>A maps to NM_001198801.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:21306896 A>T maps to NM_001198801.1 Y85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:21268371 C>A maps to NM_001198801.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:21191716 C>A maps to NM_001198801.1 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:21268605 T>A maps to NM_001198801.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:21268710 T>A maps to NM_001198801.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:103804718 C>A maps to NM_183004.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99980852 C>A maps to NM_015904.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:99995878 G>A maps to NM_015904.3 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:99976701 C>T maps to NM_015904.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:99976813 C>T maps to NM_015904.3 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr20:33867857 G>A maps to NM_002212.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr18:48513136 G>C maps to NM_018696.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:48513136 G>T maps to NM_018696.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr18:48500917 C>T maps to NM_018696.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:8028582 G>A maps to ENST00000351593 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:23762136 C>A maps to ENST00000359598 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:23704924 G>A maps to ENST00000359598 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:23701600 G>A maps to ENST00000359598 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr9:23705015 G>A maps to ENST00000359598 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:23762202 A>T maps to ENST00000359598 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:11565621 G>A maps to NM_001420.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:11568958 C>T maps to NM_001420.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:11565616 C>T maps to NM_001420.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:11565535 C>A maps to NM_001420.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:50610799 G>T maps to NM_021952.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:50610672 C>A maps to NM_021952.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:50610780 C>A maps to NM_021952.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:50661257 C>A maps to NM_021952.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:50666681 C>T maps to NM_021952.3 N325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:50659563 C>A maps to NM_021952.3 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:41507914 G>T maps to NM_172373.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr4:140005301 G>A maps to NM_006874.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:139981551 G>A maps to ENST00000379550 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:129200829 C>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:129201450 A>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:129206303 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr23:129206318 G>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:129200732 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:129205071 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:37770692 C>A maps to NM_052906.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:37771373 G>C maps to NM_052906.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:47496437 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:47497342 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:47497453 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:205588202 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589515 C>A maps to NM_001973.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:205589654 C>T maps to NM_001973.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:18576368 G>A maps to NM_006532.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:18561706 G>A maps to NM_006532.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr15:44068349 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:36934499 G>T maps to NM_014800.9 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:37264515 G>T maps to NM_014800.9 I223I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:36917704 G>T maps to NM_014800.9 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:37382249 C>A maps to NM_014800.9 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:45003280 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:45002145 C>T maps to ENST00000439931 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:107518318 C>A maps to NM_018712.3 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:107521058 A>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:141461452 T>C maps to NM_153702.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:141446701 T>C maps to NM_153702.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:85590289 G>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:73467601 T>A maps to ENST00000358929 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:73480296 C>T maps to ENST00000358929 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:73459564 C>T maps to ENST00000358929 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr19:11665066 C>T maps to NM_032377.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:11665120 C>T maps to NM_032377.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:11005667 G>A maps to NM_017770.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:103988648 A>T maps to NM_152310.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr10:103988654 C>G maps to NM_152310.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:80626441 T>C maps to NM_022726.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr6:80629226 C>T maps to NM_022726.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:80634725 C>A maps to NM_022726.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:80636030 A>C maps to NM_022726.3 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:80634725 C>A maps to NM_022726.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr6:80626435 A>C maps to NM_022726.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:80634698 C>T maps to NM_022726.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr6:80635961 G>T maps to NM_022726.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr18:33734898 C>T maps to ENST00000442325 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:31531348 C>T maps to ENST00000395934 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr11:31671712 G>T maps to ENST00000395934 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:31531534 A>C maps to ENST00000395934 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:48517426 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:79387375 G>C maps to NM_022159.3 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:79401978 C>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:79403964 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:79383617 C>A maps to NM_022159.3 G527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:79404938 A>G maps to NM_022159.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:79392732 A>T maps to NM_022159.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:79383317 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:79357262 G>A maps to NM_022159.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:79387396 T>A maps to NM_022159.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:153609422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:153609452 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153608324 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:153608665 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr23:153608672 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:153608049 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1826130 G>T maps to NM_001010865.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:1825151 C>A maps to NM_001010865.1 C196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:1825091 C>T maps to NM_001010865.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr22:29650276 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:101091000 C>G maps to ENST00000397927 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:101183241 T>G maps to ENST00000397927 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:101090976 G>A maps to ENST00000397927 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:101063284 G>T maps to ENST00000397927 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr7:101183181 G>T maps to ENST00000397927 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr7:101188640 C>A maps to ENST00000397927 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:27301992 G>T maps to NM_007046.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:2891214 G>T maps to NM_032048.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr18:2891639 C>A maps to NM_032048.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2891555 C>T maps to NM_032048.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:2892119 T>C maps to NM_032048.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr18:2913353 C>T maps to NM_032048.2 Y1038Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:2885090 C>A maps to NM_032048.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:39990773 C>A maps to NM_052846.1 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:39991416 G>C maps to NM_052846.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:39992302 G>T maps to NM_052846.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:39990939 G>A maps to NM_052846.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:39991454 G>A maps to NM_052846.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:39992361 C>A maps to NM_052846.1 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:100380642 T>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100367276 A>T maps to NM_001008707.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr14:100376584 G>T maps to NM_001008707.1 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:100331977 C>T maps to NM_001008707.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:100374054 A>G maps to NM_001008707.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:46124836 G>A maps to NM_001193268.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46124785 C>A maps to NM_001193268.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:46124872 C>T maps to NM_001193268.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62375671 C>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62373359 T>C maps to ENST00000278845 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62378704 C>T maps to ENST00000278845 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:42530317 A>G maps to NM_019063.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:42530453 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:42522519 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:42552611 T>C maps to NM_019063.3 H720H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:89161766 T>A maps to ENST00000380664 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr14:89087623 T>G maps to ENST00000380664 R1679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:89181355 C>A maps to ENST00000380664 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:89220987 C>T maps to ENST00000380664 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:13367623 A>G maps to NM_001423.2 *158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:48830830 G>T maps to NM_001425.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:48830118 G>T maps to NM_001425.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:6921872 C>T maps to ENST00000381407 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:6928182 C>T maps to ENST00000381407 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr19:6928171 G>T maps to ENST00000381407 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:6926403 C>T maps to ENST00000381407 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:6924744 C>A maps to ENST00000381407 C618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:6937292 G>T maps to ENST00000381407 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:6903851 C>T maps to ENST00000381407 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr19:6937388 C>T maps to ENST00000381407 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:6913761 G>A maps to ENST00000381407 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:6896448 C>A maps to ENST00000381407 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:14875406 G>A maps to NM_013447.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:14866618 C>A maps to NM_013447.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:14854510 G>T maps to NM_013447.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr19:14875275 C>T maps to NM_013447.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr19:14865884 C>A maps to NM_013447.2 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:14876337 G>A maps to NM_013447.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr19:14854556 C>A maps to NM_013447.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:14749074 C>A maps to NM_032571.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr10:119307664 G>T maps to NM_004098.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:119604044 C>T maps to NM_001426.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:155255090 G>A maps to NM_001427.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:225707047 C>T maps to ENST00000284563 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:225699551 C>A maps to ENST00000284563 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:225700577 G>A maps to ENST00000284563 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:71497576 C>A maps to NM_031889.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:71508510 C>T maps to NM_031889.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:71508555 T>A maps to NM_031889.2 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:71508840 T>A maps to NM_031889.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:71510526 C>T maps to NM_031889.2 T1128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr5:73931476 C>T maps to NM_003633.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:94862454 G>T maps to NM_015036.2 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:94862741 A>G maps to NM_015036.2 *501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:94862628 C>G maps to NM_015036.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr9:130586702 G>T maps to NM_001114753.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:130586660 C>G maps to NM_001114753.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:130588882 C>T maps to NM_001114753.1 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr9:130580452 G>T maps to NM_001114753.1 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr9:130581093 G>C maps to NM_001114753.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:77073538 C>G maps to NM_001042573.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:77077086 G>A maps to NM_001042573.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:77079623 C>T maps to NM_001042573.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:77081424 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:77077074 A>T maps to NM_001042573.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:77078117 G>T maps to NM_001042573.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:77079626 G>T maps to NM_001042573.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:77082417 C>G maps to NM_001042573.1 S740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr17:77076421 G>A maps to NM_001042573.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:77079561 A>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:8934895 G>C maps to NM_001428.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:8931950 C>T maps to NM_001428.2 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4856126 G>T maps to NM_053013.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:4857124 C>A maps to NM_053013.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:83381179 G>A maps to NM_021204.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr4:83381179 G>T maps to NM_021204.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr18:697317 G>C maps to ENST00000319815 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr13:43930153 G>T maps to NM_001127615.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:43798205 G>A maps to NM_001127615.1 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:43935508 G>T maps to NM_001127615.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr13:43935436 A>T maps to NM_001127615.1 C120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:43933985 C>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr13:43839532 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:43934143 C>T maps to NM_001127615.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:129771316 G>T did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr23:129837187 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:129801716 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:129837134 C>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr23:129771260 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:129759371 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:129799676 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:129799708 C>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:129759317 G>A did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:129801709 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:129771231 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:129759362 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:129813549 C>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:129771341 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:111441429 T>A maps to NM_001977.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr4:111480848 G>T maps to NM_001977.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr4:111412257 C>T maps to NM_001977.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:111441522 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:111470762 G>T maps to NM_001977.3 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:111464012 G>T maps to NM_001977.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:132171232 G>T maps to NM_006208.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:132173313 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:132168932 G>T maps to NM_006208.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:132195452 T>A maps to NM_006208.2 S537S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z049-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:120608146 C>T maps to NM_006209.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:120608212 C>A maps to NM_006209.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr8:120594687 G>T maps to NM_006209.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:120638811 C>T maps to NM_006209.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:120613650 C>A maps to NM_006209.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr8:120575253 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:120575107 C>A maps to NM_006209.3 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:120580445 G>T maps to NM_006209.3 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:132043461 G>T maps to NM_005021.3 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:131973769 G>A maps to NM_005021.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:131958538 G>A maps to NM_005021.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:46129365 T>C maps to NM_021572.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:46135474 C>A maps to NM_021572.4 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:46135474 C>A maps to NM_021572.4 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:185018488 G>A maps to NM_153343.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:77708903 G>T maps to NM_178543.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:77705080 C>T maps to NM_178543.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:77710997 G>A maps to NM_178543.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:77710992 C>T maps to NM_178543.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:77710988 C>T maps to NM_178543.3 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr22:40139817 C>A maps to NM_152512.3 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:97605317 C>T maps to NM_001098175.1 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:139945770 T>C maps to NM_203468.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:139943246 G>A maps to NM_203468.1 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:40468908 G>A maps to NM_001248.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:23302000 G>A maps to NM_004901.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:74439635 G>A maps to NM_001249.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr20:25187890 C>G maps to NM_001247.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr9:140332725 G>T maps to NM_001033113.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:27760973 T>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr3:27760112 G>A maps to ENST00000449599 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:27758587 C>A maps to ENST00000449599 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41573856 C>T maps to NM_001429.3 Q2048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41572504 G>A maps to NM_001429.3 E1678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:41573106 G>T maps to NM_001429.3 E1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr22:41568562 G>T maps to NM_001429.3 E1505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr22:41489046 C>G maps to NM_001429.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr22:41574497 G>A maps to NM_001429.3 Q2261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:41566408 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr22:41513608 G>T maps to NM_001429.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:132514350 G>C maps to ENST00000333577 L1865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:132504686 G>T maps to ENST00000333577 T1493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:132498100 G>T maps to ENST00000333577 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr12:132490798 G>T maps to ENST00000333577 A1062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:132472366 G>T maps to ENST00000333577 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:132491378 A>T maps to ENST00000333577 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:132466836 G>A maps to ENST00000333577 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:132562163 G>A maps to ENST00000333577 Q3142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:132466653 G>A maps to ENST00000333577 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr12:132496109 A>G maps to ENST00000333577 K1160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:132522602 G>T maps to ENST00000333577 E2093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:132546779 C>T maps to ENST00000333577 V2706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:132476771 G>T maps to ENST00000333577 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr12:132547171 C>T maps to ENST00000333577 Q2790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:132505711 G>T maps to ENST00000333577 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:132534887 C>T maps to ENST00000333577 L2443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr12:132537940 G>C maps to ENST00000333577 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:132466665 G>A maps to ENST00000333577 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:132546758 G>A maps to ENST00000333577 T2699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:132562034 G>T maps to ENST00000333577 V3099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:132514299 G>A maps to ENST00000333577 P1848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:46609130 C>T maps to NM_001430.4 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:46611729 G>T maps to NM_001430.4 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr2:46611666 C>T maps to NM_001430.4 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:46607469 G>C maps to NM_001430.4 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:29435867 C>T maps to NM_001166005.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:34797801 G>T maps to NM_012156.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:34778239 C>T maps to NM_012156.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:34807690 G>A maps to NM_012156.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:34797438 G>A maps to NM_012156.2 E566E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:34809853 C>T maps to NM_012156.2 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr20:34770227 C>T maps to NM_012156.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:131247752 C>A maps to NM_001431.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:131277562 A>G maps to NM_001431.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr6:131206322 G>A maps to NM_001431.3 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr6:131191137 A>G maps to NM_001431.3 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:5416023 G>A maps to NM_012307.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:5419721 C>G maps to NM_012307.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:5397197 C>A maps to NM_012307.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:5434023 C>T maps to NM_012307.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr18:5396313 C>G maps to NM_012307.2 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:5489095 C>A maps to NM_012307.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr18:5406940 C>G maps to NM_012307.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr18:5443839 G>A maps to NM_012307.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr18:5489113 C>A maps to NM_012307.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:5397299 C>G maps to NM_012307.2 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr18:5395684 C>A maps to NM_012307.2 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr18:5398033 G>A maps to NM_012307.2 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:111570403 G>T maps to NM_022140.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:111531406 T>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:111540178 G>C maps to NM_022140.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:112025333 T>C maps to NM_019114.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr9:111956511 G>T maps to NM_019114.3 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:112018504 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:111936880 G>A maps to NM_019114.3 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:112004013 G>A maps to NM_018424.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:111962561 C>A maps to NM_019114.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:120885287 G>A maps to NM_020909.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:120831674 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:120848000 G>T maps to NM_020909.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:43489634 G>C maps to NM_000119.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:43513010 C>A maps to NM_000119.2 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:43507497 G>T maps to NM_000119.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr15:43494130 G>A maps to NM_000119.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr15:43494106 G>T maps to NM_000119.2 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:32594781 T>A maps to NM_025209.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:32561035 C>T maps to NM_025209.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:47601118 G>A maps to ENST00000426238 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:47600709 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:37960402 G>A maps to NM_017549.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:75178860 T>A maps to ENST00000413830 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143096453 C>T maps to NM_005232.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:143098638 T>A maps to NM_005232.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:143096456 G>A maps to NM_005232.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:38227521 G>A maps to NM_001099439.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:38201006 G>A maps to NM_001099439.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:38227455 C>T maps to NM_001099439.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:38227380 C>T maps to NM_001099439.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:38227422 C>T maps to NM_001099439.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:38230654 C>T maps to NM_001099439.1 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:38184331 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:38227380 C>T maps to NM_001099439.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:38227569 C>A maps to NM_001099439.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:38227512 G>T maps to NM_001099439.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:38227386 G>T maps to NM_001099439.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:38227287 G>A maps to NM_001099439.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:16464842 C>T maps to NM_004431.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:16459783 C>T maps to NM_004431.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:89498499 A>T maps to NM_005233.5 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:89390123 G>T maps to NM_005233.5 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:89390221 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:89499353 C>A maps to NM_005233.5 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:89448577 C>A maps to NM_005233.5 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:89390950 C>T maps to NM_005233.5 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:89391034 G>T maps to NM_005233.5 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:89391112 G>T maps to NM_005233.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr3:89499478 G>C maps to NM_005233.5 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr3:89259010 G>A maps to NM_005233.5 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:89468361 T>C maps to NM_005233.5 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:89499397 G>T maps to NM_005233.5 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:89521733 C>G maps to NM_005233.5 Y937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr3:89456470 G>A maps to NM_005233.5 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:89390084 C>A maps to NM_005233.5 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:89499487 C>A maps to NM_005233.5 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:89445101 C>A maps to NM_005233.5 Y474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:89390221 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr3:89390959 C>T maps to NM_005233.5 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:89259173 C>A maps to NM_005233.5 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:89499325 G>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr2:222294679 G>T maps to NM_004438.3 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:222322703 G>T maps to NM_004438.3 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:222301813 G>T maps to NM_004438.3 Y701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:222429102 C>A maps to NM_004438.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:66280038 G>T maps to NM_004439.5 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:66535310 G>T maps to NM_004439.5 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:66467643 C>A maps to NM_004439.5 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:66467530 G>T maps to NM_004439.5 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:66201707 A>G maps to NM_004439.5 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:66280008 G>T maps to NM_004439.5 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr4:66467914 G>T maps to NM_004439.5 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:66467427 C>A maps to NM_004439.5 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:66356314 T>A maps to NM_004439.5 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:66270111 G>A maps to NM_004439.5 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr4:66230804 T>A maps to NM_004439.5 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr4:66217255 C>A maps to NM_004439.5 G787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:66467608 G>T maps to NM_004439.5 C220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:66356284 C>T maps to NM_004439.5 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:66270132 G>T maps to NM_004439.5 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:66218758 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:66356383 A>G maps to NM_004439.5 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:66467727 C>A maps to NM_004439.5 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:66361121 G>T maps to NM_004439.5 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:66201746 G>T maps to NM_004439.5 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:66535295 G>T maps to NM_004439.5 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:66286283 C>G did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:66467427 C>A maps to NM_004439.5 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:66509146 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:66213921 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr4:66201746 G>T maps to NM_004439.5 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97311550 G>T maps to NM_001080448.2 G828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:96963114 G>T maps to NM_001080448.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:97185323 C>A maps to ENST00000514100 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:97167417 G>T maps to NM_001080448.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:96706223 C>T maps to NM_001080448.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:97167530 C>A maps to NM_001080448.2 Y617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:97467451 C>T maps to NM_001080448.2 V1100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:97356778 C>A maps to NM_001080448.2 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:97185282 A>T maps to ENST00000514100 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:97202814 T>C maps to NM_001080448.2 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:97167455 C>A maps to NM_001080448.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:96533505 G>T maps to NM_001080448.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr3:97251209 G>T maps to NM_001080448.2 G737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:94066636 C>T maps to NM_004440.3 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:94120813 G>T maps to NM_004440.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:94120642 C>T maps to NM_004440.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:94066482 G>T maps to NM_004440.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:94120261 A>T maps to NM_004440.3 C263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:94120375 G>T maps to NM_004440.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:22915541 G>T maps to NM_020526.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:22927467 C>T maps to NM_020526.3 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:22895779 A>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:22902780 C>T maps to NM_020526.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:22920042 C>A maps to NM_020526.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:22927966 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:22924193 G>C maps to NM_020526.3 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:22927867 G>T maps to NM_020526.3 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:22903329 C>A maps to NM_020526.3 C260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:22903140 C>A maps to NM_020526.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:22924650 G>T maps to NM_020526.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:134898708 A>T maps to NM_004441.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:134920488 C>G maps to NM_004441.4 Y768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:134967156 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:134851646 G>T maps to NM_004441.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:134960129 C>T maps to NM_004441.4 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:134920437 G>T maps to NM_004441.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:134898723 C>G maps to NM_004441.4 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:134873066 G>A maps to NM_004441.4 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:134967255 G>T maps to NM_004441.4 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr3:134670689 C>T maps to NM_004441.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:134880945 G>A maps to NM_004441.4 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:134670793 C>A maps to NM_004441.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:134960098 C>A maps to NM_004441.4 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:134851754 G>C maps to NM_004441.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:134911493 G>T maps to NM_004441.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:134885844 C>A maps to NM_004441.4 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:134968219 G>T maps to NM_004441.4 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:134851772 C>T maps to NM_004441.4 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr3:134851891 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:23191472 C>G maps to ENST00000400191 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:23191569 G>T maps to ENST00000400191 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:23111388 C>T maps to ENST00000400191 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:23239050 C>G maps to ENST00000400191 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:23236972 C>A maps to ENST00000400191 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:184295456 C>T maps to NM_004443.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:184295234 G>T maps to NM_004443.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr3:184294835 G>T maps to NM_004443.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:184290794 G>A maps to NM_004443.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr3:184290476 C>A maps to NM_004443.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:100411605 C>G maps to NM_004444.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:100411611 C>G maps to NM_004444.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:100405019 C>T maps to NM_004444.4 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:100417242 C>A maps to NM_004444.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:100421304 C>A maps to NM_004444.4 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr7:100403235 G>A maps to NM_004444.4 D855D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:100420124 G>A maps to NM_004444.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:100421848 C>A maps to NM_004444.4 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr7:142568572 C>A maps to NM_004445.3 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142565366 G>A maps to NM_004445.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142562016 C>A maps to NM_004445.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:142563341 C>G maps to NM_004445.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:142568608 C>A maps to NM_004445.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr7:142562292 G>T maps to NM_004445.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:142566875 G>T maps to NM_004445.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:142562012 G>A maps to NM_004445.3 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:142563377 C>T maps to NM_004445.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:142566026 C>G maps to NM_004445.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:142566361 G>T maps to NM_004445.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:142566455 G>T maps to NM_004445.3 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:142564290 G>T maps to NM_004445.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr7:142566851 G>T maps to NM_004445.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:142561930 C>A maps to NM_004445.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:142566454 G>C maps to NM_004445.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:226030139 G>T maps to NM_001136018.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:27380004 C>G maps to ENST00000458037 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:27364420 G>T maps to ENST00000458037 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr8:27401270 G>C maps to ENST00000458037 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:27378398 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr19:15338809 G>A maps to NM_001142886.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:92515964 A>T maps to NM_173567.4 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:92511170 G>T maps to NM_173567.4 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:92528641 C>A maps to NM_173567.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:37033586 C>A maps to NM_014805.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:37034181 C>G maps to NM_014805.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr3:37033440 T>C maps to NM_014805.3 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:37033434 A>C maps to NM_014805.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:56196892 C>T maps to NM_001130071.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:56189959 G>A maps to NM_001130071.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:19186824 G>T maps to NM_014964.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr7:100319325 G>A maps to NM_000799.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:144947334 C>A maps to NM_031308.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:144940386 C>G maps to NM_031308.1 T2345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr8:144940512 G>A maps to NM_031308.1 A2303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr8:144946467 G>A maps to NM_031308.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:144944967 C>A maps to NM_031308.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:144943140 G>T maps to NM_031308.1 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr8:144940554 C>G maps to NM_031308.1 A2289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:144943194 C>A maps to NM_031308.1 R1409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr8:144940911 T>C maps to NM_031308.1 K2170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:144941166 C>A maps to NM_031308.1 V2085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:220153471 T>C maps to NM_004446.2 T1222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:51875245 G>T maps to NM_001981.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:51829697 G>C maps to NM_001981.2 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:51913717 C>A maps to NM_001981.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:16487936 G>C maps to ENST00000455140 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16535929 C>A maps to ENST00000455140 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr19:16548579 C>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr19:16504810 G>A maps to ENST00000455140 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:16515464 C>T maps to ENST00000455140 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:16539512 C>A maps to ENST00000455140 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:15774345 C>A maps to NM_004447.5 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:55597559 G>A maps to NM_133180.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:55591905 C>T maps to NM_017729.3 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:722495 C>A maps to NM_022772.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:721683 G>T maps to NM_022772.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:726340 C>T maps to NM_022772.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:721611 G>T maps to NM_022772.3 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:724777 C>T maps to NM_022772.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:720163 C>T maps to NM_022772.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110294766 C>T maps to NM_139053.1 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:110300459 G>A maps to NM_139053.1 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr1:110300958 G>T maps to NM_139053.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:43462493 G>T maps to NM_001002264.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr13:43500531 T>A maps to NM_001002264.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:56277674 C>A maps to NM_000502.4 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56272419 C>T maps to NM_000502.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56280469 G>A maps to NM_000502.4 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:56280503 C>A maps to NM_000502.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:56274427 C>T maps to NM_000502.4 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:56270729 A>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:56274463 G>A maps to NM_000502.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:56277622 C>T maps to NM_000502.4 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:56277676 G>A maps to NM_000502.4 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr17:56272479 C>T maps to NM_000502.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:56280472 C>T maps to NM_000502.4 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr17:56274298 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:91371910 G>T maps to NM_004950.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:91372012 T>A maps to NM_004950.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:91371880 C>G maps to NM_004950.4 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr17:27182138 G>A maps to NM_005702.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:96139401 G>A maps to NM_016442.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:96239249 G>T maps to NM_001130140.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:96224886 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:96253167 G>A maps to NM_001130140.1 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:48687821 G>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:48687655 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:48687961 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:48687840 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:48687841 G>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:37876037 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:37865604 C>T maps to NM_004448.2 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr17:37871592 G>A maps to NM_004448.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:37866372 C>T maps to NM_004448.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr17:37866339 G>T maps to NM_004448.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:65334266 G>A maps to ENST00000506030 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:56487889 C>T maps to NM_001982.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:56488238 G>C maps to NM_001982.2 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:56479038 A>T maps to NM_001005915.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:56493519 G>A maps to NM_001982.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:56477556 C>G maps to NM_001982.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:212288913 G>T maps to NM_005235.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:212248510 G>A maps to NM_005235.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:212522552 C>A maps to NM_005235.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:212251682 G>A maps to NM_005235.2 Q1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:212530124 C>T maps to NM_005235.2 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:212537982 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:212251643 G>T maps to NM_005235.2 R1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:212589908 C>T maps to NM_005235.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:212589919 C>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:212251616 C>A maps to NM_005235.2 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:213403194 G>T maps to NM_005235.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr2:212589823 C>A maps to NM_005235.2 G240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:212578299 C>A maps to NM_005235.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:212537945 C>A maps to NM_005235.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:212426696 C>T maps to NM_005235.2 E806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:212248725 G>A maps to NM_005235.2 Q1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:212587157 T>G maps to NM_005235.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:212652752 C>A maps to NM_005235.2 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:1137188 G>T maps to NM_178040.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:1289830 C>T maps to NM_178040.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr12:1346069 G>A maps to NM_178040.2 Q829Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:1481100 G>A maps to NM_178040.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:1291231 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:1192398 C>T maps to NM_178040.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:56468699 T>A maps to ENST00000460849 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:56468915 T>A maps to ENST00000460849 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr3:55768824 G>T maps to ENST00000460849 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr3:55733404 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:45923667 C>T maps to NM_202001.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:45912959 C>G maps to NM_001983.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:128018851 G>A maps to NM_000122.1 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:128050383 T>A maps to NM_000122.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:14028124 A>T maps to NM_005236.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr13:103527857 C>T maps to NM_000123.2 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr13:103518707 G>T maps to NM_000123.2 G766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:50667199 G>A maps to NM_000124.2 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:50736570 C>A maps to ENST00000515869 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr10:50732560 T>A maps to ENST00000515869 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr10:50667127 T>C maps to NM_000124.2 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:50691562 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr10:50681629 G>A maps to NM_000124.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr10:50732791 G>A maps to ENST00000515869 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:50686482 G>A maps to NM_000124.2 R735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:71426903 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:71425004 T>C did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:71425454 T>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:71425015 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:71428456 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:71426846 T>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr23:71427305 C>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:71428460 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:71424864 C>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:71424944 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:71427654 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:71425636 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:60183311 C>A maps to NM_000082.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:75246764 G>A maps to NM_001432.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:75246776 G>A maps to NM_001432.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:42753390 G>A maps to NM_006494.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:29524530 C>T maps to NM_016570.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr12:29498438 C>A maps to NM_016570.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr14:69847287 G>A maps to NM_004450.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:44820665 C>T maps to NM_024066.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:44750539 C>T maps to NM_024066.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:618724 C>A maps to NM_207332.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:54045060 C>A maps to NM_015701.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:54041745 T>A maps to NM_015701.3 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr8:37611492 A>T maps to NM_007175.6 K294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:37602156 G>T maps to NM_007175.6 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158178130 G>A maps to NM_001009959.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:158178193 C>T maps to NM_001009959.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:158178033 G>T maps to NM_001009959.1 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5805686 C>T maps to NM_024896.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:62135164 G>A maps to NM_001433.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:62131672 G>T maps to NM_001433.3 C630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:62131639 G>A maps to NM_001433.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:62175544 C>T maps to NM_001433.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr17:62131717 C>A maps to NM_001433.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:62144143 G>A maps to NM_001433.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:23718373 C>T maps to NM_033266.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr16:23716364 G>T maps to NM_033266.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:23712311 G>A maps to NM_033266.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:23713532 C>A maps to NM_033266.3 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:23718102 G>A maps to NM_033266.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:23713520 T>C maps to NM_033266.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:23718358 G>C maps to NM_033266.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:23718183 T>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:23722321 T>A maps to NM_033266.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:23713777 G>C maps to NM_033266.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:23713795 G>A maps to NM_033266.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:23706078 C>T maps to NM_033266.3 E738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:23724580 C>T maps to NM_033266.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:23713771 G>T maps to NM_033266.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:23702674 G>A maps to NM_033266.3 C864C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr16:23702632 C>T maps to NM_033266.3 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:23706574 C>A maps to NM_033266.3 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:23711920 C>A maps to NM_033266.3 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:53119001 C>T maps to NM_014584.1 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:53119805 C>A maps to NM_014584.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:236399087 C>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:236384261 G>A maps to NM_019891.3 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:112460059 C>T maps to NM_006817.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:102814755 C>A maps to NM_015051.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr9:102861098 G>A maps to NM_015051.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:8074128 G>C maps to NM_018948.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr18:19146167 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr18:19110321 A>G maps to NM_052911.2 N835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr18:19153653 G>C maps to NM_052911.2 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr18:19147949 T>A maps to NM_052911.2 K546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13714430 C>A maps to NM_016649.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:13695815 T>A did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr20:13753261 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:54281294 C>T maps to NM_007036.4 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:53663491 T>C maps to NM_012291.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:53663689 C>T maps to NM_012291.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr12:53684208 C>T maps to NM_012291.4 R1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:53673604 C>T maps to NM_012291.4 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:53686093 G>A maps to NM_012291.4 V1943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:53687195 C>T maps to NM_012291.4 R2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:53670893 C>T maps to NM_012291.4 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:6511765 G>A maps to NM_031475.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:239040096 C>T maps to NM_194312.2 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:239040063 C>T maps to NM_194312.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:239025608 G>C maps to NM_194312.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:239039221 C>A maps to NM_194312.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:239039106 C>A maps to NM_194312.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152265374 C>A maps to NM_001122741.1 G276G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-8119-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:152129106 G>C maps to NM_001122741.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr6:152201856 C>A maps to NM_001122741.1 C237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr6:152129052 C>A maps to NM_001122741.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:152129211 C>T maps to NM_001122741.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:64735615 A>G maps to NM_001437.2 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:64727422 C>T maps to NM_001437.2 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:95680240 G>T maps to NM_017697.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:68265393 G>C maps to NM_024939.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:68265156 T>G maps to NM_024939.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:76928948 G>A maps to NM_004452.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:76966234 C>T maps to NM_004452.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr14:76906055 C>T maps to NM_004452.3 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:216824330 C>G maps to NM_001438.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:216737684 C>T maps to NM_001438.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216850619 G>T maps to NM_001438.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:216850757 G>T maps to NM_001438.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:216737621 T>A maps to NM_001438.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:216850478 C>A maps to NM_001438.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:216850649 G>A maps to NM_001438.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:216850550 C>T maps to NM_001438.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:216737648 G>T maps to NM_001438.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:216850616 C>A maps to NM_001438.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:216850420 G>A maps to NM_001438.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:216741351 C>A maps to NM_001438.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:103495019 C>G did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:103495004 C>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:103495441 C>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:103498979 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:103495447 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:103498884 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:103495384 C>G did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:103495259 G>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:103497485 T>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:103494975 C>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:103499224 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:103495213 A>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:103495216 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:103494997 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56531638 C>G maps to NM_001184796.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:158552763 C>G maps to NM_020728.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:158580784 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:158531730 C>G maps to NM_020728.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:158534325 G>A maps to NM_020728.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:138188970 G>T maps to NM_031913.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr3:138188930 G>A maps to NM_031913.3 W511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:138183185 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:67632269 C>A maps to NM_019002.3 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:67630779 G>A maps to NM_019002.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:51853646 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:159627913 G>A maps to NM_004453.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:159601638 T>C maps to NM_004453.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr4:159627455 G>C maps to NM_004453.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:22824221 T>C maps to NM_018638.4 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr12:22813995 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:22778505 G>T maps to NM_018638.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:204110461 G>A maps to NM_018208.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128333508 G>T maps to NM_001143820.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:128359245 G>A maps to NM_001143820.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:128356000 G>C maps to NM_001143820.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:128359202 G>A maps to NM_001143820.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:128360369 G>A maps to NM_001143820.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:40194595 A>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr21:40191521 C>T maps to NM_005239.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:13971168 G>A maps to NM_004956.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:13971304 A>G maps to NM_004956.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr7:13971232 G>A maps to NM_004956.4 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:13950918 G>A maps to NM_004956.4 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:36133535 C>T maps to ENST00000222279 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:157106123 G>A maps to NM_001145312.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157069147 G>T maps to NM_001004341.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:157062485 G>T maps to NM_001004341.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:157068985 G>T maps to NM_001004341.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:41622669 C>T maps to NM_001079675.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:12022454 G>C maps to NM_001987.4 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:12022773 G>T maps to NM_001987.4 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:36334710 C>G maps to NM_016135.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:5721079 A>T maps to NM_153717.2 K94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:5812715 G>T maps to NM_153717.2 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:5811336 A>T maps to NM_153717.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr4:5800410 G>A maps to NM_153717.2 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:5754651 G>T maps to NM_153717.2 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr4:5754639 G>A maps to NM_153717.2 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr4:5755632 G>A maps to NM_153717.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:5755572 G>T maps to NM_153717.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr4:5800494 G>T maps to NM_153717.2 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr4:5798754 G>T maps to NM_153717.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:5758008 G>T maps to NM_153717.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:5733208 T>C maps to NM_153717.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:5642296 T>A maps to NM_147127.4 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:5564842 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:5586495 G>A maps to NM_147127.4 Q971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:5570313 C>A maps to NM_147127.4 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr4:5624430 C>T maps to NM_147127.4 E778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:5624460 C>A maps to NM_147127.4 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:29632168 G>T maps to NM_006495.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:93170109 A>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:93091371 C>T maps to NM_005665.4 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:7916417 C>T maps to NM_001159944.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:100563831 T>C maps to NM_016337.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:74003852 G>A maps to NM_001988.2 F1811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:74005010 G>A maps to NM_001988.2 F1425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr17:74006261 C>T maps to NM_001988.2 K1008K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr17:74007748 C>A maps to NM_001988.2 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr17:74019390 G>A maps to NM_001988.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr17:74005484 C>A maps to NM_001988.2 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:18284946 G>A maps to NM_001145127.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:18286155 G>C maps to NM_001145127.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:18286156 G>T maps to NM_001145127.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:18285003 G>C maps to NM_001145127.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:27282822 G>A maps to NM_001989.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:27283044 C>A maps to NM_001989.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:27285815 C>A maps to NM_001989.3 Y332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:27285722 C>T maps to NM_001989.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:176945401 C>T maps to NM_001080458.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr2:176947073 C>T maps to NM_001080458.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr2:176948243 G>T maps to NM_001080458.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:176946953 G>C maps to NM_001080458.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:176946938 G>T maps to NM_001080458.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:176948096 A>T maps to NM_001080458.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr22:29668238 G>A maps to NM_013986.3 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr15:41476287 T>C maps to NM_152596.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:69703223 G>T maps to NM_001193363.1 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:69695690 T>A maps to NM_001193363.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:242035503 A>T maps to NM_006027.4 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:242042434 C>T maps to NM_006027.4 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:242030244 A>T maps to NM_006027.4 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:242035553 A>T maps to NM_006027.4 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:242035580 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:242042435 C>A maps to NM_006027.4 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:56726658 A>G maps to NM_018261.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:56724546 C>T maps to NM_018261.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:56726644 A>T maps to NM_018261.3 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:56738124 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:486757 C>G maps to NM_018303.4 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:572553 C>T maps to NM_018303.4 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:497486 C>T maps to NM_018303.4 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:637752 C>T maps to NM_018303.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:637807 G>T maps to NM_018303.4 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:549212 C>A maps to NM_018303.4 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr6:532538 G>T maps to NM_018303.4 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:556007 G>A maps to NM_018303.4 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:454085 G>T maps to ENST00000315013 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:453845 G>A maps to ENST00000315013 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:457102 G>T maps to ENST00000315013 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr5:458015 C>G maps to ENST00000315013 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:466931 A>T maps to ENST00000315013 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr5:446388 G>A maps to ENST00000315013 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:453845 G>A maps to ENST00000315013 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:453716 G>T maps to ENST00000315013 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr16:67221374 G>A maps to NM_178516.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:45721529 C>T maps to NM_138568.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:45721553 G>T maps to NM_138568.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:45721577 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:45721541 C>T maps to NM_138568.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:45731238 G>A maps to NM_138568.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:132990803 A>G maps to NM_021807.3 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:132937928 C>G maps to NM_021807.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:94688134 A>T maps to NM_019053.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:94679737 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:94818034 C>T maps to NM_019053.4 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:94594582 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:72945354 C>T maps to NM_015189.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:72742213 C>T maps to NM_015189.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:72802698 T>A maps to NM_015189.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:74099486 G>A maps to NM_001145297.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:74080605 C>A maps to NM_001145297.2 G641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:74080606 C>A maps to NM_001145297.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:74084854 G>C maps to NM_001145297.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:231473127 C>A maps to NM_175876.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:231472294 G>A maps to NM_175876.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:38548420 C>T maps to NM_005107.3 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:99203014 C>G maps to NM_016046.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:11159854 G>A maps to NM_001001998.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:133569300 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:37780831 G>C maps to NM_016042.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr8:145134931 C>T maps to NM_019037.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr13:37583434 A>T maps to NM_181503.2 *277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:122722598 C>G maps to NM_001034194.1 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:122734442 A>T maps to NM_001034194.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr4:122723065 G>T maps to NM_001034194.1 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr4:122724172 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:108380886 G>A maps to NM_015065.2 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:108381672 C>A maps to NM_015065.2 E1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:108380299 G>C maps to NM_015065.2 Y1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:108382213 T>A maps to NM_015065.2 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:108382615 T>A maps to NM_015065.2 S1206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:108381279 C>A maps to NM_015065.2 E1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:108385582 G>A maps to NM_015065.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:118831992 C>A maps to NM_000127.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:119123234 G>A maps to NM_000127.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:44265762 C>T maps to NM_000401.3 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:44129288 C>T maps to NM_000401.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:28574376 G>T maps to NM_001440.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:28573839 G>T maps to NM_001440.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:28574047 C>T maps to NM_001440.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr8:28574373 G>A maps to NM_001440.2 W266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:72184100 G>T maps to NM_000503.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:72127697 T>G maps to NM_000503.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:72229802 G>A maps to NM_000503.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:72211874 G>A maps to NM_000503.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:72111604 C>A maps to NM_000503.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:72111643 G>T maps to NM_000503.4 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72127687 T>A maps to NM_000503.4 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr8:72267065 G>A maps to NM_000503.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:72182001 A>C maps to NM_000503.4 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:72184040 C>A maps to NM_000503.4 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr8:72111649 C>T maps to NM_000503.4 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:45717914 G>A maps to ENST00000360649 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:45702912 C>A maps to ENST00000360649 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:28362170 G>C maps to NM_001990.2 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:133785996 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:133836474 C>A maps to ENST00000452339 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:133783562 C>A maps to ENST00000452339 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr6:133767824 T>C maps to ENST00000452339 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115102 T>A maps to ENST00000370616 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:66115228 A>G maps to ENST00000370616 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:66054070 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:66005980 A>G maps to ENST00000370616 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:66204802 C>A maps to ENST00000370616 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:66115211 C>T maps to ENST00000370616 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:66044985 C>A maps to ENST00000370616 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:66094393 C>G did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:66205195 G>T maps to ENST00000370616 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:66063350 C>A maps to ENST00000370616 G487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:66205156 G>T maps to ENST00000370616 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:66205195 G>T maps to ENST00000370616 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:66112478 G>T maps to ENST00000370616 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr6:66054008 G>T maps to ENST00000370616 C507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr6:66205099 A>T maps to ENST00000370616 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr6:66063423 T>A maps to ENST00000370616 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:66112375 A>T maps to ENST00000370616 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:66063350 C>A maps to ENST00000370616 G487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:40872351 C>T maps to ENST00000264646 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:40857174 C>T maps to ENST00000264646 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:148544311 T>A maps to NM_004456.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:159206351 C>T maps to NM_001111077.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr6:159188460 G>A maps to NM_001111077.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:160970031 G>C maps to NM_016946.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176831230 C>T maps to NM_000505.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:176832079 G>A maps to NM_000505.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:176830338 G>A maps to NM_000505.3 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:176830357 C>T maps to NM_000505.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:6175038 G>A maps to NM_000129.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:6305707 G>A maps to NM_000129.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:6175085 T>G maps to NM_000129.3 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:6145983 G>T maps to NM_000129.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:6266854 G>C maps to NM_000129.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:6266976 C>A maps to NM_000129.3 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:6225018 C>T maps to NM_000129.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:6152140 T>A maps to NM_000129.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr6:6174855 T>C maps to NM_000129.3 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr6:6145902 T>C maps to NM_000129.3 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:6318846 G>A maps to NM_000129.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:6182292 T>A maps to NM_000129.3 K463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:6167689 C>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:6196056 T>C maps to NM_000129.3 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:6266992 G>C maps to NM_000129.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:6175038 G>T maps to NM_000129.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:6305758 G>C maps to NM_000129.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:197021762 C>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:197036344 C>T maps to NM_001994.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:197009737 T>A maps to NM_001994.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:197029494 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:197031045 A>G maps to NM_001994.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:197021820 C>A maps to NM_001994.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:197019965 T>A maps to NM_001994.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:197026188 C>T maps to NM_001994.2 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:197026414 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:197025027 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:197024934 C>A maps to NM_001994.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:197019869 G>A maps to NM_001994.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:197021788 C>T maps to NM_001994.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:197030944 C>T maps to NM_001994.2 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:197026509 T>A maps to NM_001994.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:46750357 G>T maps to NM_000506.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:76028403 A>T maps to NM_001992.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:76029213 C>A maps to NM_001992.3 C388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:75914018 G>A maps to NM_004101.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:75913973 G>T maps to NM_004101.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:75914183 C>T maps to NM_004101.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:94998771 C>G maps to NM_001993.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:169492509 T>C maps to ENST00000367796 T1996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:169489848 T>A maps to ENST00000367796 P2039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:169511450 G>T maps to ENST00000367796 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:169510784 G>T maps to ENST00000367796 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:169526010 G>T maps to ENST00000367796 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:169511382 C>T maps to ENST00000367796 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:169510972 G>A maps to ENST00000367796 Q1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:169511239 G>A maps to ENST00000367796 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:169528469 C>T maps to ENST00000367796 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:169493095 A>T maps to ENST00000367796 Y1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:169519077 T>A maps to ENST00000367796 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:169510439 T>C maps to ENST00000367796 P1301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:169519149 G>A maps to ENST00000367796 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:169528502 C>A maps to ENST00000367796 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr1:169529933 G>T maps to ENST00000367796 Y148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:113772898 G>C maps to NM_000131.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr13:113768230 C>T maps to NM_000131.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:113771896 G>T maps to NM_000131.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:113773183 C>A maps to NM_000131.3 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr13:113773000 C>A maps to NM_000131.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:113771152 G>A maps to NM_000131.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:154065971 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:154225252 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:154157321 C>A did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr23:154128188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:154159069 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:154088833 T>C did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:154157831 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:154157975 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:154156921 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:154132271 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:154157068 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:154065929 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:154157434 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:154158603 T>C did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:154227863 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:154157793 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:154157621 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr23:154157941 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:154157089 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:154182271 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:154157134 T>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:154194881 C>G did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:154158120 C>T did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr23:154159065 G>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:154197710 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:154221308 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:154157497 C>G did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr23:154197822 C>G did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:154091368 C>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:154158271 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:154132599 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:154158124 T>C did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:154221272 T>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:154225367 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:154156963 C>T did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:154159594 A>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:154159042 C>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:154133103 A>C did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:154159112 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:154133183 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:154091474 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:154157596 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:154157733 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:154158693 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:154225289 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:154158631 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr23:154088754 A>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:154158689 T>G did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:154225358 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:154250790 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:154157365 T>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:154128183 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:154221351 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:154213043 C>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:154159699 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:154132668 T>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:154158166 C>A did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr23:154185267 G>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:154130389 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:154158986 T>C did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:154065907 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:154158071 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:154159814 C>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:154176161 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:154132243 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:138623302 G>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:138612945 T>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:138644073 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:138644076 T>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:138642943 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:138644186 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:138633376 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:138643680 A>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:138630530 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:138643881 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:138642898 G>T did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr23:138630557 A>G did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:138643930 G>C did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:138633337 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:138612956 C>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:138633375 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:138644048 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:138643698 G>T did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:138643871 A>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:138642966 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:138642935 G>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:138644085 C>G did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:138644089 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:138612973 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:46867857 C>T maps to NM_001441.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:46871355 C>T maps to NM_001441.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:46871922 C>G maps to NM_001441.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:46871940 C>T maps to NM_001441.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:57318977 C>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:57337122 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:57337067 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:57405213 C>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:57405082 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:57407422 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:88425739 C>T maps to NM_001443.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:88424069 C>T maps to NM_001443.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr2:88424033 G>A maps to NM_001443.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:82441717 C>A maps to NM_001105281.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:82441684 G>T maps to NM_001105281.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:82437305 G>T maps to NM_001105281.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:82195598 A>G did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:159640747 G>A maps to NM_001040442.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:70052377 G>T maps to NM_003824.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:70049624 G>A maps to NM_003824.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr11:61579954 G>A maps to NM_013402.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:61608000 C>T maps to NM_004265.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:61608139 C>G maps to NM_004265.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:61641286 C>A maps to NM_021727.3 *446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr11:61644994 G>A maps to NM_021727.3 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr11:61645009 C>T maps to NM_021727.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:72875707 G>A maps to ENST00000310226 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:72888694 G>A maps to ENST00000310226 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:72888697 G>A maps to ENST00000310226 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr17:72888694 G>T maps to ENST00000310226 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:51049382 T>A maps to NM_007051.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:50957419 G>A maps to NM_007051.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:51171477 C>A maps to NM_007051.2 G213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:50941261 G>A maps to NM_007051.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:175919293 G>A maps to NM_014613.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:175923619 C>A maps to NM_014613.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:175927108 C>T maps to NM_014613.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:80445443 C>T maps to NM_000137.1 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:80464561 T>C maps to NM_000137.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:80460462 G>A maps to NM_000137.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr16:1877418 G>A maps to NM_001018104.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:97749975 C>A maps to NM_199336.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:97757242 C>A maps to NM_199336.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:97751934 C>A maps to NM_199336.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:138351857 G>C maps to NM_001033030.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:138340357 C>A maps to NM_001033030.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:50284483 C>A maps to NM_012306.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:50282943 G>A maps to NM_012306.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:50291868 G>A maps to NM_012306.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:50264430 C>A maps to NM_012306.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr12:50284471 G>T maps to NM_012306.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:207087299 A>T maps to NM_005449.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:293212 C>G maps to NM_182705.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:130742371 A>G maps to NM_001035254.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr9:130710648 C>T maps to NM_001035254.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:109167359 T>A maps to NM_001010883.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:55172571 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:55170247 G>C did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:55185585 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:55185585 G>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr5:14601072 G>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:14610341 C>T maps to NM_019018.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:14601319 A>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:14678874 T>C maps to NM_138348.4 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:14681700 C>T maps to NM_138348.4 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:58552960 G>A maps to ENST00000474531 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr3:58552368 G>C maps to ENST00000474531 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:14816389 C>A maps to NM_031453.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14563218 G>C maps to NM_031453.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr9:74481837 G>C maps to NM_016014.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:74477497 C>A maps to NM_016014.2 *294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:111801144 C>T maps to NM_001177996.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:111801042 C>A maps to NM_001177996.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr22:42473528 G>T maps to NM_001002034.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:59059694 C>T maps to NM_147189.2 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:59058926 G>A maps to NM_147189.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:59059079 G>T maps to NM_147189.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:59059643 G>T maps to NM_147189.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr8:59059511 C>T maps to NM_147189.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:45599 C>T maps to NM_001077710.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr2:45668 C>A maps to NM_001077710.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:45521 C>T maps to NM_001077710.2 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:58920199 C>T maps to NM_198847.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:58920346 C>T maps to NM_198847.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:58920301 A>T maps to NM_198847.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:58892466 A>T maps to NM_198947.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr20:2819729 T>C did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr20:2816299 G>T maps to NM_022760.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:47629392 C>A maps to NM_138371.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr12:47629772 C>A maps to NM_138371.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:47629610 G>A maps to NM_138371.1 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:47629133 C>G maps to NM_138371.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:38879975 G>T maps to NM_138389.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38937412 T>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:38945162 G>A maps to NM_138389.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr4:38910316 G>T maps to NM_138389.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:153406764 C>A maps to ENST00000442256 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:153414480 C>G maps to ENST00000442256 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:153407843 C>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:153382472 C>T maps to ENST00000442256 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr5:153381905 G>A maps to ENST00000442256 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:143573179 G>A maps to NM_014719.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr22:50752664 G>C maps to NM_001001794.3 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr17:47794986 G>A maps to NM_030802.3 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:203630352 C>T maps to NM_173511.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:203630378 C>T maps to NM_173511.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:203630412 C>T maps to NM_173511.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr22:45723877 G>C maps to NM_017911.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:208488973 G>T maps to ENST00000272839 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:96278482 C>T maps to ENST00000333936 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:96320267 C>T maps to ENST00000333936 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr9:96320932 G>T maps to ENST00000333936 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr9:96305726 C>T maps to ENST00000333936 H739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:170627005 G>T maps to NM_032448.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:170657263 A>G maps to NM_032448.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:170626879 C>T maps to NM_032448.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:170626894 G>T maps to NM_032448.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr6:170632318 C>G maps to NM_032448.1 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr6:170627218 A>G maps to NM_032448.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:54159203 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:54161288 C>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:54209078 G>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:54209177 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:54209049 C>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:54160417 A>G did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:54107839 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:54107827 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:54159248 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:54161373 A>G did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:54209130 G>C did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:54161385 G>A did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr23:54107802 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:133922823 G>T did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr23:133941654 T>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:133988157 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25744118 G>T maps to NM_152704.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr13:25744257 G>A maps to NM_152704.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:25744473 C>A maps to NM_152704.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:25744193 C>A maps to NM_152704.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:25744311 G>T maps to NM_152704.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:63411862 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:63410855 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:63411302 C>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:63411300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:63411365 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:63412180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:63412181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:63412037 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:63409900 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:63412938 T>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:63411088 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:63412784 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:63411429 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:63410827 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:63411981 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:63409825 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:63410733 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:63413105 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:63412379 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:63411179 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:63412890 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:63410714 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:63409802 T>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:63412795 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:63412376 C>G did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:63411356 A>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:63411910 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:63410467 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:63411141 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:63412079 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:63412080 C>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:63412532 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:63411864 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:63410256 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:63410390 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:63412014 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:63412878 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:63411834 A>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:63410546 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:63411897 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:63412646 T>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:63411186 G>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:63410528 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:63412927 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:63411317 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:63410914 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:63411754 T>C did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:63412427 G>C did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:131521153 C>A maps to NM_001105195.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:131520420 C>A maps to NM_001105195.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:131521381 C>A maps to NM_001105195.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131520622 C>T maps to NM_001105195.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:131520565 C>T maps to NM_001105195.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr2:131521594 C>T maps to NM_001105195.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:131521385 G>T maps to NM_001105195.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:131520172 G>T maps to NM_001105195.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:131519959 G>C maps to NM_001105195.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:131521417 G>T maps to NM_001105195.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:131520862 C>A maps to NM_001105195.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:131521516 A>T maps to NM_001105195.1 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:131520208 G>A maps to NM_001105195.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:131520082 C>T maps to NM_001105195.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:131520776 G>T maps to NM_001105195.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:131521631 G>T maps to NM_001105195.1 G663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:131521309 G>T maps to NM_001105195.1 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:131521156 C>A maps to NM_001105195.1 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr13:51805510 G>T maps to NM_145019.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr13:51855295 C>A maps to NM_145019.2 C551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr13:51854786 C>T maps to NM_145019.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:225266346 G>T maps to NM_001122779.1 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:17534378 C>G maps to NM_138401.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:22985288 T>A maps to NM_032581.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:22999961 G>A maps to NM_032581.3 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:201857027 T>A maps to NM_173822.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:201853121 G>C maps to NM_173822.3 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:134166553 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:134166460 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:134166522 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:134166646 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:134186108 G>T did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:134186111 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:134156365 C>G did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:134156333 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:134156203 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:134156228 C>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:134156268 C>G did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:134156269 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:134156352 T>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:134156259 A>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:132241749 G>A maps to NM_001085365.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:130948087 G>A maps to ENST00000409255 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:130948088 G>T maps to ENST00000409255 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:184764488 G>A maps to NM_052966.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:184767323 C>A maps to NM_052966.2 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:184764686 C>T maps to NM_052966.2 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:184764143 C>T maps to NM_052966.2 Q918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:184764796 C>A maps to NM_052966.2 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:184764953 G>A maps to NM_052966.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:184777291 G>A maps to NM_052966.2 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:130270747 C>A maps to NM_022833.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr9:130289574 G>A maps to NM_022833.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:17660251 G>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr19:17644448 G>T maps to ENST00000335393 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:17653057 G>T maps to ENST00000335393 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:17644490 T>C maps to ENST00000335393 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:184062427 G>T maps to NM_144635.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:143053909 G>A maps to NM_001031690.2 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr7:143053837 C>A maps to NM_001031690.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:143053717 G>A maps to NM_001031690.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr7:143055983 C>G maps to NM_001031690.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:143053912 T>A maps to NM_001031690.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:92965006 G>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:92964467 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:92964562 G>C did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:92965125 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:92964539 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:92965024 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:92964819 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:92964478 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:220047171 G>T maps to NM_024293.4 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:16481130 G>A maps to NM_001034850.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr5:16616834 G>C maps to NM_001034850.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:16572212 T>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:16477888 G>A maps to NM_001034850.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:16477805 G>C maps to NM_001034850.1 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:16475068 G>A maps to NM_001034850.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:40761279 G>A maps to NM_178126.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr6:71190693 C>A maps to NM_001162529.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:71235312 T>C maps to NM_001162529.1 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:71234772 T>C maps to NM_001162529.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr6:71242878 C>T maps to NM_001162529.1 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:71236167 T>C maps to NM_001162529.1 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:139158254 C>A maps to NM_015912.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:139255225 A>G maps to NM_015912.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:139263163 G>T maps to NM_015912.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:139153549 G>T maps to NM_015912.3 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:139164944 C>A maps to NM_015912.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:139160790 G>A maps to NM_015912.3 H1140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:139209900 G>A maps to NM_015912.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:139268930 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:139155346 G>A maps to NM_015912.3 D1182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:139165276 C>A maps to NM_015912.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:139155261 G>T maps to NM_015912.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:139164563 A>G maps to NM_015912.3 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:139278032 C>A maps to NM_015912.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:139165276 C>A maps to NM_015912.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:139209828 A>T maps to NM_015912.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:139164092 G>T maps to NM_015912.3 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139164526 C>A maps to NM_015912.3 G731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:139268978 T>A maps to NM_015912.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:139263226 G>T maps to NM_015912.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:139380194 G>T maps to NM_015912.3 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:139164173 G>T maps to NM_015912.3 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr8:139277944 C>G did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:139160903 T>A maps to NM_015912.3 K1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:139164689 G>T maps to NM_015912.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:139164584 C>A maps to NM_015912.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:139158276 G>T maps to NM_015912.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:139163633 C>A maps to NM_015912.3 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:139163753 A>T maps to NM_015912.3 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:139164698 G>C maps to NM_015912.3 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr8:139255182 A>G did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr8:139165448 C>T maps to NM_015912.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:139180141 C>T maps to NM_015912.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr8:139164869 A>G maps to NM_015912.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr8:139160883 T>C maps to NM_015912.3 E1109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:139209822 C>A maps to NM_015912.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:139144922 G>A maps to NM_015912.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:139158276 G>C maps to NM_015912.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:139144988 G>A maps to NM_015912.3 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:139164809 G>T maps to NM_015912.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:139163765 A>T maps to NM_015912.3 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:139180267 G>T maps to NM_015912.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:89950665 G>T maps to NM_014883.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:89772322 G>A maps to NM_014883.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:89660225 C>T maps to NM_014883.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:89649737 C>A maps to NM_014883.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:89680016 T>C maps to NM_014883.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:137346773 G>A maps to NM_016603.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:137354123 G>A maps to NM_016603.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:61014170 C>A maps to ENST00000442566 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:61112107 G>C maps to ENST00000442566 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:61011384 C>T maps to ENST00000442566 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:61022235 C>A maps to ENST00000442566 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:61112134 G>A maps to ENST00000442566 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:61028384 G>A maps to ENST00000442566 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr10:61014164 A>G maps to ENST00000442566 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr4:187088123 C>G maps to ENST00000356371 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:187075717 T>G maps to ENST00000356371 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:187077231 G>T maps to ENST00000356371 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:187078866 G>T maps to ENST00000356371 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:187086566 C>G maps to ENST00000356371 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:187086524 C>T maps to ENST00000356371 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:53454950 C>G did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:55077353 G>T maps to NM_176782.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:55078370 C>A maps to NM_176782.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:177156556 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:177156523 C>A maps to ENST00000425383 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:177161929 C>A maps to ENST00000425383 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:175530278 G>A maps to NM_001079529.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:175530279 G>T maps to NM_001079529.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:175528063 C>T maps to NM_001079529.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:175530273 G>T maps to NM_001079529.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:175528580 G>T maps to NM_001079529.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:175530233 G>T maps to NM_001079529.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:177466386 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:18928120 G>A maps to NM_153707.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr9:18950802 C>T maps to NM_153707.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr9:18928736 G>T maps to NM_153707.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:18929018 C>T maps to NM_153707.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:18928801 C>A maps to NM_153707.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:18928120 G>A maps to NM_153707.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr9:18941821 A>T maps to NM_153707.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr15:82574553 A>T maps to NM_001008226.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr13:108518770 G>A maps to NM_001080396.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:108518056 C>A maps to NM_001080396.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr13:107862935 A>G maps to NM_001080396.2 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:68749570 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:68725731 A>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:68725733 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr23:68749636 G>T did not map to a codon.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr23:68725634 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:68749733 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:68749625 G>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:68725550 G>T did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr23:68749485 A>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:68749662 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:68725527 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:68749623 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:6240208 C>A maps to NM_032127.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:6240219 G>A maps to NM_032127.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:6245629 G>C maps to NM_032127.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:6245022 C>A maps to NM_032127.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr11:6244450 G>C maps to NM_032127.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:116621055 A>T maps to NM_020940.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:62066779 C>A maps to ENST00000404929 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:62066701 A>G maps to ENST00000404929 D479D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:74401000 C>T maps to NM_152445.1 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr14:74409271 G>A maps to NM_152445.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:122126161 C>T maps to NM_014367.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:179783245 C>T maps to NM_173509.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:136444266 C>A maps to NM_001080515.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr8:79609709 G>A maps to NM_016010.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:75537518 G>C maps to NM_024643.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75537607 C>G maps to NM_024643.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:75538400 C>T maps to NM_024643.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:75537425 G>A maps to NM_024643.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:11301838 G>T maps to NM_053279.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr2:131829434 G>A maps to NM_001009993.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:74109749 C>G maps to NM_015566.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr15:98995156 G>A maps to NM_182562.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:98995129 C>G maps to NM_182562.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:98995108 T>A maps to NM_182562.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr15:98995201 C>A maps to NM_182562.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:118970309 G>A maps to ENST00000420106 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:118969671 C>T maps to ENST00000420106 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:118970246 A>T maps to ENST00000420106 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15296878 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:15256191 G>T maps to NM_001010924.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr10:15263030 A>T maps to NM_001010924.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:15255672 C>A maps to NM_001010924.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr10:15256428 C>T maps to NM_001010924.1 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:15290662 C>A maps to NM_001010924.1 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:15290740 C>T maps to NM_001010924.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:15256601 T>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:15255468 C>A maps to NM_001010924.1 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr10:15326030 G>A maps to NM_001010924.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:15256341 G>C maps to NM_001010924.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:15255360 A>T maps to NM_001010924.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:187626437 C>A maps to NM_177454.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:187627262 C>T maps to NM_177454.3 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:187626988 T>A maps to NM_177454.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:187627400 G>T maps to NM_177454.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:187604952 A>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:187627078 C>A maps to NM_177454.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:187627366 A>T maps to NM_177454.3 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr16:771922 C>T maps to NM_023933.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:10227602 C>A maps to NM_199133.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:84393380 G>A maps to NM_139076.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:222922903 G>A maps to NM_207468.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:222920373 G>T maps to NM_207468.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:222923345 G>C maps to NM_207468.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr10:102706854 G>A maps to NM_001136123.1 W998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr10:102721666 T>C maps to NM_018121.3 *1174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:102677017 G>A maps to NM_001136123.1 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:102683759 A>G maps to NM_001136123.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:97543649 G>A maps to ENST00000417561 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:29222071 C>T maps to NM_199280.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:29247039 C>T maps to NM_199280.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:29274844 G>C maps to NM_199280.2 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:29225483 G>A maps to NM_199280.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:45481231 T>G maps to ENST00000361462 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:45475265 G>A maps to ENST00000361462 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:45523632 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr14:45501513 A>G maps to ENST00000361462 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:45523677 A>G maps to ENST00000361462 R1495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr14:45431674 C>T maps to ENST00000361462 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:135418890 G>T maps to NM_205855.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:135418862 G>A maps to NM_205855.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:135418830 G>T maps to NM_205855.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr7:135418866 T>A maps to NM_205855.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:94395377 C>A maps to NM_138344.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:94394801 G>T maps to NM_138344.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:94394792 G>T maps to NM_138344.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr14:94394693 C>T maps to NM_138344.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr14:94394960 T>A maps to NM_138344.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:43616453 C>T maps to NM_001101376.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:119301337 G>A maps to NM_024581.4 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:119327767 G>A maps to NM_024581.4 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:49997106 C>T maps to NM_032130.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:35719354 C>A maps to NM_152481.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:15821092 G>A maps to NM_024948.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:15883598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:30915111 A>G maps to ENST00000509504 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:30915195 C>T maps to ENST00000509504 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:30890075 G>A maps to NM_032222.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:30868292 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:30890105 C>T maps to NM_032222.2 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr9:72006542 A>T maps to NM_001127608.1 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:155223709 C>T maps to ENST00000368370 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:155223913 C>T maps to ENST00000368370 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:155217712 C>A maps to ENST00000368370 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:155217713 T>A maps to ENST00000368370 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:15406279 G>A maps to NM_145301.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:15449100 G>A maps to NM_145301.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:91230571 A>G maps to NM_001145065.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:91549340 A>T maps to NM_001145065.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:91645124 G>T maps to NM_001145065.1 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:91229852 G>T maps to NM_001145065.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:86131529 C>A maps to ENST00000372088 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:2661631 A>T maps to ENST00000324666 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:2702198 G>T maps to ENST00000324666 E1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr4:2698292 G>A maps to ENST00000324666 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:176951842 A>G maps to ENST00000442143 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:150377828 C>G maps to NM_152394.3 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:150391822 G>T maps to NM_152394.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:150421643 C>T maps to NM_152394.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr16:698177 C>A maps to NM_138418.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:698149 G>A maps to NM_138418.2 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:128974032 G>C maps to NM_001039762.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr10:128974491 C>T maps to NM_001039762.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:159076789 C>T maps to NM_001128424.1 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:159052015 A>T maps to NM_001128424.1 L425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:159091957 G>T maps to NM_001128424.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr4:159076891 C>T maps to NM_001128424.1 W332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:159091672 G>T maps to NM_001128424.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr4:159092506 C>A maps to NM_001128424.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:103411550 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:103434286 A>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:103434360 C>G did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:103432892 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:103431192 G>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:103431140 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:103431139 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:103420445 G>C did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:103411603 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:103411598 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:68587941 G>T maps to NM_213609.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:62148787 C>A maps to NM_178539.3 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:62104192 G>C maps to NM_178539.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:113266600 C>T maps to NM_001004440.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr22:49042484 G>T maps to ENST00000336769 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:49042449 C>A maps to ENST00000336769 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:179013191 G>A maps to NM_014864.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:47919964 G>T maps to NM_018232.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:46248087 G>C maps to ENST00000399588 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:46222875 G>T maps to ENST00000399588 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:89118102 G>C maps to ENST00000330762 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:89118065 T>A maps to ENST00000330762 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr10:89118183 T>C maps to ENST00000330762 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:97088022 G>C maps to NM_017561.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:97082561 G>A maps to NM_017561.1 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:97088124 G>T maps to NM_017561.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr9:97082699 G>T maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr9:97081022 G>C maps to NM_017561.1 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:124672364 C>A maps to NM_001029888.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:124672367 C>A maps to NM_001029888.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr6:116837031 T>A maps to NM_153711.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr6:116784477 C>A maps to NM_001010919.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:116784477 C>T maps to NM_001010919.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:116784532 C>T maps to NM_001010919.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:88939886 T>C maps to ENST00000298786 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:88911170 C>T maps to ENST00000298786 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:10671679 A>G maps to NM_022068.2 L2701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr18:10696470 G>T maps to NM_022068.2 A2185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr18:10672703 C>T maps to NM_022068.2 G2663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr18:10672736 G>C maps to NM_022068.2 V2652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:10681677 G>A maps to NM_022068.2 Q2474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:10691236 G>C maps to NM_022068.2 L2332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr18:10680251 G>A maps to NM_022068.2 H2519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:10671666 G>T maps to NM_022068.2 R2706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr18:10680335 T>C maps to NM_022068.2 K2491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:153736185 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:42718991 G>T maps to ENST00000398652 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:42729093 A>T maps to ENST00000398652 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr21:42719024 A>C maps to ENST00000398652 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:120991229 C>A maps to NM_014888.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:120991241 G>C maps to NM_014888.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr7:120990538 T>A maps to NM_014888.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:58639443 G>A maps to NM_138805.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr3:58639473 T>A maps to NM_138805.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:58620044 C>A maps to NM_138805.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:110594384 G>A maps to NM_033088.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:110589343 G>T maps to NM_033088.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:129096470 T>A maps to ENST00000450266 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:129099405 G>T maps to ENST00000450266 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:129091574 C>G maps to ENST00000450266 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr7:129093068 T>C maps to ENST00000450266 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr7:129096341 C>T maps to ENST00000450266 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:20879648 G>A maps to NM_207334.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:120889069 A>C maps to NM_207009.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:120882984 C>T maps to NM_207009.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:27332766 G>A maps to NM_052943.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:27332470 C>G maps to NM_052943.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118166263 A>T maps to NM_017709.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:79698552 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:79698583 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:79698088 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:79698090 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:79698194 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:79699122 C>A did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr23:79699184 C>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:79698295 T>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:79698359 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:79698697 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:79698638 G>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:79698668 T>G did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:79698804 A>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:79698949 A>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:79698119 C>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:79699021 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:79698555 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:34148384 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:34148600 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:34149136 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:34149860 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:34149594 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:34148326 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:34150063 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:34148218 T>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:34149362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:34150180 C>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr23:34148897 G>T did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr23:34149051 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:34148421 C>A did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr23:34149570 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:34148839 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:34150080 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:34148120 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:34149639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:34149562 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:34149848 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:34149299 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:34150341 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:34148157 C>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:34148513 G>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:34149550 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:34148617 T>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:34150216 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:34148333 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:34149207 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:34149721 G>C did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:34149859 G>T did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:34149182 T>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:34149659 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:34148497 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:34148957 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:34148839 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:34149389 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:34149088 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:34149653 G>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:34149386 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:34150177 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:34150220 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:34150221 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:34150216 T>C did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:34149572 C>A did not map to a codon.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr23:34148326 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:34148684 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:34149639 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:34149832 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:34150161 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:34149264 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:34149271 A>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:34148019 C>A did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:34148696 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:34149739 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:34149283 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:34149685 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:34150014 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:34149867 G>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:34149868 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:34148132 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:34149194 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:34148119 G>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:34149291 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:34150260 G>T did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr23:34148548 C>G did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:34148073 A>T did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:34148984 G>T did not map to a codon.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr23:34148210 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:34150257 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:34150281 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:34148748 C>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:34148764 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:34149898 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:34149101 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:34149593 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:34150078 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:34148039 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:34149546 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:34961501 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:34961141 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:34961455 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:34961692 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:34961279 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:34961432 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:34962648 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:34961918 C>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:34961909 C>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:34961911 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:34961803 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:34961739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:34961676 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:34961711 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:34961436 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:34961614 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:34961521 C>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:34961735 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:34962202 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:34961092 G>C did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:34960963 C>A did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:34961244 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:34962303 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:34961595 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:34961973 C>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:34961703 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:34961918 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:34962802 G>C did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:34962751 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:34962074 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:34962858 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:34961517 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:34962736 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:34961845 C>G did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:34962817 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:34962492 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:34962612 T>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:34961343 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:34961432 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:34962517 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:34961677 G>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:34961678 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:34961692 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:34962110 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:34962319 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:34961112 G>T did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:34962536 G>C did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:34962537 G>T did not map to a codon.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr23:34962129 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:34961581 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:34962227 C>A did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:34961950 C>A did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:34961811 C>G did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:34962789 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:34961512 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:34962865 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:34961568 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:34961169 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:34961212 G>T did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:34962076 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:34961848 G>T did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:34962454 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:34961215 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:34961123 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:34962664 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:34962885 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:34961617 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:34961692 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:34961935 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:34961214 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:34961163 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:37027143 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:37028189 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:37029324 G>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr23:37028495 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:37027550 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:37028232 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:37028466 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:37028485 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:37027666 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:37026517 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:37027039 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:37029516 A>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:37028541 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:37029163 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:37028941 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:37028014 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:37028756 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:37026966 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:37027513 C>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:37028077 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:37029324 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:37026938 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:37026657 C>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:37028266 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:37027911 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:37026556 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:37029345 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:37027103 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:37026686 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:37028383 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:37028697 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:37028809 C>A did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr23:37027424 C>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:37027567 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:37028862 C>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:37028867 A>G did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:37026573 G>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:37027802 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:37028442 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:37028468 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:37026731 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:37028417 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:37027102 T>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:37028206 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:37028399 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:37028553 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:37028949 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:37027679 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:37028345 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:37026731 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:37028629 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:37028666 G>A did not map to a codon.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37026698 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37026699 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37027117 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37027215 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37027472 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37027473 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:37028280 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:37028889 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:37029545 T>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:37028838 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:37027387 G>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:37028395 G>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr23:37028516 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:37028223 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:37028251 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:37026779 G>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:37027490 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:37027959 A>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:37026966 G>C did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:37027908 C>G did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:37027928 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:37027420 C>G did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:37027648 C>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:37027566 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:37026966 G>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:37028453 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:37028853 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:37028949 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:37027523 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:37027758 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:37593534 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:16740725 A>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:130891659 C>A maps to NM_016623.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153678641 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:153674842 A>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:153678636 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:153678569 A>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:153677102 G>C did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:3850197 G>A maps to NM_012135.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:1657193 C>A maps to NM_001174070.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:126312149 G>C maps to NM_014661.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:136562750 C>A maps to NM_138419.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:26153312 T>C maps to NM_001099626.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114401093 G>C maps to ENST00000424269 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:114393654 G>A maps to ENST00000424269 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:114392896 G>A maps to ENST00000424269 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:114393721 A>G maps to ENST00000424269 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:114550399 T>C maps to NM_182495.5 N16N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:114569356 G>C maps to NM_182495.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:114569275 C>A maps to NM_182495.5 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:114569362 G>A maps to NM_182495.5 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:114569051 G>T maps to NM_182495.5 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:114569408 C>T maps to NM_182495.5 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:101540716 G>T maps to NM_145037.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:114453179 G>T maps to NM_001077639.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:114453674 A>T maps to NM_001077639.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:114453233 C>T maps to NM_001077639.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:114441863 G>T maps to NM_001077639.1 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:114442042 G>T maps to NM_001077639.1 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:30041746 G>A maps to NM_031478.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:30041830 C>A maps to NM_031478.4 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr16:30037143 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr23:152860003 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:29972986 C>A maps to ENST00000269209 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:29867047 C>T maps to ENST00000269209 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:29867398 C>A maps to ENST00000269209 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:29867329 C>A maps to ENST00000269209 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr18:29867443 G>C maps to ENST00000269209 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:177226495 C>A maps to NM_021165.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:177250489 G>T maps to NM_021165.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:177249933 G>A maps to NM_021165.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:177199203 C>T maps to NM_021165.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:177247897 T>A maps to NM_021165.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:177242682 C>A maps to NM_021165.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:177199215 T>C maps to NM_021165.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:177250480 C>T maps to NM_021165.2 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:177199077 G>T maps to NM_021165.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:177242682 C>T maps to NM_021165.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:177249712 C>T maps to NM_021165.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:177226441 G>C maps to NM_021165.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:177199113 C>G maps to NM_021165.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:177250066 C>T maps to NM_021165.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:190203535 C>A maps to NM_199051.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:190067752 C>A maps to NM_199051.1 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:190067231 C>A maps to NM_199051.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:190250804 G>T maps to NM_199051.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:190234117 G>T maps to NM_199051.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:190067567 G>T maps to NM_199051.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:190250720 C>A maps to NM_199051.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:190067912 G>T maps to NM_199051.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:190067975 G>A maps to NM_199051.1 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr1:190068053 G>T maps to NM_199051.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:190067744 C>A maps to NM_199051.1 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:190067231 C>G maps to NM_199051.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:190129907 C>G maps to NM_199051.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:190068002 G>T maps to NM_199051.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr1:190068155 G>A maps to NM_199051.1 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr1:190250880 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:190195449 T>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:190067159 T>C maps to NM_199051.1 K763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:190203574 G>T maps to NM_199051.1 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:190067381 G>T maps to NM_199051.1 Y689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:190234084 C>T maps to NM_199051.1 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:190234089 C>A maps to NM_199051.1 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:190067354 T>A maps to NM_199051.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:190067330 G>A maps to NM_199051.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:190067807 G>T maps to NM_199051.1 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:190423850 G>T maps to NM_199051.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:190423812 C>A maps to NM_199051.1 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:190423903 A>G maps to NM_199051.1 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:190067482 G>T maps to NM_199051.1 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:190068101 G>T maps to NM_199051.1 C449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:31435744 T>C maps to NM_001135812.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:59064388 C>T maps to NM_001040450.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:59064337 C>T maps to NM_001040450.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:59139569 C>T maps to NM_001040450.1 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:6351053 C>A maps to NM_001195228.1 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:67575921 C>A maps to NM_001193523.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr16:67574549 G>A maps to NM_001193523.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:67574537 T>C maps to NM_001193523.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:67576769 C>G maps to NM_001193523.1 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:24843407 C>T maps to NM_014722.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr20:49225885 C>T maps to NM_080829.2 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr20:49218950 G>A maps to NM_080829.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:49232616 C>T maps to NM_080829.2 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr9:139617466 C>G maps to NM_152421.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:139616662 G>A maps to NM_152421.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:72103818 G>T maps to NM_001044369.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr18:72109264 G>A maps to NM_001044369.2 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:119410765 C>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:119410809 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:119438317 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:119427896 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:119438207 A>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:119438294 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:119410884 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr13:114504649 T>A maps to NM_182614.2 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:114514731 G>A maps to NM_182614.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:212798306 C>T maps to NM_153606.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr1:212798864 C>T maps to NM_153606.3 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:156590417 C>T maps to NM_130899.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156589904 C>A maps to NM_130899.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr5:156589538 A>G maps to NM_130899.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr5:156589499 G>C maps to NM_130899.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:100042083 C>A maps to NM_153364.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:100042479 A>G maps to NM_153364.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:100042539 G>A maps to NM_153364.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:100042191 C>A maps to NM_153364.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:100042149 C>A maps to NM_153364.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr14:67665012 C>A maps to NM_173526.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr19:50979474 C>T maps to ENST00000391816 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:50979146 C>T maps to ENST00000391816 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:128363285 C>T maps to NM_032599.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:128369989 C>A maps to NM_032599.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:78338686 A>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:78269058 A>T maps to NM_198549.2 K160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:78269043 G>T maps to NM_198549.2 G155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:78332045 G>T maps to NM_198549.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr9:131802878 G>T maps to NM_032809.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:39887060 G>T maps to ENST00000377642 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:39887510 C>A maps to ENST00000377642 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:39888178 C>A maps to ENST00000377642 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:40705717 T>G maps to NM_001083124.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:40702835 C>T maps to NM_001083124.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:43625487 C>A maps to NM_001145196.1 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:43627705 G>A maps to NM_001145196.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:43627783 A>T maps to NM_001145196.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:43625221 T>C maps to NM_001145196.1 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:43629301 G>T maps to NM_001145196.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:43628677 C>A maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:43627174 T>A maps to NM_001145196.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:43626160 G>A maps to NM_001145196.1 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:43627842 G>T maps to NM_001145196.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:43625383 G>T maps to NM_001145196.1 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:43627842 G>T maps to NM_001145196.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:43627843 G>T maps to NM_001145196.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:43629261 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:43627804 G>A maps to NM_001145196.1 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:43630578 T>A maps to NM_001145196.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:43627644 C>A maps to NM_001145196.1 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:43630515 T>C maps to NM_001145196.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr9:43625071 G>A maps to NM_001145196.1 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr9:43627228 C>A maps to NM_001145196.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:90535242 A>C maps to NM_001145124.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr9:90535184 T>C maps to NM_001145124.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:90535904 C>A maps to NM_001145124.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:90535545 C>A maps to NM_001145124.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:28081708 C>T maps to NM_001143912.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:134136571 G>A maps to NM_033387.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:134151419 G>A maps to NM_033387.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:166039590 G>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:59813561 A>G maps to NM_152450.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:94731843 C>A maps to NM_152548.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:87498775 A>T maps to NM_016033.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:87487183 T>G did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:124204099 G>T maps to NM_032899.4 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:124195476 C>G maps to NM_032899.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:54735196 A>T maps to NM_001010872.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:54806245 C>A maps to NM_001010872.1 S826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54805190 C>A maps to NM_001010872.1 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:54805295 G>T maps to NM_001010872.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr6:54806261 G>A maps to NM_001010872.1 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:54806252 T>C maps to NM_001010872.1 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr6:54805943 C>G maps to NM_001010872.1 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:54805920 G>T maps to NM_001010872.1 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:54805280 T>C maps to NM_001010872.1 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:54804554 A>T maps to NM_001010872.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:54805229 C>A maps to NM_001010872.1 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:33876671 G>T maps to NM_178468.4 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr20:33874535 G>T maps to NM_178468.4 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:33875233 G>T maps to NM_178468.4 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:33876761 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr20:33879675 G>T maps to NM_178468.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:33875147 G>T maps to NM_178468.4 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:33875105 C>A maps to NM_178468.4 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37580397 G>C maps to NM_030919.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr20:37581024 C>T maps to NM_030919.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr20:37570621 C>T maps to NM_030919.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:37576644 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:37580962 T>C maps to NM_030919.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:37580295 C>T maps to NM_030919.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:49116500 C>T maps to NM_017708.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:40417815 C>A maps to NM_138435.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr22:40417509 C>A maps to NM_138435.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:18881049 T>A maps to NM_001039999.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:18882132 C>A maps to NM_001039999.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:18882138 C>A maps to NM_001039999.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr17:18882042 G>C maps to NM_001039999.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:18881946 G>A maps to NM_001039999.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:18882018 T>C maps to NM_001039999.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:14774291 C>A maps to NM_145175.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr2:14774243 C>A maps to NM_145175.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:5145515 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:17601329 G>T maps to NM_016255.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:8377323 G>T maps to NM_018088.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:8374975 G>T maps to NM_018088.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:8374864 G>A maps to NM_018088.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:8375100 G>A maps to NM_018088.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:8375359 C>T maps to NM_018088.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:124798767 A>G maps to NM_144963.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:124810415 C>T maps to NM_144963.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:124801878 A>T maps to NM_144963.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:94717156 C>T maps to ENST00000452913 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:33817276 C>T maps to ENST00000395190 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:33820592 C>A maps to ENST00000395190 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:38766384 A>G maps to NM_173611.2 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:38895994 G>C maps to NM_174905.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:8761699 T>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:8764316 T>C did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:8759375 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:8767094 C>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:9000421 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:8998401 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:9000186 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:13061249 G>C did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:13061039 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:13061340 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:13061294 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:89818611 G>A maps to NM_000135.2 H1000H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:89828399 G>A maps to NM_000135.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:14883070 C>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr23:14861791 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:14871183 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:14882910 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:14863235 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:14883040 G>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:14861872 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:14882880 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr23:14882879 C>T did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr9:97873897 C>T maps to NM_000136.2 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:10107089 G>T maps to NM_033084.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:10084738 T>C maps to NM_033084.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:10106487 C>T maps to NM_033084.3 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:10105579 G>T maps to NM_033084.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:35428395 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:22647319 C>A maps to NM_022725.3 E13*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8301-01A-11D-2284-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:22646798 G>A maps to NM_022725.3 A186A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-93-8067-01A-11D-2284-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:22647209 A>C maps to NM_022725.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:35076824 T>A maps to NM_004629.1 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:35075049 T>A maps to NM_004629.1 K504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr15:89811674 G>C maps to NM_001113378.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr15:89811675 G>T maps to NM_001113378.1 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:89824527 G>T maps to NM_001113378.1 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:89824489 C>T maps to NM_001113378.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:89833461 C>T maps to NM_001113378.1 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:58468385 C>A maps to NM_001114636.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:58425716 A>T maps to NM_001114636.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:58431270 C>T maps to NM_001114636.1 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:45645709 T>C maps to NM_020937.2 D1251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr14:45642256 G>C did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr14:45605539 T>C maps to NM_020937.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:45605261 C>T maps to NM_020937.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:45633768 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr14:45642256 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:45644331 C>G maps to NM_020937.2 S792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:45644915 C>T maps to NM_020937.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:45644561 G>T maps to NM_020937.2 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:45645484 C>T maps to NM_020937.2 F1176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr14:45609896 A>T maps to NM_020937.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:45645575 A>T maps to NM_020937.2 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:163055369 A>T maps to NM_004460.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:163051220 G>T maps to NM_004460.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr2:163031436 C>A maps to NM_004460.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr2:163066497 C>T maps to NM_004460.2 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:13722000 C>T maps to NM_032228.5 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:13734521 C>T maps to NM_032228.5 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:29423408 C>A maps to NM_018099.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:29474838 G>A maps to NM_018099.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr12:29469918 T>C maps to NM_018099.3 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:29486594 T>C maps to NM_018099.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:29486612 C>T maps to NM_018099.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:29460702 A>C maps to NM_018099.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:29450054 C>G maps to NM_018099.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:29446405 C>G maps to NM_018099.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr12:29486609 C>A maps to NM_018099.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:99092213 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:99092922 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:98865612 C>G maps to NM_005766.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:242350540 G>A maps to NM_014808.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:242347007 C>T maps to NM_014808.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:242402802 G>T maps to NM_014808.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:242380814 C>T maps to NM_014808.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:13035002 C>T maps to NM_004461.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:13035801 C>T maps to NM_004461.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:13035486 G>A maps to NM_004461.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr19:13035516 C>T maps to NM_004461.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:13034990 G>A maps to NM_004461.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:13039358 G>A maps to NM_004461.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:223513512 A>C maps to NM_005687.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:223488431 G>A maps to NM_005687.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:223488992 G>A maps to NM_005687.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:172635119 G>A maps to NM_000639.1 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:172633495 A>G maps to NM_000639.1 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:172635155 A>C maps to NM_000639.1 *282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:172628583 G>T maps to NM_000639.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:80048841 C>A maps to NM_004104.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:150774062 C>T maps to NM_006712.3 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:170428514 C>A maps to NM_024622.3 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:170417033 T>C maps to NM_024622.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:207652824 G>T maps to NM_014929.3 G587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:7866921 G>T maps to NM_024091.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:3129680 T>C maps to NM_021826.4 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3128051 T>A maps to NM_021826.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr20:3127520 C>A maps to NM_021826.4 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:187627768 G>A maps to ENST00000260147 Y1071Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:187527367 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:187522508 C>A maps to ENST00000260147 E3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:187532545 T>A maps to ENST00000260147 K3286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:187539601 G>C maps to ENST00000260147 S2716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:187531124 C>A maps to ENST00000260147 E3303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:187539050 G>A maps to ENST00000260147 Q2900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:187629892 C>A maps to ENST00000260147 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:187541781 C>T maps to ENST00000260147 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:187540188 C>A maps to ENST00000260147 T2520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr4:187518152 C>A maps to ENST00000260147 E4184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr4:187518153 C>A maps to ENST00000260147 A4183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:187630810 G>C maps to ENST00000260147 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:187518258 C>A maps to ENST00000260147 T4148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr4:187517919 C>A maps to ENST00000260147 P4261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr4:187521112 C>G maps to ENST00000260147 T4017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr4:187628359 C>A maps to ENST00000260147 T874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:187557215 C>A maps to ENST00000260147 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:150947283 A>G maps to NM_001447.2 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:150934204 T>C maps to NM_001447.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:150946773 G>A maps to NM_001447.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:150905490 C>T maps to NM_001447.2 L3448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:150923859 G>T maps to NM_001447.2 V2276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr5:150947208 G>A maps to NM_001447.2 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:150948239 C>A maps to NM_001447.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr5:150931117 G>A maps to NM_001447.2 I1402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:150885494 G>A maps to NM_001447.2 P4227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:150900903 C>G maps to NM_001447.2 T3750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:150922515 G>T maps to NM_001447.2 Y2724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:150921888 A>T maps to NM_001447.2 A2933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:150932773 C>A maps to NM_001447.2 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:150924903 C>A maps to NM_001447.2 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:150921909 C>A maps to NM_001447.2 A2926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:150947982 C>A maps to NM_001447.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:150885485 C>T maps to NM_001447.2 L4230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:150947877 C>T maps to NM_001447.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:150943132 T>G maps to NM_001447.2 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:150920178 A>T maps to NM_001447.2 T2996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:150945879 G>A maps to NM_001447.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:150946569 T>G maps to NM_001447.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr5:150920131 G>T maps to NM_001447.2 S3012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:150946785 A>G maps to NM_001447.2 C569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr5:150947475 G>A maps to NM_001447.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:150923130 A>G maps to NM_001447.2 T2519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:92534617 C>G maps to ENST00000298047 V2813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:92534272 C>A maps to ENST00000298047 V2698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:92533466 G>T maps to ENST00000298047 E2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:92535010 C>A maps to ENST00000298047 A2944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:92538487 G>C maps to ENST00000298047 V3022V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:92086010 G>T maps to ENST00000298047 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:92532334 G>T maps to ENST00000298047 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:92085739 G>A maps to ENST00000298047 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:92531047 C>A maps to ENST00000298047 I1623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:92616191 G>T maps to ENST00000298047 T4190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:92087587 G>T maps to ENST00000298047 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92086801 C>G maps to ENST00000298047 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:92087705 C>T maps to ENST00000298047 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92086705 G>T maps to ENST00000298047 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:92616482 C>G maps to ENST00000298047 P4287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:92616380 G>T maps to ENST00000298047 V4253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:92531038 A>T maps to ENST00000298047 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:92534533 C>T maps to ENST00000298047 A2785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:92086400 A>T maps to ENST00000298047 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:92532562 C>G maps to ENST00000298047 G2128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr11:92087326 C>A maps to ENST00000298047 C683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:92532886 C>T maps to ENST00000298047 D2236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616311 C>A maps to ENST00000298047 V4230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:92616506 C>A maps to ENST00000298047 C4295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92086966 T>C maps to ENST00000298047 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:92531737 G>A maps to ENST00000298047 V1853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:92616228 A>T maps to ENST00000298047 K4203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:92088373 G>T maps to ENST00000298047 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:92534671 C>G maps to ENST00000298047 T2831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:92088205 C>G maps to ENST00000298047 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:92543063 G>A maps to ENST00000298047 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:92535004 G>T maps to ENST00000298047 V2942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr11:92534899 G>C maps to ENST00000298047 T2907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:92086101 C>A maps to ENST00000298047 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:92085847 T>C maps to ENST00000298047 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:92590414 G>T maps to ENST00000298047 E3801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:92569868 G>T maps to ENST00000298047 R3408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:92600169 G>T maps to ENST00000298047 R3974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:92616116 C>A maps to ENST00000298047 I4165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:92616430 C>A maps to ENST00000298047 S4270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:92564950 C>A maps to ENST00000298047 S3215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:92086879 G>A maps to ENST00000298047 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:92620172 G>A maps to ENST00000298047 G4315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:92531098 C>T maps to ENST00000298047 S1640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92526084 G>T maps to ENST00000298047 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:92257848 C>T maps to ENST00000298047 Y1114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:92523212 G>T maps to ENST00000298047 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:92543183 T>C maps to ENST00000298047 Y3141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:92086456 C>T maps to ENST00000298047 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:92531674 A>T maps to ENST00000298047 A1832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:92534236 A>G maps to ENST00000298047 P2686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr11:92087427 C>G maps to ENST00000298047 S717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:92087374 G>A maps to ENST00000298047 K699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:92616395 C>T maps to ENST00000298047 G4258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:92623877 G>T maps to ENST00000298047 E4457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:92590377 A>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr11:92615963 G>A maps to ENST00000298047 V4114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:92258097 C>A maps to ENST00000298047 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:92507249 G>C maps to ENST00000298047 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:92087122 C>T maps to ENST00000298047 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:92616356 C>A maps to ENST00000298047 S4245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr11:92624095 C>A maps to ENST00000298047 G4529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:92600139 G>A maps to ENST00000298047 A3964A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr11:92568123 T>C maps to ENST00000298047 A3320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:92523185 G>A maps to ENST00000298047 E1471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:126240610 C>T maps to NM_024582.4 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:126336492 G>T maps to NM_024582.4 V2125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126320036 G>A maps to NM_024582.4 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:126402751 G>T maps to NM_024582.4 R4225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:126411518 C>A maps to NM_024582.4 T4514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:126384716 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:126373591 G>T maps to NM_024582.4 V3807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:126369619 C>T maps to NM_024582.4 S2483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:126240577 C>T maps to NM_024582.4 T1004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr4:126241325 G>T maps to NM_024582.4 E1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:126372424 A>T maps to NM_024582.4 P3418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:126239596 G>A maps to NM_024582.4 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:126241675 G>C maps to NM_024582.4 G1370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:126372631 C>A maps to NM_024582.4 T3487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr4:126389826 C>T maps to NM_024582.4 G4020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr4:126389832 G>C maps to NM_024582.4 R4022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:126355442 A>T maps to NM_024582.4 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:126242333 T>C maps to NM_024582.4 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:126411338 A>G maps to NM_024582.4 P4454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:126372721 C>G maps to NM_024582.4 V3517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:126238360 G>T maps to NM_024582.4 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:126370375 A>G maps to NM_024582.4 K2735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:126389778 G>A maps to NM_024582.4 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:126239638 G>T maps to NM_024582.4 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:126372394 C>A maps to NM_024582.4 I3408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr4:126372502 C>T maps to NM_024582.4 I3444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr4:126411344 G>T maps to NM_024582.4 S4456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:126408531 T>C maps to NM_024582.4 D4283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:126373661 G>T maps to NM_024582.4 E3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:126397369 A>T maps to NM_024582.4 P4084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:126408612 G>A maps to NM_024582.4 G4310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:126370480 C>T maps to NM_024582.4 A2770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:126373553 G>T maps to NM_024582.4 G3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:126411329 T>C maps to NM_024582.4 C4451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:126371596 T>A maps to NM_024582.4 S3142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:126240569 G>T maps to NM_024582.4 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:126372403 G>T maps to NM_024582.4 V3411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:126239215 G>A maps to NM_024582.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr4:126372961 A>T maps to NM_024582.4 T3597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:126411836 T>C maps to NM_024582.4 Y4620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr4:126239167 T>A maps to NM_024582.4 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr4:126328084 T>C maps to NM_024582.4 S1786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:126389832 G>C maps to NM_024582.4 R4022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:126411545 G>C maps to NM_024582.4 L4523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr23:150890398 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:150889934 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:150889972 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:73910943 C>A maps to ENST00000389570 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:73919583 C>A maps to ENST00000389570 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:16096938 C>T maps to NM_017556.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:16091648 G>A maps to NM_017556.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:45943049 C>A maps to ENST00000348697 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:45944566 C>T maps to ENST00000348697 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:45996262 G>T maps to ENST00000348697 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr22:45929725 G>T maps to ENST00000348697 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr3:13678059 C>A maps to NM_001165035.1 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:13669356 G>T maps to NM_001165035.1 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:13663315 C>A maps to NM_001165035.1 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr3:13649592 C>T maps to NM_001165035.1 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:92353591 G>A maps to ENST00000267620 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:112942901 G>A maps to NM_153214.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:112896308 T>C did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:112942862 C>T maps to NM_153214.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48800777 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:48738906 A>G maps to NM_000138.4 C1928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:48766500 G>C maps to NM_000138.4 Y1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:48755288 G>A maps to NM_000138.4 I1738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr15:48752479 T>C maps to NM_000138.4 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:127666357 G>A maps to NM_001999.3 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:127595290 G>T maps to NM_001999.3 P2865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127670447 C>A maps to NM_001999.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:127697427 C>A maps to NM_001999.3 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:127609547 G>T maps to NM_001999.3 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:127641272 G>T maps to NM_001999.3 I1868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:127610316 C>A maps to NM_001999.3 L2551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:127730961 T>A maps to NM_001999.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:127681115 C>A maps to NM_001999.3 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:127638772 C>A maps to NM_001999.3 E1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:127686665 G>T maps to NM_001999.3 I902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:127644939 T>A maps to NM_001999.3 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:127685645 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:127647595 G>T maps to NM_001999.3 P1643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr5:127595458 G>A maps to NM_001999.3 L2809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr5:127671177 A>T maps to NM_001999.3 Y1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:127712451 G>T maps to NM_001999.3 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:127624233 G>C maps to NM_001999.3 S2218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:127800504 C>G maps to NM_001999.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:127728882 G>A maps to NM_001999.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127595410 G>T maps to NM_001999.3 I2825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127648324 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:127782299 C>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:127641203 T>C maps to NM_001999.3 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:127714527 A>G maps to NM_001999.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:127614378 G>T maps to NM_001999.3 A2431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:127641323 T>A maps to NM_001999.3 I1851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:127705000 C>A maps to NM_001999.3 G708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:127640703 G>A maps to NM_001999.3 Y1915Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:127595227 C>A maps to NM_001999.3 L2886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:127595197 T>A maps to NM_001999.3 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:127744478 G>T maps to NM_001999.3 C322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr5:127712544 A>G maps to NM_001999.3 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr5:127705027 C>G did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:127800597 C>A maps to NM_001999.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:127614381 A>T maps to NM_001999.3 T2430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:8196579 C>A maps to NM_032447.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:8148209 C>T maps to NM_032447.3 E2378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:8194189 G>T maps to NM_032447.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:8176861 G>A maps to NM_032447.3 H1320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:8131063 G>A maps to NM_032447.3 I2723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:8137012 C>G maps to NM_032447.3 S2669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:8191429 G>A maps to NM_032447.3 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:8196638 G>A maps to NM_032447.3 Q597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:8190788 G>T maps to NM_032447.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:8138146 G>A maps to NM_032447.3 C2579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr19:8130961 G>A maps to NM_032447.3 G2757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:8152787 G>T maps to NM_032447.3 R2180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:97325680 G>T maps to NM_003837.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:30676241 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr19:9921643 C>A maps to NM_017703.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:102608498 C>T maps to NM_145032.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:102517934 A>G maps to NM_145032.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:102604003 G>T maps to NM_145032.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:102566796 C>A maps to NM_145032.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr10:104182722 C>T maps to NM_024326.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:745063 G>A maps to NM_153350.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:746838 C>T maps to NM_153350.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:107216862 G>A maps to NM_001163315.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr5:107684232 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5540693 G>A maps to ENST00000312577 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:5540615 G>A maps to ENST00000312577 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:5521543 G>A maps to NM_024963.4 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30937209 C>T maps to NM_001099784.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:33415413 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:37457328 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:37437683 T>A maps to NM_032875.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr17:37455264 C>A maps to NM_032875.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr13:77595701 C>G maps to NM_012158.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr6:99374723 G>A maps to NM_012160.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:99322154 C>A maps to NM_012160.3 *622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr6:99374672 A>G maps to NM_012160.3 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:145581358 G>A maps to NM_012162.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:145579331 C>A maps to NM_012162.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr8:145579641 T>C maps to NM_012162.1 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:15928062 C>A maps to NM_012304.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:15937085 C>T maps to NM_012304.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:15928575 C>A maps to NM_012304.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:15936988 G>T maps to NM_012304.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:15928305 C>A maps to NM_012304.3 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:15928464 G>C maps to NM_012304.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:15937075 C>G maps to NM_012304.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:15936871 C>A maps to NM_012304.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:15937147 C>A maps to NM_012304.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:15936787 C>T maps to NM_012304.3 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:15936922 C>A maps to NM_012304.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr5:15937087 G>T maps to NM_012304.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr5:15937192 G>A maps to NM_012304.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:15928578 C>A maps to NM_012304.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:15936691 C>T maps to NM_012304.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:15936703 G>T maps to NM_012304.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:15936733 G>T maps to NM_012304.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:15616167 G>A maps to NM_012304.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr5:15616176 C>T maps to NM_012304.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:15928182 C>A maps to NM_012304.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:15936775 G>T maps to NM_012304.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:15937168 C>A maps to NM_012304.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:15928158 C>A maps to NM_012304.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr9:37541465 T>C maps to NM_012166.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr9:37537271 C>T maps to NM_012166.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:37516040 G>A maps to NM_012166.2 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:48059589 C>A maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:71740731 G>A maps to NM_001142958.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr18:71797820 C>T maps to NM_001142958.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:71796716 T>C maps to NM_001142958.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:71797721 G>A maps to NM_001142958.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:28309951 T>C maps to NM_172366.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:28304790 C>T did not map to a codon.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr19:39435613 G>A maps to ENST00000448145 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:5956139 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr10:5965659 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:5956209 G>T maps to NM_032807.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:5978519 C>G maps to NM_032807.3 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:5969491 G>A maps to NM_032807.3 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:5948306 A>T maps to NM_032807.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr10:5965634 C>T maps to NM_032807.3 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:5956209 G>T maps to NM_032807.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:100197670 G>T maps to NM_012172.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:413122 T>C maps to NM_183421.1 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:39517530 C>T maps to NM_178820.3 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:39517605 G>A maps to NM_178820.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:33790517 G>A maps to NM_012175.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:33777463 G>A maps to NM_012175.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:87367538 C>A maps to NM_024735.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr16:87376481 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:39870664 G>T maps to NM_203301.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:55817594 C>T maps to NM_152231.1 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:55817173 G>A maps to NM_152231.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:230861623 A>T maps to NM_174899.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr5:147782065 A>G maps to NM_205836.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:147807316 G>T maps to NM_205836.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:147819232 G>A maps to NM_205836.1 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:147806774 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:6690698 G>T maps to NM_153230.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:6683888 C>T maps to NM_153230.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:6683345 T>A maps to NM_153230.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:6684113 G>A maps to NM_153230.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:41934093 C>T maps to NM_012176.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:41934063 C>G maps to NM_012176.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:121341475 C>A maps to NM_016298.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:121340500 C>A maps to NM_016298.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:121341053 G>T maps to NM_016298.3 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:121341064 T>C maps to NM_016298.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:121341581 G>T maps to NM_016298.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:121341391 A>T maps to NM_016298.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:73492452 G>T maps to ENST00000295133 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:73491151 G>C maps to ENST00000295133 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:73491082 C>T maps to ENST00000295133 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:101153929 G>T maps to NM_001029860.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr8:101153656 A>G maps to NM_001029860.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:101153695 G>A maps to NM_001029860.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:101153038 T>A maps to NM_001029860.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:11718336 C>T maps to ENST00000376768 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:11718920 G>T maps to ENST00000376768 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr1:11716116 G>A maps to ENST00000376768 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:196311059 A>G maps to NM_001105573.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr17:37099078 C>A maps to NM_001008777.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:37118262 T>G maps to NM_001008777.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:18681911 C>T maps to ENST00000395665 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr17:18675853 C>T maps to ENST00000395665 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:18651356 A>G maps to ENST00000395665 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:171318469 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:48416854 G>T maps to NM_207102.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:48421035 T>C maps to NM_207102.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:123550108 G>C maps to NM_012164.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:123535118 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:103384539 G>A maps to ENST00000331272 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr9:139835796 C>A maps to NM_018998.2 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:153303397 C>G maps to NM_001013415.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr4:153249468 C>A maps to NM_033632.2 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:153253846 G>A maps to NM_033632.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr4:153332523 C>T maps to NM_033632.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr4:153332618 C>A maps to NM_033632.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:153332825 G>A maps to NM_033632.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:153268137 G>A maps to NM_033632.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:153259072 C>A maps to NM_033632.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:12805681 C>T maps to ENST00000380339 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:207135630 G>T maps to NM_001170631.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:207135639 C>A maps to NM_001170631.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr1:207135833 G>A maps to NM_001170631.1 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207135747 G>T maps to NM_001170631.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55401198 C>T maps to NM_002000.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:55399575 A>T maps to NM_002000.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr19:55385750 C>T maps to NM_002000.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:55396755 G>A maps to NM_002000.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:159277562 A>G maps to ENST00000368115 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:159277621 C>G maps to ENST00000368115 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:159275976 G>T maps to ENST00000368115 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:159277574 A>G maps to ENST00000368115 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:159277712 A>G maps to ENST00000368115 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:159275776 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:161187845 C>A maps to NM_004106.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:161188690 G>A maps to NM_004106.1 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:161188513 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:161188715 G>T maps to NM_004106.1 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7755300 C>T maps to NM_002002.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr19:7764625 T>G maps to NM_002002.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:40366229 G>A maps to NM_003890.2 C4668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:40406006 C>A maps to NM_003890.2 A1613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:40366479 G>C maps to NM_003890.2 S4585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:40421157 G>T maps to NM_003890.2 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:40419692 G>A maps to NM_003890.2 Q1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr19:40411645 T>A maps to NM_003890.2 K1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:40433635 C>A maps to NM_003890.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:40368318 C>A maps to NM_003890.2 R4343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:40433203 C>T maps to NM_003890.2 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:40434112 G>T maps to NM_003890.2 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:40433140 T>A maps to NM_003890.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr19:40367786 G>A maps to NM_003890.2 C4391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr19:40392511 G>C maps to NM_003890.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:40363171 G>A maps to NM_003890.2 G4966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:40419849 A>G maps to NM_003890.2 C1048C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr19:40421090 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:40424299 C>A maps to NM_003890.2 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:40433428 A>G maps to NM_003890.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:40424294 G>A maps to NM_003890.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:40366283 G>A maps to NM_003890.2 C4650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr19:40366202 C>A maps to NM_003890.2 P4677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:149762921 T>A maps to NM_000566.3 L325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:161476250 T>C maps to NM_001136219.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161475295 C>T maps to NM_001136219.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:161479718 G>A maps to NM_001136219.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:161479612 G>A maps to NM_001136219.1 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161647155 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:161641209 C>A maps to NM_004001.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:161641216 C>T maps to NM_004001.4 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:161641338 C>T maps to NM_004001.4 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:161599795 C>A maps to ENST00000367964 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:17877619 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:17895734 T>A did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr19:17895612 C>G maps to NM_015122.2 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:17892527 C>A maps to NM_015122.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr19:17883285 G>A maps to NM_015122.2 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:72311460 A>G maps to NM_138782.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr5:141030647 C>A maps to ENST00000354789 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:141021279 G>A maps to ENST00000354789 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:72695252 G>A maps to ENST00000409314 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:72554226 G>C maps to ENST00000409314 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:137801874 G>T maps to NM_002003.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:137804875 C>A maps to NM_002003.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:137809690 G>T maps to NM_002003.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:137801796 T>A maps to NM_002003.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:137801675 T>A maps to NM_002003.3 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr9:137808266 G>T maps to NM_002003.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:137772708 C>A maps to NM_004108.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:137778409 G>T maps to NM_004108.2 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr1:27695885 C>T maps to NM_003665.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157771894 C>G maps to NM_052938.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:157773695 G>A maps to NM_052938.4 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:157771367 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:157772173 A>G maps to NM_052938.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:157771795 G>C maps to NM_052938.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:157772446 A>G maps to NM_052938.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:157771311 G>T maps to NM_052938.4 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:157769855 A>G maps to NM_052938.4 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:157738453 G>C maps to NM_030764.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:157737279 G>A maps to NM_030764.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:157716564 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:157736726 A>T maps to NM_030764.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:157740420 C>A maps to NM_030764.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:157740394 G>A maps to NM_030764.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:157665170 T>A maps to NM_052939.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:157650552 A>G maps to NM_052939.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:157666024 G>A maps to NM_052939.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:157660279 G>A maps to NM_052939.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:157666997 C>T maps to NM_052939.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:157659675 A>T maps to NM_052939.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:157659606 G>T maps to NM_052939.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:157659672 C>G maps to NM_052939.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:157665956 G>T maps to NM_052939.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:157665242 G>T maps to NM_052939.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:157667044 G>T maps to NM_052939.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:157660306 G>C maps to NM_052939.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:157660237 G>A maps to NM_052939.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:157665122 G>T maps to NM_052939.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:157668287 C>A maps to NM_052939.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:157555976 C>G maps to NM_031282.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:157559051 G>C maps to NM_031282.2 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:157557311 G>A maps to NM_031282.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:157559210 T>C maps to NM_031282.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:157551322 G>T maps to NM_031282.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:157556222 G>T maps to NM_031282.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:157548317 C>A maps to NM_031282.2 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:157497605 A>G maps to NM_031281.2 C587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:157514256 G>T maps to NM_031281.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:157508978 G>T maps to NM_031281.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:157494129 G>C maps to NM_031281.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:157490894 C>A maps to NM_031281.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:157490887 C>A maps to NM_031281.2 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:157504437 G>T maps to NM_031281.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:157497584 G>T maps to NM_031281.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr1:157490930 C>T maps to NM_031281.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:157494102 G>A maps to NM_031281.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:157514711 T>A maps to NM_031281.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr1:157514289 G>A maps to NM_031281.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:157508894 C>A maps to NM_031281.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:157514636 G>T maps to NM_031281.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:159785242 G>T maps to NM_001004310.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:159779228 G>T maps to NM_001004310.2 G214G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:161680652 G>A maps to NM_001184866.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:161680697 C>A maps to NM_001184866.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:161681007 C>A maps to NM_001184866.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:161693310 C>G maps to NM_001002901.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:11687841 C>G maps to NM_004462.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:155288030 C>G maps to NM_001135821.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:155287751 G>A maps to NM_001135821.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:110327730 G>T maps to NM_004109.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr19:10421211 T>A maps to NM_001031734.2 K168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:111747646 C>A maps to ENST00000428306 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:111747581 C>A maps to ENST00000428306 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:72862600 C>A maps to ENST00000442102 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:72860302 T>A maps to ENST00000442102 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:72858953 G>C maps to ENST00000442102 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr17:72862630 G>A maps to ENST00000442102 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:55247312 C>A maps to NM_001012515.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr18:55238744 G>A maps to NM_001012515.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr18:55240515 G>A maps to NM_001012515.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr15:68582376 C>A maps to NM_015322.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr15:68582097 G>C maps to NM_015322.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:114860289 G>A maps to NM_020177.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:114879139 C>A maps to NM_020177.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:108290504 G>T maps to NM_005246.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:108380494 A>T maps to NM_005246.2 K610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:108134021 C>T maps to NM_005246.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr5:108203571 C>T maps to NM_005246.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:108380496 G>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:108134000 A>T maps to NM_005246.2 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:108516523 G>T maps to NM_005246.2 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:97368992 C>T maps to NM_001113382.1 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:125047561 C>A maps to NM_001039112.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:125015437 C>A maps to NM_001039112.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:125131083 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:125131931 C>T maps to NM_001039112.2 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:125072896 C>T maps to NM_001039112.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr8:125080027 G>A maps to NM_001039112.2 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:124989712 C>A maps to NM_001039112.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:125094555 A>T maps to NM_001039112.2 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:125081668 A>T maps to NM_001039112.2 K1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:125074092 G>T maps to NM_001039112.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:125052163 C>A maps to NM_001039112.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:124989823 C>T maps to NM_001039112.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr8:125061963 A>G maps to NM_001039112.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:124992819 C>T maps to NM_001039112.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:125061921 C>A maps to NM_001039112.2 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr8:124982336 C>A maps to NM_001039112.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:125109516 C>T maps to NM_001039112.2 R1567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:125047561 C>T maps to NM_001039112.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:125052197 C>G maps to NM_001039112.2 S847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr8:124968249 G>A maps to NM_001039112.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr8:125107212 T>C maps to NM_001039112.2 C1543C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:125076753 G>T maps to NM_001039112.2 P1165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:125103711 C>T maps to NM_001039112.2 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr8:125033809 C>A maps to NM_001039112.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:125131931 C>A maps to NM_001039112.2 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:124989742 G>A maps to NM_001039112.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:19184853 A>G maps to NM_152898.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:19184744 C>A maps to NM_152898.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:19184871 G>T maps to NM_152898.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:19184485 C>A maps to NM_152898.2 *167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:19184640 G>A maps to NM_152898.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:19184586 G>C maps to NM_152898.2 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:6077578 G>A maps to NM_017671.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6068531 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:6096635 C>T maps to NM_017671.4 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:53360089 C>T maps to NM_001134999.1 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:53331253 A>C maps to NM_001134999.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:63987468 C>T maps to NM_178443.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:63987476 C>G maps to NM_178443.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr15:91437238 C>T maps to NM_002005.3 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:91432604 G>T maps to NM_002005.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:186370113 G>T maps to NM_014375.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:186358297 G>T maps to NM_014375.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:125359481 A>G maps to NM_005103.4 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:125351489 G>C maps to NM_005103.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:125330418 G>A maps to NM_005103.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:121943804 G>T maps to NM_001024613.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:121942173 G>A maps to NM_001024613.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:121942892 C>T maps to NM_001024613.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr7:121942155 C>T maps to NM_001024613.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:121942155 C>T maps to NM_001024613.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:62357919 G>C maps to NM_018008.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr3:62358289 G>C maps to NM_018008.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr19:35842852 C>T maps to NM_005303.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:35941155 G>T maps to NM_005306.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:35941413 C>A maps to NM_005306.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:35940867 C>A maps to NM_005306.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:35941284 G>T maps to NM_005306.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:35849908 C>T maps to NM_005304.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35850520 G>T maps to NM_005304.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:35849878 C>A maps to NM_005304.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr4:155507347 G>C maps to NM_000508.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:155507188 G>T maps to NM_000508.3 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:155507212 G>T maps to NM_000508.3 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:155509952 G>T maps to NM_000508.3 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:155505593 A>G maps to NM_000508.3 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:155507679 C>A maps to NM_000508.3 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:155505647 C>G maps to NM_000508.3 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:155505868 C>A maps to NM_000508.3 G670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:155505869 C>T maps to NM_000508.3 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:155508743 T>A maps to NM_000508.3 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr4:155505707 A>T maps to NM_000508.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:155487753 C>T maps to NM_005141.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:155490894 C>A maps to NM_005141.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:155489561 G>T maps to NM_005141.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr4:155487072 C>T maps to NM_005141.4 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:155487639 G>A did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr4:155489646 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:54472780 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:54497807 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:54497751 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:54497770 G>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr23:54497769 C>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:54482963 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:54492143 G>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:54496520 G>C did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:54492139 G>C did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:54496845 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:54521720 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:54492127 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:54482953 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:54497779 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:54475347 T>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:54472808 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:54496628 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:54472586 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:36981396 C>A maps to NM_173558.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:95795118 T>C maps to NM_033086.2 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr9:95766311 G>C maps to NM_033086.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:95738723 G>T maps to NM_033086.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:95772595 G>T maps to NM_033086.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:32735019 G>A maps to NM_139241.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:32735364 G>A maps to NM_139241.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:32735365 G>T maps to NM_139241.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:32735076 T>C maps to NM_139241.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr12:32735175 G>T maps to NM_139241.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:14861825 G>A maps to NM_152536.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:14862089 G>A maps to NM_152536.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:14905646 G>A maps to NM_152536.3 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14862491 C>A maps to NM_152536.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr3:14862825 C>A maps to NM_152536.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:14861864 C>T maps to NM_152536.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr3:14862302 G>A maps to NM_152536.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:14862554 G>A maps to NM_152536.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:14942522 C>A maps to NM_152536.3 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:14861948 C>A maps to NM_152536.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:95602830 G>A maps to NM_018351.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:95604747 A>G maps to NM_018351.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:95603226 C>A maps to NM_018351.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:141993533 G>A maps to NM_001144935.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:44388619 G>A maps to NM_004465.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:44310632 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:44310552 G>A maps to NM_004465.1 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:192053164 G>T maps to NM_021032.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:192078250 G>T maps to NM_021032.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr3:191888340 C>T maps to NM_021032.4 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:191888364 G>A maps to NM_021032.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr3:192053248 G>T maps to NM_021032.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr3:191861869 T>C maps to NM_021032.4 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr3:191861863 A>T maps to NM_021032.4 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:137715147 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:137939713 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:137939774 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:137793048 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:137715134 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:137715044 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:137793039 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:137793018 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:137793014 G>C did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:137785246 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:137715013 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:137715141 T>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:137717644 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:137715100 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:137939742 C>G did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:137717720 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:102375180 C>A maps to NM_175929.2 *253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr13:103053980 T>C maps to NM_175929.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr13:102378992 T>G maps to NM_175929.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr23:76711919 T>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:76711989 A>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:170863158 G>C maps to NM_003862.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:170883613 G>A maps to NM_003862.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:170883631 G>A maps to NM_003862.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr5:170863179 G>A maps to NM_003862.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr5:170863215 G>A maps to NM_003862.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:123748451 G>T maps to NM_002006.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:123813427 C>A maps to NM_002006.4 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr8:16850715 C>A maps to NM_019851.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:49261404 C>A maps to NM_019113.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:49261224 G>A maps to NM_019113.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:49261320 C>T maps to NM_019113.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:49260276 G>C maps to NM_019113.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:49259513 G>T maps to NM_019113.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:4488553 G>T maps to NM_020638.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:4479565 G>A maps to NM_020638.2 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:4479832 G>T maps to NM_020638.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:4479787 G>A maps to NM_020638.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:4479625 G>A maps to NM_020638.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:69625399 G>T maps to NM_005247.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr11:69625447 G>A maps to NM_005247.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:69631162 C>A maps to NM_005247.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr11:69588223 C>T maps to NM_002007.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:81188289 C>A maps to NM_004464.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:81188268 C>A maps to NM_004464.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:81188178 G>A maps to NM_004464.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:81207591 C>T maps to NM_004464.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4554565 C>A maps to NM_020996.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:4543449 G>T maps to NM_020996.1 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:4554565 C>A maps to NM_020996.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr15:49776610 T>G maps to NM_002009.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:103534630 C>G maps to NM_033163.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr4:15937796 G>C maps to NM_005130.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:15964477 C>T maps to NM_031950.3 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr8:38314895 C>T maps to NM_001174067.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:38277221 C>A maps to NM_001174067.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:38277188 T>A maps to NM_001174067.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr8:38285497 G>A maps to NM_001174067.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:38274923 T>C maps to NM_001174067.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:38279318 C>A maps to NM_001174067.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:38314886 G>T maps to NM_001174067.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167446088 A>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:167416709 G>C maps to NM_007045.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:167417873 G>T maps to NM_007045.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:123260451 C>A maps to ENST00000351936 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr10:123279633 G>A maps to ENST00000351936 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:1807624 C>T maps to NM_000142.4 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:176522577 C>A maps to NM_213647.1 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:176520230 C>T maps to NM_213647.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:176524538 C>T maps to NM_213647.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:176517993 G>A maps to NM_213647.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:176524382 G>T maps to NM_213647.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:176522651 G>T maps to NM_213647.1 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:155528067 G>A maps to ENST00000407946 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr4:155527884 A>T maps to ENST00000407946 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:155533353 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:60125888 A>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:60125889 G>C did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr8:17743045 A>G maps to NM_201552.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:76828786 G>A maps to NM_006682.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76828894 G>A maps to NM_006682.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:76825790 G>T maps to NM_006682.2 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:27939492 G>A maps to NM_005248.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:27949653 C>T maps to NM_005248.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:27949587 G>A maps to NM_005248.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:27942116 C>T maps to NM_005248.2 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:241672064 G>A maps to NM_000143.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:241665846 C>A maps to NM_000143.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:59737984 T>A maps to NM_002012.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:135289239 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:135290729 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:135288733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:135290119 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:135288622 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:135288702 A>T did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr23:135290071 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:135288700 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:135288687 G>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:135291444 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:135292118 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:135292128 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:105977847 C>T maps to ENST00000344213 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr2:105990142 G>A maps to ENST00000344213 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:97053947 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:97052765 C>T maps to NM_020482.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:97051596 A>T maps to NM_020482.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:97053871 C>T maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr6:97063585 C>T maps to NM_020482.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr6:97053781 C>G maps to NM_020482.4 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:97063491 A>C maps to NM_020482.4 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:97052762 C>T maps to NM_020482.4 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:67266052 G>C maps to NM_013241.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr16:67267931 C>T maps to NM_013241.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr16:67271204 G>C maps to NM_013241.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:34298542 G>T maps to NM_025135.2 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:34081943 C>T maps to NM_025135.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:34298530 G>A maps to NM_025135.2 W915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr18:34174787 C>A maps to NM_025135.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr18:34298167 G>T maps to NM_025135.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:34205612 C>A maps to NM_025135.2 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr18:34335225 G>T maps to NM_025135.2 R1284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr18:34081917 C>T maps to NM_025135.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:33952675 G>A maps to NM_025135.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:34191967 G>T maps to NM_025135.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34081904 C>A maps to NM_025135.2 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:34261507 G>T maps to NM_025135.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr18:34273357 C>A maps to NM_025135.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr18:34205488 G>T maps to NM_025135.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:34191968 G>T maps to NM_025135.2 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:133780762 G>T maps to NM_001145106.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr9:133799181 C>A maps to NM_001145106.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:133779621 G>A maps to NM_001145106.1 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:27016132 C>T maps to NM_203371.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:27016682 C>T maps to NM_203371.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:27016636 G>A maps to NM_203371.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:27016336 C>A maps to NM_203371.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:65655165 C>A maps to NM_198897.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:65653135 T>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:65652446 C>A maps to NM_198897.1 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:108910757 C>A maps to NM_007076.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:108910808 C>A maps to NM_007076.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:110146372 C>T maps to NM_014845.5 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:110113827 C>G maps to NM_014845.5 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:110059537 G>T maps to NM_014845.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr6:110081455 C>A maps to NM_014845.5 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:110110874 A>T maps to NM_014845.5 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:15376213 G>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:15364371 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:15364264 T>C did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:15371242 C>T did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:15376202 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:15381327 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:164466340 T>C maps to NM_018086.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:164468116 A>C maps to NM_018086.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:164466370 C>T maps to NM_018086.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:164467882 C>A maps to NM_018086.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr2:164467546 C>A maps to NM_018086.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:50514190 G>A maps to NM_022116.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:50514654 T>A maps to NM_022116.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:50513886 C>A maps to NM_022116.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:50513041 A>G maps to NM_022116.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:50512968 C>A maps to NM_022116.3 G673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr6:76022196 G>A maps to NM_015687.2 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76124486 T>A maps to NM_015687.2 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr6:76063271 C>T maps to NM_015687.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:76124489 G>A maps to NM_015687.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr6:76023513 A>G maps to NM_015687.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:76023480 G>T maps to NM_015687.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr6:76022792 C>A maps to NM_015687.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:99568742 G>A maps to NM_001042459.1 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:99568587 G>T maps to NM_001042459.1 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr3:99568014 G>A maps to NM_001042459.1 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:54294192 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:54256688 G>T maps to NM_030917.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:54257622 A>T maps to NM_030917.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr20:42935468 C>A maps to NM_001080472.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:35640939 G>T maps to NM_014344.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:39974500 C>A maps to NM_021939.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:39974663 C>T maps to NM_021939.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr17:39973308 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:39975576 C>T maps to NM_021939.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr17:39978639 C>A maps to NM_021939.3 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:39978050 C>A maps to NM_021939.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr12:49318377 C>T maps to NM_016594.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:30065926 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:30058644 A>G maps to NM_017946.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr9:115983481 C>A maps to ENST00000446284 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:115956434 T>C maps to ENST00000446284 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:24276805 G>C maps to NM_004116.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:24276808 G>A maps to NM_004116.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr11:64011313 G>T maps to NM_057092.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:45603641 T>A maps to NM_002013.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:2910446 G>A maps to NM_002014.3 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:72755321 A>G maps to NM_003602.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:72756805 G>C did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:72754750 C>A maps to NM_003602.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr7:72742686 C>A maps to NM_003602.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr7:72744348 C>T maps to NM_003602.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:72744303 G>T maps to NM_003602.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:72756837 G>T maps to NM_003602.3 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:33014276 G>A maps to NM_007270.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:33014285 G>C maps to NM_007270.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:32097283 G>A maps to NM_022110.3 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:32096885 C>A maps to NM_022110.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr9:108397355 G>T maps to NM_006731.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:154962043 T>C maps to NM_025207.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154956262 C>T maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:154960558 C>G maps to ENST00000405236 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17127347 C>T maps to NM_144997.5 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:17117141 T>A maps to NM_144997.5 K523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:152279054 C>T maps to NM_002016.1 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152282981 G>T maps to NM_002016.1 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152283358 C>A maps to NM_002016.1 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:152281323 G>C maps to NM_002016.1 S2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152277575 G>A maps to NM_002016.1 A3262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:152281949 T>G maps to NM_002016.1 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:152276507 T>G maps to NM_002016.1 A3618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:152283734 C>A maps to NM_002016.1 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:152279609 A>G maps to NM_002016.1 S2584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152283464 C>T maps to NM_002016.1 R1299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:152277155 C>T maps to NM_002016.1 R3402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:152281969 G>T maps to NM_002016.1 R1798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:152283677 G>A maps to NM_002016.1 D1228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:152281631 T>G maps to NM_002016.1 T1910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152281931 C>T maps to NM_002016.1 Q1810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:152284187 G>T maps to NM_002016.1 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152279938 C>A maps to NM_002016.1 G2475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:152283962 C>T maps to NM_002016.1 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:152285558 T>A maps to NM_002016.1 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:152281730 G>T maps to NM_002016.1 G1877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:152283026 C>T maps to NM_002016.1 V1445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:152284041 G>C maps to NM_002016.1 S1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr1:152279738 G>A maps to NM_002016.1 A2541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:152280767 T>C maps to NM_002016.1 Q2198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr1:152280503 G>A maps to NM_002016.1 H2286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:152277575 G>T maps to NM_002016.1 A3262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:152280731 A>G maps to NM_002016.1 H2210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:152283883 C>A maps to NM_002016.1 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:152282996 G>A maps to NM_002016.1 H1455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:152282657 G>T maps to NM_002016.1 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:152285471 G>A maps to NM_002016.1 H630H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:152277653 G>T maps to NM_002016.1 S3236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:152275964 G>T maps to NM_002016.1 A3799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:152279987 A>T maps to NM_002016.1 G2458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:152279700 G>T maps to NM_002016.1 S2554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:152279738 G>T maps to NM_002016.1 A2541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:152280901 G>A maps to NM_002016.1 Q2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:152282135 G>T maps to NM_002016.1 P1742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:152282768 G>T maps to NM_002016.1 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:152284874 G>T maps to NM_002016.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:152278661 A>G maps to NM_002016.1 H2900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:152282528 A>T maps to NM_002016.1 S1611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152276228 G>T maps to NM_002016.1 L3711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152280815 C>G maps to NM_002016.1 G2182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152285525 C>T maps to NM_002016.1 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr1:152283413 T>C maps to NM_002016.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:152283877 G>A maps to NM_002016.1 Q1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:152284625 A>T maps to NM_002016.1 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:152280611 C>T maps to NM_002016.1 E2250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:152275892 G>A maps to NM_002016.1 S3823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:152276705 A>T maps to NM_002016.1 S3552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:152283722 G>T maps to NM_002016.1 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:152281399 C>A maps to NM_002016.1 G1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:152278934 A>G maps to NM_002016.1 S2809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:152286188 T>C maps to NM_002016.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152323751 G>C maps to NM_001014342.2 S2170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152329768 G>A maps to NM_001014342.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152326310 C>T maps to NM_001014342.2 Q1317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152327810 G>A maps to NM_001014342.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:152323526 G>T maps to NM_001014342.2 S2245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152324582 T>G maps to NM_001014342.2 S1893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:152325344 T>G maps to NM_001014342.2 T1639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:152324369 G>T maps to NM_001014342.2 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:152323526 G>C maps to NM_001014342.2 S2245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:152328818 T>C maps to NM_001014342.2 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:152327630 G>A maps to NM_001014342.2 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:152329305 G>T maps to NM_001014342.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:152327319 G>T maps to NM_001014342.2 S981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:152323622 G>A maps to NM_001014342.2 S2213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:152323946 G>A maps to NM_001014342.2 H2105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:152324099 G>T maps to NM_001014342.2 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:152327854 G>A maps to NM_001014342.2 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152323125 G>C maps to NM_001014342.2 S2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:152328161 T>G maps to NM_001014342.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:152329648 T>A maps to NM_001014342.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:152327651 G>A maps to NM_001014342.2 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:152326896 G>T maps to NM_001014342.2 S1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152327849 G>T maps to NM_001014342.2 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:152325707 T>A maps to NM_001014342.2 S1518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:152326859 G>T maps to NM_001014342.2 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr1:152329307 C>T maps to NM_001014342.2 Q318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:128680586 A>T maps to NM_002017.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:128638057 G>T maps to NM_002017.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr11:128680405 C>T maps to NM_002017.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:128628041 C>A maps to NM_002017.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:128677123 G>T maps to NM_002017.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:18151881 C>T maps to NM_002018.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:18150354 C>T maps to NM_002018.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:18155794 C>T maps to NM_002018.2 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:21546373 G>T maps to NM_018071.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr14:21546382 A>T maps to NM_018071.3 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr14:21548905 G>T maps to NM_018071.3 E821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:78389002 G>A maps to NM_173627.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:106300652 G>A maps to NM_175884.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:60982839 C>A maps to NM_173667.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:142487878 C>T maps to NM_207414.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:142505488 G>T maps to NM_207414.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:142480702 G>T maps to NM_207414.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:142450388 G>T maps to NM_207414.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr8:142490534 G>T maps to NM_207414.2 S255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr8:142444084 C>T maps to NM_207414.2 Q1310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:142506507 G>T maps to NM_207414.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:84607298 C>T maps to NM_001001670.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:84609107 C>A maps to NM_001001670.2 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:84609842 T>G maps to NM_001001670.2 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:84603913 C>T maps to NM_001001670.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:84606359 G>A maps to NM_001001670.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:84606401 T>C maps to NM_001001670.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr9:84605876 T>A maps to NM_001001670.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:84607512 C>T maps to NM_001001670.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:84606678 G>T maps to NM_001001670.2 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:84606977 C>T maps to NM_001001670.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr9:84608953 C>G maps to NM_001001670.2 S1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:84603852 G>T maps to NM_001001670.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:84607298 C>A maps to NM_001001670.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:84606239 C>T maps to NM_001001670.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153581772 G>C did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:153587757 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:153590121 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:153588256 G>C did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:153579292 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:153590913 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:153582820 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:153596270 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:153588196 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:153590145 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:153588367 A>G did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:153577353 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:153577354 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:153589707 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153596103 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:153581506 C>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:153585926 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:153588706 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:153593510 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153593197 C>A did not map to a codon.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr23:153588904 G>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:153599394 G>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:153595007 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:153589729 G>C did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:153589730 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153578208 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153593595 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:153591029 C>A did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:153581718 C>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:153590627 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:153590477 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:153593004 C>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:153593757 C>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:153593557 A>G did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153596390 G>A did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:153586811 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:153587762 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:153587459 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:153590133 T>G did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:153590840 T>C did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:153586886 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr23:153581234 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:153582538 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:153593021 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58154383 A>T maps to NM_001164317.1 T2503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:58080587 G>T maps to NM_001164317.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:58111326 G>C maps to NM_001164317.1 V1306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:58135871 C>G maps to NM_001164317.1 V2126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:58083618 C>T maps to NM_001164317.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:57994581 C>A maps to NM_001164317.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:57994536 G>T maps to NM_001164317.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:58124066 C>T maps to NM_001164317.1 A1671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:128470852 C>A maps to NM_001458.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128493675 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:128496862 C>T maps to NM_001458.4 N2483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:128490514 G>T maps to NM_001458.4 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:128493587 G>T maps to NM_001458.4 E2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:128491635 C>T maps to NM_001458.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:128480719 C>A maps to NM_001458.4 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:128492993 G>A maps to NM_001458.4 G2039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:128478699 G>A maps to NM_001458.4 Q418Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:128487898 G>T maps to NM_001458.4 V1479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:128486490 G>A maps to NM_001458.4 K1367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:128484761 G>A maps to NM_001458.4 A1081A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:128489394 G>A maps to NM_001458.4 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:128493820 C>T maps to NM_001458.4 I2138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:128489238 C>T maps to NM_001458.4 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr7:128494175 C>G maps to NM_001458.4 T2211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr7:128493014 C>G maps to NM_001458.4 V2046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:128491662 C>A maps to NM_001458.4 P1941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:128492670 C>T maps to NM_001458.4 L1957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:128494599 G>T maps to NM_001458.4 T2287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr7:128490866 G>A maps to NM_001458.4 R1803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:128488077 C>T maps to NM_001458.4 P1512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:128477507 C>A maps to NM_001458.4 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:128494958 G>A maps to NM_001458.4 Q2376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:128489514 G>A maps to NM_001458.4 V1694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr7:128486042 G>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:30708996 C>T maps to NM_005803.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr17:27208842 G>A maps to ENST00000394906 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:86088718 A>G maps to NM_013231.4 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:86089393 C>A maps to NM_013231.4 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:86088697 G>T maps to NM_013231.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:86088547 C>A maps to NM_013231.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:86088907 C>A maps to NM_013231.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:86088895 G>T maps to NM_013231.4 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr14:86087947 G>T maps to NM_013231.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:86088907 C>G maps to NM_013231.4 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr14:86088583 G>C maps to NM_013231.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:86089276 T>A maps to NM_013231.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:86089576 C>A maps to NM_013231.4 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr14:86089744 C>G maps to NM_013231.4 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:86089222 G>A maps to NM_013231.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr14:86088226 C>A maps to NM_013231.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:86088161 G>T maps to NM_013231.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:14306823 C>G maps to NM_198391.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr20:14306547 C>T maps to NM_198391.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:28959103 G>T maps to NM_002019.4 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:29005448 T>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:28877396 G>T maps to NM_002019.4 T1308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr13:28901628 C>T maps to NM_002019.4 K922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr13:28885794 G>A maps to NM_002019.4 F1189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr13:28896488 G>A maps to NM_002019.4 D987D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr13:28893580 G>A maps to NM_002019.4 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr13:28903860 C>T maps to NM_002019.4 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr13:29012432 T>A maps to NM_002019.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:29005429 G>A maps to NM_002019.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:28602426 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:28599081 T>C did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr13:28602365 G>A maps to NM_004119.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:28608039 G>A maps to NM_004119.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:28588650 G>T maps to NM_004119.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:28626685 C>A maps to NM_004119.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr13:28589731 G>T maps to NM_004119.2 S883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr13:28608087 G>A maps to NM_004119.2 N626N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:28644626 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180048746 C>A maps to NM_182925.4 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:180047709 C>A maps to NM_182925.4 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:180057087 C>T maps to NM_182925.4 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:180058773 C>T maps to NM_182925.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:180057744 G>T maps to NM_182925.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:180038480 T>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:213058633 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:76045407 C>A maps to NM_017791.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:76107372 C>A maps to NM_017791.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr14:76107309 T>C maps to NM_017791.2 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:2980840 G>T maps to ENST00000399667 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:2946545 C>G maps to NM_138439.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr15:33261483 C>T maps to NM_001103184.2 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:33261645 C>A maps to NM_001103184.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:33357256 C>A maps to NM_001103184.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:240497462 C>T maps to ENST00000406993 Q1710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:240256719 T>A maps to ENST00000406993 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:240371459 G>A maps to ENST00000406993 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:240371672 G>T maps to ENST00000406993 P1330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:240497407 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:240370907 C>A maps to ENST00000406993 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:240370488 C>T maps to ENST00000406993 R936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:240421288 A>T maps to ENST00000406993 I1513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:240255645 G>T maps to ENST00000406993 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:240370520 C>A maps to ENST00000406993 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:240255780 G>C maps to ENST00000406993 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:240370130 C>A maps to ENST00000406993 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:240601507 G>A maps to ENST00000406993 E1829E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:240371696 A>T maps to ENST00000406993 I1338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:240370505 C>T maps to ENST00000406993 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:240255601 A>T maps to ENST00000406993 K208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:240370727 C>A maps to ENST00000406993 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:240492662 C>A maps to ENST00000406993 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:240255982 C>T maps to ENST00000406993 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:240255696 T>C maps to ENST00000406993 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:240371124 G>T maps to ENST00000406993 G1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:43320573 C>A maps to NM_005892.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:43313571 C>T maps to NM_005892.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:153476137 T>A maps to NM_052905.3 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:153399311 G>T maps to NM_052905.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:50045836 C>G maps to NM_175736.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:50062265 C>T maps to NM_175736.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:50045883 C>A maps to NM_175736.4 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:171254535 C>A maps to NM_002021.1 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:171227349 A>T maps to NM_002021.1 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:171251410 C>A maps to NM_002021.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:171236681 G>T maps to NM_002021.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:171254424 C>A maps to NM_002021.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:171250034 C>T maps to NM_002021.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:171154953 T>G maps to NM_001460.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:171083398 A>G maps to NM_006894.5 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:171076826 C>A maps to NM_006894.5 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:171310611 C>T maps to NM_002022.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:171306561 A>G maps to NM_002022.1 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:171303750 C>T maps to NM_002022.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:171293329 G>A maps to NM_002022.1 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:171292286 G>T maps to NM_002022.1 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:203316789 C>A maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:203316984 G>A maps to NM_002023.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:203316692 G>T maps to NM_002023.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:203316863 T>A maps to NM_002023.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:147024764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:147010236 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:147011476 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:147009853 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:147030275 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:147027065 A>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:147024826 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:147019023 A>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:147014082 A>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:147018984 G>C did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:147011468 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:147011490 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:147026522 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:147026523 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:147011748 A>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:147007064 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:147014251 G>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:147106431 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:147084780 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:147062974 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:147062984 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:147084781 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:147106419 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:147084782 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:147062984 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:147063057 G>C did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:147062997 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:147063137 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:147084796 A>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:147063198 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216272027 A>G maps to NM_212482.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr2:216295506 G>A maps to NM_212482.1 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:216248812 A>T maps to NM_212482.1 T1608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:216269166 G>T maps to NM_212482.1 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:216237098 C>G did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr2:216247048 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:216262477 C>A maps to NM_212482.1 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:216285399 G>A maps to NM_212482.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:216286822 G>A maps to NM_212482.1 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:216296670 C>A maps to NM_212482.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:80708483 C>T maps to NM_022158.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:80680681 A>T maps to NM_024619.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr17:80676906 G>A maps to NM_024619.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr17:80684396 G>A maps to NM_024619.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr9:132689527 A>G maps to NM_015033.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:93965083 T>A maps to ENST00000370253 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:94014885 C>T maps to ENST00000370253 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:47774471 T>A maps to NM_015308.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:47767697 C>T maps to NM_015308.2 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:47767895 T>C maps to NM_015308.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:159642651 C>A maps to NM_032532.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:159653379 G>T maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:159653415 G>T maps to NM_032532.2 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:159653295 G>T maps to NM_032532.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:159655019 C>A maps to NM_032532.2 S1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr6:159655176 C>A maps to NM_032532.2 G1211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr6:159672373 G>T maps to NM_032532.2 P1625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:159654109 C>T maps to NM_032532.2 R856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:159687131 G>A maps to NM_032532.2 W1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:159653934 C>T maps to NM_032532.2 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:159688833 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:49777384 C>T maps to NM_001079673.1 Q1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:172052792 G>A maps to NM_022763.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:172025272 A>T maps to NM_022763.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:172115081 C>T maps to NM_022763.3 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:171830325 G>T maps to NM_022763.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:172052735 G>A maps to NM_022763.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:172065049 G>T maps to NM_022763.3 G805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:172080422 G>C maps to NM_022763.3 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:27715646 C>A maps to NM_022823.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:33330311 C>A maps to ENST00000291421 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:33333800 G>T maps to ENST00000291421 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:33333812 C>T maps to ENST00000291421 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:109270512 G>T maps to NM_001144937.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:109268417 C>T maps to NM_001144937.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:109268627 T>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr17:33454198 G>A maps to NM_017559.2 G116G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z055-01A-01W-0747-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:131008459 A>G maps to NM_133372.2 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:131055008 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:159753233 G>C maps to ENST00000379346 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:42927366 C>T maps to NM_002027.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr8:42911656 G>T maps to NM_002027.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr8:42919325 T>C maps to NM_002027.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:49186289 C>G maps to NM_004476.1 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:49221941 A>T maps to NM_004476.1 L92L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-3396-01A-01D-1553-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr11:49178266 A>G did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr11:49207298 C>A maps to NM_004476.1 G250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:49208287 C>A maps to NM_004476.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:49204728 C>A maps to NM_004476.1 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:49178306 C>A maps to NM_004476.1 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:49170213 C>A maps to NM_004476.1 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:49197487 T>A maps to NM_004476.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:89403611 G>A maps to NM_153696.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:89403575 C>A maps to NM_153696.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:89405080 C>A maps to NM_153696.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:89424613 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:89402587 A>G maps to NM_153696.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:89405071 G>T maps to NM_153696.2 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:89402665 T>C maps to NM_153696.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:89431655 T>C maps to NM_153696.2 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:89413825 A>T maps to NM_153696.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr11:71906938 A>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:71932568 C>A maps to NM_001113536.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr11:71847042 G>A maps to ENST00000442948 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr11:94040719 G>T maps to NM_001080486.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:94040827 C>T maps to NM_001080486.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:45973885 G>A did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:65660406 C>A maps to NM_005438.3 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:28635134 G>A maps to NM_005253.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:38061775 C>A maps to NM_004496.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:38060893 C>T maps to NM_004496.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:38060626 G>A maps to NM_004496.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:38061609 G>A maps to NM_004496.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:46376129 A>T maps to NM_004497.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:60297986 G>T maps to NM_012182.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr15:60297752 C>T maps to NM_012182.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr15:60298112 C>G maps to NM_012182.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:79635142 T>C maps to NM_001013735.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79635400 C>A maps to NM_001013735.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:79634848 C>T maps to NM_001013735.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:79635337 C>A maps to NM_001013735.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:79635202 G>A maps to NM_001013735.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr9:79635319 C>A maps to NM_001013735.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr9:79634671 G>T maps to NM_001013735.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr9:79635355 C>T maps to NM_001013735.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:79635202 G>C maps to NM_001013735.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:79635313 G>T maps to NM_001013735.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:1611204 G>A maps to NM_001453.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:86602191 C>G maps to NM_005251.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr16:86601303 C>A maps to NM_005251.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:47904181 G>T maps to NM_004474.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:63789367 C>T maps to NM_012183.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:116940 C>T maps to NM_207305.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:114257954 A>T maps to NM_012184.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:70177794 C>A maps to NM_001126334.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:70177785 C>A maps to NM_001126334.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:100616543 C>T maps to NM_004473.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr9:100617227 G>A maps to NM_004473.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:86545095 C>T maps to NM_001451.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr16:86544432 G>T maps to NM_001451.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:1390694 C>T maps to NM_001452.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:1390745 G>A maps to NM_001452.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr14:29237714 C>T maps to NM_005249.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr14:29237816 G>A maps to NM_005249.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:29237306 G>T maps to NM_005249.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:29237171 C>A maps to NM_005249.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:29237186 C>A maps to NM_005249.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:29237644 C>A maps to NM_005249.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:29237063 C>G maps to NM_005249.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:29237672 C>T maps to NM_005249.3 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:29237048 G>T maps to NM_005249.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr14:29237720 C>A maps to NM_005249.3 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:29237534 G>A maps to NM_005249.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:169533119 C>G maps to NM_012188.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:169533257 G>A maps to NM_012188.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:169533077 G>A maps to NM_012188.4 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:169535353 G>C maps to NM_012188.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr5:169533053 C>A maps to NM_012188.4 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr5:169533096 C>A maps to NM_012188.4 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:169535128 G>A maps to NM_012188.4 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:169535260 C>A maps to NM_012188.4 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:169533164 C>A maps to NM_012188.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr10:129537210 G>T maps to NM_207426.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:129535890 G>A maps to NM_207426.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr12:8196335 C>T maps to NM_018416.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:42744309 A>T maps to NM_001198850.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:42744123 T>C maps to NM_001198850.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:42645381 T>A maps to NM_001198850.1 *623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:4796695 G>T maps to ENST00000450194 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:4800710 C>T maps to ENST00000450194 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:4798714 G>A maps to ENST00000450194 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:80478021 G>T maps to NM_004514.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr17:80559373 A>T maps to NM_004514.3 *661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:86612496 G>A maps to NM_005250.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr16:86613132 G>T maps to NM_005250.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:86612676 G>C maps to NM_005250.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr16:86612658 G>T maps to NM_005250.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:138665315 G>A maps to NM_023067.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:138665255 G>T maps to NM_023067.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:138665135 G>C maps to NM_023067.3 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:138665396 C>G maps to NM_023067.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:138665306 C>T maps to NM_023067.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr12:2968028 A>G maps to NM_202002.1 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:26851621 C>G maps to NM_003593.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:26864297 G>A maps to NM_003593.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:48573634 A>G maps to NM_002158.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:48600428 A>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:109719545 C>A maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:109719577 G>T maps to NM_213596.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:109723223 G>C maps to NM_213596.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:109719545 C>T maps to NM_213596.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr13:41134853 G>A maps to NM_002015.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:108985208 G>A maps to NM_001455.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:70321309 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:70321151 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:70321391 C>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:70321241 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:70321242 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:70320965 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:70320770 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:70320987 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:70320854 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:70320969 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:71015117 T>C maps to NM_032682.4 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:71021827 C>G did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr3:71050203 G>C maps to NM_032682.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:71008397 T>A maps to NM_032682.4 *678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:114302189 G>A maps to NM_148898.3 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:114294036 C>A maps to NM_148898.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr7:114066583 G>A maps to NM_148898.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:114271722 T>A maps to NM_148898.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:114269984 A>G maps to NM_148898.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:49114014 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:49111898 A>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:41557831 G>T maps to NM_001012426.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:41533599 C>A maps to NM_001012426.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr6:41558066 C>T maps to NM_001012426.1 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:1313598 G>T maps to NM_033260.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:118849734 G>T maps to NM_181721.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:118851197 A>G did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:118851415 C>A maps to NM_181721.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:55651048 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:55651038 A>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:55650339 A>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:55650321 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:55650677 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:55650436 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:55650850 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:55650675 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:126144845 G>A maps to NM_017547.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr22:36886231 C>G maps to NM_001102371.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr20:30433324 G>A maps to NM_004118.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr20:30433279 G>A maps to NM_004118.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:74664033 C>G maps to NM_001112808.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:74664009 C>A maps to NM_001112808.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:74670340 G>T maps to NM_003838.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:74670276 G>A maps to NM_003838.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:52250184 G>T maps to NM_002029.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:52250112 C>G maps to NM_002029.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:52249722 G>T maps to NM_002029.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:52250121 C>A maps to NM_002029.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr19:52249893 G>A maps to NM_002029.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:52272798 C>A maps to NM_001005738.1 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52272375 C>A maps to NM_001005738.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52272423 T>C maps to NM_001005738.1 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:52272882 C>A maps to NM_001005738.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:52272483 G>T maps to NM_001005738.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:52272732 T>G maps to NM_001005738.1 Y274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:52272474 G>A maps to NM_001005738.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52327945 C>A maps to NM_002030.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52327483 C>T maps to NM_002030.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52327465 C>A maps to NM_002030.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:52328053 A>G maps to NM_002030.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:52327525 C>T maps to NM_002030.3 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:52327903 C>A maps to NM_002030.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:52327393 C>A maps to NM_002030.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:79417956 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:79447787 C>A maps to NM_025074.6 A3634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:79158661 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:79360061 A>T maps to NM_025074.6 S1791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:79343065 G>A maps to NM_025074.6 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr4:79428720 C>T maps to NM_025074.6 Q3155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:79373506 A>T maps to NM_025074.6 P2254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:79455608 G>A maps to NM_025074.6 L3644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr4:79362435 G>T maps to NM_025074.6 E1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:79387516 C>G maps to NM_025074.6 L2395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr4:79340119 G>T maps to NM_025074.6 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:79188480 G>T maps to NM_025074.6 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr4:79460482 C>T maps to NM_025074.6 F3778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:79437100 T>C maps to NM_025074.6 F3441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:79350310 C>T maps to NM_025074.6 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:79436951 G>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr4:79240018 G>T maps to NM_025074.6 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr4:79285086 C>T maps to NM_025074.6 C867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:79371404 G>T maps to NM_025074.6 G2125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:79199898 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:14797584 T>A maps to ENST00000380880 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:14823205 C>A maps to ENST00000380880 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:14848753 G>A maps to ENST00000380880 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr9:14859286 C>A maps to ENST00000380880 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:14748527 G>T maps to ENST00000380880 S1892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:14851556 G>A maps to ENST00000380880 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:14737480 A>T maps to ENST00000380880 C2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:14824822 A>T maps to ENST00000380880 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:14776137 C>A maps to ENST00000380880 V1505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:14819376 G>A maps to ENST00000380880 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr9:14808013 A>G maps to ENST00000380880 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:14746989 A>G maps to ENST00000380880 F2026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:14859202 T>C maps to ENST00000380880 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:14746968 C>A maps to ENST00000380880 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr9:14848693 A>G maps to ENST00000380880 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr9:14776191 G>A maps to ENST00000380880 I1487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:39435605 G>T maps to NM_207361.4 E2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:39454432 C>A maps to NM_207361.4 R3007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:39266238 C>A maps to NM_207361.4 T1586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:39266286 C>A maps to NM_207361.4 I1602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:39265302 A>G maps to NM_207361.4 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:39448685 G>A maps to NM_207361.4 E2748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr13:39263806 C>T maps to NM_207361.4 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:39265119 C>G maps to NM_207361.4 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:39263817 C>A maps to NM_207361.4 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:39425096 C>G maps to NM_207361.4 P2198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr13:39263979 C>T maps to NM_207361.4 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:135438788 C>T maps to ENST00000443774 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:135438866 G>C maps to ENST00000443774 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr10:135440216 G>C maps to ENST00000443774 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:135440222 G>T maps to ENST00000443774 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:135440113 T>A maps to ENST00000443774 K45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr10:135440174 G>A maps to ENST00000443774 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:135440207 G>T maps to ENST00000443774 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr6:168479734 G>T maps to NM_024919.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr6:168479735 G>T maps to NM_024919.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr6:168479585 C>A maps to NM_024919.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr9:86004517 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:85926821 C>T maps to NM_174938.4 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:85926823 T>A maps to NM_174938.4 K251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:85914068 G>C maps to NM_174938.4 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr9:85950555 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:13779903 C>A maps to NM_018027.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:13698954 C>T maps to NM_018027.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:13735909 G>A maps to NM_018027.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:13702485 T>A maps to NM_018027.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr10:13735982 C>A maps to NM_018027.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr10:13779861 A>G maps to NM_018027.3 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:69225772 G>A maps to NM_015123.1 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:69271057 C>A maps to NM_015123.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr3:69230695 T>C maps to NM_015123.1 Q735Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:44198063 C>T maps to NM_032892.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:52188725 G>T maps to ENST00000344768 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:52179251 G>T maps to ENST00000344768 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:52188790 A>T maps to ENST00000344768 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr14:52194665 A>G maps to ENST00000344768 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:131228117 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:131212509 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:131231334 A>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:131212989 T>A did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:131212857 G>C did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:131212039 C>G did not map to a codon.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr23:131212271 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:131214235 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:131212379 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:131234701 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:131234702 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:131212131 T>C did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:131219610 G>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:131212725 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:131212528 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:131212670 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:131212488 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:131219732 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:131234702 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:65167215 C>T maps to NM_031904.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:37711391 G>C maps to NM_014907.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:37746357 A>C maps to NM_014907.2 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:37745335 G>T maps to NM_014907.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr9:37746018 G>A maps to NM_014907.2 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:37730992 G>T maps to NM_014907.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:37746165 C>A maps to NM_014907.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr9:37745407 G>T maps to NM_014907.2 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr9:37732365 C>A maps to NM_014907.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:37707436 G>A maps to NM_014907.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:37724226 T>C maps to NM_014907.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:37744665 A>C maps to NM_014907.2 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr9:37732368 G>T maps to NM_014907.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:37692733 G>A maps to NM_014907.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr9:37731097 C>T maps to NM_014907.2 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr10:49440182 G>C maps to NM_001018071.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:49444597 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:49450215 A>T maps to NM_001018071.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:49440191 C>T maps to NM_001018071.3 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:49459705 G>T maps to NM_001018071.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:49450293 C>T maps to NM_001018071.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:49393667 T>A maps to NM_001018071.3 K763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:49414916 C>T maps to NM_001018071.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr10:49447709 C>T maps to NM_001018071.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:49431293 C>A maps to NM_001018071.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:49420092 C>T maps to NM_001018071.3 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr10:49450361 G>A maps to NM_001018071.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:12736344 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:12722557 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:12722585 G>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:12734336 A>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:12725740 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:12725741 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:12736248 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:12722506 C>G did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:12708434 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:12735648 G>C did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:12725669 T>A did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:12734960 G>C did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:12725754 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:12632917 C>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr23:12736240 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:12725694 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:12728531 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:12736043 T>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:12516807 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:12157101 C>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:12704278 G>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:12735830 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:12736195 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:12734878 G>C did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:12736564 A>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:12735645 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:12720053 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:12736160 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:12736161 A>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:12734442 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:12734514 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:12722576 T>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:12735848 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:12734241 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:12735852 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:12516864 C>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:12734960 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:12708424 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:12708443 A>G did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:12701694 G>A did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:12734351 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:12736289 T>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:12627908 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:12734685 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:12734827 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:100183081 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:100185117 G>A maps to NM_001013660.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:69965980 A>T maps to NM_006654.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:69968446 G>T maps to NM_006654.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:69965137 G>A maps to NM_006654.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:69968090 C>T maps to NM_006654.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:41743229 G>T maps to NM_006653.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:41740638 C>A maps to NM_006653.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:41738848 G>A maps to NM_006653.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:32783212 G>T maps to NM_023037.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:32836596 T>A maps to NM_023037.2 I2588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:32783855 T>A maps to NM_023037.2 V1470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:32745187 A>C maps to NM_023037.2 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:32868708 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr13:32776614 A>T maps to NM_023037.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr13:32835908 G>T maps to NM_023037.2 E2525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:32802629 G>T maps to NM_023037.2 P1748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr13:32848977 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr13:32731474 G>T maps to NM_023037.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:48592823 G>T maps to NM_015030.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:48569379 A>G maps to NM_015030.1 Y1018Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:48636352 A>C maps to NM_015030.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr4:48583535 C>T maps to NM_015030.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:48584627 A>T maps to NM_015030.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr4:48622704 C>A maps to NM_015030.1 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr4:48542535 C>T maps to NM_015030.1 K2043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:48622677 G>T maps to NM_015030.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:48517100 C>T maps to NM_015030.1 L2627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:48559525 C>A maps to NM_015030.1 G1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr4:48584692 G>A maps to NM_015030.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:183707256 T>A maps to NM_001463.3 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:183699581 G>T maps to NM_001463.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:183730973 C>A maps to NM_001463.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:183731174 C>A maps to NM_001463.3 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:44975464 A>T maps to NM_032135.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr14:44975065 A>T maps to NM_032135.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:44975659 T>C maps to NM_032135.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44974150 A>T maps to NM_032135.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:44976030 C>A maps to NM_032135.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:44973895 C>A maps to NM_032135.3 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:44975737 C>A maps to NM_032135.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:44975730 C>A maps to NM_032135.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:44973865 C>T maps to NM_032135.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:44974569 C>A maps to NM_032135.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:44975323 G>C maps to NM_032135.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:5642886 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:127238613 C>T maps to NM_020369.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:127240302 C>A maps to NM_020369.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:127235647 C>A maps to NM_020369.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:127235689 G>C maps to NM_020369.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:127239487 C>A maps to NM_020369.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:4307949 G>T maps to NM_024333.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr19:4312014 G>T maps to NM_024333.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:83440921 G>T maps to NM_001007122.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:83440920 G>T maps to NM_001007122.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:83451731 C>A maps to NM_001007122.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr11:30253604 C>A maps to NM_001018080.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:30253481 T>A maps to NM_001018080.1 C11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:49190599 C>A maps to NM_000145.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:49190744 G>A maps to NM_000145.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:49189949 G>T maps to NM_000145.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:49195958 C>A maps to NM_000145.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:49217718 G>T maps to NM_000145.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:49195970 A>G maps to NM_000145.3 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:49190147 C>G maps to NM_000145.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:49190510 G>C maps to NM_000145.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:49295428 C>G maps to NM_000145.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:49190936 C>T maps to NM_000145.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr2:49210286 C>A maps to NM_000145.3 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:49190831 G>T maps to NM_000145.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:49190603 G>T maps to NM_000145.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:49216158 C>A maps to NM_000145.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:49210067 G>T maps to NM_000145.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:49190563 C>A maps to NM_000145.3 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:49195910 C>T maps to NM_000145.3 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:40034008 T>A maps to NM_152597.4 K218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:40018854 C>A maps to NM_152597.4 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:40068672 G>C maps to NM_152597.4 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:186671024 G>T maps to NM_173651.2 T5753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:186670277 C>A maps to NM_173651.2 I5504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:186672479 C>A maps to NM_173651.2 I6238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:186670133 T>C maps to NM_173651.2 D5456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:186672188 A>C maps to NM_173651.2 V6141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:186672890 C>A maps to NM_173651.2 G6375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:186673097 C>T maps to NM_173651.2 F6444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:186673451 A>T maps to NM_173651.2 T6562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:186671624 T>A maps to NM_173651.2 P5953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:186672998 G>T maps to NM_173651.2 V6411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:186678573 A>G maps to NM_173651.2 K6799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:186672284 G>T maps to NM_173651.2 V6173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:186671327 C>T maps to NM_173651.2 P5854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:186673153 C>A maps to NM_173651.2 S6463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:186672737 C>A maps to NM_173651.2 T6324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr2:186680100 G>T maps to NM_173651.2 E6866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr2:186672752 T>A maps to NM_173651.2 T6329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:186670642 C>G maps to NM_173651.2 S5626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:186670280 C>A maps to NM_173651.2 T5505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:52778791 C>A maps to NM_013409.1 C56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:52779974 C>T maps to NM_013409.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:52781806 G>T maps to NM_013409.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:52780022 T>C maps to NM_013409.1 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:52778749 C>A maps to NM_013409.1 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:52779454 G>A maps to NM_013409.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr5:52779493 A>G maps to NM_013409.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:52780010 G>A maps to NM_013409.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr3:120134835 C>A maps to NM_007085.4 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:681420 G>T maps to NM_005860.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr5:132534870 G>A maps to NM_015082.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:132652221 G>A maps to NM_015082.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:132652222 G>A maps to NM_015082.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:162376241 C>A maps to NM_020116.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:163032428 T>A maps to NM_020116.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:162508658 G>T maps to NM_020116.3 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:162380416 G>A maps to NM_020116.3 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:162841555 C>A maps to NM_020116.3 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:162841739 G>A maps to NM_020116.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:162577479 A>G maps to NM_020116.3 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:162577479 A>G maps to NM_020116.3 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:162380376 G>T maps to NM_020116.3 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr21:47570080 G>A maps to ENST00000397748 C286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr21:47571591 C>A maps to ENST00000397748 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:61732336 G>T maps to NM_002032.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:31089805 G>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:31089626 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:31089830 G>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:31089981 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:31089992 C>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:31090016 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:31089889 C>A did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:31089930 A>G did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:31089958 T>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:31089959 A>C did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:49469608 G>T maps to NM_000146.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:121187927 G>T maps to NM_177478.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:121188071 C>A maps to NM_177478.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:121188314 G>T maps to NM_177478.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:121187759 G>T maps to NM_177478.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:121188293 G>T maps to NM_177478.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr5:121187741 C>A maps to NM_177478.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:53878064 A>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:48340054 G>T did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:48339588 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:48341099 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:48339683 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:48339834 A>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:48339577 A>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:48336505 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:2279092 C>T maps to NM_013393.1 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr7:2279317 G>A maps to NM_013393.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:2279287 C>G maps to NM_013393.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61897778 C>A maps to NM_017647.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:61904228 G>T maps to NM_017647.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:71319390 C>A maps to NM_018348.5 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:71318328 C>A maps to NM_018348.5 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:71318472 C>A maps to NM_018348.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:71318667 C>A maps to NM_018348.5 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71318652 C>A maps to NM_018348.5 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:71318241 C>A maps to NM_018348.5 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:71318898 C>A maps to NM_018348.5 G309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:71318217 T>A maps to NM_018348.5 K536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr16:71318472 C>A maps to NM_018348.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:71317668 G>A maps to NM_018348.5 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr16:71318328 C>A maps to NM_018348.5 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:71317673 G>C maps to NM_018348.5 S717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:37427351 G>A maps to NM_015050.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:37430667 G>A maps to NM_015050.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:78430611 C>A maps to ENST00000436586 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:78425922 G>A maps to ENST00000436586 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr1:78435672 T>A maps to ENST00000436586 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:70501838 G>T maps to NM_145059.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:70497655 G>A maps to NM_145059.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:70497128 C>T maps to NM_145059.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:70503107 G>A maps to NM_145059.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr16:70512185 C>T maps to NM_145059.2 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:70513218 T>C maps to NM_145059.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:44386526 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:154282907 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:154261736 T>A did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:154274856 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:154280017 A>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:154282871 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:154261778 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:91423350 G>T maps to NM_002569.2 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:91419748 G>T maps to NM_002569.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:91424921 C>T maps to NM_002569.2 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:31202718 G>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:31201041 C>G maps to NM_004960.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr16:31200442 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:49253551 G>A maps to NM_000148.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:49254138 C>A maps to NM_000148.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:33247176 C>A maps to ENST00000380081 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr8:33247082 T>A maps to ENST00000380081 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:75533498 C>G maps to NM_173540.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:75533399 C>T maps to NM_173540.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:49206479 C>T maps to NM_001097638.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr19:49206737 G>C maps to NM_001097638.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:94278600 G>A maps to NM_002033.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:94278000 C>A maps to NM_002033.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:5832191 C>T maps to NM_001040701.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:5832236 G>C maps to NM_001040701.1 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:5832020 C>A maps to NM_001040701.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:66188640 G>T maps to NM_178155.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr14:66096227 A>T maps to NM_178155.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:66136029 C>T maps to NM_178155.1 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr14:66096221 G>T maps to NM_178155.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:66208905 G>A maps to NM_178155.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr14:66200026 A>G maps to NM_178155.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:96651792 G>T maps to NM_006581.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:96651471 C>A maps to NM_006581.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:96651789 C>A maps to NM_006581.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:96651884 C>A maps to NM_006581.3 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:96651315 G>T maps to NM_006581.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:96651654 G>A maps to NM_006581.3 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:50314902 C>T maps to NM_025129.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:6503348 C>A maps to NM_012192.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:180675673 G>T maps to NM_005087.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:180675674 A>T maps to NM_005087.3 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:180667012 A>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:180693107 T>C maps to NM_005087.3 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:7499144 C>A maps to NM_004860.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:7496105 G>C maps to NM_004860.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:117693432 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:35657167 C>A maps to NM_001164605.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:117711079 G>T maps to NM_001164831.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:117710518 A>G maps to NM_001164831.1 *96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:39202803 C>A maps to ENST00000263405 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:39153584 T>C maps to ENST00000263405 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:39202015 G>T maps to ENST00000263405 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:39134974 T>G maps to ENST00000263405 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:39202378 G>A maps to ENST00000263405 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:39202771 G>A maps to ENST00000263405 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr5:39202549 G>T maps to ENST00000263405 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:39119120 T>C maps to ENST00000263405 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:39119033 T>C maps to ENST00000263405 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr5:39127874 A>C maps to ENST00000263405 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:39110455 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:46009261 G>A maps to NM_024513.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:46023126 C>A maps to NM_024513.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:46009514 C>T maps to NM_024513.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:46014652 C>A maps to NM_024513.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr3:46009256 T>C maps to NM_024513.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:112021337 C>G maps to NM_002037.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:112024100 T>A maps to NM_153047.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:111983135 C>A maps to NM_153047.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:90895970 G>T maps to NM_003505.1 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr7:90895394 G>A maps to NM_003505.1 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:90895179 C>T maps to NM_003505.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:90895710 C>T maps to NM_003505.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:90895850 C>T maps to NM_003505.1 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:130648390 G>T maps to NM_007197.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr12:130648188 G>A maps to NM_007197.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:130647969 C>G maps to NM_007197.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:130648251 C>A maps to NM_007197.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:130648758 G>C maps to NM_007197.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:130648983 C>G maps to NM_007197.3 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr12:130648509 G>A maps to NM_007197.3 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:42635928 G>T maps to NM_001466.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42635671 A>T maps to NM_001466.3 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:42636024 G>A maps to NM_001466.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:42636255 C>T maps to NM_001466.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr17:42635329 C>T maps to NM_001466.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:42635886 G>A maps to NM_001466.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:28378249 C>G maps to NM_017412.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:86662264 C>T maps to NM_012193.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:86666064 C>A maps to NM_012193.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:86662525 C>G maps to NM_012193.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr11:86662522 T>G maps to NM_012193.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:208633088 G>A maps to NM_003468.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr2:208632530 G>A maps to NM_003468.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr8:104330999 G>A maps to NM_003506.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:202899456 C>T maps to NM_003507.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202899447 G>C maps to NM_003507.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:202900671 C>T maps to NM_003507.1 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:202901056 A>T maps to NM_003507.1 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:202899756 G>A maps to NM_003507.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr2:202899741 C>T maps to NM_003507.1 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr2:202900125 C>T maps to NM_003507.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:35928959 C>T maps to NM_031866.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr10:35928704 G>A maps to NM_031866.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr7:72849737 C>A maps to NM_003508.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:3527757 G>T maps to NM_001136198.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:31066642 G>T maps to NM_017769.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:31077151 C>T maps to NM_017769.3 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:151166232 C>T maps to NM_198395.1 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:41052970 C>T maps to NM_000151.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr17:41063322 C>A maps to NM_000151.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr17:41063208 C>G maps to NM_000151.2 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:41052997 G>T maps to NM_000151.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:41063277 C>T maps to NM_000151.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:169764516 C>A maps to NM_021176.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:169764388 C>T maps to NM_021176.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:169764405 C>G maps to NM_021176.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:169763264 C>T maps to NM_021176.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr23:153764206 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:153762265 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:153760494 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:153760819 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:78086451 C>T maps to NM_001079804.1 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:78093090 G>A maps to NM_001079804.1 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr17:78092456 G>A maps to NM_001079804.1 T884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:144390296 G>A maps to NM_207123.2 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr11:77937571 G>A maps to NM_080491.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:77937814 G>T maps to NM_080491.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:77991883 C>A maps to NM_080491.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:77991884 C>T maps to NM_080491.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153927786 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:153944515 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:153925478 G>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:153927567 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:153940879 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153928278 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153944567 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:153941500 C>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:153941576 T>C did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:153944559 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr22:17445724 T>C maps to NM_001037814.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:17468884 C>T maps to NM_001037814.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:17447119 C>A maps to NM_001037814.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:17472979 G>T maps to NM_001037814.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr22:17488962 T>G maps to NM_001037814.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:17444713 C>T maps to NM_001037814.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr22:17450872 G>A maps to NM_001037814.1 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr22:17472946 G>A maps to NM_001037814.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr22:17443700 G>T maps to NM_001037814.1 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:29574724 G>A maps to NM_001470.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29599209 G>A maps to NM_001470.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:29591180 T>C maps to NM_001470.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:101216262 C>T maps to NM_005458.7 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:101151281 G>T maps to NM_005458.7 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr9:101235487 G>T maps to NM_005458.7 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:101148032 T>C maps to NM_005458.7 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr9:101052877 G>C maps to NM_005458.7 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr9:101061539 G>A maps to NM_005458.7 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr21:27136660 G>T maps to NM_002040.3 G315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr21:27124297 A>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr15:50581767 T>A maps to NM_005254.5 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151079675 A>C maps to NM_144618.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:151076125 C>T maps to NM_144618.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:161324187 T>C maps to NM_001127648.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:161302568 G>A maps to NM_001127648.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:161324409 C>A maps to NM_001127648.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr5:161318051 C>T maps to NM_001127648.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:161322791 C>A maps to NM_001127648.1 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:161277867 C>T maps to NM_001127648.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:161318004 C>T maps to NM_001127648.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:161324340 G>T maps to NM_001127648.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:161292748 T>C maps to NM_001127648.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:46252333 G>T maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:46305629 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:46314523 C>T maps to ENST00000507069 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:46314559 A>G maps to ENST00000507069 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:46307712 G>T maps to ENST00000507069 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:46305626 C>A maps to ENST00000507069 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:46252603 G>T maps to ENST00000507069 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:46390666 C>G maps to ENST00000507069 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:46307699 A>T maps to ENST00000507069 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:46334652 G>T maps to ENST00000507069 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr4:46388187 G>T maps to ENST00000507069 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:46252477 T>C maps to ENST00000507069 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr4:46334682 G>C maps to ENST00000507069 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:46334679 G>A maps to ENST00000507069 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:151514096 C>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:151424260 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:151336821 T>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:151358393 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:151453202 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:151376547 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:151393251 G>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:151366209 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:151336799 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:151336956 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:151533026 T>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:151358251 G>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:151366115 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:151532999 C>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:151366108 G>C did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:151358388 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:151532985 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:151424463 T>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:151358390 C>A did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:151376545 C>T did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:151376483 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:151424353 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:46973175 C>A maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:46930517 A>G maps to NM_000809.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:46930628 C>A maps to NM_000809.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:46967115 G>A maps to NM_000809.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:46967178 G>A maps to NM_000809.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr4:46967031 G>A maps to NM_000809.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr4:46967067 G>C maps to NM_000809.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:46967175 A>G maps to NM_000809.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:46994842 A>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:27193364 C>A maps to NM_000810.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:27185180 C>A maps to NM_000810.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:27159958 C>T maps to NM_000810.3 I169I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z005-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr15:27185072 C>G maps to NM_000810.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr15:27128617 C>T maps to NM_000810.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:27159948 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr15:27128316 C>T maps to NM_000810.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr15:27128525 G>T maps to NM_000810.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:27126075 T>A maps to NM_000810.3 L57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr15:27128647 C>A maps to NM_000810.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr15:27185159 C>A maps to NM_000810.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:161116292 G>T maps to NM_000811.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:161116289 G>A maps to NM_000811.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:161117359 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:161117219 A>T maps to NM_000811.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:161128526 G>T maps to NM_000811.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr5:161118971 C>A maps to NM_000811.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:161128658 C>A maps to NM_000811.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:161128706 A>T maps to NM_000811.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:161113239 G>T maps to NM_000811.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:161119184 T>A maps to NM_000811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr5:161116747 A>T maps to NM_000811.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:161113969 T>C maps to NM_000811.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:161128730 A>T maps to NM_000811.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:161128727 G>A maps to NM_000811.2 W437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:161116328 C>G maps to NM_000811.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:161113948 C>A maps to NM_000811.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:161128766 C>T maps to NM_000811.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:47408702 C>A maps to NM_000812.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:47034432 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:47427875 G>T maps to NM_000812.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:47322209 C>A maps to NM_000812.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:47428007 C>A maps to NM_000812.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:47427851 C>A maps to NM_000812.3 Y414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:47033972 G>T maps to NM_000812.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:47427731 C>A maps to NM_000812.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr4:47405417 C>T maps to NM_000812.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:160763717 T>A maps to NM_021911.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:160757982 G>A maps to NM_021911.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:26825484 C>T maps to NM_021912.4 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:26793026 C>T maps to NM_021912.4 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:26812797 T>A maps to NM_021912.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr15:26825466 T>A maps to NM_021912.4 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr15:27017581 G>A maps to NM_021912.4 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr15:26866524 C>A maps to NM_021912.4 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:26806213 G>T maps to NM_021912.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:26792939 T>A maps to NM_021912.4 *474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr15:26825520 C>A maps to NM_021912.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr15:26866462 G>A maps to NM_021912.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:26825553 C>T maps to NM_021912.4 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:26793244 C>A maps to NM_021912.4 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:26812731 G>T maps to NM_021912.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:1961435 C>T maps to NM_000815.4 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:1961092 C>A maps to NM_000815.4 C317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:151123872 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:151131076 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:151123292 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:151124234 G>C did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:151128374 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:151123539 C>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:151131056 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:151130894 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:151123379 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:151124290 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:151128368 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:46060555 G>A maps to NM_173536.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:46067559 G>A maps to NM_173536.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:46060351 C>A maps to NM_173536.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:46086070 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:46067502 A>C maps to NM_173536.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:46099302 G>T maps to NM_173536.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:46099312 C>T maps to NM_173536.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:46060348 G>A maps to NM_173536.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:46043193 C>A maps to NM_173536.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:46053441 G>T maps to NM_173536.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:46053596 A>T maps to NM_173536.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:46043114 C>A maps to NM_173536.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:46053638 C>A maps to NM_173536.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:46125840 C>G maps to NM_173536.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr4:46099216 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:46053440 C>A maps to NM_173536.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:161530944 G>T maps to NM_198903.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:161580242 C>T maps to NM_198903.2 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:161569236 C>A maps to NM_198903.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:161580233 G>T maps to NM_198903.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:161580355 C>G maps to NM_198903.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:161524721 C>T maps to NM_198903.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:161569248 C>A maps to NM_198903.2 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr5:161569182 C>A maps to NM_198903.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:27777960 G>T maps to NM_033223.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:27572005 T>A maps to NM_033223.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr15:27772630 C>T maps to NM_033223.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:27765181 G>A maps to NM_033223.4 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:27772702 G>C maps to NM_033223.4 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr15:27222208 G>A maps to NM_033223.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr15:27765253 A>G maps to NM_033223.4 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr15:27777804 C>T maps to NM_033223.4 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:27571990 G>A maps to NM_033223.4 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:170235646 T>C maps to NM_014211.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:170224481 T>A maps to NM_014211.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:170235602 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:170216195 T>C maps to NM_014211.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:151821208 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:151818272 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:151820192 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:151820150 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:151820032 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:151821225 C>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:151820166 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:151821212 C>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:151815582 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:151820221 C>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:151821551 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:151818268 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:151814001 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:151818237 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:151821408 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:151815583 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:151821179 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:151821536 G>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:151821219 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:151815581 T>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:151815585 G>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:151821065 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:151819032 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:151813999 C>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:151815611 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:151821479 C>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:151818214 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:151821300 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:151817738 C>A did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:151821589 G>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:151815620 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:89907908 A>G maps to NM_002042.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:89895077 G>A maps to NM_002042.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:89909083 G>A maps to NM_002042.3 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:89907944 G>A maps to NM_002042.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:89975452 C>A maps to NM_002043.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:89967430 G>C maps to NM_002043.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr6:89974244 C>A maps to NM_002043.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:97731231 G>A maps to NM_001105580.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr3:97720488 G>T maps to NM_001105580.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:97720471 T>A maps to NM_001105580.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:171716262 C>A maps to NM_000817.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:171687700 A>T maps to NM_000817.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:171704265 T>C maps to NM_000817.2 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:26518624 C>A maps to NM_001134366.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr10:26581847 C>A maps to NM_001134366.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr10:26575389 T>C maps to NM_001134366.1 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26559582 C>T maps to NM_001134366.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:26558095 A>G maps to NM_001134366.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:26507975 G>T maps to NM_001134366.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:26508070 C>G maps to NM_001134366.1 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:26506828 G>T maps to NM_001134366.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:26512828 C>A maps to NM_001134366.1 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:26507993 A>C maps to NM_001134366.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:26534848 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:26506849 C>A maps to NM_001134366.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr10:26581401 C>A maps to NM_001134366.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:92220653 C>T maps to NM_006705.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:92220728 G>T maps to NM_006705.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:30891520 A>C maps to NM_207359.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:30880602 C>A maps to NM_207359.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:49369623 C>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:49369625 G>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:49369622 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:49161403 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:49161409 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:49173665 A>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:49161354 G>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:49355829 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:905554 C>A maps to NM_005255.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:891921 G>A maps to NM_005255.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:891883 C>A maps to NM_005255.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30951022 C>A maps to NM_004861.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr22:30953304 G>A maps to NM_004861.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:30951245 G>A maps to NM_004861.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr22:30951464 C>G maps to NM_004861.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:242741366 C>A maps to NM_022134.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr2:242741339 A>G maps to NM_022134.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:242741369 C>T maps to NM_022134.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:242741261 G>T maps to NM_022134.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:242741256 A>T maps to NM_022134.2 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:65812811 T>A maps to NM_033036.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:65810808 G>A maps to NM_033036.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:99758405 C>A maps to NM_024637.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr7:99764166 G>T maps to NM_024637.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:99757729 G>A maps to NM_024637.4 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:99758252 G>T maps to NM_024637.4 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:99764145 G>A maps to NM_024637.4 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:88406292 C>A maps to NM_000153.2 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr14:88416220 T>A maps to NM_000153.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:88442729 C>A maps to NM_000153.2 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:49531416 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:49611951 C>T maps to NM_002044.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:38958888 T>A maps to NM_138801.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:88898456 C>T maps to NM_000512.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr16:88898417 G>A maps to NM_000512.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr16:88898456 C>A maps to NM_000512.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:33267089 G>A maps to NM_020474.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:33272143 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr18:33263451 A>G maps to NM_020474.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:153783749 G>T maps to NM_198321.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:153755918 G>C maps to NM_198321.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:153789303 G>T maps to NM_198321.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:153674470 G>A maps to NM_198321.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:155158100 A>C maps to NM_052917.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:155157977 T>A maps to NM_052917.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:155158049 G>T maps to NM_052917.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:155098677 G>A maps to NM_052917.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:155295152 T>A maps to NM_052917.2 L482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:155099251 G>T maps to NM_052917.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:154996877 A>G maps to NM_052917.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:155115578 C>T maps to NM_052917.2 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:31168709 C>A maps to NM_024572.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:31178600 C>T maps to NM_024572.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:31147091 G>T maps to NM_024572.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:31189074 G>T maps to NM_024572.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr2:31147107 G>T maps to NM_024572.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:31147627 C>A maps to NM_024572.2 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:31165109 C>T maps to NM_024572.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:31133916 G>C maps to NM_024572.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:31178780 G>A maps to NM_024572.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr2:31147627 C>A maps to NM_024572.2 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:31165066 C>A maps to NM_024572.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:230415089 G>T maps to NM_004481.3 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:230339027 G>T maps to NM_004481.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:230371792 G>T maps to NM_004481.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:230379103 G>T maps to NM_004481.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:230415080 G>C maps to NM_004481.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:230371837 C>G maps to NM_004481.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:230339027 G>A maps to NM_004481.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:230372466 A>T maps to NM_004481.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:166616012 T>A maps to NM_004482.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr12:89916916 A>G maps to NM_003774.4 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:89917072 C>A maps to NM_003774.4 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:89918167 C>T maps to NM_003774.4 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:158115853 G>T maps to NM_014568.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr2:158114728 C>T maps to NM_014568.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:158115334 G>A maps to NM_014568.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:158140946 C>T maps to NM_014568.1 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:158114938 G>A maps to NM_014568.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51753050 G>T maps to NM_007210.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:51753113 C>A maps to NM_007210.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr12:51754522 G>A maps to NM_007210.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr12:51757966 G>A maps to NM_007210.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:51773502 C>G maps to NM_007210.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr4:174216608 C>T maps to NM_017423.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:174169579 A>G maps to NM_017423.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:174216995 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:4873213 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:4872540 C>T maps to NM_017417.1 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:4848445 C>T maps to NM_017417.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:4881636 C>G maps to NM_017417.1 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:4835818 G>A maps to NM_017417.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:4835914 C>T maps to NM_017417.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:4881630 A>G maps to NM_017417.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:4829956 G>T maps to NM_017417.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr12:4874712 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:4870122 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:132688112 G>T maps to NM_001122636.1 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:132682498 C>A maps to NM_001122636.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr12:132685677 C>T maps to NM_001122636.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr14:69798188 C>A maps to NM_020692.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:69800211 A>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:16237265 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:16216666 A>T maps to NM_054110.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:16268965 C>T maps to NM_054110.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr3:16237393 C>T maps to NM_054110.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:16237422 C>T maps to NM_054110.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:11314628 C>A maps to NM_198516.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:11362512 G>A maps to NM_198516.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr11:11643071 G>A maps to NM_198516.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:11292738 C>G maps to NM_198516.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr11:11454333 C>A maps to NM_198516.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr7:151680214 G>A maps to NM_145292.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr7:151699868 C>T maps to NM_145292.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr4:173269701 C>T maps to NM_001034845.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:173804034 G>T maps to NM_001034845.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr4:173734826 C>A maps to NM_001034845.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:173734718 C>A maps to NM_001034845.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:172735813 G>A maps to NM_001034845.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr4:173232861 T>C maps to NM_001034845.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:173269724 C>T maps to NM_001034845.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:173942642 G>A maps to NM_001034845.2 W502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:172735811 C>A maps to NM_001034845.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:173873318 C>A maps to NM_001034845.2 C427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr4:173803977 C>A maps to NM_001034845.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:56688494 C>T maps to NM_033106.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:56691993 C>T maps to NM_033106.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr19:56693609 G>A maps to NM_033106.3 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:56688565 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980578 A>G maps to NM_001480.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr18:74980857 A>C maps to NM_001480.3 *350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:74962575 G>A maps to NM_001480.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:74962539 C>T maps to NM_001480.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:74962773 C>A maps to NM_001480.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr18:74962761 C>G maps to NM_001480.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:74071266 G>T maps to NM_003857.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:74071305 C>T maps to NM_003857.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:81410933 G>C did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:62396346 G>A maps to NM_198335.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62400517 C>T maps to NM_198335.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr11:62397857 G>A maps to NM_198335.2 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr11:62393612 A>G maps to NM_198335.2 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:42602976 C>A maps to NM_198141.2 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:42568591 A>T maps to NM_198141.2 K26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:115395141 G>T maps to NM_001130064.1 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr3:115395144 G>T maps to NM_001130064.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:115395297 G>T maps to NM_001130064.1 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:115395287 C>A maps to NM_001130064.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:115395233 C>G maps to NM_001130064.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:115395236 C>G maps to NM_001130064.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:115395185 C>G maps to NM_001130064.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:115395011 T>A maps to NM_001130064.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:36034290 C>G maps to NM_014364.4 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:36029296 G>T maps to NM_014364.4 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:36024470 C>G maps to NM_014364.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:57790734 C>A maps to NM_152687.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:128061358 C>A maps to NM_015635.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:128092474 A>T maps to NM_015635.2 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr9:128064471 T>G maps to NM_015635.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr9:128118029 G>T maps to NM_015635.2 E1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:110745572 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:130101922 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:30655526 A>T maps to NM_002047.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr21:34876748 T>A maps to NM_001136006.1 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr21:34911475 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:34889377 G>A maps to NM_001136006.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr21:34883583 A>G maps to NM_001136006.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr21:34876757 G>A maps to NM_001136006.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr21:34897280 G>A maps to NM_001136006.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:89560860 C>G maps to NM_002048.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:22770674 G>C maps to NM_005256.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:34072003 C>A maps to NM_139285.2 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:34072747 G>A maps to NM_139285.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr17:34072790 G>T maps to NM_139285.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:34077227 C>G maps to NM_139285.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:34072250 C>T maps to NM_139285.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:34072769 C>T maps to NM_139285.2 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:101017689 C>A maps to NM_174942.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:101018046 C>T maps to NM_174942.1 H488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:101017383 G>A maps to NM_174942.1 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:101017695 T>C maps to NM_174942.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr13:114526416 G>T maps to ENST00000357389 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:9830017 G>T maps to NM_201433.1 C318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:9850261 C>G maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:9820592 G>T maps to NM_201433.1 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:9923166 G>A maps to NM_201433.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:9923092 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:9850261 C>A maps to NM_201433.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39871798 G>T maps to NM_000805.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:48649677 C>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:48650255 C>G did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:48650829 G>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:48652248 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48649524 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:48651662 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:48650290 C>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:48652211 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:48650611 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:48650387 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:128200778 G>A maps to NM_032638.4 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:128200002 A>T maps to NM_032638.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:128204774 C>T maps to NM_032638.4 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr3:128200787 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:128205122 A>T maps to NM_032638.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:8100775 G>A maps to NM_001002295.1 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:8100535 A>T maps to NM_001002295.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:8100556 G>A maps to NM_001002295.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:8115718 T>A maps to NM_001002295.1 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:8100740 C>T maps to NM_001002295.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:8115845 A>T maps to NM_001002295.1 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:8100385 G>T maps to NM_001002295.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:8111434 G>T did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr10:8115973 C>A maps to NM_001002295.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:11607675 G>C maps to NM_002052.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:11615980 G>T maps to NM_002052.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr8:11606498 C>T maps to NM_002052.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:61039975 G>T maps to NM_080473.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr20:61040521 T>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:19780755 G>T maps to NM_005257.3 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr18:19751290 G>T maps to NM_005257.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:19612197 C>T maps to ENST00000404158 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:19611939 G>A maps to ENST00000404158 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:19606950 G>T maps to ENST00000404158 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:153789862 G>A maps to NM_020699.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:153788827 G>A maps to NM_020699.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:153782714 C>A maps to NM_020699.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:153785902 C>A maps to NM_020699.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:120884581 C>T maps to NM_176818.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:45656214 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:45661524 C>A maps to ENST00000432007 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:155208061 C>T maps to NM_001005742.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:155206035 C>T maps to NM_001005742.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:155210445 T>A maps to NM_001005742.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:155210460 G>C maps to NM_001005742.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:35738835 C>T maps to NM_020944.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr9:35738623 C>T maps to NM_020944.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:22749299 C>G maps to NM_020973.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:22748973 C>T maps to NM_020973.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:22737820 C>T maps to NM_020973.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:22820506 C>A maps to NM_020973.3 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr4:22749342 G>T maps to NM_020973.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:22737820 C>T maps to NM_020973.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:56051429 G>T maps to NM_001483.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:81640186 C>A did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr3:81695600 C>A maps to ENST00000264326 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104123115 A>G maps to NM_004193.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:104123555 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:89523825 G>A maps to NM_002053.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:89587487 C>G maps to NM_004120.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:89476649 G>C maps to NM_018284.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:89656942 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:89654378 C>T maps to NM_052941.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:89657123 G>T maps to NM_052941.4 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:89652015 C>T maps to NM_052941.4 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:89729610 C>T maps to NM_052942.3 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:89735196 G>A maps to NM_052942.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:89732128 T>C maps to NM_052942.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:89849313 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:89846102 C>T maps to NM_198460.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:89849284 C>A maps to NM_198460.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:89847478 C>T maps to NM_198460.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:89844083 A>T maps to NM_198460.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:89846020 C>T maps to NM_198460.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:89849808 G>C maps to NM_198460.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:89607331 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:89618439 C>T maps to NM_207398.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:89637474 G>A maps to NM_207398.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150864101 C>A maps to NM_001098834.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr7:150845684 G>A maps to NM_001098834.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:237074745 G>T maps to NM_001485.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:237075027 C>T maps to NM_001485.2 P192P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-86-6851-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:237076107 C>T maps to ENST00000415226 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:237074613 G>A maps to NM_001485.2 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:72631269 C>A maps to ENST00000504199 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:72623760 C>A maps to ENST00000504199 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:72620762 C>A maps to ENST00000504199 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:72618363 C>G maps to ENST00000504199 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:72622628 C>A maps to ENST00000504199 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr4:72620754 G>A maps to ENST00000504199 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr2:163215667 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr22:38212697 G>T maps to NM_001171690.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:127222943 C>T maps to NM_024523.5 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr7:127222754 C>T maps to NM_024523.5 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127222088 C>T maps to NM_024523.5 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:127224377 C>A maps to NM_024523.5 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109067568 G>C did not map to a codon.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr2:109087032 C>T maps to NM_181453.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:109092019 G>T maps to NM_181453.3 E964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr21:34136680 A>C maps to NM_016631.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:34117918 G>A maps to NM_016631.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr21:34132125 G>A maps to NM_016631.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:34117198 A>G maps to NM_016631.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr21:34132239 G>A maps to NM_016631.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:163004008 G>C maps to ENST00000233604 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:163002053 G>T maps to ENST00000233604 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:163000667 C>T maps to ENST00000233604 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:163003953 G>A maps to ENST00000233604 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:163004014 T>A maps to ENST00000233604 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:163002069 C>G maps to ENST00000233604 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr2:163004008 G>C maps to ENST00000233604 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:44190611 C>T maps to NM_000162.3 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:44192963 C>T maps to NM_000162.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44189440 C>T maps to NM_000162.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:44191929 C>T maps to NM_000162.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:44192930 G>A maps to NM_000162.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:27726406 C>A maps to NM_001486.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:27722026 G>A maps to NM_001486.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:27726467 G>T maps to NM_001486.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr2:27722062 G>A maps to NM_001486.3 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:27722062 G>A maps to NM_001486.3 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:53385714 C>A maps to NM_001498.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:53365074 G>C maps to NM_001498.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr6:53370273 C>T maps to NM_001498.3 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:53385616 T>C maps to NM_001498.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:52993252 T>C maps to NM_003643.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:52993666 A>T maps to NM_003643.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:52993300 G>T maps to NM_003643.3 Y338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:52999123 T>C did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr6:10874376 T>G maps to NM_004752.3 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:120578770 G>T maps to NM_006836.1 P1962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:120596318 C>A maps to NM_006836.1 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:120572171 C>A maps to NM_006836.1 G2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:120593436 G>C maps to NM_006836.1 V1133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:120616754 T>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:120615555 C>G did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:120612966 G>C maps to NM_006836.1 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:120589171 G>A maps to NM_006836.1 C1362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:79118028 G>T maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:79118034 G>A maps to NM_001097636.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr9:79117887 C>G maps to NM_001097636.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr9:79118112 C>G maps to NM_001097636.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:79118406 G>T maps to NM_001097636.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr9:79118130 C>G maps to NM_001097636.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:10586722 C>T maps to NM_145655.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:10529656 G>A maps to NM_145649.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr6:10557141 C>A maps to NM_001491.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:10529605 C>T maps to NM_145649.4 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:10529944 G>T maps to NM_145649.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr6:10586825 G>T maps to NM_145655.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:74325436 A>G maps to NM_016591.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:74325766 T>C maps to NM_016591.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr15:57910303 C>G maps to NM_001018090.3 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:57931724 C>G maps to NM_001018090.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:58004325 G>C maps to NM_001018090.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:74810460 G>T maps to ENST00000238018 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:74825637 T>C maps to ENST00000238018 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:74856164 C>T maps to ENST00000238018 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:74842863 G>C maps to ENST00000238018 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:75262777 C>T maps to NM_018972.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:42891924 C>A maps to NM_024034.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr20:42891868 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:118420732 C>T maps to NM_017686.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:118461305 C>A maps to NM_017686.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:118420693 C>G maps to NM_017686.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:118449204 C>G did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:118454704 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:118461336 C>T maps to NM_017686.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:48428892 C>T maps to NM_004962.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:48426593 G>A maps to NM_004962.2 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:48429501 G>T maps to NM_004962.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:48428802 C>T maps to NM_004962.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18499156 G>C maps to NM_004864.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:48414051 C>G maps to NM_016204.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr10:48414309 T>C maps to NM_016204.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:48414411 G>T maps to NM_016204.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:48416570 C>A maps to NM_016204.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:48414231 C>T maps to NM_016204.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:7843253 C>T maps to NM_020634.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:7848291 G>A maps to NM_020634.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:7848122 G>A maps to NM_020634.1 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr12:7842941 A>G maps to NM_020634.1 D209D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-55-8506-01A-11D-2393-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-75-5126-01A-01D-1753-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-78-8640-01A-11D-2393-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-6851-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:34025348 C>A maps to NM_000557.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:97156799 G>T maps to NM_001001557.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr8:97157675 C>A maps to NM_001001557.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:97156874 G>A maps to NM_001001557.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:97172695 G>T maps to NM_001001557.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:97156916 G>T maps to NM_001001557.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr8:97157009 G>A maps to NM_001001557.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr5:132200159 G>A maps to NM_005260.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:132197388 A>T maps to NM_005260.3 C419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153668785 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:153668808 A>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:153670127 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:153670946 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:153667447 A>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:153666922 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:153668830 G>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:153670993 A>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:5838738 G>A maps to NM_001494.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr10:5808593 G>A maps to NM_001494.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:37815910 A>G maps to NM_001190468.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:37815752 T>A maps to NM_001190468.1 *229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr5:37816163 C>T maps to NM_001190468.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:57311874 T>C maps to NM_182569.3 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:69645307 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:69647226 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:69647064 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:69649555 C>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:69646753 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:69649519 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:69649392 G>T did not map to a codon.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr23:69647190 G>C did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:69652157 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:69649411 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:69649359 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:76982253 G>T maps to ENST00000376217 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:76956337 G>A maps to ENST00000376217 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:76982253 G>T maps to ENST00000376217 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:75146614 G>T maps to NM_030792.6 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:75146632 A>G maps to NM_030792.6 Y579Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:58010268 G>A maps to NM_001111270.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr12:58007843 C>T maps to NM_001111270.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007141 G>A maps to NM_001111270.1 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:58007228 G>T maps to NM_001111270.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:58009404 C>A maps to NM_001111270.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:58006845 C>G maps to NM_001111270.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:58008536 G>T maps to NM_001111270.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:58009771 C>A maps to NM_001111270.1 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:650507 C>A maps to NM_015721.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:649338 T>C maps to NM_015721.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:154278850 T>A maps to NM_015465.3 K1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr5:154270921 A>G maps to NM_015465.3 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:154292551 G>A maps to NM_015465.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:45593434 C>T maps to NM_024707.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:14038376 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:14038430 G>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:14027090 C>A did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:14038354 C>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:17955605 C>T maps to NM_001130009.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:17962032 A>T maps to NM_001130009.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:42992461 G>C maps to NM_002055.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:42992767 G>T maps to NM_002055.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:42990678 C>T maps to NM_002055.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:42988814 G>A maps to NM_002055.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr17:42990791 G>T maps to NM_002055.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr17:42988740 C>A maps to NM_002055.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:92941702 G>A maps to NM_005263.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr1:92941660 G>A maps to NM_005263.3 C398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:135864467 G>T maps to NM_004188.4 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:135865280 C>A maps to NM_004188.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:135864569 G>A maps to NM_004188.4 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr9:135863738 G>T maps to NM_004188.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:158366914 G>T maps to ENST00000264263 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:158409160 C>T maps to ENST00000264263 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:74032774 G>C maps to NM_032380.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:13487029 C>A maps to NM_018988.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr6:13365723 C>A maps to NM_018988.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:13364976 A>C maps to NM_018988.2 *391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:67709825 G>A maps to NM_030819.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:67719579 G>A maps to NM_030819.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:67709087 C>A maps to NM_030819.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:69565627 T>A maps to ENST00000357308 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:69577253 C>A maps to ENST00000357308 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr5:179734238 C>A maps to NM_005110.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:179763575 A>G maps to NM_005110.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr10:117885021 G>T maps to NM_005264.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:117885009 G>A maps to NM_005264.4 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr10:117884825 G>A maps to NM_005264.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:117856244 G>A maps to NM_005264.4 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:137589487 G>A maps to NM_001496.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:137600049 G>A maps to NM_001496.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:55214929 A>C maps to NM_207410.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55264236 T>C maps to NM_207410.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:55216093 T>C maps to NM_207410.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr6:55223838 G>T maps to NM_207410.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:55264012 T>C maps to NM_207410.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:55198717 G>T maps to NM_207410.2 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr6:55196615 G>A maps to NM_207410.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:38026075 G>T maps to ENST00000381756 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr22:38026924 A>T maps to ENST00000381756 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:23491169 G>A maps to NM_015044.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:23498077 C>A maps to NM_015044.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr16:23491167 C>A maps to NM_015044.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73238542 C>T maps to NM_138619.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:73242604 C>G maps to NM_138619.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:73238913 C>A maps to NM_138619.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:30538474 G>A maps to NM_024051.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:85777723 G>A maps to NM_000821.4 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:63930052 T>C maps to NM_003878.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:63927973 C>A maps to NM_003878.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:38876353 G>T maps to NM_152657.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:34937809 G>T maps to NM_024835.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr17:34923615 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:34913137 T>C maps to NM_024835.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr20:33451277 G>A maps to NM_178026.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:23967074 G>T maps to NM_178311.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:61995376 G>T maps to NM_000515.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:61994764 G>A maps to NM_000515.3 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:61995230 G>T maps to NM_000515.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr17:61994725 G>A maps to NM_000515.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:61994795 G>T maps to NM_000515.3 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:61958248 C>T maps to NM_002059.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:61958481 C>T maps to NM_002059.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:61958486 C>A maps to NM_002059.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:61958499 G>T maps to NM_002059.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr17:61957643 G>T maps to NM_022558.2 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:40344962 G>A maps to NM_032484.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:40344700 T>A maps to NM_032484.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40344577 C>T maps to NM_032484.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr17:40344664 G>A maps to NM_032484.4 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:85901330 C>T maps to ENST00000436406 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:85904648 C>G maps to ENST00000436406 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:42718754 C>A maps to NM_000163.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:42689016 C>A maps to NM_000163.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:42711436 A>C maps to NM_000163.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:42719333 T>A maps to NM_000163.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr20:35885253 G>A maps to NM_021081.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr20:35882715 G>A maps to NM_021081.4 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:31014633 G>T maps to NM_000823.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:31008551 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:31013714 C>G maps to NM_000823.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:31013667 A>T maps to NM_000823.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:31011703 C>T maps to NM_000823.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:172165765 G>A maps to NM_198407.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:172166173 C>A maps to NM_198407.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:172165384 C>T maps to NM_004122.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:172165528 G>T maps to NM_198407.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:172163025 G>T maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:172165687 G>A maps to NM_198407.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:172165807 G>T maps to NM_198407.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:59603315 G>T maps to NM_005142.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:59604818 G>C maps to NM_005142.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:100280382 G>A maps to NM_022574.4 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:233626120 T>C maps to ENST00000373566 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:233671354 C>T maps to ENST00000373566 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:150416162 G>T maps to NM_130759.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:150417235 G>A maps to NM_130759.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:150417565 C>T maps to NM_130759.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:150417415 G>A maps to NM_130759.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:150417442 G>A maps to NM_130759.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:150417698 C>T maps to NM_130759.3 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:150389569 G>T maps to NM_015660.2 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:150389578 G>T maps to NM_015660.2 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:150389685 A>G maps to NM_015660.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150389658 G>A maps to NM_015660.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:150269487 C>T maps to ENST00000430830 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:150270129 T>G maps to ENST00000430830 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:150269946 C>A maps to ENST00000430830 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr7:150269610 C>T maps to ENST00000430830 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:150269502 T>C maps to ENST00000430830 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:150266998 C>T maps to ENST00000430830 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:150267033 A>T maps to ENST00000430830 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:150439478 C>A maps to ENST00000447239 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:150439288 T>A maps to ENST00000447239 L57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:150439758 C>A maps to ENST00000447239 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:150439808 G>A maps to ENST00000447239 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:150325195 G>T maps to ENST00000438845 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:150324821 C>A maps to ENST00000438845 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:150325328 G>A maps to ENST00000438845 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr7:150325355 G>A maps to ENST00000438845 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:150324907 C>A maps to ENST00000438845 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:150217450 T>A maps to NM_153236.3 L130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:150217136 G>T maps to NM_153236.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:150217517 C>A maps to NM_153236.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:150171184 C>T maps to NM_175571.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:150163824 C>A maps to NM_175571.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150174228 G>T maps to NM_175571.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:150171415 G>T maps to NM_175571.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:150174462 G>A maps to NM_175571.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:150171652 G>A maps to NM_175571.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:150174421 T>C maps to NM_175571.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:150174810 C>T maps to NM_175571.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:150174513 G>T maps to NM_175571.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:102423877 T>C did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr5:102432326 C>T maps to NM_017676.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:25405909 G>T maps to NM_021067.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:85712181 A>G maps to NM_016095.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr16:58438631 G>A maps to NM_001126129.1 *256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:41394733 G>A maps to NM_032336.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:41387777 G>T maps to NM_032336.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:47044561 C>A maps to NM_004123.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:14593766 G>T maps to NM_202470.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:78511975 C>G maps to NM_017655.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:3586948 C>A maps to NM_133261.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:3586647 G>A maps to NM_133261.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:46178074 G>C maps to NM_000164.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:46184988 G>T maps to NM_000164.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:46180281 G>T maps to NM_000164.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:27910596 C>A maps to NM_001085454.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:121768043 C>T maps to NM_000165.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:121768688 C>T maps to NM_000165.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:121768116 G>T maps to NM_000165.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:90605635 G>A maps to NM_032602.1 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr6:90605650 C>A maps to NM_032602.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:35260117 C>A maps to NM_002060.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:35260488 G>C maps to NM_002060.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:35260567 C>T maps to NM_002060.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:35260671 C>A maps to NM_002060.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr1:147230939 C>T maps to NM_005266.5 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:147230976 C>A maps to NM_005266.5 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:147230605 C>T maps to NM_005266.5 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:147380414 G>A maps to NM_005267.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:147380378 C>T maps to NM_005267.4 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:147380357 C>G maps to NM_005267.4 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:147380447 C>T maps to NM_005267.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:147380738 C>T maps to NM_005267.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:147381149 G>C maps to NM_005267.4 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:39340851 G>A maps to NM_030772.4 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:39340852 G>A maps to NM_030772.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:39341673 G>A maps to NM_030772.4 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:39341358 G>A maps to NM_030772.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39341323 G>C maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr1:39340941 G>A maps to NM_030772.4 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:70443679 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:70443954 G>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:70444127 A>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr13:20763171 G>T maps to NM_004004.5 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr13:20763552 C>A maps to NM_004004.5 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:35250701 C>T maps to NM_001005752.1 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:35227241 G>A maps to NM_153212.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:35227226 G>A maps to NM_153212.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:35227310 C>A maps to NM_153212.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:35227625 G>A maps to NM_153212.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:35227442 C>T maps to NM_153212.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223434 A>G maps to NM_005268.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:35223473 A>G maps to NM_005268.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:35223536 C>A maps to NM_005268.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:87994540 G>T maps to NM_198568.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:87993959 C>G maps to NM_198568.2 *224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:87994036 C>T maps to NM_198568.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:87994525 G>C maps to NM_198568.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:87993967 G>T maps to NM_198568.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:42882275 G>A maps to NM_001080383.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42883059 G>A maps to NM_001080383.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr17:42882972 G>A maps to NM_001080383.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:42883089 C>G maps to NM_001080383.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:42882321 A>T maps to NM_001080383.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:228346301 C>G maps to NM_020435.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:99526853 G>A maps to NM_181538.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr7:99526820 C>T maps to NM_181538.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:35045188 C>T maps to NM_020660.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:35044819 C>A maps to NM_020660.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:35044897 C>T maps to NM_020660.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:35045110 T>G maps to NM_020660.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr15:35045464 G>T maps to NM_020660.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:35896752 C>A maps to NM_153368.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:30726206 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:30709247 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:30739035 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:30736711 A>C did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:30709268 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:30714173 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:30738764 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:30715864 T>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:80328604 A>G maps to NM_033214.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:80328019 T>A maps to NM_033214.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:80329141 C>A maps to NM_033214.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:141896418 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:141904808 C>A maps to NM_001039547.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:69204658 A>T maps to NM_019617.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:100653083 C>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:100653423 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:100662734 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:100653522 A>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:100656783 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:100653865 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:100662854 C>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:100662860 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:100653787 C>A did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:100658908 C>G did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr3:33055582 G>A maps to NM_000404.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:33063129 T>A maps to NM_000404.2 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:220104939 G>A maps to NM_024506.3 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134217326 G>A maps to NM_138342.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr11:134238565 G>T maps to NM_138342.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr11:134158729 G>A maps to NM_001080407.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:134182307 C>A maps to NM_001080407.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:8062111 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:8099878 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr7:8125954 C>G maps to NM_138426.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:8125840 G>A maps to NM_138426.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:6604785 T>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:6553454 C>A maps to NM_000170.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:6554778 C>A maps to NM_000170.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:6602205 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:6604784 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr9:6605136 C>T maps to NM_000170.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:6604636 G>A maps to NM_000170.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr9:6540060 G>T maps to NM_000170.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:6620263 C>T maps to NM_000170.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:51696917 T>C maps to NM_181789.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:131271367 G>T maps to NM_001003722.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:74526855 T>C maps to NM_012201.5 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:74537460 G>A maps to NM_012201.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:74530505 C>A maps to NM_012201.5 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:74525009 C>A maps to NM_012201.5 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:74524931 C>T maps to NM_012201.5 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr16:74526921 G>A maps to NM_012201.5 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:74525039 C>G maps to NM_012201.5 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr16:74506310 T>C did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr12:57861140 C>A maps to NM_005269.2 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:57861952 G>T maps to NM_005269.2 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:57857531 C>A maps to NM_005269.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:57864592 C>T maps to NM_005269.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:57863407 C>G maps to NM_005269.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:121744023 G>C maps to NM_005270.4 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:121748104 C>T maps to NM_005270.4 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:121743870 C>T maps to NM_005270.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:121554949 G>T maps to NM_005270.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:121747029 T>C maps to NM_005270.4 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:121747077 G>T maps to NM_005270.4 G1196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:121726410 G>T maps to NM_005270.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:121747416 G>A maps to NM_005270.4 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:121746687 G>T maps to NM_005270.4 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:121732615 C>T maps to NM_005270.4 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:42005030 G>A maps to NM_000168.5 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:42004992 T>A maps to NM_000168.5 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:42006186 C>T maps to NM_000168.5 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:42005085 G>A maps to NM_000168.5 N1195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:42004818 G>T maps to NM_000168.5 T1284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:42006171 G>C maps to NM_000168.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:42065848 A>C maps to NM_000168.5 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:42005523 G>C maps to NM_000168.5 Y1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:42085016 C>A maps to NM_000168.5 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr7:42005256 G>A maps to NM_000168.5 H1138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr7:42005277 C>A maps to NM_000168.5 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr7:42005352 T>A maps to NM_000168.5 A1106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:42005868 C>A maps to NM_000168.5 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:42079716 G>A maps to NM_000168.5 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:42005961 C>A maps to NM_000168.5 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr7:42088288 G>A maps to NM_000168.5 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr7:42064964 C>T maps to NM_000168.5 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr12:75875684 G>T maps to NM_006851.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:75807463 A>T maps to ENST00000378692 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:36148588 G>A maps to NM_022343.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:36147843 C>A maps to NM_022343.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:53974960 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:54060031 G>A maps to NM_147193.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:4382450 C>G maps to NM_032575.2 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:3937123 T>A maps to NM_001042413.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:3879428 C>T maps to NM_001042413.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:92730114 A>T maps to NM_053274.2 L432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:92755851 T>C maps to NM_053274.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:48629474 G>C did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:48629390 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:48629411 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:39047363 C>A maps to NM_002062.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:39046937 G>C maps to NM_002062.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:39025254 C>T maps to NM_002062.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr6:39053761 C>G maps to NM_002062.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:39046124 G>A maps to NM_002062.3 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:39046943 C>A maps to NM_002062.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:9791284 G>T maps to NM_004246.1 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr17:9739736 T>G maps to NM_004246.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:9729481 C>A maps to NM_004246.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:9745933 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:9792952 C>G maps to NM_004246.1 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:151271896 A>G maps to NM_001146040.1 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:151239473 G>T maps to NM_001146040.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:151231154 G>C maps to NM_001146040.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr5:151234688 G>T maps to NM_001146040.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:14627194 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:14550470 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:14599448 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:14550389 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:14599491 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:14748433 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:14748447 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:14599362 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:14627185 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:14748343 C>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:14548214 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:14625332 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:14622518 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:14592612 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:14627122 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:14599504 T>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:14550435 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:14748353 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:14627262 T>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:14708873 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:14627265 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:14627159 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:14599451 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:14748489 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:14550452 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:14625389 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:14592453 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:14625350 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:14625360 T>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:175688111 A>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:175636718 A>T maps to NM_006529.2 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr4:175598276 C>G maps to NM_006529.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:102962324 G>A did not map to a codon.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr23:102979088 C>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:102979533 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:102979520 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:102974189 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:102979907 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:102968472 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:102977172 G>A did not map to a codon.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr23:102974029 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:102979155 T>A did not map to a codon.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr23:102974034 C>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:102979196 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:102979083 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:102974074 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:102979466 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:102968474 A>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:102962360 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:102968567 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:158041791 C>T maps to NM_001166060.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:158074126 G>T maps to NM_001166060.1 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:158091630 G>A maps to NM_001166060.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:158073915 C>T maps to NM_001166060.1 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:158091863 G>A maps to NM_001166060.1 W493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr5:95152246 C>A maps to NM_002064.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:193065772 C>T maps to NM_016066.3 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:131958333 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:131973128 A>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr10:131965193 A>G maps to NM_006541.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:131959181 C>G maps to NM_006541.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:96010438 A>T maps to NM_016417.2 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:191827618 C>G maps to NM_014905.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:56867049 G>T maps to NM_013267.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:129373262 C>A maps to ENST00000442111 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:129431966 C>T maps to ENST00000442111 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:129360513 G>T maps to ENST00000442111 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:129432000 G>T maps to ENST00000442111 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr12:129431954 G>T maps to ENST00000442111 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:129442185 C>T maps to ENST00000442111 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:183942809 C>A maps to NM_015101.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:183909712 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:183920144 C>A maps to NM_015101.2 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:183933059 G>T maps to NM_015101.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:183913402 C>A maps to NM_015101.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:183920139 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:183907987 C>T maps to NM_015101.2 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:138516185 G>T maps to NM_182974.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:104388147 G>T maps to NM_031302.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr12:104393231 C>T maps to NM_031302.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:104390539 C>T maps to NM_031302.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:104408806 C>A maps to NM_031302.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:4692554 C>A maps to NM_001014985.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:48183813 C>T maps to NM_015711.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:48184100 C>T maps to NM_015711.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr19:48183886 C>G maps to NM_015711.3 S487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:48201947 G>T maps to NM_015711.3 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:48254358 C>G maps to NM_015710.4 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:88820736 C>A maps to NM_005271.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr23:120181911 A>G did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:120182569 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:120181572 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:120181691 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:120183090 C>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:120182195 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:120182427 C>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:120182770 A>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:120181570 G>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:120182248 T>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:120182417 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:120182838 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:120181614 C>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr23:120182372 G>T did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr23:120182373 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:120182831 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:120181629 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:120182640 A>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:182353653 G>A maps to NM_002065.5 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:182355391 C>T maps to NM_002065.5 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:58491926 C>A maps to NM_201648.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:58478070 G>T maps to NM_201648.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:58480243 A>T maps to NM_201648.2 L102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:58482865 C>A maps to NM_201648.2 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:58480263 G>T maps to NM_201648.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr11:58480242 T>C maps to NM_201648.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:58482881 G>T maps to NM_201648.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:58722739 G>A maps to NM_080661.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:58723388 G>C maps to NM_080661.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:58723475 C>T maps to NM_080661.2 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:58711089 G>A maps to NM_080661.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr11:58723296 G>T maps to NM_080661.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:58604650 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:58604597 T>C maps to NM_145016.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58604549 T>C maps to NM_145016.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:58605832 G>T maps to NM_145016.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr11:58602126 G>T maps to NM_145016.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:52324423 G>T maps to NM_145262.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52324414 C>G maps to NM_145262.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:4882009 C>T maps to NM_032569.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:150632803 C>T maps to NM_000405.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr2:70106038 A>G did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr6:2116019 G>T maps to NM_001500.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:1930450 A>T maps to NM_001500.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:1960205 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:1624765 G>A maps to NM_001500.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:29037044 C>T maps to NM_006582.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:29030803 T>C maps to NM_006582.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:19749276 T>C maps to NM_016573.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr19:19748830 G>A maps to NM_016573.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:19740855 T>C maps to NM_016573.2 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:143928045 G>T maps to NM_002066.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:143928000 C>A maps to NM_002066.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:143921918 C>A maps to NM_002066.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:49759190 G>A maps to NM_013334.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:16279042 G>A maps to NM_006877.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr14:24707944 C>T maps to ENST00000348719 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:155632278 C>A maps to NM_003875.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:155628514 A>C maps to NM_003875.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:155649576 C>A maps to NM_003875.2 Y528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr3:155628910 C>T maps to NM_003875.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:155643028 G>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:3113344 C>T maps to NM_002067.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr7:2771078 G>A maps to NM_007353.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:63049633 G>A maps to NM_006572.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:79818430 G>T maps to NM_002069.5 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:79846621 C>A maps to NM_002069.5 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:110134686 A>T maps to NM_006496.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr18:11752921 C>T maps to NM_182978.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:11752921 C>A maps to NM_182978.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:56388844 C>A maps to NM_020988.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:56226146 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:56377777 G>T maps to NM_138736.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:56377843 G>T maps to NM_138736.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:56226257 C>A maps to NM_020988.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:56374810 G>T maps to NM_138736.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:56388952 C>T maps to NM_020988.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:56226489 T>A maps to NM_020988.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr16:56377860 G>T maps to NM_138736.2 *355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:57430251 G>A maps to NM_080425.2 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:57430245 G>A maps to NM_080425.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:57415310 C>T maps to NM_016592.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:57485074 T>C maps to NM_080425.2 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:57429240 C>A maps to NM_080425.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr20:57430038 C>T maps to NM_080425.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57415373 C>T maps to NM_016592.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:57415490 G>A maps to NM_016592.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:57429150 C>A maps to NM_080425.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:57415334 C>A maps to NM_016592.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr20:57474034 C>T maps to NM_080425.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:57484271 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:50230587 C>T maps to NM_000172.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:110146651 G>T maps to NM_005272.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:80091553 G>T maps to NM_001102386.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr22:23438484 C>T maps to NM_002073.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr22:23437950 G>T maps to NM_002073.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr22:23438505 G>A maps to NM_002073.2 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:23438544 C>A maps to NM_002073.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:1721832 C>G did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:1720624 G>A maps to NM_002074.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:100275137 G>A maps to NM_005273.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:100275741 A>T maps to NM_005273.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:180670767 G>T maps to NM_006098.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:180665098 C>T maps to NM_006098.4 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:179131211 G>A maps to NM_021629.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:179138685 C>T maps to NM_021629.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr15:52418242 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:52472024 C>A maps to NM_016194.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr9:36227306 G>A maps to NM_001128227.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:36217418 G>A maps to NM_001128227.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:93555526 A>G maps to NM_004126.3 *74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62476248 G>T maps to NM_012202.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:235747042 G>C maps to NM_004485.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:235715444 G>C maps to NM_004485.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:93540199 G>A maps to NM_021955.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:30515039 C>A maps to NM_005275.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:38034453 G>A maps to NM_013285.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:38048523 G>C maps to NM_013285.2 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:38048465 G>A maps to NM_013285.2 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr23:54578085 A>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:54574705 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:54581095 G>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:54569697 G>C did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:54578809 G>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:54578127 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:54578049 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:54578050 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:54578156 G>C did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:54567806 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:54584912 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:85924771 G>A maps to NM_006433.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:85923142 C>G maps to NM_006433.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42930897 C>T maps to NM_018960.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:231406678 G>T maps to NM_014236.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:231406609 G>C maps to NM_014236.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:231403467 C>T maps to NM_014236.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:44713077 T>C maps to NM_138335.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:102153822 G>C maps to NM_024312.4 Y1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:102160037 A>C maps to NM_024312.4 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:102183813 A>T maps to NM_024312.4 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr12:102158579 T>C maps to NM_024312.4 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:3025466 G>T maps to NM_001501.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:68606248 G>T maps to NM_000406.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr4:68606439 G>A maps to NM_000406.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:68606374 A>T maps to NM_000406.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:68619558 G>T maps to NM_000406.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:65141689 T>A maps to ENST00000418919 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:127651472 C>T maps to NM_002077.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:127651447 C>A maps to NM_002077.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:127674181 C>A maps to NM_002077.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:131020132 C>G maps to NM_004486.4 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131019540 G>A maps to NM_004486.4 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:131028133 G>A maps to NM_004486.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:131027929 C>T maps to NM_004486.4 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr9:131023763 C>T maps to NM_004486.4 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:100551821 G>A maps to ENST00000266746 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:133357452 C>T maps to NM_005895.3 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:133360731 C>G maps to NM_001172557.1 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:133353278 G>A maps to NM_005895.3 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:133375048 G>T maps to NM_005895.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:133357431 C>T maps to NM_005895.3 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:133398681 G>A maps to NM_005895.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:133365816 C>T maps to NM_005895.3 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr12:133353246 T>C maps to NM_005895.3 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:133372566 C>A maps to NM_005895.3 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37379194 G>T maps to NM_001172713.1 S2137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:37365368 C>T maps to NM_001172713.1 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:37365450 G>T maps to NM_001172713.1 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:37367526 C>T maps to NM_001172713.1 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:37381673 G>T maps to NM_001172713.1 V2167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:37369957 G>A maps to NM_001172713.1 L2019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:93299471 C>T maps to NM_005113.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:93263811 G>A maps to NM_005113.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:74368266 C>A maps to NM_001038640.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:72953684 G>C maps to NM_018652.4 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr15:75562494 G>T maps to NM_001164404.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:75586707 G>T maps to NM_001145224.1 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:121396160 G>A maps to ENST00000393667 Q3004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr3:121412610 T>C maps to ENST00000393667 E2253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:121412825 G>A maps to ENST00000393667 Q2182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:121417265 C>A maps to ENST00000393667 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:121413584 C>A maps to ENST00000393667 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:121433815 G>C maps to ENST00000393667 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:121435662 T>C maps to ENST00000393667 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:121416858 C>A maps to ENST00000393667 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:121395774 G>A maps to ENST00000393667 Q3048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:167761281 G>A maps to NM_014498.3 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:167813019 C>A maps to NM_014498.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:167754670 G>A maps to NM_014498.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:167754632 C>T maps to NM_014498.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:167728112 C>A maps to NM_014498.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:167750316 C>T maps to NM_014498.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:88651389 C>A maps to ENST00000376023 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:88692461 T>A maps to ENST00000376023 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:32126341 C>G maps to NM_022130.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:32126341 C>A maps to NM_022130.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:32143956 T>A maps to NM_022130.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:204172023 G>A maps to NM_198447.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:21661495 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:21665282 C>A maps to NM_016072.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:155726843 G>A maps to ENST00000368331 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:155735058 G>C maps to ENST00000368331 S1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:155735335 G>A maps to ENST00000368331 Q1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:155735477 G>A maps to ENST00000368331 F1262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:155740887 G>A maps to ENST00000368331 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:155744856 C>T maps to ENST00000368331 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr1:155753799 G>A maps to ENST00000368331 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:155747448 T>G maps to ENST00000368331 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:117884488 A>G maps to NM_020399.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:170521422 A>G maps to NM_152281.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:170501309 G>A maps to NM_152281.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr1:170501348 C>T maps to NM_152281.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:171822342 C>T maps to NM_015530.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:28811678 A>G did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:45017937 C>T maps to NM_054022.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr10:101163361 C>A maps to NM_002079.2 G275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr8:37794536 A>T maps to NM_152413.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:37795162 A>G maps to NM_152413.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:58757762 G>A maps to NM_002080.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:20329601 C>A maps to NM_001007240.1 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr16:20329667 G>A maps to NM_001007240.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:20335216 C>A maps to NM_001007240.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:20331681 G>A maps to NM_001007240.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:20322603 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:20331622 G>T maps to NM_001007240.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:20327354 G>T maps to NM_001007240.1 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:20331721 C>T maps to NM_001007240.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr16:20335276 G>A maps to NM_001007240.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr16:20335183 C>A maps to NM_001007240.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr16:20331616 G>T maps to NM_001007240.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr16:20330958 G>T maps to NM_001007240.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:20322603 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:20327338 G>C maps to NM_001007240.1 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr16:20337678 C>T maps to NM_001007240.1 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:194117475 C>G maps to NM_004488.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr3:194117509 G>C maps to NM_004488.2 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:194118855 G>C maps to NM_004488.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr3:194117577 C>T maps to NM_004488.2 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:55526376 G>T maps to NM_001083899.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:55543669 C>G maps to NM_001083899.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:55530018 C>A did not map to a codon.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:55543710 C>A maps to NM_001083899.1 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128780875 C>G maps to NM_000174.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:167025040 G>T maps to NM_005814.1 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:167038195 C>T maps to NM_005814.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:167024211 C>A did not map to a codon.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr1:167042702 G>A maps to NM_005814.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:167023627 G>T maps to NM_005814.1 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:167038354 C>T maps to NM_005814.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:167038192 G>T maps to NM_005814.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:167024211 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:167032842 G>A maps to NM_005814.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:145138041 G>T maps to NM_003801.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:145140568 C>T maps to NM_003801.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:145138896 G>C maps to NM_003801.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:113920500 C>A maps to NM_020918.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:113920365 G>A maps to NM_020918.4 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:113913355 G>A maps to NM_020918.4 C813C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:113932820 C>A maps to NM_020918.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr10:113933467 C>A maps to NM_020918.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:96690295 C>T maps to NM_207328.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:96690280 G>T maps to NM_207328.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:33602646 C>T maps to NM_018025.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:33597740 A>T maps to NM_018025.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:33597773 G>T maps to NM_018025.2 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:217793633 T>C maps to NM_018040.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:217783677 C>A maps to NM_018040.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr17:42513913 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:42478466 C>T maps to NM_001002909.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr17:42477875 C>T maps to NM_001002909.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr17:42477152 C>T maps to NM_001002909.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:56558437 G>A maps to NM_001127236.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr5:56542958 G>T maps to NM_001127236.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:99773221 C>G maps to NM_152742.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:99773278 G>T maps to NM_152742.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:99769769 C>A maps to NM_152742.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:99771578 G>A maps to NM_152742.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:133087217 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:132730524 T>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:132887563 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:133087111 T>C did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:132795804 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:132887745 G>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:132887865 G>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:133087119 C>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:133119398 G>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:132670152 C>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:132887814 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:133087158 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:132548852 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:132445406 G>C did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:132437211 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:132438834 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:132473342 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:132548910 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:132548939 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:132548940 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:132436997 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:132437227 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:132436930 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:132458534 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:132439937 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:132548850 G>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr23:132439840 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:132458434 T>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:132445319 T>A did not map to a codon.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr23:132458559 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:132473341 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:92345960 G>C maps to NM_004466.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:93518664 G>A maps to NM_004466.4 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr13:92345801 C>A maps to NM_004466.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:92560220 C>A maps to NM_004466.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:93518616 A>T maps to NM_004466.4 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:92560247 C>T maps to NM_004466.4 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr13:92797108 T>A maps to NM_004466.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr13:92346008 G>T maps to NM_004466.4 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr13:92346129 G>T maps to NM_004466.4 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:94482404 A>T did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr13:95050857 C>T maps to NM_005708.3 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr13:95050794 G>C maps to NM_005708.3 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr13:94482698 C>A maps to NM_005708.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:93879810 C>T maps to NM_005708.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr13:94482632 C>T maps to NM_005708.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr20:5542131 T>A maps to NM_019593.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:5538642 C>A maps to NM_019593.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:157406195 C>A maps to NM_000408.4 Y246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:1132476 C>T maps to NM_001505.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:1131903 C>G maps to NM_001505.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr14:63784564 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:63779817 C>A maps to ENST00000314140 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr14:63784521 G>A maps to ENST00000314140 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:67431987 G>T maps to NM_020806.4 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:34884874 G>T maps to NM_000175.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr19:34868424 C>T maps to NM_000175.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:144297308 C>T maps to NM_178172.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:144297146 G>T maps to NM_178172.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:144297149 C>T maps to NM_178172.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:48972657 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:48976098 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:48972136 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:48973404 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:48973450 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:48972242 A>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:48972290 C>A did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:48978830 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:24462986 T>C maps to NM_001503.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:24473859 C>T maps to NM_001503.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:24437452 G>A maps to NM_001503.2 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:24448430 G>A maps to NM_001503.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:176561959 C>A maps to NM_005277.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:176622814 A>C maps to NM_005277.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr4:176594890 G>T maps to NM_005277.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:176561342 C>T maps to NM_005277.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:176556088 A>T maps to NM_005277.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:176622829 C>A maps to NM_005277.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:176622817 G>T maps to NM_005277.3 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:176561297 C>T maps to NM_005277.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:13825813 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:13834963 T>C did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:13795472 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:13825876 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:13825878 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:27857778 C>A maps to NM_007266.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:27212600 C>A maps to NM_018066.3 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr1:27216425 G>A maps to NM_018066.3 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:23313758 C>T maps to ENST00000435486 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23299710 G>T maps to ENST00000435486 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr7:23293803 G>A maps to ENST00000435486 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:23299725 C>T maps to ENST00000435486 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr7:23293807 C>T maps to ENST00000435486 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:23293863 G>T maps to ENST00000435486 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:23300115 C>A maps to ENST00000435486 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:207041254 C>A maps to NM_005279.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr2:207040990 C>A maps to NM_005279.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:136112901 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:136113091 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:136112792 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:136113648 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:136113726 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:136112734 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:136112888 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:136113761 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:136113087 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:136112641 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:136113028 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:136112471 A>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:136112643 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:136113263 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:136112695 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:136113087 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:136112485 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:136113000 T>G did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:136113328 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:136113329 G>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:136112510 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:136112984 G>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:136113698 A>C did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:136113640 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:136112639 A>G did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:132842043 A>T maps to NM_001136557.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:6732043 G>C maps to NM_001080452.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:123186930 G>T maps to NM_177551.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:123201017 C>T maps to NM_006018.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:46977115 C>A maps to ENST00000283297 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:46977835 G>A maps to ENST00000283297 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:47649584 C>A maps to NM_153839.6 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:47646725 C>T maps to NM_153839.6 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr6:47646773 A>G maps to NM_153839.6 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:135432427 T>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:135439864 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:135427822 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:135455193 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:135433622 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:135428830 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:135433700 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:135430447 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:135430860 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:135445640 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:135487936 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:135430552 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:135431526 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:135432389 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:135487953 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:135427277 T>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:135405116 G>C did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:135429457 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:135427339 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:135427840 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:135428175 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:135431851 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:135482020 A>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:135429738 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:135431049 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:135431649 C>G did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:135432187 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:135428675 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:135427079 A>C did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:135432047 T>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr23:135485477 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:135428012 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:135428500 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:135431945 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:135430792 C>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:135487997 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:135482264 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:135443690 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:135429848 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:135429795 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:135432070 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:135427234 C>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:135496330 G>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:135405178 G>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr23:135431751 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:135431922 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:135430881 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:135482181 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:135430311 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:135428833 T>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:135455095 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:135405536 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:135431490 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:135426737 T>C did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr23:135487990 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:135455155 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:135430301 A>C did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:135405429 G>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:135426563 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:135428318 A>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:135438315 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:135430005 G>A did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:135405146 G>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:135455107 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:135426904 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:135432563 G>A did not map to a codon.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr23:135432397 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:135427291 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:135428791 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:135429321 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:135431456 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:135488007 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:135427277 T>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:135429897 T>C did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:135429707 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:135432216 A>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:135427666 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:135432282 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:135429308 T>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:135429309 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:135405268 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:135428166 A>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:135405347 G>C did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:135405348 G>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:135445702 C>T did not map to a codon.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr23:135432476 T>G did not map to a codon.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr23:135431149 C>T did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr23:135429203 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:135428121 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:135428900 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:135485468 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:135485478 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:135429208 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:135429355 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:135429356 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:135431522 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:135474496 A>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:135469963 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:135482014 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:135427293 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:135432184 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:135496330 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:135428924 T>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:135429136 C>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:135487936 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:135426944 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:135430518 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:135431774 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:135430933 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:135455156 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:135431278 C>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:135482066 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:135427302 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:135427806 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:135429885 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:135431879 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:135443671 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:135485474 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:135487977 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:135432318 A>G did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:135430971 A>C did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:135427291 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:135428207 T>C did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:135428952 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:135426567 A>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:135431006 T>A did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:135430453 A>G did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:135488053 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:135430382 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:135427713 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:135429186 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:135426803 T>C did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:135428780 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:135432100 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:135404983 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr23:135426724 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr23:135427688 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:135438285 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:135427726 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:135453629 A>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:135431297 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:26534165 G>T maps to NM_001145168.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:26534033 G>C maps to NM_001145168.1 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:26533739 C>T maps to NM_001145168.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:26536637 G>C maps to NM_001145168.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:26535930 C>A maps to NM_001145168.1 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:47681877 G>T maps to NM_153838.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:47682756 C>T maps to NM_153838.3 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:47681808 C>A maps to NM_153838.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47682165 G>T maps to NM_153838.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:47682492 C>T maps to NM_153838.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:47675034 C>A maps to NM_153838.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:47684540 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:47682215 C>G maps to NM_153838.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:46826210 C>A maps to NM_015234.4 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:46849192 G>A maps to NM_015234.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr6:46826924 G>C maps to NM_015234.4 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr6:46828609 G>A maps to NM_015234.4 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:129518862 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:129518637 G>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:129519240 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:129518923 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:129518708 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:129518895 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr23:129519183 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:27333097 G>T maps to NM_005288.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:27333928 C>A maps to NM_005288.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:27333673 G>A maps to NM_005288.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr13:27333688 C>A maps to NM_005288.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:27333175 G>T maps to NM_005288.3 C263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:27333190 C>A maps to NM_005288.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr13:27333463 G>T maps to NM_005288.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95335954 C>T maps to NM_181745.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:134940763 C>T maps to ENST00000368577 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr10:134916247 A>T maps to ENST00000368577 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:134916292 C>A maps to ENST00000368577 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:134912261 C>T maps to ENST00000368577 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:37692864 C>T maps to NM_032777.9 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:37691585 G>T maps to NM_032777.9 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:37672446 C>T maps to NM_032777.9 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:37693151 C>A maps to NM_032777.9 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:37691582 C>T maps to NM_032777.9 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr8:37687464 C>G maps to NM_032777.9 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:37687410 C>T maps to NM_032777.9 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:37686462 G>A maps to NM_032777.9 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:37687389 G>A maps to NM_032777.9 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:37688279 G>A maps to NM_032777.9 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:37693265 C>T maps to NM_032777.9 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:37686426 C>T maps to NM_032777.9 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:37687023 C>A maps to NM_032777.9 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:22436932 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:22390173 C>G maps to NM_145290.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr4:22389441 G>A maps to NM_145290.2 N1284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:22394314 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:22415262 G>A maps to NM_145290.2 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:22389681 G>A maps to NM_145290.2 N1204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:22389608 C>A maps to NM_145290.2 E1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:22390065 G>A maps to NM_145290.2 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:22389996 T>A maps to NM_145290.2 T1099T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr4:22394280 G>A maps to NM_145290.2 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr4:22390733 G>A maps to NM_145290.2 Y900Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:22422625 T>A maps to NM_145290.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:142732544 G>A maps to NM_198569.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:142711478 G>A maps to NM_198569.2 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr6:142732478 A>T maps to NM_198569.2 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:142725013 G>T maps to NM_198569.2 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:100387876 C>A maps to NM_032787.2 Y688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:100362477 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:100364804 C>T maps to NM_032787.2 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr3:100328801 C>A maps to NM_032787.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:100356150 G>A maps to NM_032787.2 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr3:100378576 G>T maps to NM_032787.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:100373990 G>C maps to NM_032787.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:105518392 G>T maps to NM_013345.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:105518182 G>T maps to NM_013345.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:105517528 G>A maps to NM_013345.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:131605421 C>T maps to NM_198827.3 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:131590397 C>G maps to NM_198827.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:131488756 A>T maps to NM_198827.3 K391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:131622689 C>G maps to NM_198827.3 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:131593297 A>G maps to NM_198827.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:131487746 G>T maps to NM_198827.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:131602945 C>A maps to NM_198827.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:131623759 G>A maps to NM_198827.3 W859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:131487809 G>A maps to NM_198827.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:131476885 C>T maps to NM_198827.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:59930495 T>C maps to NM_022571.5 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:59930847 G>T maps to NM_022571.5 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:64054307 C>T maps to NM_001170726.1 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:236341795 G>T maps to NM_003272.3 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:236341875 C>G maps to NM_003272.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:20043323 G>T maps to NM_001002911.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:20043587 G>T maps to NM_001002911.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:20043968 G>T maps to NM_001002911.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:20043221 C>A maps to NM_001002911.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:20043935 G>T maps to NM_001002911.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:20043437 G>T maps to NM_001002911.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:20043245 C>A maps to NM_001002911.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:20043560 G>A maps to NM_001002911.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:37780669 G>A maps to NM_181791.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:37780048 C>A maps to NM_181791.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:37780618 G>T maps to NM_181791.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:37780318 G>T maps to NM_181791.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:37780846 C>T maps to NM_181791.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:37780441 C>A maps to NM_181791.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:37780442 C>T maps to NM_181791.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72368432 C>G maps to ENST00000440684 G1324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:72368402 G>T maps to ENST00000440684 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:72368429 G>T maps to ENST00000440684 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:72368676 G>T maps to ENST00000440684 E1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:72368048 G>T maps to ENST00000440684 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:72368384 G>T maps to ENST00000440684 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:72368471 C>A maps to ENST00000440684 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:72368039 G>T maps to ENST00000440684 V1193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:72367925 C>A maps to ENST00000440684 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:9728836 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:9693873 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:131487497 G>T maps to NM_207364.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:131487509 C>A maps to NM_207364.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:131487639 G>T maps to NM_207364.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:131486900 G>T maps to NM_207364.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:131487176 C>A maps to NM_207364.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:154147119 G>A maps to NM_001038705.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:154146867 G>A maps to NM_001038705.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:154055652 G>C maps to NM_001038705.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:154146578 C>A maps to NM_001038705.1 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:154147230 C>A maps to NM_001038705.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:154055988 C>T maps to NM_001038705.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:154147308 C>A maps to NM_001038705.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:154146876 C>A maps to NM_001038705.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:154139016 A>G maps to NM_001038705.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:154147338 A>T maps to NM_001038705.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:154139073 C>A maps to NM_001038705.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:154146525 C>A maps to NM_001038705.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:154147359 C>A maps to NM_001038705.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:154147311 G>A maps to NM_001038705.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:154146870 C>A maps to NM_001038705.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:98251065 C>A maps to NM_005290.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:98251875 A>T maps to NM_005290.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr5:94956179 G>C maps to NM_199243.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:94956173 C>T maps to NM_199243.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:94956164 A>T maps to NM_199243.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:145894569 G>T maps to NM_194251.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr5:145895385 C>T maps to NM_194251.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:67219556 C>A maps to NM_206997.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:6313831 G>A maps to NM_207370.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:6313999 C>A maps to NM_207370.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:6314815 C>A maps to NM_207370.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:175301047 C>G maps to NM_152529.5 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr2:175335283 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:119905558 C>A maps to NM_153002.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119900181 G>T maps to NM_153002.2 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:119887087 C>A maps to NM_153002.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:119905591 G>A maps to NM_153002.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr3:119886714 G>T maps to NM_153002.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr3:119905503 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr3:119885887 C>G maps to NM_153002.2 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:9164642 G>A maps to NM_024980.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:25886828 T>C maps to NM_020752.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:25464426 C>T maps to NM_020752.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:25510016 G>T maps to NM_020752.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:25887425 C>A maps to NM_020752.2 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:25887653 T>A maps to NM_020752.2 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:25888181 C>A maps to NM_020752.2 I1209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr10:25887761 T>A maps to NM_020752.2 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr10:25887906 G>T maps to NM_020752.2 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:25887284 G>A maps to NM_020752.2 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr10:25885718 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:25883265 G>T maps to NM_020752.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:25887285 G>T maps to NM_020752.2 E911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:25755614 G>T maps to NM_020752.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:25887176 G>T maps to NM_020752.2 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:25886703 G>T maps to NM_020752.2 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr10:25887578 T>A maps to NM_020752.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr10:25887710 T>A maps to NM_020752.2 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:25887468 A>T maps to NM_020752.2 K972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:25701353 G>T maps to NM_020752.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:25886723 C>A maps to NM_020752.2 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:25861769 C>T maps to NM_020752.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:25887914 G>T maps to NM_020752.2 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr10:25701315 C>T maps to NM_020752.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:25887239 A>T maps to NM_020752.2 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr10:25887190 C>A maps to NM_020752.2 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:169802236 C>T maps to NM_014373.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:168055035 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:168065746 T>A maps to NM_153832.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:168066240 G>A maps to NM_153832.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:168073830 C>T maps to NM_153832.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr12:6933928 T>C maps to NM_019858.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:6936230 T>G maps to NM_019858.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:128408647 C>T maps to NM_005291.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:128408863 C>A maps to NM_005291.2 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:128409115 C>T maps to NM_005291.2 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:128408737 C>G maps to NM_005291.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:128408416 C>A maps to NM_005291.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:145583397 G>T maps to NM_024531.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:145583751 G>A maps to NM_024531.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:145583766 C>T maps to NM_024531.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:4937817 G>A maps to NM_017986.3 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:53106886 G>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:53106003 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:53106627 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:53106004 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr23:53106253 T>C did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:78426623 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:78426924 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:78426598 C>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:78426507 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:78426661 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:78427093 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:78426677 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:78426916 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr23:78427196 G>A did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr23:78427043 C>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:78427234 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:78427210 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:78426677 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:78427053 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:78427450 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:78426603 C>A did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:78427205 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:78426764 G>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:78427265 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:78427216 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:78426720 C>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr15:40093559 C>A maps to NM_007223.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr15:40093560 C>T maps to NM_007223.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr15:40093670 C>A maps to NM_007223.1 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:36498904 G>C maps to ENST00000398597 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:36484369 C>T maps to ENST00000398597 E1695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr17:36499177 C>T maps to ENST00000398597 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr17:36485943 G>T maps to ENST00000398597 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:36483817 G>A maps to ENST00000398597 N1879N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr13:95271524 G>C maps to NM_180989.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr13:95273341 C>T maps to NM_180989.4 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr13:95279404 A>T maps to NM_180989.4 K435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:57389031 G>A maps to NM_007264.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:57389145 C>A maps to NM_007264.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815043 G>A maps to NM_006143.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815115 G>A maps to NM_006143.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:12815159 G>A maps to NM_006143.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:125797432 G>A maps to NM_005294.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:125797759 T>C maps to NM_005294.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:107115455 G>A maps to NM_005295.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:107115749 C>G maps to NM_005295.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:200843049 G>T maps to NM_005298.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:200842881 G>C maps to NM_005298.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:200843049 G>C maps to NM_005298.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:200842959 C>A maps to NM_005298.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:200842206 G>T maps to NM_005298.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:125426471 C>A maps to NM_153442.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:125426522 C>T maps to NM_153442.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:125426342 C>A maps to NM_153442.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:71804186 G>T maps to NM_018971.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:27720713 C>T maps to NM_005281.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:27720809 C>T maps to NM_005281.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:167570896 C>G maps to NM_005299.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:167571268 C>A maps to NM_005299.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr6:167571238 C>T maps to NM_005299.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:51274315 C>T maps to NM_001506.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:51274423 G>T maps to NM_001506.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51274756 T>A maps to NM_001506.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:51274219 G>T maps to NM_001506.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:51274267 G>T maps to NM_001506.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:51274165 C>T maps to NM_001506.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:41555022 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:41555239 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:41554924 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:41554924 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:41554970 C>G did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:41555275 G>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:41555241 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:241570037 C>G maps to NM_001195381.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr2:241569659 G>A maps to NM_001195381.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:241569992 G>A maps to NM_001195381.1 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:124386712 C>A maps to NM_005302.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:202092444 C>T maps to NM_004767.3 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:133175301 G>T maps to NM_001508.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:133174632 C>T maps to NM_001508.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:46094545 C>A maps to NM_005282.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:46094749 G>A maps to NM_005282.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:46094524 C>A maps to NM_005282.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46094343 C>A maps to NM_005282.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:46094047 C>T maps to NM_005282.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:60620763 G>T maps to NM_004778.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:105859085 G>T maps to NM_007227.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:105859316 C>A maps to NM_007227.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:105858713 C>T maps to NM_007227.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:105859053 C>A maps to NM_007227.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:105858590 C>G maps to NM_007227.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:105858896 C>G maps to NM_007227.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:105858395 C>A maps to NM_007227.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:150348571 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:150348519 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:150349061 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:150349062 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:150349617 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:150345267 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:150349227 A>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:150349292 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:150349626 C>A did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:150349244 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:150349261 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:150348991 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:150348438 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:150349712 C>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:150348611 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:150349604 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:150349876 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:150348939 G>T did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:150349640 C>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:150349407 C>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:150349408 C>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:150348411 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:150345291 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:150349268 A>T did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:150349711 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:150345293 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:150349444 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:150348991 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:150349474 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:174417407 G>C maps to NM_005684.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:174417608 C>T maps to NM_005684.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:174418079 G>C maps to NM_005684.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:231774828 C>A maps to NM_005683.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:231775563 G>A maps to NM_005683.3 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:231774762 G>A maps to NM_005683.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:57689438 C>T maps to NM_005682.5 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:57684225 G>C maps to NM_005682.5 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:57689408 C>T maps to NM_005682.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:57689861 C>G maps to NM_005682.5 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:57685481 C>T maps to NM_005682.5 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:110300857 C>A maps to ENST00000414000 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:110300596 G>T maps to ENST00000414000 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr6:110301346 C>T maps to ENST00000414000 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr6:110301370 G>T maps to ENST00000414000 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:110085967 C>A maps to NM_031936.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:110086057 G>T maps to NM_031936.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:110086456 C>A maps to NM_031936.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:110086321 G>T maps to NM_031936.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:97247544 C>A maps to NM_030784.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr6:97246785 C>T maps to NM_030784.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:97247415 T>A maps to NM_030784.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:97247457 G>A maps to NM_030784.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:19031947 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:19027765 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:19031888 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:19046302 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:19031920 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:19027776 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:19020987 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:19009092 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:19042028 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:19013081 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:19018033 C>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:19051730 C>T did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr23:19022897 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:19045369 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:19045377 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:19031914 G>C did not map to a codon.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr14:88477376 C>T maps to NM_003608.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr14:88477961 C>T maps to NM_003608.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:91700938 G>T maps to ENST00000238699 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:54080405 G>A maps to NM_006794.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:47845054 G>T maps to NM_018485.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:8588828 C>A maps to NM_080819.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:8588915 C>A maps to NM_080819.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:8582789 G>T maps to NM_080819.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:123214565 C>G maps to NM_032554.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:41586497 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:41586983 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:41586806 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:41586833 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:94113617 G>A maps to NM_016540.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:94113890 A>G maps to NM_016540.3 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:94113677 G>C maps to NM_016540.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:94134233 G>C maps to NM_016540.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr11:94126760 G>T maps to NM_016540.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:112724476 C>A maps to NM_018970.6 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:112724005 C>A maps to NM_018970.6 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:112724233 A>T maps to NM_018970.6 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:101005565 C>T maps to NM_022049.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:101005397 C>A maps to NM_022049.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr1:101004788 G>T maps to NM_022049.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:57712137 C>A maps to NM_170776.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr16:57717907 C>T maps to NM_170776.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:90012411 C>A maps to NM_032119.3 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:90025572 C>A maps to NM_032119.3 S3514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:89953779 G>T maps to NM_032119.3 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:90040908 G>A maps to NM_032119.3 W3532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90021006 T>G maps to NM_032119.3 L3337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:90085635 A>T maps to NM_032119.3 R4671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:89923107 C>A maps to NM_032119.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:90059177 G>T maps to NM_032119.3 T4059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:90052968 A>T maps to NM_032119.3 A3977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:89933648 C>T maps to NM_032119.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:89999480 G>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr5:90106985 C>T maps to NM_032119.3 F5303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:90001259 T>A maps to NM_032119.3 Y2810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:90079735 C>T maps to NM_032119.3 I4505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:89923459 G>T maps to NM_032119.3 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:90281196 G>T maps to NM_032119.3 E6004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr5:90015942 G>T maps to NM_032119.3 G3176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:89989937 C>T maps to NM_032119.3 F2455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:89949443 A>G maps to NM_032119.3 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:89938741 C>T maps to NM_032119.3 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:90106335 G>T maps to NM_032119.3 E5087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:90074413 A>C maps to NM_032119.3 S4279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:89990066 G>T maps to NM_032119.3 V2498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:89933561 G>T maps to NM_032119.3 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:89933729 G>T maps to NM_032119.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:89933730 G>T maps to NM_032119.3 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:90149127 A>G maps to NM_032119.3 P5744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:101909098 A>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:101909156 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:101912715 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:101911403 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:101910159 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:101910160 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:101911150 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:101909065 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:101910400 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:101910103 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:101911165 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:101910919 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:101912228 A>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:101912051 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:101910822 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:101909738 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:101911007 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:101910605 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:101912303 G>C did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr23:101909506 T>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:101909022 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:101911736 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:101911812 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:101911200 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:101911167 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:101969998 G>C did not map to a codon.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr23:101970800 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:101972044 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:101970464 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:101969992 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:101969871 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:101970220 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:101970101 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:101971405 G>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:101970547 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:101971042 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:101971016 G>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:101970386 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:101972245 G>T did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:101970714 C>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:101970907 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:101971019 A>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr23:101970072 A>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:101970568 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:101971084 A>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:101971024 G>C did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:13061537 C>T maps to NM_003979.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:19883615 G>T maps to NM_016235.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr16:19884023 C>G maps to NM_016235.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr16:19873157 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:72436646 T>C maps to NM_022036.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:117149992 C>A maps to NM_148963.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:117128029 G>A maps to NM_148963.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:117127976 C>T maps to NM_148963.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:117113760 A>G maps to NM_148963.2 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:117121860 G>C maps to NM_148963.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:117128060 G>C maps to NM_148963.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:117121788 G>A maps to NM_148963.2 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:117113849 C>A maps to NM_148963.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:117121857 C>T maps to NM_148963.2 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr6:117128108 G>T maps to NM_148963.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr6:117113985 G>T maps to NM_148963.2 C700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:176025500 C>A maps to NM_052899.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:176025659 C>A maps to NM_052899.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:176026460 C>T maps to NM_052899.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:47000058 G>T maps to NM_014696.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:46999947 G>T maps to NM_014696.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr4:90169158 G>A maps to NM_198281.2 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:90170589 C>T maps to NM_198281.2 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:90169241 G>A maps to NM_198281.2 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:90169635 A>G maps to NM_198281.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:7216392 G>A maps to NM_004489.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr17:7216946 G>A maps to NM_004489.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:139228960 C>T maps to NM_001145638.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:139228912 G>A maps to NM_001145638.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr8:145730155 C>G maps to NM_005309.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:46943705 C>T maps to NM_133443.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:49395530 C>A maps to NM_000581.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:28501898 C>T maps to NM_001509.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:28500164 G>T maps to NM_001509.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:28478651 G>T maps to NM_182701.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:53072382 G>T maps to NM_015696.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:54456890 C>T maps to NM_001008397.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:54456927 T>A maps to NM_001008397.2 L104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:54456043 G>A maps to NM_001008397.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr5:54460036 G>A maps to NM_001008397.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:35500181 G>T maps to NM_020895.3 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:35501098 G>T maps to NM_020895.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:35512614 G>T maps to NM_020895.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123471180 C>T maps to ENST00000456860 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123477486 T>G maps to ENST00000456860 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:123471195 G>T maps to ENST00000456860 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:123471226 C>A maps to ENST00000456860 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:123484226 G>A maps to ENST00000456860 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:123489403 G>T maps to ENST00000456860 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:123485516 C>A maps to ENST00000456860 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:123480518 A>T maps to ENST00000456860 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:113658765 G>A maps to NM_017577.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:113659179 G>C maps to NM_017577.4 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:113634611 T>A maps to NM_017577.4 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:113634668 T>C maps to NM_017577.4 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:125824488 A>T did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr22:47054117 C>T maps to NM_015124.2 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr22:47063992 G>T maps to NM_015124.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr22:47069607 G>A maps to NM_015124.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr22:47022848 G>C maps to NM_015124.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40365464 C>A maps to NM_004810.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr22:40366980 G>T maps to NM_004810.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr22:40365423 G>T maps to NM_004810.2 G234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:52407513 C>A maps to NM_181711.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:50660723 C>A maps to NM_005311.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr7:50737523 T>C maps to NM_005311.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:50771566 C>A maps to NM_005311.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:50799977 C>G maps to NM_005311.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:50771535 G>T maps to NM_005311.4 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:165364994 C>T maps to NM_004490.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:165404187 G>A maps to NM_004490.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:165365353 C>A maps to NM_004490.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:165351034 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:165353988 T>C maps to NM_004490.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:165353976 C>A maps to NM_004490.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:73316466 G>C maps to NM_002086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:37903137 G>A maps to ENST00000445327 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr17:37902041 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:37902406 C>T maps to ENST00000445327 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8513-01A-11D-2393-08 chr17:37903086 C>T maps to ENST00000445327 H535H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:37902033 C>T maps to ENST00000445327 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:11716527 C>T maps to NM_014668.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:11750921 G>A maps to NM_014668.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:11756767 G>T maps to NM_014668.3 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:11756755 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:11728878 G>T maps to NM_014668.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr2:11725912 G>T maps to NM_014668.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:11738001 C>T maps to NM_014668.3 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr2:11733208 C>T maps to NM_014668.3 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:11758582 C>G maps to NM_014668.3 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:11750900 G>T maps to NM_014668.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:11737991 T>C maps to NM_014668.3 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:11751087 G>T maps to NM_014668.3 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:11725324 A>T maps to NM_014668.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:33023328 C>A maps to NM_013372.6 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:240656702 G>T maps to NM_022469.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:10132274 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:10102597 G>C maps to NM_198182.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:10101348 G>A maps to NM_198182.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:102570808 C>T maps to NM_024915.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr8:102570829 G>T maps to NM_024915.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:102589633 A>C did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:102656357 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:102570769 G>T maps to NM_024915.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:24663022 C>G maps to NM_021180.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr1:24658014 G>A maps to NM_021180.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:24663232 C>T maps to NM_021180.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:153182037 C>T maps to NM_001114183.1 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:153144083 G>T maps to NM_001114183.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:153065835 C>A maps to NM_001114183.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5055-01A-01D-1625-08 chr5:153149874 G>T maps to NM_001114183.1 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr5:153149963 G>A maps to NM_001114183.1 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:153149975 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr5:153029905 G>A maps to NM_001114183.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:153144050 C>A maps to NM_001114183.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:153035389 A>G maps to NM_001114183.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:153065883 C>T maps to NM_001114183.1 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:158257769 G>A maps to NM_000826.3 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:158283986 G>T maps to NM_000826.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158233870 A>G maps to NM_000826.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:158284151 A>T maps to NM_000826.3 K870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:158282245 A>G maps to NM_001083619.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr4:158281078 G>A maps to NM_000826.3 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:158257623 C>T maps to NM_000826.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:158262430 C>A maps to NM_000826.3 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:158224836 A>T maps to NM_000826.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:158281226 C>A maps to NM_000826.3 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:158281202 T>A maps to NM_000826.3 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:158282692 C>T maps to NM_000826.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:158224767 T>C maps to NM_000826.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:158256938 C>A maps to NM_000826.3 Y461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr4:158282203 C>G maps to NM_001083619.1 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:158142864 A>T maps to NM_000826.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:158234011 C>T maps to NM_000826.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:158224785 C>T maps to NM_000826.3 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:122616717 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:122616706 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:122528861 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:122319799 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:122318469 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:122537343 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:122387171 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:122616871 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:122387161 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:122616713 T>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:122616714 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:122528961 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:122532555 C>A did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr23:122598955 G>C did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:122561799 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:122460065 T>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:122387355 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:122319787 A>G did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:122616857 G>A did not map to a codon.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr23:122319829 G>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:122532603 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:122616860 A>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:122551484 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:122537304 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:122538598 T>G did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:122551378 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:122551379 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:105623719 T>A maps to NM_000829.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:105836688 C>G maps to NM_001077243.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:105795123 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:105850453 G>C maps to NM_000829.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr11:105795453 C>A maps to NM_000829.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:105483078 C>T maps to NM_000829.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:105623851 G>T maps to NM_000829.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:105623794 C>A maps to NM_000829.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:105758264 T>C maps to NM_000829.3 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:105797465 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:105623806 C>T maps to NM_000829.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:87373322 G>T maps to NM_017551.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr10:87487668 G>A maps to NM_017551.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:87482851 G>A maps to NM_017551.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:87379646 G>T maps to NM_017551.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:87362238 G>T maps to NM_017551.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:87966292 G>C maps to NM_017551.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr10:87373268 G>A maps to NM_017551.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:88123743 G>T maps to NM_017551.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:87489350 C>T maps to NM_017551.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:87362371 C>T maps to NM_017551.2 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:87482881 C>A maps to NM_017551.2 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:87407154 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:87379727 C>T maps to NM_017551.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:87373337 G>T maps to NM_017551.2 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr10:87489352 C>A maps to NM_017551.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr10:87628789 C>A maps to NM_017551.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr10:87628877 C>A maps to NM_017551.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:87615794 G>T maps to NM_017551.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr10:87966382 C>A maps to NM_017551.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:94343932 T>C maps to NM_001510.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:94411877 G>T maps to NM_001510.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:94690495 A>T maps to NM_001510.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94436365 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:94690558 G>C maps to NM_001510.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:94344040 C>A maps to NM_001510.2 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:94690552 G>A maps to NM_001510.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr4:94316765 C>A maps to NM_001510.2 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:94006215 C>A maps to NM_001510.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:94690558 G>T maps to NM_001510.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:94006167 C>G maps to NM_001510.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:94411925 C>A maps to NM_001510.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:94006320 T>C maps to NM_001510.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:94547571 T>C maps to NM_001510.2 D782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr4:94690474 C>A maps to NM_001510.2 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:94690474 C>A maps to NM_001510.2 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:94159550 A>G maps to NM_001510.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:94436523 G>T maps to NM_001510.2 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:94006430 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:94693372 G>T maps to NM_001510.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31023524 G>A maps to ENST00000327783 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:30949367 G>T maps to ENST00000327783 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr21:31062243 G>C maps to ENST00000327783 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr21:31066377 C>A maps to ENST00000327783 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr21:30959741 C>T maps to ENST00000327783 W579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr21:31027159 G>T maps to ENST00000327783 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:30927397 G>T maps to ENST00000327783 S861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:31062099 C>G maps to ENST00000327783 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr21:30949385 T>A maps to ENST00000327783 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31045362 G>C maps to ENST00000327783 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr21:31015274 C>A maps to ENST00000327783 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr21:31027132 G>T maps to ENST00000327783 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:102250222 C>G maps to NM_021956.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:102503455 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:102372529 G>A maps to NM_021956.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:102134197 C>A maps to NM_021956.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:102074321 A>T maps to NM_021956.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:102516385 A>C maps to NM_021956.4 *909Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:102503232 A>T maps to NM_021956.4 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr6:102266252 G>T maps to NM_021956.4 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:102483430 C>A maps to NM_021956.4 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr6:101847170 G>T maps to NM_021956.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr6:102516290 A>T maps to NM_021956.4 K878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr6:102134227 G>A maps to NM_021956.4 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr6:102307313 C>A maps to NM_021956.4 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:37267484 G>T maps to NM_000831.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:37291208 G>A maps to NM_000831.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37271747 C>A maps to NM_000831.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:37324780 G>T maps to NM_000831.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:37307393 G>T maps to NM_000831.3 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:37356599 C>T maps to NM_000831.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:37271783 G>A maps to NM_000831.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:37307528 G>A maps to NM_000831.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:37325576 G>T maps to NM_000831.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:37282789 C>A maps to NM_000831.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr1:37346265 C>G maps to NM_000831.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:37307539 C>A maps to NM_000831.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:37307504 C>T maps to NM_000831.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:37307351 C>T maps to NM_000831.3 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:120702642 G>T maps to NM_014619.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120831680 G>T maps to NM_014619.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:120776195 C>T maps to NM_014619.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:120732756 C>T maps to NM_014619.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:120690597 C>T maps to NM_014619.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:120833379 C>A maps to NM_014619.2 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr11:120707501 A>C maps to NM_014619.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:120702729 C>A maps to NM_014619.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:42510925 C>T maps to NM_002088.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:42566720 C>A maps to NM_002088.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:42558060 G>T maps to NM_002088.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:42509974 G>T maps to NM_002088.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:42560891 G>T maps to NM_002088.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:140058265 C>A maps to ENST00000371546 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:140058238 C>T maps to ENST00000371546 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:140036577 C>G maps to ENST00000371546 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:140057043 C>T maps to ENST00000371546 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:140040200 C>A maps to ENST00000371546 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr9:140055650 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:140059720 C>T maps to ENST00000371546 F912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:9934561 C>A maps to NM_000833.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:9934525 G>A maps to NM_000833.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:9857329 G>T maps to NM_000833.3 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:9943737 C>A maps to NM_000833.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:10031859 G>A maps to NM_000833.3 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:9857857 G>A maps to NM_000833.3 N1181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:9857311 G>A maps to NM_000833.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr16:9857956 C>T maps to NM_000833.3 P1148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr16:9858028 C>T maps to NM_000833.3 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:10032408 C>A did not map to a codon.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr16:9923438 G>A maps to NM_000833.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9934798 G>T maps to NM_000833.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:9984902 G>T maps to NM_000833.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr16:9934804 T>A maps to NM_000833.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:9892236 C>A maps to NM_000833.3 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:10031979 G>A maps to NM_000833.3 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr16:10274037 G>A maps to NM_000833.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:9858085 G>T maps to NM_000833.3 Y1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr16:9857944 C>T maps to NM_000833.3 Q1152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:13719973 G>T maps to NM_000834.3 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:13716361 C>T maps to NM_000834.3 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:13717203 G>T maps to NM_000834.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:13906651 G>A maps to NM_000834.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:13717084 G>A maps to NM_000834.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:13720198 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:13768117 G>C maps to NM_000834.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:13906582 G>T maps to NM_000834.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:13717312 G>T maps to NM_000834.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr12:13769540 G>T maps to NM_000834.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr12:13761686 C>G maps to NM_000834.3 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr12:13716715 G>T maps to NM_000834.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:13717030 G>A maps to NM_000834.3 D1047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:13716150 C>A maps to NM_000834.3 E1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:13715932 C>A maps to NM_000834.3 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr17:72846416 G>A maps to NM_000835.3 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:72846027 G>A maps to NM_000835.3 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:48908349 G>A maps to NM_000836.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:48925193 C>G maps to NM_000836.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr19:48922563 C>T maps to NM_000836.2 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:48925067 G>A maps to NM_000836.2 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:104433277 G>C maps to NM_133445.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:104449332 G>C maps to NM_133445.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:104433247 G>T maps to NM_133445.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:104449374 C>A maps to NM_133445.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:104432626 G>A maps to NM_133445.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr9:104433160 A>G maps to NM_133445.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr9:104432377 C>T maps to NM_133445.2 K772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr9:104499832 G>A maps to NM_133445.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:104499955 C>A maps to NM_133445.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:104499982 C>A maps to NM_133445.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:104390580 T>G maps to NM_133445.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:104499661 G>T maps to NM_133445.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:104448920 C>A maps to NM_133445.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:104448969 G>T maps to NM_133445.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:104449473 A>T maps to NM_133445.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:1008896 G>A maps to NM_138690.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:1004960 G>A maps to NM_138690.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:1008895 C>A maps to NM_138690.1 S891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:145065525 C>T maps to NM_001009184.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr12:66773166 C>T maps to ENST00000359742 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr12:66911694 T>A maps to ENST00000359742 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:66788001 C>G maps to ENST00000359742 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:66765479 C>T maps to ENST00000359742 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:66935727 C>A maps to ENST00000359742 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:14547154 C>T maps to ENST00000507975 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:14552739 G>T maps to ENST00000507975 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:14564538 C>A maps to ENST00000507975 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:14567023 C>A maps to ENST00000507975 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr3:14558607 G>T maps to ENST00000507975 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:48832428 C>A did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:48858615 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48849921 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:48831664 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:114324003 T>A maps to NM_002929.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:3029697 C>T maps to NM_182982.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121086100 T>A maps to NM_005308.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:121184540 C>T maps to NM_005308.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:121212277 C>G maps to NM_005308.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr10:121212763 G>A maps to NM_005308.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr10:121196209 C>A maps to NM_005308.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:176867987 G>T maps to NM_002082.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:176857960 C>T maps to NM_002082.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:176863128 C>T maps to NM_002082.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:176867753 C>T maps to NM_002082.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:141535732 T>C maps to NM_139209.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47422324 C>T maps to NM_004491.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr19:47422256 C>T maps to NM_004491.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:47503857 G>A maps to NM_004491.4 P1471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:47422311 C>G maps to NM_004491.4 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:47424933 C>G maps to NM_004491.4 S1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:47422372 G>A maps to NM_004491.4 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr19:47422057 C>T maps to NM_004491.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:47424278 C>T maps to NM_004491.4 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:47422558 C>T maps to NM_004491.4 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr19:47422510 G>A maps to NM_004491.4 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:146720538 G>A maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:146351043 C>T maps to NM_000838.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:146755227 G>T maps to NM_000838.3 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:146480565 C>A maps to NM_000838.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:146747739 A>G maps to NM_001114329.1 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:146480614 C>A maps to NM_000838.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr6:146719959 A>T maps to NM_000838.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:146708031 C>A maps to NM_000838.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr6:146351141 C>A maps to NM_000838.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:146351144 C>A maps to NM_000838.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:146755352 C>A maps to NM_000838.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:146720637 C>T maps to NM_000838.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr6:146720433 G>C maps to NM_000838.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:146708033 G>C maps to NM_000838.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:51749621 T>A maps to NM_000839.3 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:51743226 G>A maps to NM_000839.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:51746994 G>T maps to NM_000839.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:86416433 T>G did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:86416286 G>T maps to NM_000840.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:86415734 C>T maps to NM_000840.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:86415677 C>A maps to NM_000840.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:86416073 C>A maps to NM_000840.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:86415743 C>G maps to NM_000840.2 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:86479846 C>T maps to NM_000840.2 T851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:86415917 C>G maps to NM_000840.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:86394874 C>T maps to NM_000840.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr7:86394907 T>C maps to NM_000840.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:33996101 C>G maps to NM_000841.1 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:34008346 G>T maps to NM_000841.1 Y449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr6:34008364 G>C maps to NM_000841.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:34003717 G>T maps to NM_000841.1 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:88330420 T>C maps to NM_001143831.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:88301012 G>C maps to NM_001143831.2 S613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:88300588 G>T maps to NM_001143831.2 C754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:88301014 G>A maps to NM_001143831.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:88323859 G>T maps to NM_001143831.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:88583078 C>G maps to NM_001143831.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:88780622 T>A maps to NM_001143831.2 K140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:88780893 C>G maps to NM_001143831.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:88337920 C>A maps to NM_001143831.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:88300348 G>T maps to NM_001143831.2 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:88780896 A>C maps to NM_001143831.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:88780590 G>A maps to NM_001143831.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:88300450 G>T maps to NM_001143831.2 I800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:88323888 G>T maps to NM_001143831.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr11:88338055 G>C maps to NM_001143831.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr11:88300585 G>A maps to NM_001143831.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:178418426 G>A maps to NM_000843.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:178408744 C>T maps to NM_000843.3 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:178413229 G>A maps to NM_000843.3 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr5:178418468 G>T maps to NM_000843.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:178417680 G>A maps to NM_000843.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:178413313 G>T maps to NM_000843.3 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:178416023 G>T maps to NM_000843.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:178413547 C>A maps to NM_000843.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:178417646 C>A maps to NM_000843.3 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:178419045 G>A maps to NM_000843.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:178416023 G>T maps to NM_000843.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620494 G>T maps to NM_181874.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:7620935 C>G maps to NM_181874.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:6903104 C>A maps to NM_181874.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:6903371 G>C maps to NM_181874.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:7620878 T>C maps to NM_181874.2 Y762Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:7620335 C>A maps to NM_181874.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:7620455 C>T maps to NM_181874.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:7340369 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:7503363 G>C maps to NM_181874.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:7503303 C>T maps to NM_181874.2 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:7494357 C>T maps to NM_181874.2 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:7620395 G>T maps to NM_181874.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:7340512 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:7620125 G>A maps to NM_181874.2 W511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:7620332 C>T maps to NM_181874.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:7728044 C>T maps to NM_181874.2 N900N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:7348223 C>A maps to NM_181874.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:7348274 G>C maps to NM_181874.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr3:7620593 C>A maps to NM_181874.2 C667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:126173584 T>C maps to NM_001127323.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:126173710 G>T maps to NM_001127323.1 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:126544738 T>G did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:126173023 T>A maps to NM_001127323.1 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:126173449 G>A maps to NM_001127323.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:126410119 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:126173878 C>A maps to NM_001127323.1 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:126086279 C>A maps to NM_001127323.1 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr7:126542709 G>A maps to NM_001127323.1 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:126883159 G>A maps to NM_001127323.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:126882808 G>T maps to NM_001127323.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:126086288 G>A maps to NM_001127323.1 F856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:126882943 C>G maps to NM_001127323.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr7:126883249 G>T maps to NM_001127323.1 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:126086183 G>T maps to NM_001127323.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:126086156 C>A maps to NM_001127323.1 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:126542594 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:126882964 C>A maps to NM_001127323.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:126746691 C>A maps to NM_001127323.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr17:42429562 C>T maps to NM_002087.2 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:42429562 C>T maps to NM_002087.2 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr18:56892961 C>A maps to NM_002091.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr4:7062753 C>T maps to NM_025196.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:148730754 A>T maps to NM_152407.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:16142117 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:16170415 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:16142310 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:16168632 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:16142295 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:16170423 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:16168616 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:16168470 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:16168472 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:71698942 T>A maps to NM_002092.3 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:71690059 C>T maps to NM_002092.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:48956134 C>T maps to NM_031485.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:42895637 C>T maps to NM_001080476.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:42965057 T>C maps to NM_001080476.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:42895465 G>A maps to NM_001080476.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:43032469 A>T maps to NM_001080476.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr4:42895396 G>T maps to NM_001080476.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr22:19136548 C>T maps to NM_005315.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:38126821 G>T maps to NM_178171.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr17:38122057 C>T maps to NM_178171.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:38130566 C>T maps to NM_178171.4 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr17:38122576 G>T maps to NM_178171.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:38127853 C>T maps to NM_178171.4 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr17:38066034 G>A maps to NM_001165958.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:130760959 G>A maps to NM_031415.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr8:130789752 T>A maps to NM_031415.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:130789794 G>C maps to NM_031415.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:144644998 G>T maps to NM_024736.6 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr8:144642895 G>A maps to NM_024736.6 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:13243461 G>A maps to NM_001080555.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:13238119 C>G maps to NM_001080555.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:13240940 G>A maps to NM_001080555.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr12:13243746 C>T maps to NM_001080555.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr12:13237957 G>T maps to NM_001080555.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:27840243 T>A maps to NM_001109763.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr16:27840113 C>A maps to NM_001109763.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3627903 A>T maps to NM_031965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:3627255 G>T maps to NM_031965.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:119720925 G>A maps to NM_002093.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:119812254 G>C maps to NM_002093.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:119582445 G>A maps to NM_002093.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr16:11980743 T>C maps to NM_002094.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:51488069 C>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:51488469 T>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:51488282 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:51486782 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:51486790 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:51487924 G>C did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:51487182 A>C did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr23:51487853 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:30567404 T>A maps to NM_000637.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:30560721 G>A maps to NM_000637.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:30550565 T>A maps to NM_000637.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:33539580 C>T maps to NM_000178.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:33533874 G>C maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:52664028 G>T maps to NM_145740.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:52659011 G>A maps to NM_145740.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:52657704 G>T maps to NM_145740.3 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr6:52701068 G>T maps to NM_153699.1 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:106647734 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:110231319 G>A maps to ENST00000369823 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr10:106039208 G>T maps to NM_183239.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:106057397 C>T maps to NM_183239.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:24323169 C>T maps to NM_000854.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:77796650 A>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:28368063 G>T maps to NM_145657.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr13:28368022 G>T maps to NM_145657.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:144966222 G>T maps to NM_001164629.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:144714906 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:144710379 T>A maps to NM_001164629.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:144903178 C>A maps to NM_001164629.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:81659000 T>C maps to NM_015859.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:48848036 G>T maps to NM_172311.2 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:48874181 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:48873883 C>T maps to NM_172311.2 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:59944430 G>A maps to NM_004492.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:120469410 A>T maps to NM_005513.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:120469791 C>G maps to NM_005513.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:120489650 A>G maps to NM_005513.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:6387449 C>A maps to NM_002096.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:6380975 G>A maps to NM_002096.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:18354718 G>A maps to NM_005316.3 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:18363154 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:30876867 C>T maps to NM_001517.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:30880222 C>T maps to NM_001517.4 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:73927186 G>T maps to NM_016328.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr7:73927301 G>T did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:73969506 C>T maps to NM_016328.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:73944211 G>A maps to NM_016328.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:74004250 A>T maps to NM_016328.2 K813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:27476637 G>A maps to NM_001520.3 F1766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:27476786 C>A maps to NM_001520.3 E1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:27492446 C>T maps to NM_001520.3 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:27544623 C>T maps to NM_001520.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:27549127 T>C maps to NM_001520.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr16:27475737 T>C maps to NM_001520.3 A1925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr16:27518345 C>A maps to NM_001520.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr16:27497464 T>A maps to NM_001520.3 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:27544610 C>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr16:27483124 C>T maps to NM_001520.3 K1490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:27472817 G>A maps to NM_001520.3 F2061F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr16:27499674 C>T maps to NM_001520.3 W1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:27509023 C>A maps to NM_001520.3 G762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:27549550 C>A maps to NM_001520.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:27481436 G>A maps to NM_001520.3 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr16:27481532 G>A maps to NM_001520.3 A1570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr16:27500984 C>T maps to NM_001520.3 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:27497404 C>A maps to NM_001520.3 R1257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:27565995 G>T maps to NM_001521.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:135555141 C>G maps to NM_012204.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:135554778 C>T maps to NM_012204.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr9:135564266 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135933285 G>A maps to NM_001122823.1 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:135933327 T>C maps to NM_001122823.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:135926347 G>T maps to NM_001122823.1 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr22:39104847 A>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:89984397 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr6:43593174 G>A maps to NM_019096.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:43589436 G>T maps to NM_019096.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:43592281 G>A maps to NM_019096.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:43591805 C>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr19:17451851 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:17452464 G>T maps to NM_133644.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr19:17450396 C>T maps to NM_133644.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr19:17452005 G>T maps to NM_133644.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr10:1046795 C>G maps to NM_012341.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr10:1034430 C>G maps to NM_012341.2 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:60773886 G>A maps to NM_015666.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46708078 C>T maps to NM_016426.6 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr22:46704788 G>T maps to NM_016426.6 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr22:46712019 G>T maps to NM_016426.6 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr22:46724731 C>G maps to NM_016426.6 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:46709785 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:42146547 C>T maps to NM_000409.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:42162527 C>A maps to NM_002098.5 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:108672524 C>A maps to NM_005459.3 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:42620421 C>T maps to NM_007102.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:42619207 C>A maps to NM_007102.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:106579320 C>A maps to ENST00000282249 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:106681096 T>C maps to ENST00000282249 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:106558340 A>C maps to ENST00000282249 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:106680948 T>A maps to ENST00000282249 K488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:106579341 C>T maps to ENST00000282249 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:106647304 C>A maps to ENST00000282249 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:106647305 C>A maps to ENST00000282249 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr11:106810512 G>A maps to ENST00000282249 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:106558346 A>G maps to ENST00000282249 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:106810227 A>G maps to ENST00000282249 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr11:106680826 A>C maps to ENST00000282249 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:106558442 C>A maps to ENST00000282249 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr11:106681008 T>G maps to ENST00000282249 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:106810473 T>G maps to ENST00000282249 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:106558445 C>A maps to ENST00000282249 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:106680717 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:156651381 A>T maps to NM_001130684.1 *691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:156634680 C>G maps to NM_001130684.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:156634495 G>T maps to NM_001130684.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:156634248 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:156727535 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:156715005 A>T did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr4:156680961 G>T maps to ENST00000502959 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:14778849 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:14804339 C>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr12:14774060 G>A maps to NM_004963.3 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:14809551 C>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:14834320 A>G maps to NM_004963.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:14766089 C>T maps to NM_004963.3 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:7915565 C>T maps to NM_000180.3 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:7910408 C>T maps to NM_000180.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:108708513 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:108673615 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:108718454 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:108625420 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:108684681 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:108628500 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:108708603 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:108684588 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:108628438 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:108631742 G>T did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:108638635 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:108631888 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:108652339 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:108641893 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:108697068 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:108619372 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:108684663 T>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:108684623 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:108673535 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:108708534 A>G did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:108696811 G>T did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:108619376 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:108696734 T>C did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:108635215 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:108684638 A>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:108652297 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:108619335 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:108636225 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:108719011 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:108631805 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:44693768 G>T maps to NM_021927.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:44683137 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:44682780 C>T maps to NM_021927.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:228333278 G>A maps to ENST00000366720 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:228335202 G>T maps to ENST00000366720 R182R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-86-8056-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:65426033 C>G maps to NM_000181.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:65429375 G>A maps to NM_000181.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:65429343 G>A maps to NM_000181.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:65441052 G>T maps to NM_000181.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:65444835 G>A maps to NM_000181.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:65435325 C>T maps to NM_000181.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:42491396 C>A maps to NM_173601.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:73004334 G>A maps to NM_001080393.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr3:148711956 C>T maps to NM_004130.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:2773086 G>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:2799176 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:2772126 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:2773171 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:2779568 C>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:45946097 C>G maps to NM_152312.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:45948931 A>C maps to NM_152312.3 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr4:145038045 C>G maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:145039891 T>C maps to NM_002099.6 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:144918703 G>T maps to ENST00000283128 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:127453520 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:127451437 A>G maps to ENST00000356887 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr2:127453711 T>C maps to NM_002101.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:144797934 G>T maps to NM_198682.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr19:49485990 C>A maps to NM_002103.4 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:49473871 C>G maps to NM_002103.4 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:21713402 C>A maps to NM_021957.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:21728835 C>G maps to NM_021957.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr12:21712054 T>A maps to NM_021957.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23345106 C>T maps to NM_022482.3 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr20:23350780 G>T maps to NM_022482.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:54398578 A>G maps to NM_006144.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:25101072 A>C maps to ENST00000382542 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:25101303 C>A maps to ENST00000382542 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr14:25102224 G>T maps to ENST00000382542 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr14:25101279 C>T maps to ENST00000382542 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:25075913 G>T maps to NM_033423.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:25077586 G>T maps to NM_033423.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:54326300 A>T maps to NM_002104.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:549789 G>T maps to NM_005317.2 *258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:48723268 C>T maps to NM_181788.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:129270134 C>A maps to NM_153833.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr3:129034607 G>T maps to NM_006026.3 G46G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-7659-01A-11D-2063-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-8585-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:134724750 G>T maps to NM_138610.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:71851670 G>A maps to NM_018649.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:103267881 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:103268140 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:103268101 G>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:103268200 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:103268202 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:103267314 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:103267966 A>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:103268066 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:9307142 G>T did not map to a codon.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr1:9324039 G>A maps to NM_004285.3 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr1:9323859 C>T maps to NM_004285.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:9324756 C>A maps to NM_004285.3 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:43019610 G>T maps to NM_012205.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr10:115335695 C>A maps to NM_004132.3 C88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:105192074 G>A maps to NM_020771.3 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:105280921 T>A maps to NM_020771.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:105192069 C>T maps to NM_020771.3 E826E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-93-8067-01A-11D-2284-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:108935702 G>A maps to ENST00000351726 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:26457192 T>C maps to NM_000182.4 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr2:26486305 G>T maps to NM_000183.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:1872978 C>A maps to NM_005326.4 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:96389478 G>C maps to NM_002108.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:96371727 C>A maps to NM_002108.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:35775839 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:153857484 G>C maps to NM_004821.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:7920966 C>A maps to NM_017545.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr20:7915176 G>T maps to NM_017545.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:7886946 G>C maps to NM_017545.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr20:7866403 G>A maps to NM_017545.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr20:7894995 T>C maps to NM_017545.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr20:7915152 G>A maps to NM_017545.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr20:7866451 G>A maps to NM_017545.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr20:7875871 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:119925579 G>T maps to ENST00000361035 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:119925535 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:119927429 C>A maps to ENST00000361035 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:39890457 G>C maps to ENST00000310778 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:39884046 C>A maps to ENST00000310778 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:39888997 G>T maps to ENST00000310778 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:39890640 G>T maps to ENST00000310778 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:39881303 C>T maps to ENST00000310778 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:39883374 C>A maps to ENST00000310778 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:82940335 G>T maps to NM_001884.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:82937539 G>T maps to NM_001884.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:82937481 C>A maps to NM_001884.3 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:82948629 G>T maps to NM_001884.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:82948641 T>G maps to NM_001884.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:156593863 C>G maps to NM_021817.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr15:89421482 C>T maps to NM_178232.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr15:89422411 C>A maps to NM_178232.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr15:89421299 C>T maps to NM_178232.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr15:89421265 G>A maps to NM_178232.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19371793 G>T maps to NM_023002.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:19371852 T>A maps to NM_023002.2 K85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:19369647 G>A maps to NM_023002.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:19369410 G>A maps to NM_023002.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr19:19369374 G>T maps to NM_023002.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140059417 C>G maps to NM_002109.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:140076792 A>G maps to NM_012208.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr5:140076936 G>T maps to NM_012208.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:140075360 C>T maps to NM_012208.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52220290 C>T maps to NM_001523.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52222629 C>T maps to NM_001523.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:52222511 C>A maps to NM_001523.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:52216703 G>T maps to NM_001523.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:122641152 G>T maps to NM_005328.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:122626809 G>T maps to NM_005328.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:122641019 C>T maps to NM_005328.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr8:122626831 G>C maps to NM_005328.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr8:122641355 T>C maps to NM_005328.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:122641477 G>A maps to NM_005328.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:122626660 G>A maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:122626872 C>A maps to NM_005328.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:69148655 A>T maps to NM_005329.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:69143831 G>A maps to NM_005329.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:69148367 G>A maps to NM_005329.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:172841108 C>T maps to NM_003642.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:172822980 C>T maps to NM_003642.3 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr18:43708087 G>C maps to NM_138443.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:2242154 A>C maps to NM_024511.5 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:2238062 T>A maps to NM_024511.5 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:2242225 G>A maps to NM_024511.5 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:2242523 C>T maps to NM_024511.5 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:2242366 C>A maps to NM_024511.5 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:23424311 G>A maps to NM_017815.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36109806 G>T maps to NM_015302.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:36109869 G>A maps to NM_015302.1 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:19078171 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:19080547 C>A maps to NM_017645.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:19063029 T>C maps to NM_017645.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:152734676 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:152721765 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:152721025 G>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:152734614 C>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:152734615 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:152721788 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:152721052 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:152721062 A>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:152719879 C>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:152721781 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:152721101 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:152721041 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156482497 A>T maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:156476070 T>A maps to NM_001173393.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:156479504 C>A maps to NM_001173393.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:156469676 C>A maps to NM_001173393.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:156482497 A>G maps to NM_001173393.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:156464270 G>A maps to NM_001173393.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:156533887 G>T maps to NM_032782.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:156533647 G>T maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:156535949 C>A maps to NM_032782.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr5:156531728 T>C maps to NM_032782.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:154247909 G>T maps to NM_006118.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:5246902 G>A maps to NM_000518.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:5255304 A>G maps to NM_000519.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:5255394 C>T maps to NM_000519.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:5290848 C>A maps to NM_005330.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:5290731 C>T maps to NM_005330.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:5290727 C>A maps to NM_005330.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:5290842 G>T maps to NM_005330.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:5289755 A>T maps to NM_005330.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:5274632 G>T maps to ENST00000399563 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:5275653 G>A maps to ENST00000399563 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:5274541 C>A maps to ENST00000399563 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:106826353 T>C maps to NM_012257.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:106841862 C>G maps to NM_012257.3 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:135360765 C>T maps to NM_006620.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr16:202964 C>A maps to NM_005332.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:11132992 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:11136728 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:11139772 G>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:11139854 C>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:11130218 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153217334 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153222984 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:153230085 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:153220718 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:153224148 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:153219070 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:153223607 G>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:153220035 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:153227706 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:153220589 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:153229609 G>T did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:153219909 G>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:153225259 C>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:153236138 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:153220567 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:153221644 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153222927 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:153218231 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:153220003 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:153215716 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:153220167 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153223312 A>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153225596 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153225597 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:153215762 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:153227747 G>A did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:153219759 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:153216378 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:153217515 G>T did not map to a codon.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr23:153228789 G>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:153222781 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153221827 G>C did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:153221720 G>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:153221811 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:153215988 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:153215032 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:153220945 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:104473247 G>T maps to NM_013320.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:104458364 G>A maps to NM_013320.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:30659584 G>A maps to NM_002110.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr20:30662468 G>T maps to NM_002110.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr20:30674476 A>G maps to NM_002110.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:30672332 G>T maps to NM_002110.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr20:30689306 C>A maps to NM_002110.3 Y522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:30689291 C>A maps to NM_002110.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:30672296 C>T maps to NM_002110.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:121350946 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:121353095 C>T maps to NM_005335.4 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:45262154 C>A maps to NM_021072.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:45262663 G>A maps to NM_021072.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:45262889 C>A maps to NM_021072.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr5:45645553 A>G maps to NM_021072.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:45645682 T>G maps to NM_021072.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:45645391 G>T maps to NM_021072.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:45353207 C>A maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:45262352 C>T maps to NM_021072.2 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:45262166 T>C maps to NM_021072.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:45262168 G>T maps to NM_021072.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:45262862 A>G maps to NM_021072.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:45262466 C>T maps to NM_021072.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr5:45262358 C>A maps to NM_021072.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:45262604 G>A maps to NM_021072.2 C697C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:45267337 T>A maps to NM_021072.2 K546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr5:45645421 A>T maps to NM_021072.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:45262382 C>G maps to NM_021072.2 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:45396641 G>C maps to NM_021072.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:45303719 T>C maps to NM_021072.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:45262697 C>T maps to NM_021072.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:45262787 G>A maps to NM_021072.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:45262235 C>A maps to NM_021072.2 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:45396632 G>T maps to NM_021072.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:45695937 C>A maps to NM_021072.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:45262442 C>T maps to NM_021072.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:45396683 G>A maps to NM_021072.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:45262208 T>C maps to NM_021072.2 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr5:45262727 C>G maps to NM_021072.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:45262304 C>G maps to NM_021072.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:45645630 C>A maps to NM_021072.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:45262241 G>C maps to NM_021072.2 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:155253817 C>T maps to NM_020897.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:155254544 G>A maps to NM_020897.1 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:155257692 G>T maps to NM_020897.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:155254515 C>T maps to NM_020897.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:155252499 G>T maps to NM_020897.1 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:73617679 C>A maps to NM_005477.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:73617521 A>G maps to NM_005477.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:73660113 C>A maps to NM_005477.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:73624564 G>A maps to NM_005477.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:32084918 A>G maps to NM_001525.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:32085283 C>T maps to NM_001525.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:55145159 T>A maps to NM_001526.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:55113464 C>T maps to NM_001526.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:55113435 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:55119931 A>G did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr6:55113506 G>A maps to NM_001526.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:55128553 C>T maps to NM_001526.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr6:55039537 A>G maps to NM_001526.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:55039414 C>T maps to NM_001526.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:55128532 C>T maps to NM_001526.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:36394805 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:32796424 G>T maps to NM_004964.2 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:13543373 C>T maps to NM_024827.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:114279811 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr6:114262224 G>A maps to ENST00000398283 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:114279888 G>A maps to ENST00000398283 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:141014504 G>A maps to NM_003883.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:239990287 C>G maps to NM_006037.3 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:239974809 C>A maps to NM_006037.3 E1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:240066312 G>T maps to NM_006037.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr2:240036976 C>T maps to NM_006037.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:239975196 G>A maps to NM_006037.3 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:240066303 T>A maps to NM_006037.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:240111690 C>A maps to NM_006037.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:240085566 A>G maps to NM_006037.3 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr17:42169749 C>A maps to NM_001015053.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:42169821 C>T maps to NM_001015053.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:42169193 G>A maps to NM_001015053.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:48682426 T>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:48681321 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:48665047 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:48663849 C>G did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:48663850 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48666689 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:48663928 G>C did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:48661317 C>G did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:48673863 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:48681413 A>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:48683009 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:48678625 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr23:48661576 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:48681202 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:48188623 C>G maps to NM_015401.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:71791952 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:18832987 G>A maps to NM_178425.2 W745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:19015565 G>T maps to NM_178425.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:18687613 T>A maps to NM_178425.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:19015513 C>A maps to NM_178425.2 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:18688194 C>A maps to NM_178425.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:18705918 G>T maps to NM_178425.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:18687589 A>G maps to NM_178425.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:18705894 G>A maps to NM_178425.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:18706011 G>C maps to NM_178425.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:18669104 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:18993770 G>A maps to NM_178425.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:18875118 G>A maps to NM_178425.2 Q832Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:18975530 C>A maps to NM_178425.2 S968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:18687493 C>T maps to NM_178425.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:18625114 G>A maps to NM_178425.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:18687574 T>C maps to NM_178425.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:18669010 C>T maps to NM_178425.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:19035667 G>T maps to NM_178425.2 E1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:18767261 G>T maps to NM_178425.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:19015534 A>T maps to NM_178425.2 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:18914118 G>C maps to NM_178425.2 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr7:18788725 C>T maps to NM_178425.2 R670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:18688116 C>T maps to NM_178425.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr7:18630020 G>T maps to NM_178425.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr7:18630021 G>T maps to NM_178425.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr7:18684406 C>A maps to NM_178425.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:18625072 G>T maps to NM_178425.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:50546388 G>T maps to NM_002112.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr15:50535204 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:50534960 C>T maps to NM_002112.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:50534774 G>T maps to NM_002112.3 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr15:50535002 G>T maps to NM_002112.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr15:50534987 C>A maps to NM_002112.3 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:156713552 C>A maps to NM_001126050.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:156721200 C>T maps to NM_004494.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:22569971 G>C maps to NM_138574.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:22569902 C>T maps to NM_138574.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:22569815 C>T maps to NM_138574.2 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:4499588 G>A maps to ENST00000301284 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:4498881 G>A maps to ENST00000301284 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:6995375 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:6995464 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:6995489 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:7023811 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:7023768 C>A did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:7023807 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:242169567 G>T maps to NM_005336.3 Y1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242179036 G>A maps to NM_005336.3 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr2:242203864 G>A maps to NM_005336.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:242187459 C>A maps to NM_005336.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:242179420 G>A maps to NM_005336.3 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:83599331 G>C did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:83723703 G>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:83724065 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:83599426 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:83616486 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:83730298 T>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:83599335 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:83724223 T>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:83730390 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:83723644 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:83581268 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:83723855 T>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:83581278 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:83724131 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:83591884 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:83695582 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:83723631 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:83724071 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:83581203 A>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:83723980 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:83599265 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:236723046 C>A maps to NM_018072.5 A1579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:236762788 T>A maps to NM_018072.5 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:236737627 T>A maps to NM_018072.5 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:236730017 G>A maps to NM_018072.5 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:236740142 C>G maps to NM_018072.5 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:236766622 C>A maps to NM_018072.5 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:236727848 C>T maps to NM_018072.5 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr1:236734871 G>T maps to NM_018072.5 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:801406 C>G maps to NM_017802.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:794430 C>T maps to NM_017802.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr7:803546 G>T maps to NM_017802.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:803465 G>T maps to NM_017802.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:769460 C>T maps to NM_017802.3 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:73964916 G>T maps to ENST00000334988 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:31795410 G>A maps to ENST00000389961 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr14:31774299 A>G maps to ENST00000389961 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:31778293 A>T maps to ENST00000389961 L1506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr14:31855776 G>A maps to ENST00000389961 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:37289110 C>T maps to NM_019024.1 W556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:37234210 T>G maps to NM_019024.1 R1587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:37227728 C>A maps to NM_019024.1 E1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:37302746 G>A maps to NM_019024.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:37304052 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:58127024 C>T maps to NM_022070.4 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:58134603 C>T maps to NM_022070.4 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:58144874 G>A maps to NM_022070.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:145235187 G>T maps to NM_032450.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:145246688 G>A maps to NM_032450.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:41004552 A>G maps to ENST00000296803 C1364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:41045868 G>C maps to ENST00000296803 Y606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:41012738 A>T maps to ENST00000296803 C1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:40999794 T>A maps to ENST00000296803 A1524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr5:41004594 G>T maps to ENST00000296803 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:41054866 A>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:41038948 G>T maps to ENST00000296803 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:41054883 A>T maps to ENST00000296803 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:41061780 C>T maps to ENST00000296803 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:41058238 C>A maps to ENST00000296803 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:41015532 C>A maps to ENST00000296803 E979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:41055875 A>T maps to ENST00000296803 L334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:41008744 G>A maps to ENST00000296803 Q1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:41004913 G>T maps to ENST00000296803 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr14:31585575 C>A maps to NM_015382.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr14:31598244 G>A maps to NM_015382.2 S1444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:31613400 T>C maps to NM_015382.2 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:31597040 G>C maps to NM_015382.2 S1644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:31604166 C>A maps to NM_015382.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:31597941 C>T maps to NM_015382.2 L1545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:93244261 A>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:93242722 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:93256104 G>T maps to ENST00000446394 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:45474215 G>T maps to NM_024602.5 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:43484003 G>A maps to NM_015052.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:43548607 C>T maps to NM_015052.3 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:43594284 G>A maps to NM_015052.3 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43484129 C>G maps to NM_015052.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:43548637 G>T maps to NM_015052.3 G1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:43508596 G>T maps to NM_015052.3 E998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:43484720 G>T maps to NM_015052.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:43531768 A>G maps to NM_015052.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:43360300 G>A maps to NM_015052.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:43447276 G>T maps to NM_015052.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:43483874 C>A maps to NM_015052.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:43590133 C>A maps to NM_015052.3 R1447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr7:43484529 G>T maps to NM_015052.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:43436450 A>G maps to NM_015052.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:43519206 A>G did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:43484585 G>A maps to NM_015052.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:43484555 G>A maps to NM_015052.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:43519228 C>T maps to NM_015052.3 N1040N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr7:43360232 G>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:43546841 T>C maps to NM_015052.3 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:43484468 G>C maps to NM_015052.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:43590132 G>A maps to NM_015052.3 W1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:43540316 C>A maps to NM_015052.3 R1153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:43590048 G>C maps to NM_015052.3 T1418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:197106926 A>G maps to NM_020760.1 G1177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:197184182 A>G maps to NM_020760.1 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:197183363 G>T maps to NM_020760.1 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:197297865 A>C maps to NM_020760.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:197143299 C>A maps to NM_020760.1 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:197105192 G>A maps to NM_020760.1 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:197183690 A>T maps to NM_020760.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:197143335 C>A maps to NM_020760.1 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:124731845 G>A maps to NM_020733.1 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:124731532 T>A maps to NM_020733.1 K964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr3:124746193 C>A maps to NM_020733.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:124732514 G>A maps to NM_020733.1 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr3:124746162 C>A maps to NM_020733.1 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:66698700 C>T maps to NM_033647.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:66698689 C>T maps to NM_033647.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:66703494 A>T maps to NM_033647.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:66718822 C>T maps to NM_033647.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:66704009 T>C maps to NM_033647.2 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:66703640 A>G maps to NM_033647.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:96333865 A>G maps to NM_018063.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr10:96341153 G>A maps to NM_018063.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr10:96361377 A>T maps to NM_018063.3 *839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:96306164 G>T maps to NM_018063.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr4:84374726 C>T maps to NM_133636.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:185941604 G>A maps to NM_001029887.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:185940983 G>T maps to NM_001029887.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:185941817 C>T maps to NM_001029887.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:65197254 G>C maps to NM_014877.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:65146101 C>A did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr17:65156438 G>C maps to NM_014877.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:65120093 G>A maps to NM_014877.3 Q1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:65110478 C>T maps to NM_014877.3 K1293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr17:65103322 G>A maps to NM_014877.3 R1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:65174827 C>T maps to NM_014877.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr17:65103683 G>A maps to NM_014877.3 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr17:65144704 G>A maps to NM_014877.3 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:100689760 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:100693000 C>A maps to NM_018437.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124805827 C>T maps to NM_152722.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:124793652 G>T maps to NM_152722.4 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:124794833 G>T maps to NM_152722.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:124793276 C>A maps to NM_152722.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr11:124792301 G>T maps to NM_152722.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:92844777 G>C maps to ENST00000453812 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:65409586 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:65423336 A>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:65423351 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:65392257 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:65409582 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:65427132 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:65427990 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:65393449 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:65420571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:65486407 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:65427075 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:65417598 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:65413470 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:65428008 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:65413395 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:65417579 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:65475971 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:65474944 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:65417555 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:65420493 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:65427034 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:65415022 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:65428068 G>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:65480002 A>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:65427104 G>C did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:65475991 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:65480098 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:65474908 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:65392222 A>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:65390519 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:65476105 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:65423255 A>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:65412037 G>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:65476096 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:65417596 C>G did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:65390482 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:65390483 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:65479981 C>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:65418785 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:65480009 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:65480069 C>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:65479948 A>G did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:65423228 G>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:65480055 C>A did not map to a codon.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr23:65423205 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:65393569 C>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:65423251 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:65413415 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr23:65417587 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:65427051 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:65411973 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:65480039 C>A did not map to a codon.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr23:65412111 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:65486330 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:65413396 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:65476012 G>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:65420512 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:93797495 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:93806600 A>T maps to NM_001098672.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93803633 T>A maps to NM_001098672.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93806537 G>A maps to NM_001098672.1 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:93844083 C>A maps to NM_001098672.1 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:93796812 G>T maps to NM_001098672.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:93754596 G>A maps to NM_001098672.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr11:93822101 C>T maps to NM_001098672.1 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:93837764 A>G maps to NM_001098672.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:93808442 G>T maps to NM_001098672.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:93822026 C>A maps to NM_001098672.1 Y729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:124789651 T>A maps to NM_001037558.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr11:124789729 C>G maps to NM_001037558.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:64045284 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:64067495 T>A maps to ENST00000261887 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:63988516 G>A maps to ENST00000261887 Q1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:28361809 C>A did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28375357 G>A maps to NM_004667.4 V4251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:28458893 C>T maps to NM_004667.4 L2260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:28375307 C>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:28360586 C>T maps to NM_004667.4 A4570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:28478364 A>G maps to NM_004667.4 F1534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr15:28460847 G>A maps to NM_004667.4 L2043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr15:28419688 C>T maps to NM_004667.4 V3303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr15:28443873 C>A maps to NM_004667.4 V2586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr15:28362195 G>A maps to NM_004667.4 L4459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:28510961 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:28463680 G>A maps to NM_004667.4 C1994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:28377244 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:28391470 T>A maps to NM_004667.4 V3640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:28465738 C>A maps to NM_004667.4 G1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:28510996 G>A maps to NM_004667.4 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr15:28465649 C>T maps to NM_004667.4 L1931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:28501137 T>A maps to NM_004667.4 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:28447505 T>C maps to NM_004667.4 A2489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:28493760 G>A maps to NM_004667.4 Q1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:28508178 G>A maps to NM_004667.4 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:28511032 G>A maps to NM_004667.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr15:28513741 G>T maps to NM_004667.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr15:28514450 G>A maps to NM_004667.4 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr15:28465775 T>A maps to NM_004667.4 P1889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:28441683 G>A maps to NM_004667.4 V2681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:28387464 C>T maps to NM_004667.4 W3873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:89576323 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr4:89602476 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:69793919 G>A maps to NM_022079.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:69726543 C>A maps to NM_022079.2 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr10:69699383 T>C maps to NM_022079.2 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr10:69684944 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:69793922 C>A maps to NM_022079.2 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:89414160 A>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:89410314 A>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:89334305 C>T maps to NM_017912.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:89358918 G>T maps to NM_017912.3 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:56974112 G>A maps to NM_014685.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:35674869 G>A maps to NM_022373.4 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:6304609 C>A maps to NM_001024598.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:6305548 C>A maps to NM_001024598.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:935137 G>C maps to NM_001142467.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:935104 G>C maps to NM_001142467.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:934951 C>T maps to NM_001142467.1 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:2461330 C>T maps to NM_001010926.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:57233790 T>C maps to NM_003865.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:72668121 G>A maps to ENST00000457859 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr15:72638940 G>T maps to ENST00000457859 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:74011443 C>T maps to NM_000521.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:80391652 G>A maps to NM_173620.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:43227345 G>A maps to NM_006460.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:43227462 G>A maps to NM_006460.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:43227532 G>T maps to NM_006460.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr17:43226679 C>A maps to NM_006460.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:43246806 C>T maps to NM_144608.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:80679297 G>A maps to NM_001040708.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:80679498 G>A maps to NM_001040708.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:80679288 A>G maps to NM_001040708.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:126080722 C>A maps to NM_012259.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:126080785 G>T maps to NM_012259.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr6:126080809 C>T maps to NM_012259.2 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr6:126080326 A>G maps to NM_012259.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:126080668 C>T maps to NM_012259.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:126080623 G>A maps to NM_012259.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:145416842 C>G maps to NM_213653.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:145415333 G>C maps to NM_213653.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:145415732 A>T maps to NM_213653.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:91818089 C>T maps to NM_001017975.3 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:91727808 T>C maps to NM_001017975.3 E1409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:91728124 C>A maps to NM_001017975.3 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:91851360 C>A maps to NM_001017975.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:91816379 A>G maps to NM_001017975.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:91816322 G>T maps to NM_001017975.3 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:91816428 C>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:91784848 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:91844038 T>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:91850783 T>C maps to NM_001017975.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:91851285 T>C maps to NM_001017975.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:91779020 G>C maps to NM_001017975.3 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:91844619 T>A maps to NM_001017975.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:91845680 A>T maps to NM_001017975.3 L329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:120389379 C>T did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:120394668 A>C maps to NM_000187.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81332037 A>G maps to NM_000601.4 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:81388035 G>A maps to NM_000601.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:81334810 A>G maps to NM_000601.4 Y635Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:81335059 G>T maps to NM_000601.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:81386503 C>T maps to ENST00000453018 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:81399224 C>A maps to NM_000601.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:81374422 G>T maps to NM_000601.4 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr7:81335604 G>C maps to NM_000601.4 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:81392078 A>T maps to NM_000601.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:81355308 T>A maps to NM_000601.4 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:81388017 A>G maps to NM_000601.4 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:81372699 G>T maps to NM_000601.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:81388089 T>C maps to NM_000601.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:81381505 C>T maps to NM_000601.4 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:81374412 C>A maps to NM_000601.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:81355322 C>A maps to NM_000601.4 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:3451121 C>T maps to ENST00000511533 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:3444490 A>T maps to ENST00000511533 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:3446353 T>A maps to ENST00000511533 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr4:3444598 G>A maps to ENST00000511533 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:3451001 C>T maps to ENST00000511533 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:3447973 G>A maps to ENST00000511533 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:3447889 C>T maps to ENST00000511533 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:79662892 C>T maps to NM_004712.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:79660583 G>C maps to NM_004712.4 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr8:43025813 C>T maps to ENST00000458501 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr8:43028854 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:43016641 C>G maps to ENST00000458501 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:43025732 G>T maps to ENST00000458501 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:210761418 G>A maps to NM_001170580.1 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:210796993 G>A maps to NM_001170580.1 W457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr1:210761256 A>T maps to NM_001170580.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:210637921 C>G maps to NM_001170580.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:210536200 G>T maps to NM_001170580.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr3:42734572 G>C maps to NM_020707.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:42738368 C>A maps to NM_020707.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:42739108 G>T maps to NM_020707.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:145627700 C>T maps to NM_022475.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:100118679 G>T maps to NM_001127258.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:100135224 C>G maps to NM_032425.4 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr14:100119150 C>T maps to NM_001127258.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:100118596 G>T maps to NM_001127258.1 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:100118877 C>T maps to NM_001127258.1 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:222717099 C>G maps to NM_024746.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:222717027 C>T maps to NM_024746.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:222717204 C>G maps to NM_024746.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:222696209 T>C maps to NM_024746.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:222712051 G>A maps to NM_024746.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222696184 T>A maps to NM_024746.3 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:222712015 C>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:222721266 C>T maps to NM_024746.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:222700384 C>A maps to NM_024746.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108095391 C>G maps to NM_007072.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:100515505 C>A maps to NM_033055.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:100547674 G>A maps to NM_033055.2 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:100527432 G>A maps to NM_033055.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:27565833 C>A maps to NM_152740.3 *337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21800809 C>T maps to NM_015094.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:21800488 G>T maps to NM_015094.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:62199166 G>T maps to ENST00000394997 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:102300525 C>A maps to ENST00000442724 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:46815501 G>T maps to NM_152795.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:46808500 G>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:119002577 G>T maps to NM_198971.1 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:118997722 C>T maps to NM_198971.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:126298797 C>T maps to NM_138571.4 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:75186956 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:75187481 G>A maps to NM_005338.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:75191384 C>T maps to NM_005338.4 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:75174064 C>A maps to NM_005338.4 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr1:114511087 C>T maps to ENST00000426820 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:114483770 G>T maps to ENST00000426820 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:114483043 G>T maps to ENST00000426820 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:114483823 G>A maps to ENST00000426820 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:139416275 C>G maps to NM_022740.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:139416617 C>A maps to NM_022740.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:139297962 T>A maps to NM_022740.4 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:33308673 T>G maps to NM_005734.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:33373333 G>C maps to NM_005734.3 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:33308506 C>T maps to NM_005734.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:33375023 C>T maps to NM_005734.3 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:40886709 A>T maps to NM_144685.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:40886385 G>C maps to NM_144685.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:40886803 G>T maps to NM_144685.3 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr22:19382002 G>A maps to NM_003325.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr16:30005265 A>T maps to NM_003609.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:27834893 C>A maps to NM_005322.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26056239 C>T maps to NM_005319.3 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:26056401 C>T maps to NM_005319.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:26235026 G>T maps to NM_005320.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:26234543 C>T maps to NM_005320.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:26235143 T>C maps to NM_005320.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:26156938 C>G maps to NM_005321.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr6:26156806 G>A maps to NM_005321.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:26157076 G>A maps to NM_005321.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:26157277 G>A maps to NM_005321.2 *220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:26157275 T>A maps to NM_005321.2 *220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr6:26107823 G>A maps to NM_005323.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:26108234 C>G maps to NM_005323.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:25726494 C>T maps to NM_170745.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:26033502 C>T maps to NM_003513.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:26033627 C>A maps to NM_003513.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr6:26199201 G>A maps to NM_021065.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:26217274 C>T maps to NM_021052.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr6:26217426 G>A maps to NM_021052.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr6:26217249 A>G maps to NM_021052.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:27100921 C>G maps to NM_021064.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:27115266 G>A maps to NM_080596.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:27115083 G>A maps to NM_080596.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:27114999 G>A maps to NM_080596.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:27776052 C>A maps to NM_003509.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:27776295 C>T maps to NM_003509.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:27782452 G>T maps to NM_021066.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr6:27806012 G>A maps to NM_003510.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:26043588 C>T maps to NM_021062.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:26043663 G>A maps to NM_021062.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr6:26124096 C>T maps to NM_003526.2 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:26158618 C>T maps to NM_138720.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr6:26158708 G>T maps to NM_138720.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:26158555 C>A maps to NM_138720.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:26158711 G>A maps to NM_138720.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:26158660 G>C maps to NM_138720.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:26199999 G>T maps to NM_003522.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:26216649 G>A maps to NM_003518.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr6:26216577 G>A maps to NM_003518.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:26251898 C>T maps to NM_003524.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:26251946 G>A maps to NM_003524.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr6:26252141 G>C maps to NM_003524.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:27100274 G>A maps to NM_021058.3 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:27114529 C>T maps to NM_080593.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:27114211 G>A maps to NM_080593.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:27775546 C>G maps to NM_003519.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:27775537 G>A maps to NM_003519.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:27775344 C>A maps to NM_003519.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr6:27782889 G>A maps to NM_003521.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr6:27782890 A>T maps to NM_003521.2 K24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:27806486 G>A maps to NM_003520.3 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:27861500 C>G maps to NM_003527.4 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:26031934 C>T maps to NM_003537.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:26032249 G>T maps to NM_003537.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:26032180 C>T maps to NM_003537.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr6:26032180 C>T maps to NM_003537.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:26031996 C>A maps to NM_003537.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:26032162 G>T maps to NM_003537.3 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr6:26032018 C>T maps to NM_003537.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr6:26031934 C>T maps to NM_003537.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26045848 C>T maps to NM_003531.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr6:26045817 G>A maps to NM_003531.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:26197385 T>A maps to NM_003530.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:26197136 G>A maps to NM_003530.3 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:26197310 C>T maps to NM_003530.3 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr6:26225699 G>A maps to NM_003532.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:26225651 G>A maps to NM_003532.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr6:26225791 G>T maps to NM_003532.2 *137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:26250491 G>A maps to NM_021018.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:26250503 C>G maps to NM_021018.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr6:26271321 G>A maps to NM_003534.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:26271399 C>T maps to NM_003534.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr6:27777977 C>A maps to NM_003536.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:27839853 C>T maps to NM_003533.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:27858294 C>G maps to NM_003535.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:26104360 C>T maps to NM_003542.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:26104273 G>T maps to NM_003542.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr6:26189082 C>T maps to NM_003539.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr6:26189154 G>A maps to NM_003539.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:26240784 G>C maps to NM_003540.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:26240949 C>G maps to NM_003540.3 Y99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:27107278 G>A maps to NM_003495.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:27799269 G>T maps to NM_003541.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:27840994 C>A maps to NM_003546.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:149859276 G>A maps to NM_175065.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:149858523 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:149858691 C>G maps to NM_003517.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:149858832 C>A maps to NM_003517.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:149858805 G>A maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:149858559 C>T maps to NM_003517.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:149858579 C>A maps to NM_003517.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:149858787 C>T maps to NM_003517.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:149858700 G>C maps to NM_003517.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:149857920 G>T maps to NM_003528.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:149783725 G>A maps to ENST00000427880 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:149783680 G>A maps to ENST00000427880 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr1:149783692 G>T maps to ENST00000427880 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr1:149783692 G>A maps to ENST00000427880 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:228645212 G>C maps to NM_033445.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:228645164 G>T maps to NM_033445.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:228646195 C>T maps to NM_175055.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:228646150 G>T maps to NM_175055.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:228612716 G>A maps to NM_003493.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:228612813 C>T maps to NM_003493.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:228612921 G>A maps to NM_003493.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:12120864 A>T maps to NM_002114.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:12122959 A>T maps to NM_002114.2 K978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:12163742 G>T maps to NM_002114.2 G2402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:12123582 C>T maps to NM_002114.2 H1185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:12161912 G>T maps to NM_002114.2 T2243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:12123027 C>T maps to NM_002114.2 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:12124183 A>T maps to NM_002114.2 K1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:12120883 C>T maps to NM_002114.2 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:12123905 C>G maps to NM_002114.2 S1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr6:12163814 C>T maps to NM_002114.2 L2426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:143091671 C>A maps to NM_006734.3 E1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:143081223 T>C maps to NM_006734.3 K2067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:143092971 G>A maps to NM_006734.3 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:143081589 G>A maps to NM_006734.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:143093748 C>G maps to NM_006734.3 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:143080971 G>C maps to NM_006734.3 Y2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:143092506 C>T maps to NM_006734.3 P1123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:143091738 G>A maps to NM_006734.3 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:143080986 G>A maps to NM_006734.3 P2146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:143081427 C>T maps to NM_006734.3 Q1999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:143091915 C>A maps to NM_006734.3 S1320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:42049868 G>T maps to NM_024503.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:41978897 G>A maps to NM_024503.3 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:41978900 G>A maps to NM_024503.3 C1997C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:42048658 C>A maps to NM_024503.3 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:42048155 C>A maps to NM_024503.3 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:41979190 G>A maps to NM_024503.3 Q1901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:71103608 G>T maps to ENST00000439900 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:71075715 C>T maps to NM_033496.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:71078720 C>T maps to NM_000188.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:71103677 G>A maps to ENST00000439900 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:71142368 C>T maps to ENST00000439900 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr10:71136839 C>T maps to ENST00000439900 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr10:71158542 G>T maps to ENST00000439900 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr10:71160863 G>T maps to ENST00000439900 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:75117983 C>T maps to NM_000189.4 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr2:75094767 G>T maps to NM_000189.4 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:75109284 C>G maps to NM_000189.4 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:75100443 A>T maps to NM_000189.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:75116482 G>T maps to NM_000189.4 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:176308304 C>G maps to NM_002115.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:176310846 G>A maps to NM_002115.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:176308745 C>T maps to NM_002115.2 Q780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:176317680 G>A maps to NM_002115.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:176316700 G>A maps to NM_002115.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr5:176317671 C>A maps to NM_002115.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr5:176318131 C>T maps to NM_002115.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:71000487 C>A maps to NM_025130.3 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr10:71026381 C>T maps to NM_025130.3 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:71021020 C>T maps to NM_025130.3 F781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:71005912 C>T maps to NM_025130.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:37853635 G>A maps to NM_181786.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:37854656 C>T maps to NM_181786.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:37838715 G>A maps to NM_181786.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:37854242 C>T maps to NM_181786.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:37854343 G>A maps to NM_181786.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr6:29911193 C>T maps to ENST00000376806 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:29911150 G>A maps to ENST00000376806 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr6:32917486 G>A maps to NM_006120.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:32918371 T>C maps to NM_006120.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr6:32920761 G>A maps to NM_006120.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:32906655 T>A maps to NM_002118.4 K48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:32976018 G>T maps to NM_002119.3 Y34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:32975901 C>T maps to NM_002119.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:32975250 G>A maps to NM_002119.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:33037433 G>A maps to NM_033554.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr6:33036444 C>T maps to NM_033554.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:33052925 G>T maps to NM_002121.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32609932 C>T maps to NM_002122.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32713751 C>T maps to NM_020056.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:32713634 T>A maps to NM_020056.4 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr6:32632626 C>T maps to ENST00000374943 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:32629936 T>C maps to ENST00000374943 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:32629749 C>A maps to ENST00000374943 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:32411566 A>T maps to NM_019111.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:32411097 A>T maps to NM_019111.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:32548583 G>T maps to NM_002124.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30460193 G>C maps to NM_005516.5 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr6:29691471 G>A maps to NM_001098479.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29692181 C>T maps to NM_001098479.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:29693317 G>C maps to NM_001098479.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:29797611 C>A maps to ENST00000376828 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:29796362 C>G maps to ENST00000376828 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr21:38137444 A>G maps to NM_000411.5 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr21:38302559 T>A maps to NM_000411.5 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:53345166 G>C maps to NM_002126.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:148789206 T>A maps to NM_003071.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:148791110 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:148760061 C>A maps to NM_003071.3 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:221057722 G>T maps to NM_021958.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:221057823 C>T maps to NM_021958.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:221057700 T>G maps to NM_021958.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:221053270 G>T maps to NM_021958.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:221057557 C>A maps to NM_021958.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30142618 T>C maps to NM_178581.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:30136874 G>T maps to NM_178581.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:118960401 G>C maps to NM_000190.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:186077689 A>T maps to NM_031935.2 P3650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:186086594 A>T maps to NM_031935.2 P3896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:185931767 T>C maps to NM_031935.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:186050511 G>T maps to NM_031935.2 G2925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:186036966 A>G maps to NM_031935.2 V2569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186113344 C>A maps to NM_031935.2 C4655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:186158652 C>T maps to NM_031935.2 L5517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:185834870 A>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:186064395 C>A maps to NM_031935.2 S3439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:186120335 G>T maps to NM_031935.2 G4871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:185972976 G>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:186121912 G>T maps to NM_031935.2 R4976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:186062711 G>T maps to NM_031935.2 T3369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:186084073 C>A maps to NM_031935.2 V3800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:186057108 G>T maps to NM_031935.2 G3137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:185986170 T>C maps to NM_031935.2 C1756C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:186086242 C>G maps to NM_031935.2 V3893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr1:186094763 A>T maps to NM_031935.2 G4176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr1:186056717 G>T maps to NM_031935.2 E3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:186008857 A>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:186008914 G>A maps to NM_031935.2 P2028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:186051995 G>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:186092347 C>A maps to NM_031935.2 V4165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:186010215 G>T maps to NM_031935.2 V2084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:185962391 C>A maps to NM_031935.2 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:185959563 G>A maps to NM_031935.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:186113374 A>T maps to NM_031935.2 T4665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:186099672 C>T maps to NM_031935.2 N4358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:186083240 T>A maps to NM_031935.2 A3754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:186141244 G>T maps to NM_031935.2 E5266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:186143733 A>G maps to NM_031935.2 P5301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:185939625 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:186143743 C>A maps to NM_031935.2 R5305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:185939527 G>A maps to NM_031935.2 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:185992226 A>C maps to NM_031935.2 T1897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:186094787 A>G maps to NM_031935.2 S4184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:186158956 G>T maps to NM_031935.2 E5619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:186106047 A>C maps to NM_031935.2 R4521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:186008060 A>T maps to NM_031935.2 S1984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:186055508 A>T maps to NM_031935.2 K3006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:185976346 G>A maps to NM_031935.2 G1521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:186059942 G>T maps to NM_031935.2 G3261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:185964205 G>A maps to NM_031935.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:185815173 A>T maps to NM_031935.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:186114889 G>T maps to NM_031935.2 G4815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:186120874 G>T maps to NM_031935.2 G4966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr1:186062652 G>T maps to NM_031935.2 E3350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:186084543 C>A maps to NM_031935.2 Y3853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:186113752 C>T maps to NM_031935.2 S4728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:77771519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:174254254 C>G maps to NM_002129.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:174254281 G>A maps to NM_002129.3 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:150156301 C>A did not map to a codon.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:150155702 G>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:150154607 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:34330166 G>A maps to NM_145205.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:34330268 C>G maps to NM_145205.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:34330331 G>T maps to NM_145205.4 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:55300460 C>A maps to NM_019036.2 *371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr6:55441929 G>A maps to NM_019036.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr6:55304312 G>T maps to NM_019036.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr5:74646702 A>G maps to NM_000859.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43298641 C>T maps to NM_002130.6 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:43299015 C>A maps to NM_002130.6 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:43297158 T>C maps to NM_002130.6 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr5:43294158 C>T maps to NM_002130.6 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:120301894 T>A maps to NM_005518.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:120301853 A>T maps to NM_005518.3 L246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:120307035 G>A maps to NM_005518.3 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:120306918 G>T maps to NM_005518.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:26545674 C>T maps to NM_006353.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:26545529 A>G maps to NM_006353.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:80375303 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:80375301 A>C did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:80370642 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:35661296 G>T maps to NM_001003681.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:35661014 C>T maps to NM_001003681.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr22:35661238 G>T maps to NM_001003681.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:1080514 G>T maps to NM_012292.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr19:1080514 G>A maps to NM_012292.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:162909665 C>T maps to NM_001142556.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:162900477 G>A maps to NM_001142556.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:162917454 A>G maps to NM_001142556.1 Q674Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:35779115 C>A maps to NM_002133.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr22:35789560 G>A maps to NM_002133.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr22:35789500 C>G maps to NM_002133.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:173491285 A>T maps to NM_015980.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:173534486 G>C maps to NM_015980.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:124909092 C>A maps to NM_005519.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr10:124907980 C>T maps to NM_005519.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:124909257 G>T maps to NM_005519.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr10:124909219 C>A maps to NM_005519.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:1748975 A>T maps to ENST00000382711 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr12:121437353 C>T maps to NM_000545.5 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr17:36064924 T>C maps to NM_000458.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:43058193 A>T maps to ENST00000338692 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr20:42984467 C>T maps to NM_175914.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:42984470 G>C maps to NM_175914.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:43058301 C>A maps to ENST00000338692 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43042430 G>C maps to ENST00000338692 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:43058238 C>T maps to ENST00000338692 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr20:43052919 G>T maps to NM_178850.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:76472699 C>A maps to NM_004133.4 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:76472577 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:76471132 C>G maps to NM_004133.4 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:76471159 G>T maps to NM_004133.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:76465284 C>T maps to NM_004133.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:76470885 A>T maps to NM_004133.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:76456115 G>T maps to NM_004133.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:137089548 G>A maps to NM_006805.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:54675628 A>G maps to NM_031157.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:53217178 A>G maps to NM_001011725.1 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:53217011 G>T maps to NM_001011725.1 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:53216791 G>A maps to NM_001011725.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:26240190 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:178080265 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:178081585 A>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr2:178081320 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:178081298 C>T maps to NM_194247.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:12907902 T>C maps to NM_001013631.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12907643 G>T maps to NM_001013631.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:12907839 T>A maps to NM_001013631.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr4:83279892 C>A maps to NM_031370.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:179044534 G>C maps to NM_005520.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:100667365 C>A did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:100667240 A>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:100667713 T>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:100667365 C>G did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:100667051 G>T did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:100667388 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:100667614 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr9:86586852 C>A maps to NM_031262.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr9:86591966 C>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:39340507 C>T maps to ENST00000221419 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:23648099 T>A maps to ENST00000414299 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:23667393 T>A maps to ENST00000414299 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:245022669 C>A maps to NM_031844.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:245018902 C>T maps to NM_031844.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:245025940 A>G maps to NM_031844.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:245023748 G>C maps to NM_031844.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:245027245 C>A maps to NM_031844.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:41774164 C>A maps to NM_007040.3 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:41778032 G>T maps to NM_007040.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:41778020 C>T maps to NM_007040.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr19:41778105 G>T maps to NM_007040.3 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr11:62489324 G>A maps to NM_001079559.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:83347645 C>A maps to NM_031372.2 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr4:83350666 G>C maps to NM_031372.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:83350671 G>A maps to NM_031372.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:38811069 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:38796435 C>A maps to NM_138394.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:38809124 T>A maps to NM_138394.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:38812887 A>G maps to NM_138394.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:78697766 C>T maps to NM_004272.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:78746811 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:83544129 C>T maps to NM_199330.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:83527842 G>A maps to NM_199330.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr15:83561535 C>T maps to NM_199330.1 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:19042356 C>T maps to NM_004838.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:19043761 G>A maps to NM_004838.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:60328549 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:60287597 A>T maps to NM_015888.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:60324149 A>G maps to NM_015888.4 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr1:60314855 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:60324669 A>C maps to NM_015888.4 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:60312833 G>A maps to NM_015888.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr19:12878663 G>A maps to NM_013312.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:12877044 G>C maps to NM_013312.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:12874184 G>A maps to NM_013312.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:12874185 G>A maps to NM_013312.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:42828542 G>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:42841830 G>A maps to NM_032410.3 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:42852779 T>C maps to NM_032410.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:42868488 A>G maps to NM_032410.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:42841872 A>T maps to NM_032410.3 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:57514942 C>A maps to NM_032495.5 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:150689611 A>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:150691946 A>C did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:150684032 T>A maps to NM_032132.4 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:150679040 C>T maps to NM_032132.4 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:27135408 C>A maps to NM_005522.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:27134301 C>A maps to NM_005522.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:27213049 C>A maps to NM_018951.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:27212968 C>A maps to NM_018951.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:27213043 C>A maps to NM_018951.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr7:27213367 G>T maps to NM_018951.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr7:27213841 A>G maps to NM_018951.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:27213850 G>T maps to NM_018951.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr7:27211518 C>T maps to NM_018951.3 *411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr7:27224661 C>A maps to NM_005523.5 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr7:27224463 G>A maps to NM_005523.5 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:27238773 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:27239054 G>T maps to NM_000522.4 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:27237954 C>A maps to NM_000522.4 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:27238952 G>A maps to NM_000522.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27238026 A>C maps to NM_000522.4 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:27238816 C>A maps to NM_000522.4 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:27140485 T>C maps to NM_006735.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:27141897 C>T maps to NM_006735.3 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:27141753 G>T maps to NM_006735.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:27147962 G>T maps to NM_153631.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:27147987 G>T maps to NM_153631.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:27147953 G>T maps to NM_153631.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:27149788 G>T maps to NM_153631.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:27147938 G>T maps to NM_153631.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr7:27147854 C>A maps to NM_153631.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27147571 C>A maps to NM_153631.2 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:27148136 G>T maps to NM_153631.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:27147794 G>T maps to NM_153631.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:27148328 G>T maps to NM_153631.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:27147767 G>A maps to NM_153631.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr7:27148127 G>T maps to NM_153631.2 Y246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:27147655 G>A maps to NM_153631.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:27148286 G>T maps to NM_153631.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:27149899 C>A maps to NM_153631.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr7:27147767 G>A maps to NM_153631.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:27147914 G>T maps to NM_153631.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:27168918 T>C maps to NM_002141.4 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:27183100 G>T maps to NM_019102.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:27183049 C>A maps to NM_019102.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:27182926 C>A maps to NM_019102.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:27187266 C>G maps to NM_024014.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:27185360 G>C maps to NM_024014.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:27186945 C>T maps to NM_024014.2 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr7:27185327 G>A maps to NM_024014.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:27187137 C>T maps to NM_024014.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:27196008 C>G maps to NM_006896.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr7:27194806 C>G maps to NM_006896.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:27194647 G>A maps to NM_006896.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:27205034 C>T maps to NM_152739.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:27204521 G>T maps to NM_152739.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46607741 G>C maps to NM_002144.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr17:46607987 G>A maps to NM_002144.3 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:46804190 C>T maps to NM_006361.5 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:46804355 G>A maps to NM_006361.5 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:46805353 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:46804334 G>A maps to NM_006361.5 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:46620954 G>A maps to NM_002145.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:46628224 G>T maps to NM_002146.4 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:46628508 G>A maps to NM_002146.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr17:46654112 G>T maps to NM_024015.4 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:46669780 C>T maps to NM_002147.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:46669807 C>T maps to NM_002147.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46673819 C>A maps to NM_018952.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:46685326 C>A maps to NM_004502.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:46685422 G>T maps to NM_004502.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr17:46685368 C>T maps to NM_004502.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:46691844 G>A maps to NM_024016.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:46703205 C>A maps to NM_024017.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:46703127 C>T maps to NM_024017.4 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:46700308 G>T maps to NM_024017.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:46703289 C>G maps to NM_024017.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:54379591 C>A maps to NM_017409.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:54379777 G>T maps to NM_017409.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:54379645 C>A maps to NM_017409.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:54369070 G>T maps to NM_014212.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:54369109 G>A maps to NM_014212.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr12:54367256 G>T maps to NM_014212.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:54333328 C>T maps to NM_017410.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:54448763 C>A maps to NM_153633.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:54447720 G>T maps to NM_153633.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:54423643 C>T maps to NM_004503.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr12:54403334 T>C maps to NM_022658.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr12:54394136 C>T maps to NM_006897.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:54396361 C>G maps to NM_006897.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:176982208 G>A maps to NM_002148.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:176982040 C>A maps to NM_002148.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:176981699 G>T maps to NM_002148.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:176982217 C>A maps to NM_002148.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:176983898 C>A maps to NM_002148.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176972319 C>A maps to NM_021192.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:176973686 C>A maps to NM_021192.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:176965451 C>G maps to NM_021193.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:176965280 C>A maps to NM_021193.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:176964639 C>A maps to NM_021193.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:176965463 G>A maps to NM_021193.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:176965304 G>C maps to NM_021193.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:176964684 C>A maps to NM_021193.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:176958399 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:176957938 C>T maps to NM_000523.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:176958061 G>A maps to NM_000523.3 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:176959355 G>A maps to NM_000523.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:177036401 C>T maps to NM_006898.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr2:177034069 G>A maps to NM_006898.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:177034075 C>A maps to NM_006898.4 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:177034261 C>A maps to NM_006898.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:177016753 C>A maps to NM_014621.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:176995547 C>T maps to NM_019558.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:176996315 C>T maps to NM_019558.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:176988901 G>T maps to NM_014213.3 *353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:176988788 C>T maps to NM_014213.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:176988215 G>A maps to NM_014213.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:72094554 G>A maps to NM_005143.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:21071462 T>A maps to NM_016287.3 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:21083702 G>A maps to NM_016287.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:21099997 C>A maps to NM_016287.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:21074148 C>A did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:21071535 C>G maps to NM_016287.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:33354566 C>G maps to NM_002143.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:33354702 C>G maps to NM_002143.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:10560059 C>A maps to NM_002149.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:40148228 C>T maps to NM_016257.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:122284812 A>T maps to NM_002150.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:122295275 G>T maps to NM_002150.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:122284984 C>T maps to NM_002150.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:175443104 T>C maps to NM_000860.4 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr4:175416761 A>T maps to NM_000860.4 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:95223335 G>A maps to NM_014485.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr4:95229826 G>A maps to NM_014485.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:35556238 G>T maps to NM_182983.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:35551689 G>T maps to NM_182983.2 L260L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L4-A4E5-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr19:35550652 G>C maps to NM_182983.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:72110412 C>A maps to ENST00000228226 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:133609243 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:100189562 C>T maps to NM_000195.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr10:100185700 A>T maps to NM_000195.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:148847542 G>T maps to NM_032383.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:148857789 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr22:26860503 T>C maps to NM_022081.4 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:26864522 C>T maps to NM_022081.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:26872993 T>A maps to NM_022081.4 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr22:26861449 G>A maps to NM_022081.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:26875275 T>C maps to NM_022081.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:26849255 G>A maps to NM_022081.4 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:18330608 C>A maps to NM_181507.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:18301446 G>C maps to NM_181507.1 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:18327040 C>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:18306903 G>A maps to NM_181507.1 C980C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:18330503 A>T maps to NM_181507.1 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:18339330 G>C maps to NM_181507.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:18330572 G>A maps to NM_181507.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826163 G>C maps to NM_024747.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:103826181 A>G maps to NM_024747.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr10:103827454 C>T maps to NM_024747.4 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:84216630 G>A maps to NM_006665.5 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:100995382 G>A maps to NM_021828.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:100374726 C>G maps to NM_021828.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr10:100380390 G>A maps to NM_021828.4 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:100995408 T>A maps to NM_021828.4 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:100995442 G>A maps to NM_021828.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr10:100481487 C>A maps to NM_021828.4 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6461960 C>G did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr11:6459661 T>G maps to NM_000613.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:6453033 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:21977318 C>T maps to NM_005144.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:21976734 C>G maps to NM_005144.4 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr8:21977360 G>A maps to NM_005144.4 C963C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:21984808 T>A maps to NM_005144.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:21978724 A>T maps to NM_005144.4 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:21978633 A>G maps to NM_005144.4 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:49657762 T>C maps to NM_002152.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:186383975 G>T maps to NM_000412.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:186395104 C>A maps to NM_000412.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr3:186383963 C>T maps to NM_000412.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:186395386 C>T maps to NM_000412.2 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:11301700 G>T maps to NM_001098211.1 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:175111180 T>G maps to NM_001131055.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr5:175111018 G>A maps to NM_001131055.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:175110496 C>G maps to NM_001131055.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:175110361 C>A maps to NM_001131055.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:175111255 G>C maps to NM_001131055.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:175110316 C>T maps to NM_001131055.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:175110325 C>A maps to NM_001131055.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:60791982 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:60791901 C>A maps to ENST00000317393 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:60791828 C>A maps to ENST00000317393 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:60793636 C>A maps to ENST00000317393 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:60791199 G>C maps to ENST00000317393 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:22048810 G>T maps to NM_021624.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:22040785 G>T maps to NM_021624.3 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:22057267 G>T maps to NM_021624.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:152187997 G>C maps to NM_001009931.1 S2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:152187576 C>G maps to NM_001009931.1 G2176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152193134 G>A maps to NM_001009931.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:152188095 G>A maps to NM_001009931.1 Y2003Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:152191539 G>T maps to NM_001009931.1 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:152191867 G>C maps to NM_001009931.1 S746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:152191896 T>A maps to NM_001009931.1 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152192918 G>A maps to NM_001009931.1 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191000 G>T maps to NM_001009931.1 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:152191908 C>T maps to NM_001009931.1 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:152191361 G>T maps to NM_001009931.1 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:152193050 C>A maps to NM_001009931.1 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:152187705 G>A maps to NM_001009931.1 Y2133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:152191806 G>A maps to NM_001009931.1 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:152188104 G>T maps to NM_001009931.1 S2000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:152193063 G>T maps to NM_001009931.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:152191803 T>A maps to NM_001009931.1 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:152191374 C>T maps to NM_001009931.1 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:152191728 G>T maps to NM_001009931.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:152191932 G>A maps to NM_001009931.1 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:152190894 T>G maps to NM_001009931.1 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:152187606 G>C maps to NM_001009931.1 S2166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:152188036 G>T maps to NM_001009931.1 S2023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:152188192 G>C maps to NM_001009931.1 S1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:152191740 G>A maps to NM_001009931.1 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:152192016 G>A maps to NM_001009931.1 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:152188170 G>T maps to NM_001009931.1 G1978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:152187690 A>T maps to NM_001009931.1 S2138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:152193474 A>G maps to NM_001009931.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:152193468 G>T maps to NM_001009931.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:152188248 G>T maps to NM_001009931.1 G1952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:152187602 G>A maps to NM_001009931.1 Q2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:20818971 C>A maps to NM_022460.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:20823687 G>A maps to NM_022460.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:20824501 T>C maps to NM_022460.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:87569261 C>G maps to NM_012262.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr4:11401182 C>A maps to NM_005114.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:11400758 C>A maps to NM_005114.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:11401446 G>T maps to NM_005114.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr16:22926315 C>A maps to NM_006043.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:22826314 G>C maps to NM_006043.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr16:22926637 C>A maps to NM_006043.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr16:22826293 C>A maps to NM_006043.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:13399540 G>T maps to NM_006042.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:14248434 G>T maps to NM_006041.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:25704415 G>A maps to NM_006040.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr16:26147181 G>A maps to NM_006040.2 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr16:26147247 C>A maps to NM_006040.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:26147229 C>A maps to NM_006040.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:26147292 C>A maps to NM_006040.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr16:26147397 A>G maps to NM_006040.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:114383949 G>A maps to NM_153612.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:114378978 G>A maps to NM_153612.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:114378648 C>T maps to NM_153612.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr6:114383988 C>T maps to NM_153612.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr6:114383970 G>T maps to NM_153612.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr6:114379170 C>G maps to NM_153612.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:114379203 C>A maps to NM_153612.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr6:114378735 C>T maps to NM_153612.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr6:114379191 G>C maps to NM_153612.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr16:1961983 G>A maps to ENST00000454677 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:131803195 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:131762608 A>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:131762521 T>C did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:131803196 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:97485037 C>T maps to NM_153456.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:209878313 C>A maps to NM_005525.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:209879154 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:209880127 C>T maps to NM_005525.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:209907802 C>A maps to NM_005525.2 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:209878374 G>T maps to NM_005525.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr1:209878375 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:53459278 A>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:53459012 C>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr4:88312132 C>T maps to NM_016245.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:43775600 A>G maps to NM_016142.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:49316527 C>A maps to NM_016246.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr19:49339626 C>A maps to NM_016246.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr16:82131863 C>T maps to NM_002153.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:99006652 C>T maps to NM_000197.1 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr9:99006664 G>A maps to NM_000197.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:118814642 G>A maps to NM_000414.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:118835178 C>T maps to NM_000414.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr5:118861718 G>C did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:118824885 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:120050200 C>T maps to ENST00000235547 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:120056731 C>A maps to ENST00000235547 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:120056649 G>A maps to ENST00000235547 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:119965137 G>A maps to NM_000198.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:119958095 C>A maps to NM_000198.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:119964840 G>T maps to NM_000198.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:30999231 G>T maps to NM_025193.3 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:84163917 G>A maps to NM_031463.4 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:84163260 C>A maps to NM_031463.4 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:115216389 C>T maps to NM_032303.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:145535023 C>A maps to NM_005526.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45033780 G>T maps to NM_007031.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr21:45053212 C>G maps to NM_007031.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr21:45012208 C>A maps to NM_007031.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:56565353 C>A maps to NM_001080439.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr19:16268357 C>G maps to NM_032855.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:16268597 A>G maps to NM_032855.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:102548770 G>T maps to NM_001017963.2 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:44219847 C>T maps to NM_007355.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr6:44221293 G>T maps to NM_007355.2 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118451918 C>T maps to NM_025015.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr10:118460543 G>A maps to NM_025015.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:118458210 T>A maps to NM_025015.2 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:118464789 C>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:3726566 G>T maps to NM_052970.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr20:3730745 C>T maps to NM_052970.4 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr21:15746075 G>A maps to NM_006948.4 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr21:15746218 G>A maps to NM_006948.4 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:31779551 C>T maps to NM_005527.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr14:65008151 G>A maps to NM_021979.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439556 G>T maps to NM_002154.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:132439654 G>A maps to NM_002154.3 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:128751909 C>T maps to ENST00000438626 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:128719865 T>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr4:128722949 G>A maps to ENST00000438626 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr4:128719836 G>A maps to ENST00000438626 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:161495986 C>T maps to NM_002155.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:161494894 C>A maps to NM_002155.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:161495341 C>T maps to NM_002155.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:161495728 C>A maps to NM_002155.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:161494984 G>C maps to NM_002155.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:161495870 C>T maps to NM_002155.3 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:122930823 C>T maps to NM_006597.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:122931359 C>A maps to NM_006597.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:122929363 T>A maps to NM_006597.3 K500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:137897271 G>A maps to NM_004134.6 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:54405719 C>A maps to NM_016126.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:16342122 C>A maps to ENST00000375714 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:16343585 C>A maps to ENST00000375714 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:122478135 C>T maps to NM_024610.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:55777550 G>C maps to NM_012267.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:64683514 C>G maps to NM_014181.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:198363419 C>T maps to NM_199440.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:198367822 G>T maps to NM_002157.2 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:22222418 C>T maps to NM_005529.5 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:22181235 C>A maps to NM_005529.5 P2052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:22174313 C>T maps to NM_005529.5 P2631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:22174304 G>A maps to NM_005529.5 I2634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:22188550 C>A maps to NM_005529.5 G1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr1:22179192 C>A maps to NM_005529.5 G2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:22172955 G>A maps to NM_005529.5 L2767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:22178155 G>A maps to NM_005529.5 P2347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:22202156 G>A maps to NM_005529.5 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:22211355 C>A maps to NM_005529.5 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr1:22176569 C>T maps to NM_005529.5 W2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:22173049 G>C maps to NM_005529.5 S2736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:22205521 C>A maps to NM_005529.5 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:22168095 G>C maps to NM_005529.5 T3088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr1:22202225 C>A maps to NM_005529.5 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:22205116 G>A maps to NM_005529.5 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr1:22176602 G>A maps to NM_005529.5 L2459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:31735713 C>T maps to NM_006644.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:31735659 G>T maps to NM_006644.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:31719732 C>A maps to NM_006644.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:31712651 A>T maps to NM_006644.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr13:31713010 C>A maps to NM_006644.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr13:31729697 A>G maps to NM_006644.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr13:31712587 G>A maps to NM_006644.2 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:135592242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:135593310 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:135594123 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:135585092 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:135593099 C>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:135593998 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:135586541 G>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:135593507 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:135592351 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:135581828 G>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:135585005 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:135593334 A>T did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr23:135592249 G>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:135592352 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:135581827 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:135592993 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:135581841 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr23:135579987 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:63256397 G>C maps to NM_000524.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:63256622 G>T maps to NM_000524.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:63256718 G>T maps to NM_000524.2 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:63257441 G>T maps to NM_000524.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:63256991 G>A maps to NM_000524.2 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:63256904 G>C maps to NM_000524.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:63256361 A>G maps to NM_000524.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:63256859 C>T maps to NM_000524.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:78172322 C>A maps to NM_000863.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:78172305 G>T maps to NM_000863.1 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:78172235 G>T maps to NM_000863.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:78172175 G>T maps to NM_000863.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:23520675 G>A maps to NM_000864.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:23520466 G>T maps to NM_000864.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:87725345 G>A maps to NM_000865.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:87725672 C>T maps to NM_000865.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:87725648 G>T maps to NM_000865.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:87725102 G>A maps to NM_000865.2 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr6:87725612 G>A maps to NM_000865.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:88039964 C>G maps to NM_000866.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:88040363 T>A maps to NM_000866.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:88040643 A>T maps to NM_000866.3 K249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:88040744 G>A maps to NM_000866.3 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:88040760 G>T maps to NM_000866.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:88040471 C>T maps to NM_000866.3 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:47409238 G>A maps to NM_000621.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:47469741 G>A maps to NM_000621.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:47409208 C>A maps to NM_000621.3 R393R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-6774-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:47409355 G>T maps to NM_000621.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:47469795 G>T maps to NM_000621.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr13:47409076 C>T maps to NM_000621.3 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:231973422 C>T maps to NM_000867.4 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:231988311 C>T maps to NM_000867.4 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:114141569 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:114141512 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:114141542 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:114141545 T>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:113965912 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:114141327 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:114141303 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:114141822 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:114141350 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:114141296 T>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:113965883 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:113965829 T>G did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:113965990 C>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:114082671 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:113965976 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:114141857 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:113965705 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:113965954 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:113860403 G>T maps to NM_213621.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:113848527 C>T maps to NM_213621.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:113857445 C>A maps to NM_213621.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113803680 C>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:113816738 G>A maps to NM_006028.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:113803682 G>T maps to NM_006028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:113775683 G>A maps to NM_006028.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:113803760 C>T maps to NM_006028.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:183773962 A>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:183772674 G>A maps to NM_130770.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:183772675 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:183776233 C>A maps to NM_130770.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:183777423 C>A maps to NM_130770.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:183774068 G>T maps to NM_130770.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:183778022 C>A maps to NM_130770.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:183754232 C>T maps to NM_001145143.1 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:183822694 C>T maps to NM_182589.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:183824453 C>A maps to NM_182589.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:183818337 C>T maps to NM_182589.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:183823737 C>A maps to NM_182589.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:147928400 A>T maps to NM_001040173.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:147889329 G>C maps to NM_001040173.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:147830797 C>A maps to NM_001040169.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr5:147889551 A>T maps to NM_001040173.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:147902825 C>T maps to NM_001040173.2 W146*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:154862941 G>C maps to NM_024012.2 R111R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4430-01A-02D-1265-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-17-Z010-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:154862698 C>A maps to NM_024012.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:154876088 C>T maps to NM_024012.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr7:154875950 G>A maps to NM_024012.2 R276R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8089-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:154862761 G>A maps to NM_024012.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:154875863 G>T did not map to a codon.
Multiple mappings detected for codon TCGA-73-4666-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr7:154876112 C>T maps to NM_024012.2 N330N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-86-8073-01A-11D-2238-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-8073-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:154862857 C>A maps to NM_024012.2 A83A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-NJ-A4YQ-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:92617179 C>G maps to NM_019859.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr10:92616927 C>A maps to NM_019859.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:124271530 G>C maps to NM_002775.4 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:124271509 G>T maps to NM_002775.4 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:124268282 A>T maps to NM_002775.4 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr10:124266401 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:74758069 A>T maps to NM_013247.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:8307712 T>C maps to NM_053044.3 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr4:8305913 G>A maps to NM_053044.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr8:38835597 C>A maps to NM_153692.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:38835502 C>A maps to NM_153692.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:38840065 C>T maps to NM_153692.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:3201609 G>A maps to NM_002111.6 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:3156081 G>A maps to NM_002111.6 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:3231756 C>T maps to NM_002111.6 A2751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr4:3176671 G>C did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:3235053 C>G maps to NM_002111.6 L2810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:3107097 G>T maps to NM_002111.6 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr4:3129174 C>T maps to NM_002111.6 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:3211675 G>T maps to NM_002111.6 S2138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:3137636 G>T maps to NM_002111.6 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:3148598 G>T maps to NM_002111.6 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3176789 C>T maps to NM_002111.6 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr4:3129108 G>A maps to NM_002111.6 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr21:33318468 C>T maps to NM_014586.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:33296871 C>T maps to NM_014586.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:33296886 C>T maps to NM_014586.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:33296934 C>T maps to NM_014586.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:33296973 C>A maps to NM_014586.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:33297030 C>T maps to NM_014586.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr21:33340620 C>T maps to NM_014586.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr7:48007447 G>A maps to NM_004507.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:48015208 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:656683 C>G maps to NM_148959.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:656539 C>A maps to NM_148959.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:53574723 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:53644082 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:53576029 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:53675170 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:53563455 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:53578369 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:53585706 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:53578392 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:53634607 T>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:53591626 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:53610528 T>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:53672298 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:53641576 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:53563172 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:53578044 C>G did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:53578102 C>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:53577915 G>C did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:53591665 C>G did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:53616619 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:53607905 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:53579741 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:53655811 G>C did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:53566628 T>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:53634597 C>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:53573738 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:53571561 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:53571683 C>G did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:53591560 C>G did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:53596786 C>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:53642719 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:53643939 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:53617987 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:53672341 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:53607797 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:53674395 A>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:53578037 C>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:53578300 C>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:53611278 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:53571709 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:53560974 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:53644370 G>A did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:53610523 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:53571670 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:53652123 G>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:53585704 C>G did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:53612060 T>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:53561121 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:53596698 A>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:53579702 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:53574892 G>C did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:53610739 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:53581871 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:53629546 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:53621554 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:53641507 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:53616744 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:53661216 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:111099151 G>A maps to NM_001040107.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:111088014 C>T maps to NM_001040107.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:111099121 C>T maps to NM_001040107.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:50338078 G>A maps to NM_153281.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:50340019 G>C maps to NM_153281.1 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr3:50357599 C>T maps to NM_033158.4 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr7:123516998 C>T maps to NM_012269.2 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:123514853 G>T maps to NM_012269.2 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:123508869 C>G maps to NM_012269.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:123514870 T>A maps to NM_012269.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:123516863 C>A maps to NM_012269.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr7:123516998 C>T maps to NM_012269.2 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr16:71007833 G>T maps to NM_032821.2 A1708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70934908 C>A maps to NM_032821.2 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:70935047 C>G maps to NM_032821.2 R2968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70977729 C>T maps to NM_032821.2 L2217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:71212911 G>A maps to NM_032821.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:71015294 T>C maps to NM_032821.2 T1502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:71096191 G>T maps to NM_032821.2 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:70935047 C>T maps to NM_032821.2 R2968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr16:70891749 G>A maps to NM_032821.2 F4050F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr16:70841740 G>T maps to NM_032821.2 Y5035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:70935008 T>C maps to NM_032821.2 V2981V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:70908241 G>T maps to NM_032821.2 I3637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:71218765 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:71015344 C>A maps to NM_032821.2 G1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr16:70972617 A>T maps to NM_032821.2 R2297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:70902625 G>A maps to NM_032821.2 I3718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:71007820 C>A maps to NM_032821.2 G1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:71098634 G>A maps to NM_032821.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr16:70841494 C>A maps to NM_032821.2 G5117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr16:71212866 G>C maps to NM_032821.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:70917955 G>T maps to NM_032821.2 V3281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:70954808 C>T maps to NM_032821.2 A2489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:118918744 C>A maps to NM_001130991.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr11:118925327 G>A maps to NM_001130991.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:118926252 C>G maps to NM_001130991.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:21526335 G>A maps to NM_000415.2 L17L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4397-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:94973091 G>A maps to ENST00000375660 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:95019070 T>A maps to ENST00000375660 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:94985760 G>A maps to ENST00000375660 N1142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:220307775 G>T maps to NM_018060.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:220298647 T>C maps to NM_018060.3 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:220284191 G>T maps to NM_018060.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:220284168 G>T maps to NM_018060.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:220310247 G>T maps to NM_018060.3 G682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:220275469 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:88731894 T>A maps to NM_004967.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:88731894 T>C maps to NM_004967.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:88731900 C>A maps to NM_004967.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:82950158 C>A maps to NM_015525.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr6:82936911 G>T maps to NM_015525.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:82950119 C>A maps to NM_015525.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:82910356 T>G maps to NM_015525.2 V953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr7:8198168 T>A maps to ENST00000422063 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr7:8181393 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:203644315 C>T maps to NM_138468.4 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:203653589 G>A maps to NM_138468.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:203682251 C>T maps to NM_138468.4 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:203644329 G>A maps to NM_138468.4 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:10395636 C>G maps to NM_000201.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:10395693 G>C maps to NM_000201.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:10395857 C>T maps to NM_000201.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:10444649 G>C maps to NM_002162.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:10449400 G>A maps to NM_002162.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:10397792 G>A maps to NM_001544.3 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:10402219 G>A maps to NM_003259.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:52871149 C>T maps to NM_016513.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:204801540 A>T maps to NM_012092.3 K2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr21:45658371 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr21:45656864 G>T maps to ENST00000400379 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:19838365 G>T maps to NM_001546.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:94230103 T>A did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr10:94297240 G>A maps to NM_004969.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:94228660 C>A maps to NM_004969.3 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:209104695 C>A maps to NM_005896.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:90634803 C>T maps to NM_002168.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr20:2641184 G>A maps to NM_006899.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr20:2641146 C>T maps to NM_006899.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr20:2641350 C>A maps to NM_006899.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr20:2644633 C>A maps to NM_006899.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153051700 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:153052270 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:153052969 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:153051377 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:153055721 C>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:153055713 C>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:1089974 T>A maps to NM_004508.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:1088654 C>A maps to NM_004508.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:39872814 C>A maps to NM_194294.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:148568623 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:148564644 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:148585761 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:148568578 C>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:148564645 G>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr23:148577944 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:148579783 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:148578032 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:997817 G>A maps to NM_000203.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:994667 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:13264218 G>T maps to NM_004907.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:13264099 C>T maps to NM_004907.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:30711922 G>A maps to NM_003897.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr18:44683866 C>A maps to NM_016097.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:181058373 G>T maps to NM_016545.4 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:181058755 A>T maps to NM_016545.4 K240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:6658969 G>A maps to NM_001193457.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:6650691 G>C maps to NM_001193457.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:6664535 C>A maps to NM_001193457.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:159023408 A>T maps to ENST00000295809 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:159021488 T>C maps to ENST00000295809 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:159021489 G>T maps to ENST00000295809 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:158986357 C>A maps to ENST00000295809 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:158990201 A>C maps to ENST00000295809 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr14:94582777 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:94568238 A>T maps to NM_206949.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:94568259 A>G maps to NM_206949.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:41166313 T>A maps to NM_005533.4 *289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:79128522 T>A maps to NM_006417.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:79121117 G>T maps to NM_006417.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:79107492 G>T maps to NM_006820.2 *453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:79102760 C>T maps to NM_006820.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:79094634 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:27994969 T>G maps to NM_022873.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:163174655 C>A maps to NM_022168.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:163144752 G>T maps to NM_022168.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:163174535 G>A maps to NM_022168.2 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:91144224 C>A maps to NM_001010987.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:91144372 C>A maps to NM_001010987.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:91143648 A>G maps to NM_001010987.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:91144395 C>T maps to NM_001010987.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr10:91144407 C>A maps to NM_001010987.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:91065721 G>A maps to NM_001547.4 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:91177354 C>G maps to NM_012420.2 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:315103 G>T maps to ENST00000328221 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:314315 G>A maps to ENST00000328221 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:309044 C>T maps to NM_006435.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:319882 A>T maps to NM_021034.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:298709 G>A maps to NM_001025295.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr9:21206910 G>A maps to NM_002171.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:21206546 T>A maps to NM_002171.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:21239472 C>T maps to NM_002172.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr9:21216752 T>G maps to NM_002173.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr9:21217274 G>T maps to NM_002173.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:21385304 C>A maps to NM_000605.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:21166572 C>A maps to NM_002175.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:21166254 C>T maps to NM_002175.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:21187074 A>T maps to NM_021068.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr9:21304742 G>T maps to NM_002169.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr9:21350556 A>T maps to NM_021002.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr9:21350775 G>T maps to NM_021002.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:21350616 G>T maps to NM_021002.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:21201912 G>A maps to NM_021057.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr9:21409375 T>C maps to NM_002170.3 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr9:21409696 C>T maps to NM_002170.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:34632983 G>T maps to NM_207585.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:21077532 G>T maps to NM_002176.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr9:21077495 C>A maps to NM_002176.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr9:21077631 G>C maps to NM_002176.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr12:68551691 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr12:68551692 C>A maps to NM_000619.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:137519416 G>A maps to NM_000416.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:137519524 C>G maps to NM_000416.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:137524822 C>G maps to ENST00000367735 *187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:137519720 G>C maps to NM_000416.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr21:34805027 T>C maps to ENST00000381995 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr21:34799248 C>T maps to ENST00000381995 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:112112291 G>T maps to NM_001007245.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr7:112090829 G>C maps to NM_001007245.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:50327637 G>A maps to ENST00000336089 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:129233291 G>T maps to NM_052985.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:129195285 G>T maps to NM_052985.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:129196947 G>T maps to NM_052985.2 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr3:129236351 C>T maps to NM_052985.2 I1153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1573702 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:1608042 C>A maps to NM_014714.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:1621514 G>A maps to NM_014714.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:1652540 G>A maps to NM_014714.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:1634397 C>T maps to NM_014714.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:1574790 G>A maps to NM_014714.3 V997V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:27669193 G>C maps to NM_015662.1 S1563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:27707129 A>T maps to NM_015662.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:27707894 C>A maps to NM_015662.1 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:27704106 C>A maps to NM_015662.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:27700894 C>A maps to NM_015662.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr2:27676910 G>A maps to NM_015662.1 Q1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:118428530 T>A maps to NM_020153.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr20:42265859 G>T maps to NM_016004.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr3:107938419 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:26990193 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:27062667 G>C maps to NM_025103.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:159998597 T>A maps to ENST00000483754 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:159976352 G>C maps to ENST00000483754 S936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:110618327 G>A maps to NM_014055.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr12:110581238 T>A maps to NM_014055.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:69353824 C>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:69366621 A>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:65622918 T>C maps to NM_004884.3 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65622727 A>T maps to NM_004884.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:65622131 G>T maps to NM_004884.3 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:65621814 G>T maps to NM_004884.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr15:65621254 C>A maps to NM_004884.3 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr15:65623005 G>T maps to NM_004884.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:65688241 C>A maps to NM_020962.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:65677327 C>A maps to NM_020962.1 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65681619 A>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr15:65682491 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr15:65682626 C>T maps to NM_020962.1 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:65702612 C>A maps to NM_020962.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:65678330 C>T maps to NM_020962.1 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:65677372 C>A maps to NM_020962.1 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr15:65702514 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr15:65684550 C>A maps to NM_020962.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:65686836 G>A maps to NM_020962.1 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:102796284 C>A maps to NM_000618.3 *154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:99442823 C>T maps to NM_000875.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:99459971 G>T maps to NM_000875.3 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:99459899 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:99465613 G>C maps to NM_000875.3 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:99251007 G>T maps to NM_000875.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:99459973 G>A maps to NM_000875.3 E690E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:99434578 G>T maps to NM_000875.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:2156600 G>T maps to NM_001127598.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:2161379 C>A maps to NM_001127598.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:2156609 G>T maps to NM_001127598.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:47118739 G>C maps to NM_006546.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr17:47121402 G>A maps to NM_006546.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:47115535 C>T maps to NM_006546.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:47109329 C>G maps to NM_006546.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr17:47075133 C>T maps to NM_006546.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr17:47117316 A>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:47122351 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:47115589 C>A maps to NM_006546.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:185369905 G>A maps to NM_006548.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr3:185390391 G>A maps to NM_006548.4 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr3:185390421 G>A maps to NM_006548.4 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr3:185364842 G>A maps to NM_006548.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:23387343 G>T maps to NM_006547.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:23391090 C>A maps to NM_006547.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:23509711 G>T maps to NM_006547.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:160494946 C>T maps to NM_000876.2 H1702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:160482938 G>T maps to NM_000876.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:160485481 C>T maps to NM_000876.2 N1312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:160485538 C>T maps to NM_000876.2 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr6:160494947 G>T maps to NM_000876.2 G1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:160477508 G>A maps to NM_000876.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:160468235 A>G maps to NM_000876.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr16:1841460 G>A maps to NM_001146006.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:1842109 G>C maps to NM_001146006.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:45931535 C>A maps to NM_000596.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:45930251 G>A maps to NM_000596.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:217526666 C>A maps to NM_000597.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr2:217498632 C>T maps to NM_000597.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:45957003 G>T maps to NM_001013398.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:45954451 C>T maps to NM_001013398.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:38610235 A>G maps to NM_001552.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:217543650 G>T maps to NM_000599.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:217541566 C>T maps to NM_000599.3 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:53494881 C>A maps to NM_002178.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:57906996 C>T maps to NM_001553.1 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46733630 C>T maps to NM_198541.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:46627240 G>T maps to NM_207393.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:46543513 C>T maps to NM_001002923.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:201196046 C>A maps to NM_001164586.1 P3608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:201185762 C>A maps to NM_001164586.1 T3159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:201185814 C>A maps to NM_001164586.1 R3177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:201196322 C>A maps to NM_001164586.1 T3700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:201196295 G>T maps to NM_001164586.1 T3691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:201182427 G>T maps to NM_001164586.1 E2803*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4390-01A-02D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:71532177 G>T maps to NM_144646.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:23915734 C>A maps to NM_020070.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr22:23915548 C>G maps to NM_020070.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr22:23915742 G>A maps to NM_020070.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr22:23915506 G>T maps to NM_020070.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr22:23915772 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr22:23237849 A>T maps to ENST00000410090 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:23237855 C>A maps to ENST00000410090 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr22:23237862 G>T maps to ENST00000410090 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:23237597 C>T maps to ENST00000410090 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:23237657 G>T maps to ENST00000410090 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:23237576 T>G maps to ENST00000410090 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:23237663 T>C maps to ENST00000410090 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr22:23235923 G>A maps to ENST00000410090 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:51826948 C>A maps to NM_001101372.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:51826945 G>T maps to NM_001101372.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:51827008 G>T maps to NM_001101372.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:130419769 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:130409257 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:130416703 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:130415732 C>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr23:130417144 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:130412614 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:130412659 T>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:130409601 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:130407899 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:130408769 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:130409974 C>A did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr23:130416521 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:130409232 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:130411033 G>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:130416644 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:130410114 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:130411006 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:130407892 T>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:130420591 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:130412048 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:130419305 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:130419877 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:130417037 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:130411123 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:130412476 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:130419899 T>C did not map to a codon.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr23:130412682 G>A did not map to a codon.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr23:130416700 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:130408704 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:130420643 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:130416667 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:130417005 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:130410950 C>A did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:130408757 C>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:130410141 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:130409618 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:130409619 C>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr23:130409660 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:130413276 A>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:130416557 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:130410952 G>C did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:130419786 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr23:130419263 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:130410141 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:151163171 T>A maps to NM_178822.4 K1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:151163145 G>A maps to NM_178822.4 F1541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:151164576 C>A maps to NM_178822.4 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:151163927 C>A maps to NM_178822.4 G1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:151155694 G>A maps to NM_178822.4 P2218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151156245 G>A maps to NM_178822.4 L2035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:151162965 G>T maps to NM_178822.4 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:151164626 C>A maps to NM_178822.4 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:151166318 C>A maps to NM_178822.4 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:151166889 C>G maps to NM_178822.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:151154763 G>A maps to NM_178822.4 R2529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:151161240 G>A maps to NM_178822.4 L1832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:151163028 G>A maps to NM_178822.4 Y1580Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr3:151164417 G>A maps to NM_178822.4 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:151156156 G>T maps to NM_178822.4 G2064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:118623643 G>A maps to NM_152538.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:118621428 C>A maps to NM_152538.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:118624497 C>A maps to NM_152538.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:118624545 G>T maps to NM_152538.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:18691925 G>T maps to NM_032880.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:18688690 C>A maps to NM_032880.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:18554485 G>T maps to NM_032880.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:18735860 G>T maps to NM_173588.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr11:18743147 G>A maps to NM_173588.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:18731901 G>C maps to NM_173588.3 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:18732286 C>A maps to NM_173588.3 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:18740269 G>T maps to NM_173588.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:117131682 C>A maps to NM_001542.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:117122425 A>G maps to NM_001542.2 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117127642 C>A maps to NM_001542.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:117122167 C>G maps to NM_001542.2 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:117142848 T>A maps to NM_001542.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:117156399 G>A maps to NM_001542.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:117122230 A>G maps to NM_001542.2 D1059D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:117150687 G>T maps to NM_001542.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:117146447 G>A maps to NM_001542.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:117131613 C>A maps to NM_001542.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr21:41151017 C>T maps to NM_001080444.1 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr21:41143095 C>A maps to NM_001080444.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr21:41137705 C>A maps to NM_001080444.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:41151218 T>C maps to NM_001080444.1 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr16:21658802 G>T maps to NM_005849.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:160061723 C>T maps to NM_052868.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:160063848 G>T maps to NM_052868.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:160064707 G>A maps to NM_052868.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:159900161 C>T maps to NM_001135050.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:133790154 C>A maps to NM_014987.1 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:133795690 C>T maps to NM_014987.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:133790343 C>A maps to NM_014987.1 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:133792461 A>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:133790609 C>A maps to NM_014987.1 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:133791249 G>A maps to NM_014987.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:133790970 C>A maps to NM_014987.1 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr11:133805951 G>A maps to NM_014987.1 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:133789935 G>T maps to NM_014987.1 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:133801380 T>A maps to NM_014987.1 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:133799597 A>G maps to NM_014987.1 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:133807298 A>T maps to NM_014987.1 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:219922302 G>T maps to NM_002181.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:219920416 C>A maps to NM_002181.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:219920021 C>A maps to NM_002181.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140037230 T>G maps to NM_006083.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140038605 G>T maps to NM_006083.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:99020243 C>A maps to NM_153687.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:111663783 T>A maps to NM_003640.3 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:111668632 C>T maps to NM_003640.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr9:111659269 T>C maps to NM_003640.3 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:111681116 T>A maps to NM_003640.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr9:111673440 G>T maps to NM_003640.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr9:111689718 C>T maps to NM_003640.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:111658817 A>G maps to NM_003640.3 Y898Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:42162702 A>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr8:42174362 G>T maps to NM_001556.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42186653 G>T maps to NM_001556.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:42146231 C>T maps to NM_001556.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42176905 G>T maps to NM_001556.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:42179668 C>G maps to NM_001556.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:206653243 A>G maps to NM_014002.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:206649521 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:206647747 G>A maps to NM_014002.3 R54R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-99-7458-01A-11D-2036-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153780354 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:153780266 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:50444255 G>A maps to NM_006060.3 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:50367288 G>T maps to NM_006060.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:50450322 G>T maps to NM_006060.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:50459427 C>A maps to NM_006060.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr7:50450265 C>T maps to NM_006060.3 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:117864125 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:34640769 G>T maps to ENST00000433395 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:159711624 G>T maps to NM_000882.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr5:158747500 G>A maps to NM_002187.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:18170763 G>A maps to NM_005535.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr19:18194272 A>G maps to NM_005535.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:67795268 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:67816659 C>T maps to NM_001559.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:67804385 G>A maps to NM_001559.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:67795396 C>T maps to NM_001559.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:67795366 T>A maps to NM_001559.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:67816614 G>C maps to NM_001559.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr5:131995901 C>A maps to NM_002188.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:117907896 C>G did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:117900508 G>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:117883721 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:114250290 T>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:114245311 A>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:114249015 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:114251747 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:114244192 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:114242541 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr23:114242516 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:114242497 C>T did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr23:114249118 G>C did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr23:114249131 G>A did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr23:114250374 G>A did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:114250331 G>C did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:114250372 G>C did not map to a codon.
Alternatively spliced codon TCGA-69-7979-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:142643088 A>T maps to NM_000585.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr10:6002510 G>A maps to NM_002189.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:5995117 C>T maps to NM_002189.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:81592381 C>A maps to NM_172217.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr15:81592195 C>T maps to NM_172217.3 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr15:81578128 C>A maps to NM_172217.3 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:81585041 G>T maps to NM_172217.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:81598782 G>A maps to NM_172217.3 T1234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:81572083 C>T maps to NM_172217.3 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:81571978 C>A maps to NM_172217.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:81592486 G>T maps to NM_172217.3 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:52054021 C>A maps to NM_002190.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr6:52054068 G>T maps to NM_002190.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr6:52052546 C>T maps to NM_002190.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr6:52054017 C>G maps to NM_002190.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr6:52053903 C>A maps to NM_002190.2 C94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:52052534 G>T maps to NM_002190.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:52103574 G>T maps to NM_052872.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:52103658 G>A maps to NM_052872.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr22:17586479 G>C did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:53880623 C>T maps to NM_018725.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr3:9975222 G>T maps to NM_153461.2 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:57132510 C>T maps to NM_017563.3 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr3:57130438 G>A maps to NM_017563.3 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:57136546 G>A maps to NM_017563.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr3:57132269 G>A maps to NM_017563.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:9950948 C>T maps to NM_153483.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:9952836 G>A maps to NM_153483.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr22:50437718 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:103013213 G>A maps to NM_003855.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:103010926 A>G did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:102992515 A>T maps to NM_003855.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:102992474 G>T maps to NM_003855.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:103013337 G>T maps to NM_003855.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr2:102992414 A>T maps to NM_003855.2 K173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr2:103010990 G>T maps to NM_003855.2 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:103040328 C>A maps to NM_003853.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:103040547 A>C maps to NM_003853.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:103053769 G>A maps to NM_003853.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr2:103040347 G>T maps to NM_003853.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:103068358 A>G maps to NM_003853.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:103068613 G>T maps to NM_003853.2 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr2:103063626 G>T maps to NM_003853.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:113588988 G>T maps to NM_000576.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:113588913 G>T maps to NM_000576.2 Y184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:113832766 G>A maps to NM_032556.4 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:113832387 A>G maps to NM_032556.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:113820089 C>A maps to NM_173170.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:113820124 G>T maps to NM_173170.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:113765485 G>A maps to NM_014440.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:113675248 C>T maps to NM_014439.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:113676326 G>T maps to NM_014439.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:113788646 A>T maps to NM_173178.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:113742496 C>A maps to NM_019618.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:113742502 C>A maps to NM_019618.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:113742624 G>T maps to NM_019618.2 *170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:113736270 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:102792909 A>T maps to NM_000877.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:190362169 A>T maps to NM_002182.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:190345226 C>T maps to NM_002182.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:190362059 G>T maps to NM_002182.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:29417356 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:29301283 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:29417341 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:29938086 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:29938085 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:29938103 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:29938181 G>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:29417271 G>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:29938178 G>C did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:29973556 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:29301282 G>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:29414548 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:29973707 A>G did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:29973567 T>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:29935702 A>C did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:29301255 G>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:29414537 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:29938084 G>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:29973905 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:29972707 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:29973522 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:29973850 G>C did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:29301213 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:29417280 A>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:28807535 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:29973777 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:105010958 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:105011535 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:104512089 G>C did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:104961394 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:105011609 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:105011393 G>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr23:105010968 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:104440259 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:105011540 A>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:104512135 A>C did not map to a codon.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr23:104728315 G>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:104440286 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:105011563 C>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:104961437 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:104984578 G>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:105011473 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:104992969 G>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:104992978 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:104440386 T>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:105011294 C>A did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr23:104440392 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:104993095 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:102968096 G>T maps to NM_016232.4 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr2:102957268 C>A maps to NM_016232.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:102964543 T>A maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:102956626 A>G maps to NM_016232.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:102959634 A>G maps to NM_016232.4 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:102956658 C>A maps to NM_016232.4 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr2:102968275 C>A maps to NM_016232.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:113887237 G>T maps to NM_173841.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr4:123377318 T>A maps to NM_000586.3 K63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:123377358 C>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:207041894 G>T maps to NM_018724.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:207039226 T>C maps to NM_018724.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr6:137322793 G>A maps to NM_014432.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:137325892 T>C maps to NM_014432.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:137323090 C>T maps to NM_014432.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:136728999 G>T maps to NM_144717.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:136699371 C>G maps to NM_144717.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:27460063 G>T maps to NM_181079.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:27441409 C>A maps to NM_181079.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:27455948 G>A maps to NM_181079.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:27456537 C>G maps to NM_181079.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:27455867 G>T maps to NM_181079.4 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:27460309 C>A maps to NM_181079.4 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:27457348 C>A maps to NM_181079.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:27454427 C>A maps to NM_181079.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr16:27445755 G>T maps to NM_181079.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:27456034 C>A maps to NM_181079.4 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr16:27448889 C>A maps to NM_181079.4 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:68646304 G>T maps to NM_020525.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:24447963 G>A maps to NM_021258.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:24463711 G>A maps to NM_021258.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:24463756 C>A maps to NM_021258.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:24465125 C>T maps to NM_021258.2 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:137466886 A>T maps to NM_052962.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:56733602 C>T maps to NM_016584.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:67705956 C>A maps to NM_144701.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:67685288 G>T maps to NM_144701.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:67685345 T>C maps to NM_144701.2 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:67648552 C>G maps to NM_144701.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:67648609 C>A maps to NM_144701.2 Y153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:67685375 T>C maps to NM_144701.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr14:23842380 A>T maps to NM_022789.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:23842336 C>T maps to NM_022789.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:23842407 C>A maps to NM_022789.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:68619521 G>A maps to NM_018402.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:68595651 A>T maps to NM_018402.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28515336 A>G maps to NM_145659.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:28513377 G>A maps to NM_145659.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:28518120 C>A maps to NM_145659.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr16:28511130 G>T maps to NM_145659.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:14153293 G>T maps to NM_004843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:14153284 C>A maps to NM_004843.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:14162996 C>T maps to NM_004843.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:39734505 G>T maps to ENST00000392072 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:39735474 G>A maps to ENST00000392072 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39788641 C>A maps to NM_172140.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:39789086 G>A maps to NM_172140.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:6104075 G>A maps to NM_000417.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:6066300 C>T maps to NM_000417.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:6060059 C>G maps to NM_000417.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:6063567 G>T maps to NM_000417.2 C152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:6104106 G>C maps to NM_000417.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr10:6066216 C>A maps to NM_000417.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:70331303 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:70327593 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:70328488 A>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:70327652 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:70330843 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:70331294 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:122657104 G>A maps to NM_001014336.1 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:55201964 C>A maps to NM_139017.4 C367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:55179016 C>A maps to NM_139017.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr5:55164713 C>T maps to NM_139017.4 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:55209303 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:55212557 G>A maps to NM_139017.4 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:55204135 G>A maps to NM_139017.4 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:55168205 C>T maps to NM_139017.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119199 G>T maps to ENST00000416912 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:3119311 G>T maps to ENST00000416912 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr16:3119262 C>G maps to ENST00000416912 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr16:3119035 C>T maps to ENST00000416912 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr16:70690951 C>G maps to NM_152456.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:1471273 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:1471346 C>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:1499949 C>G did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:1460678 G>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:1471284 G>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr23:1464319 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:1499969 C>G did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:1471250 G>A did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr23:1464276 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr23:1475146 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50397695 C>A maps to NM_172374.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:50397677 G>A maps to NM_172374.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:50394673 C>T maps to NM_172374.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:27373905 C>T maps to NM_000418.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:27356217 G>T maps to NM_000418.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:27373981 G>T maps to NM_000418.2 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr16:27367204 G>T maps to NM_000418.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27374556 A>G maps to NM_000418.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr16:27373725 C>G maps to NM_000418.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:3136994 A>G maps to NM_000564.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:3134046 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr3:3111909 C>A maps to NM_000564.3 *421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:22766895 C>T maps to NM_000600.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr7:22771062 C>T maps to NM_000600.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:154422456 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:154401817 G>T maps to NM_000565.2 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:154437777 G>T maps to NM_000565.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:79645959 A>T maps to NM_000880.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:35873613 C>A maps to NM_002185.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:35874617 C>A maps to NM_002185.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:35876377 C>A maps to NM_002185.2 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:35871287 C>A maps to NM_002185.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:35871200 A>G maps to NM_002185.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:35874575 C>A maps to NM_002185.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:35873613 C>A maps to NM_002185.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:35876368 C>A maps to NM_002185.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:35873731 G>T maps to NM_002185.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:35867449 A>G maps to NM_002185.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:35857136 G>T maps to NM_002185.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr5:35876368 C>T maps to NM_002185.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:135231469 G>A maps to NM_000590.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:135229726 T>C maps to NM_000590.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:155232672 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:155235137 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:155234199 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:155234099 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:155233194 A>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:155235121 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:155233518 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:155235035 C>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:155233497 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:155239570 G>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:155233372 A>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:155235829 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:155239750 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:155239557 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:155237271 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:155233456 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:121712503 C>A maps to ENST00000344209 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:121720217 G>A maps to ENST00000344209 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr3:121712587 G>A maps to ENST00000344209 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:166904655 G>T maps to NM_199351.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:166904586 C>A maps to NM_199351.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:166891879 C>A maps to NM_199351.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:166927015 C>A maps to NM_199351.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:166896402 G>T maps to NM_199351.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:166904640 G>A maps to NM_199351.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:166904631 G>C maps to NM_199351.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:166904535 A>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:153635229 G>C maps to NM_004515.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:153640496 C>A maps to NM_004515.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:10799239 G>T maps to NM_017620.2 G817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:6630368 C>T maps to NM_001014795.1 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:15230305 G>T maps to NM_006844.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15233751 A>T maps to NM_006844.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:31477920 C>A maps to NM_144981.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:110526648 C>A maps to NM_032549.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:86406603 C>T maps to NM_006839.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:86386709 T>C maps to NM_006839.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:75932167 C>G maps to NM_018285.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:131102211 G>T maps to NM_033416.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:43923552 C>A maps to NM_175882.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr17:43922517 C>A maps to NM_175882.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:43923270 C>T maps to NM_175882.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:43923924 C>T maps to NM_175882.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43922292 C>T maps to NM_175882.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:43923726 G>A maps to NM_175882.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:43923159 C>A maps to NM_175882.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:82572880 T>A maps to NM_001144878.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr18:12009891 G>T maps to NM_014214.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:57905850 C>G maps to NM_017813.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:57876396 G>C maps to NM_017813.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:57878816 C>G maps to NM_017813.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr8:57905880 G>A maps to NM_017813.3 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:128049522 G>A maps to NM_000883.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:128040392 G>A maps to NM_000883.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr3:49062559 T>A maps to NM_000884.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:76715025 C>A maps to NM_001563.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:76728563 T>A maps to NM_001563.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:76713659 A>T maps to NM_001563.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:76660392 G>T maps to NM_001563.2 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:76744340 C>T maps to NM_001563.2 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:76728443 G>A maps to NM_001563.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:76744337 C>T maps to NM_001563.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr6:76751682 C>A maps to NM_001563.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:76751661 C>T maps to NM_001563.2 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:100963142 C>A maps to NM_016247.2 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:100976421 C>G maps to NM_016247.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:101038617 G>A maps to NM_016247.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:100949990 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:100994514 C>A maps to NM_016247.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:100962534 C>T maps to NM_016247.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr3:100961628 G>A maps to NM_016247.2 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:100961604 C>A maps to NM_016247.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:100961619 C>A maps to NM_016247.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr3:100963434 T>C maps to NM_016247.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:105037099 C>A maps to NM_032727.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:105048116 G>A maps to NM_032727.3 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr10:105037909 G>A maps to NM_032727.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:62582841 C>G maps to NM_176877.2 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62321802 C>T maps to NM_176877.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:62455858 T>A maps to NM_176877.2 Y1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:62626588 G>T maps to NM_176877.2 L1796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:62231975 C>A maps to NM_176877.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr1:62293119 A>G maps to NM_176877.2 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:62626578 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:62261223 A>T maps to NM_176877.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:61913163 G>T maps to NM_001040694.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:61897766 G>A maps to NM_001040694.1 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:61897760 G>T maps to NM_001040694.1 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:61897382 G>T maps to NM_001040694.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:61897892 G>A maps to NM_001040694.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:61897667 G>A maps to NM_001040694.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr14:105169538 C>T maps to ENST00000252520 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:105176006 C>G maps to ENST00000252520 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr13:111367798 C>T maps to NM_005537.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:111372014 C>T maps to NM_005537.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr13:111372068 C>G maps to NM_005537.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:111368347 G>C maps to NM_005537.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:120606713 G>T maps to NM_019071.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:6772255 C>G maps to NM_001127582.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:242651390 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:242644134 G>T maps to NM_032329.4 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:242650847 G>A maps to NM_032329.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220439497 A>G maps to NM_002191.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:41730009 G>T maps to NM_002192.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:41729268 C>T maps to NM_002192.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:41739732 C>T maps to NM_002192.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr7:41729712 C>T maps to NM_002192.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr7:41739638 C>A maps to NM_002192.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:41729271 G>T maps to NM_002192.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:41739855 C>T maps to NM_002192.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr2:121104186 C>T maps to NM_002193.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:121107308 G>T maps to NM_002193.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:57828905 C>T maps to NM_005538.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr12:57843177 C>A maps to NM_005538.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr12:57843450 A>T maps to NM_005538.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:57850273 G>T maps to NM_031479.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:30795406 C>A maps to NM_006774.4 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:41377596 C>T maps to NM_017553.1 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:41387984 T>C maps to NM_017553.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:41342252 T>C maps to NM_017553.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr15:41347501 C>A maps to NM_017553.1 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:41347447 C>A maps to NM_017553.1 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr15:41275984 T>A maps to NM_017553.1 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr18:33048703 G>A maps to NM_001098817.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:206874386 G>A maps to NM_017759.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:206869931 C>A maps to NM_017759.4 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:191236091 G>T maps to NM_002194.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:99169338 C>T maps to NM_001134224.1 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:99182489 A>C did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:99180084 G>T maps to NM_001134224.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:99156081 C>G maps to NM_001134224.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:99193583 C>T maps to NM_001134224.1 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr2:99172083 G>A maps to NM_001134224.1 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:143003332 G>T maps to NM_003866.2 C831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:143129580 T>A maps to NM_003866.2 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:143130047 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:143114322 C>T maps to NM_003866.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:143045851 C>T maps to NM_003866.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:143033800 T>A maps to NM_003866.2 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:143081564 C>T maps to NM_003866.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:143326436 C>T maps to NM_003866.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:143130115 G>T maps to NM_003866.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr4:143114337 G>A maps to NM_003866.2 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr4:143007364 C>A maps to NM_003866.2 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr4:143159165 T>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:143033732 A>G maps to NM_003866.2 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr4:143043279 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:38339794 C>T maps to ENST00000373026 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:38411523 T>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:38341285 T>A maps to ENST00000373026 K674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:38331515 C>A maps to ENST00000373026 E891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:38397645 T>A maps to ENST00000373026 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:234072374 G>A maps to ENST00000359570 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:234072548 A>C maps to ENST00000359570 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:233925274 C>A maps to ENST00000359570 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:234106842 C>T maps to ENST00000359570 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:234091101 C>A maps to ENST00000359570 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr2:233995346 G>A maps to ENST00000359570 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:234113074 G>A maps to ENST00000359570 E1093E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:234106824 C>A maps to ENST00000359570 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:31522646 C>G maps to ENST00000331075 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr22:31529924 C>A maps to ENST00000331075 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr17:1417236 C>A maps to NM_016532.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr11:71946218 C>T maps to NM_001567.3 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:71944744 G>T maps to NM_001567.3 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:71948809 G>C maps to NM_001567.3 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:2181168 C>A maps to NM_001185098.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:2181117 G>T maps to NM_001185098.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:15197460 G>T maps to NM_001031853.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:15197586 C>T maps to NM_001031853.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:15243084 G>T maps to NM_001031853.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:15197340 C>G maps to NM_001031853.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:15243093 T>A maps to NM_001031853.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:15199881 T>A maps to NM_001031853.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:15212340 T>A maps to NM_001031853.3 L272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr11:15243057 C>T maps to NM_001031853.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr11:15243127 C>T maps to NM_001031853.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:15267456 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:15212251 G>T maps to NM_001031853.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:15170755 C>G maps to NM_001031853.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:15260576 C>T maps to NM_001031853.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:15199872 C>A maps to NM_001031853.3 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr11:15134021 C>A maps to NM_001031853.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:15212245 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:15222461 C>T maps to NM_001031853.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:15197517 C>A maps to NM_001031853.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:15197533 C>A maps to NM_001031853.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:155093400 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:118860813 G>T maps to NM_016133.2 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:17927680 C>T maps to NM_005543.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:20349228 G>A maps to NM_002196.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:20350197 C>A maps to NM_002196.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr14:36005114 C>A maps to NM_032594.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:7267398 C>A maps to NM_000208.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:7125476 G>T maps to NM_000208.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:7117069 G>A maps to NM_000208.2 S1382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr19:7152777 C>T maps to NM_000208.2 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:7125392 G>A maps to NM_000208.2 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:7166354 C>A maps to NM_000208.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:7143016 G>A maps to NM_000208.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:7150531 G>C maps to NM_000208.2 S748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:156810733 G>T maps to NM_014215.2 T1275T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-5899-01A-11D-1625-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-55-8506-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:156811943 G>A maps to NM_001007792.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:156812255 G>C maps to NM_014215.2 V1057V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:156814031 G>A maps to NM_014215.2 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr1:156816536 G>A maps to NM_014215.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156810665 C>T maps to NM_014215.2 *1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:156815424 C>T maps to NM_014215.2 A720A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-97-7554-01A-11D-2036-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-97-7937-01A-11D-2167-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MP-A4TF-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:156811946 G>T maps to NM_001007792.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:156823912 C>A maps to NM_014215.2 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:156816443 C>A maps to NM_014215.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr7:1535816 G>A maps to ENST00000389470 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:1524940 G>A maps to ENST00000389470 A1214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:1512765 C>T maps to ENST00000389470 G2218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:1519958 G>A maps to ENST00000389470 F1560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:1523718 G>A maps to ENST00000389470 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:1538655 C>A maps to ENST00000389470 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:1521020 C>A maps to ENST00000389470 V1436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:106604351 T>C maps to NM_020395.3 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:59962346 G>A maps to NM_020748.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:59958410 C>A maps to NM_020748.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:60003897 A>T maps to NM_020748.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:153740269 C>T maps to ENST00000428986 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:153740180 G>T maps to ENST00000428986 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:153745744 G>A maps to ENST00000428986 *1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:77671418 C>A maps to NM_033547.3 G226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:77635797 C>T maps to NM_033547.3 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr11:77618830 G>A maps to NM_033547.3 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:77632421 G>A maps to NM_033547.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr11:77705650 G>A maps to NM_033547.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr11:77618828 T>C maps to NM_033547.3 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:77630018 T>A maps to NM_033547.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr11:62417107 G>A maps to NM_030628.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:62415211 G>T maps to NM_030628.1 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr11:62416147 G>A maps to NM_030628.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62416482 C>A maps to NM_030628.1 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:51942032 T>C maps to NM_012141.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:51969544 G>C maps to NM_012141.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:212148540 T>C maps to NM_015434.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:212180033 G>A maps to NM_015434.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr1:212118197 G>C maps to NM_015434.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:95888300 G>A did not map to a codon.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr8:95837231 T>G maps to NM_017864.2 L81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:95839952 A>T maps to NM_017864.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:95862155 G>C maps to NM_017864.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:28654151 G>C maps to NM_018250.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:128632152 G>T maps to NM_015693.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:128584606 G>A maps to NM_015693.3 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr3:49764842 A>T maps to NM_153273.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:48726008 G>A maps to ENST00000395509 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:33690859 A>G maps to NM_054111.4 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:33703156 T>A maps to NM_054111.4 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:154521138 C>T maps to NM_001130700.1 L191L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-86-A4JF-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:59956112 A>G maps to NM_152230.4 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:59956229 T>A maps to NM_152230.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:61922991 G>A maps to NM_001134779.1 K965K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:61923141 C>T maps to NM_001134779.1 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:44429989 A>C maps to NM_014652.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:24655131 C>T maps to ENST00000458132 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:24656910 G>A maps to ENST00000458132 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:98673308 G>C maps to NM_002271.4 A1061A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:98666431 A>T maps to NM_002271.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr13:98641394 G>A maps to NM_002271.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:9445352 G>A maps to NM_006391.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:9431504 C>T maps to NM_006391.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:30787165 G>C maps to NM_006390.3 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:30837233 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:30783814 C>A maps to NM_006390.3 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:201844050 T>G maps to NM_018085.4 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:201832720 G>C maps to NM_018085.4 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:201839916 G>A maps to NM_018085.4 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:201841971 A>T maps to NM_018085.4 K865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:201823948 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:46179937 C>A maps to NM_005897.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:46206825 G>A maps to NM_005897.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:46193420 G>A maps to NM_005897.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr1:46211801 G>A maps to NM_005897.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:95397467 G>A maps to NM_022755.5 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:237272521 G>A maps to ENST00000457693 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:237415898 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:237405862 C>A maps to ENST00000457693 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:237395534 T>C maps to ENST00000457693 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:121509046 C>T maps to NM_001023570.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:121547405 G>A maps to NM_001023570.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr3:121547450 G>A maps to NM_001023570.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:121544909 G>T maps to NM_001023570.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:32673605 C>T maps to NM_001160042.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:32672630 C>T maps to NM_001160042.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:2617907 G>C maps to NM_152558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:2608632 A>T maps to NM_152558.3 K44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:51897053 C>A maps to NM_203424.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:51864583 C>A maps to NM_001085479.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:51864789 G>A maps to NM_001085479.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:197618358 C>T maps to NM_001134435.1 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr3:197616455 T>A maps to NM_001134435.1 K443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr3:197640777 C>A maps to NM_001134435.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:67681316 C>T maps to NM_001031715.2 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr15:67553672 G>T maps to NM_001031715.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:158983077 T>A maps to NM_001042705.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:158980357 G>A maps to NM_001197113.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:91035817 C>T maps to NM_003870.3 A1501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr15:90931602 G>A maps to NM_003870.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:75885524 C>G maps to NM_006633.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:75954464 G>A maps to NM_006633.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:75979001 G>T maps to NM_006633.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:75893270 T>A maps to NM_006633.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr5:75907005 G>T maps to NM_006633.2 G507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr5:75964576 T>A maps to NM_006633.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:75948600 G>T maps to NM_006633.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:75893300 G>C maps to NM_006633.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:75893301 G>T maps to NM_006633.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:75932976 A>G maps to NM_006633.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:75936793 G>T maps to NM_006633.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:75902106 C>T maps to NM_006633.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:75979700 A>T maps to NM_006633.2 I1288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:75886332 G>A maps to NM_006633.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr5:75858377 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:75950035 G>A maps to NM_006633.2 W730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:75967607 C>T maps to NM_006633.2 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:75978941 C>A maps to NM_006633.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:156501026 C>A maps to NM_178229.4 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:156496382 C>A maps to NM_178229.4 L1597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:156510565 C>A maps to NM_178229.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:156533588 G>A maps to NM_178229.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr1:156536335 C>T maps to NM_178229.4 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:156513997 C>T maps to NM_178229.4 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:156498299 C>A did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr3:12961966 C>G maps to ENST00000429247 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:12977435 C>A maps to ENST00000429247 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:12962029 G>A maps to ENST00000429247 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:12977839 C>A maps to ENST00000429247 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:12977660 C>T maps to ENST00000429247 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:12978002 C>T maps to ENST00000429247 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:53267401 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:53280024 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:53284095 C>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:53280040 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:53277965 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:53268437 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:53277999 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:53285033 G>C did not map to a codon.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr23:53267380 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:53265578 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:53267474 C>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:53284024 A>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:53283711 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:53279981 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:247542 C>A maps to NM_001170738.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:274922 C>A maps to NM_001170738.1 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:280293 G>C maps to NM_001170738.1 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:247638 C>T maps to NM_001170738.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr12:271188 G>T maps to NM_001170738.1 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:123143030 G>A maps to NM_178827.4 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr7:123097557 G>T maps to NM_178827.4 C690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:123101659 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:123101554 G>T maps to NM_178827.4 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr7:123104949 C>T maps to NM_178827.4 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr7:123152036 C>A maps to NM_178827.4 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:123101455 T>C maps to NM_178827.4 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:123097557 G>A maps to NM_178827.4 C690C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:123105038 C>A maps to NM_178827.4 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:153284085 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:153284752 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:153279703 T>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:153279569 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:153278821 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:153284705 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:153278080 A>G did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:10219675 C>G maps to NM_001570.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:66638981 C>T maps to NM_007199.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:66622045 A>G maps to NM_007199.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:66638403 A>G maps to NM_007199.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr15:78780595 C>T maps to NM_004136.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:46387493 G>A maps to NM_015649.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:46387916 C>T maps to NM_015649.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:46388939 G>T maps to NM_015649.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr1:234744399 C>A maps to NM_182972.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr19:50167984 A>G maps to NM_001571.5 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:50165691 C>T maps to NM_001571.5 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:209965772 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:209974727 T>A maps to NM_006147.2 K11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:209961968 C>A maps to NM_006147.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:209961959 G>A maps to NM_006147.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr16:85945191 A>T maps to NM_002163.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:85946792 C>T maps to NM_002163.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:85952131 C>G maps to NM_002163.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:85936642 C>A maps to NM_002163.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr16:85936693 G>T maps to NM_002163.2 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr16:85954812 C>G maps to NM_002163.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr16:85946783 G>T maps to NM_002163.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:24632299 C>T maps to NM_006084.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr14:24632698 C>T maps to NM_006084.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:44222904 G>A maps to NM_019612.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:44223519 C>T maps to NM_019612.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:44223192 G>A maps to NM_019612.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:227663166 C>A maps to NM_005544.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:227661393 G>A maps to NM_005544.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:227660322 C>A maps to NM_005544.2 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:227660835 C>A maps to NM_005544.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr2:227659845 T>G maps to NM_005544.2 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:110438031 G>C maps to NM_003749.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:107977663 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:107979481 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:107976560 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:107976662 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:107976363 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107976645 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:107977985 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr23:107977312 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:107976486 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:107978334 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:107977955 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:107978238 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:107978287 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:107977840 A>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:107977626 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:107977757 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:107978506 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:107977780 T>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:107978160 C>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:107975922 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:107978579 C>G did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:107976098 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:107976881 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:107976353 A>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:107978199 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:107977486 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:107978596 C>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:107975899 G>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr23:107976068 G>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:107977508 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:107978466 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:107977959 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:107978077 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:107976274 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:107976298 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:107976306 G>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:107979004 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:107977373 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:107975898 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:107977502 G>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:3600723 G>A maps to NM_024337.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:3599370 G>A maps to NM_024337.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:3599619 G>A maps to NM_024337.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:3599692 G>T maps to NM_024337.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:3599343 G>C maps to NM_024337.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:3599691 C>T maps to NM_024337.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr5:2749502 C>T maps to NM_033267.4 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:2748642 T>A maps to NM_033267.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:2748675 G>A maps to NM_033267.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:2748736 G>C maps to NM_033267.4 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:2749826 G>A maps to NM_033267.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:2749642 G>T maps to NM_033267.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:54318156 C>A did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr5:1879615 A>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:1879630 G>A maps to NM_016358.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:1879807 G>A maps to NM_016358.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:54966693 G>T maps to NM_005853.5 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:55360396 C>A maps to NM_024335.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:55362639 G>T maps to NM_024335.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr16:55361653 C>T maps to NM_024335.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7816-01A-11D-2167-08 chr16:55362796 C>T maps to NM_024335.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:55360367 C>T maps to NM_024335.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr9:88887028 T>G did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:108958089 G>T maps to NM_213595.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:949578 G>T maps to NM_005101.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr15:89195510 G>A maps to NM_002201.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:89198668 G>T maps to NM_002201.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr1:156697420 C>G maps to NM_030980.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:50683564 C>A maps to NM_002202.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr15:76633473 G>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74467990 C>A maps to NM_201526.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:74468089 G>T maps to NM_201526.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr15:74425517 C>T maps to NM_001130137.1 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:74426879 A>T maps to NM_001130137.1 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:13280018 C>A maps to NM_080826.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:13279805 C>A maps to NM_080826.1 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:13279934 C>A maps to NM_080826.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr14:77942009 G>A maps to NM_199296.2 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:77950851 G>T maps to NM_199296.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:128442667 G>T maps to NM_016048.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:55967070 C>A maps to NM_024710.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr7:16348240 A>G maps to NM_001101426.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:128849007 C>T maps to ENST00000418265 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:128875700 T>G maps to ENST00000418265 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:128849433 G>A maps to ENST00000418265 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:18546131 G>T maps to NM_016368.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:33033184 C>G maps to ENST00000262650 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:33067497 A>T maps to ENST00000262650 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr20:33026419 C>T maps to ENST00000262650 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:33068417 G>T maps to ENST00000262650 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr20:33068414 T>C maps to ENST00000262650 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr20:33077154 G>A maps to ENST00000262650 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr16:47462784 C>T maps to NM_030790.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:47189630 C>A maps to NM_030790.3 *613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:2930909 A>T maps to NM_018463.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:2927443 G>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:2932972 C>T maps to NM_018463.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr12:2930954 C>T maps to NM_018463.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:2932952 G>T maps to NM_018463.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:310022 G>C maps to NM_032039.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:52201707 C>A maps to NM_181501.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:52240773 C>G maps to NM_181501.1 S1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:52211397 G>T maps to NM_181501.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:52204759 A>G maps to NM_181501.1 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:52206176 G>T maps to NM_181501.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:52216285 C>T maps to NM_181501.1 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:52206158 C>A maps to NM_181501.1 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:145539089 C>T maps to NM_003637.3 N1010N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534112 C>T maps to NM_003637.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145534243 G>T maps to NM_003637.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:145539418 G>T maps to NM_003637.3 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:145533104 G>A maps to NM_003637.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145536119 C>T maps to NM_003637.3 Q738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:145535837 C>T maps to NM_003637.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:145532168 G>T maps to NM_003637.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:145537213 T>C maps to NM_003637.3 C795C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:145537232 C>T maps to NM_003637.3 Q802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:145533109 G>A maps to NM_003637.3 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr1:145534171 G>A maps to NM_003637.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:68607987 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:68596156 G>A maps to ENST00000423218 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:68628072 G>T maps to ENST00000423218 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr15:68609659 C>T maps to ENST00000423218 R886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:68620470 G>A maps to ENST00000423218 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:68617468 C>T maps to ENST00000423218 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr5:52386428 A>C maps to NM_002203.3 *1182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:52351367 A>G maps to NM_002203.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:52360755 G>A maps to NM_002203.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:52371049 G>T did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr5:52368965 C>T maps to NM_002203.3 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:52356876 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:42452119 C>A maps to NM_000419.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:42457993 G>T maps to NM_000419.3 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:42451838 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:42455867 G>A maps to NM_000419.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:42451766 C>A maps to NM_000419.3 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:42457492 C>A maps to NM_000419.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:48153047 C>T maps to NM_002204.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:48156474 G>T maps to NM_002204.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:182347320 C>G maps to NM_000885.4 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:182344886 A>T maps to NM_000885.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:182392051 G>T maps to NM_000885.4 G790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr2:182363443 A>C maps to NM_000885.4 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:182339986 G>T maps to NM_000885.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:182359477 G>T maps to NM_000885.4 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:182399574 C>G maps to NM_000885.4 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:54797564 T>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:54799677 G>T maps to NM_002205.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:54802688 G>A maps to NM_002205.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:54802717 G>A maps to NM_002205.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr12:54801968 C>A maps to NM_002205.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:173340412 G>A maps to ENST00000264106 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:173339728 C>T maps to ENST00000264106 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:173352048 A>T maps to ENST00000264106 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:173355837 A>G maps to ENST00000264106 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:173333935 G>T maps to ENST00000264106 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:173344443 G>A maps to ENST00000264106 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:56101304 G>A maps to ENST00000347027 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:56078919 C>A maps to ENST00000347027 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr12:56090808 C>T maps to ENST00000347027 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:56092537 G>A maps to ENST00000347027 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:56094076 G>T maps to ENST00000347027 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:56088669 C>A maps to ENST00000347027 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:15714632 G>A maps to NM_003638.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:15688875 G>A maps to NM_003638.1 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:15614332 G>A maps to NM_003638.1 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:15646308 G>A maps to NM_003638.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:15689004 T>C maps to NM_003638.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:15614260 C>A maps to NM_003638.1 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:15634291 G>T maps to NM_003638.1 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr10:15697381 G>T maps to NM_003638.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr10:15614329 G>A maps to NM_003638.1 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr10:15634291 G>T maps to NM_003638.1 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:15573120 G>T maps to NM_003638.1 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:15600155 G>T maps to NM_003638.1 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:15639298 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:15617522 C>A maps to NM_003638.1 E815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr10:15760898 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:15658513 T>A maps to NM_003638.1 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr10:15655726 C>T maps to NM_003638.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:15760794 G>A maps to NM_003638.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:15617594 T>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:15655726 C>G maps to NM_003638.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr10:15614365 C>T maps to NM_003638.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr3:37512506 G>T maps to NM_002207.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:37536028 C>T maps to NM_002207.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:37536029 C>T maps to NM_002207.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:37544798 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr3:37574939 A>G maps to NM_002207.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:31419750 C>T maps to ENST00000444228 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:31425862 T>A maps to ENST00000444228 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:31409183 G>T maps to ENST00000444228 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:31414912 C>A maps to ENST00000444228 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:31427912 G>T maps to ENST00000444228 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr16:31424439 C>A maps to ENST00000444228 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:31426311 T>A maps to ENST00000444228 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:31426236 G>A maps to ENST00000444228 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:31434492 G>T maps to ENST00000444228 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr16:31429457 C>G maps to ENST00000444228 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:31427867 G>A maps to ENST00000444228 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:31434962 C>A maps to ENST00000444228 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:31414948 G>C maps to ENST00000444228 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:3655071 G>A maps to NM_002208.4 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:3657178 G>A maps to NM_002208.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:30500666 G>T maps to NM_002209.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:30516759 G>A maps to NM_002209.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:30486882 C>A maps to NM_002209.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr16:30521708 G>T maps to NM_002209.2 E846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:30500469 C>T maps to NM_002209.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr16:30500675 A>G maps to NM_002209.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:30500430 C>T maps to NM_002209.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:31336930 G>T maps to NM_001145808.1 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31332581 C>T maps to NM_001145808.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:31283250 G>C maps to NM_001145808.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr16:31332814 C>A maps to NM_001145808.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:31282350 G>T maps to NM_001145808.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:31309268 T>C maps to NM_001145808.1 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:31309100 G>T maps to NM_001145808.1 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:31308875 G>A maps to NM_001145808.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:31332904 C>T maps to NM_001145808.1 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:31339482 C>G maps to NM_001145808.1 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:31309151 G>T maps to NM_001145808.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31277364 C>A maps to NM_001145808.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:31339509 G>T maps to NM_001145808.1 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr16:31309181 G>T maps to NM_001145808.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:31340615 C>T maps to NM_001145808.1 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:187533637 G>A maps to NM_002210.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:187506202 A>G maps to NM_002210.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:187531955 G>T maps to NM_002210.3 G776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:187528563 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:31374571 G>T maps to NM_000887.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:31388319 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:31371151 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:31371362 G>T maps to NM_000887.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr16:31384695 C>T maps to NM_000887.3 Y831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr16:31372508 G>A maps to NM_000887.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:31391127 G>T maps to NM_000887.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:31373166 C>A maps to NM_000887.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:31388166 A>T maps to NM_000887.3 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr16:31383062 C>T maps to NM_000887.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:31391337 A>T maps to NM_000887.3 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr10:33217115 C>A maps to ENST00000374956 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:33209283 G>A maps to ENST00000374956 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:33221493 T>A maps to ENST00000374956 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:70521701 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:70521702 C>G did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:70524813 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:70524988 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:70524985 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:70521716 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:3939949 G>T maps to NM_170678.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:46310028 T>A maps to NM_000211.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:46330267 C>T maps to NM_000211.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr21:46321418 G>C maps to NM_000211.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr21:46311722 C>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr21:46326914 G>T maps to NM_000211.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:46308662 C>A maps to NM_000211.3 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr21:46319065 C>T maps to NM_000211.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr21:46313396 G>A maps to NM_000211.3 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:45376866 C>A maps to NM_000212.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45384960 C>T maps to NM_000212.2 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:45361944 C>T maps to NM_000212.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr17:45361972 C>A maps to NM_000212.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:45369931 C>A maps to NM_000212.2 S563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:73750666 G>A maps to NM_001005619.1 V1373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:73736481 G>A maps to NM_001005619.1 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:73735959 G>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr17:73735772 G>A maps to NM_001005619.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:124578286 C>A maps to NM_002213.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:124482529 C>T maps to NM_002213.3 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:160958300 A>G maps to NM_000888.3 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:160994644 T>A maps to NM_000888.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:161056553 G>T maps to NM_000888.3 C7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:161051902 T>G maps to NM_000888.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:53588065 G>T maps to NM_000889.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:20441684 G>T maps to NM_002214.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:20418722 T>G maps to NM_002214.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:20441522 A>G maps to NM_002214.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr7:20449247 C>A maps to NM_002214.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:20418672 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:20431052 G>T maps to NM_002214.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:20445750 A>G maps to NM_002214.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:20421492 C>T maps to NM_002214.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr13:102250507 G>T maps to NM_004791.1 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:102235681 C>A maps to NM_004791.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:102235703 C>A maps to NM_004791.1 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:102367913 G>T maps to NM_004791.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr13:102250500 A>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr13:102235703 C>A maps to NM_004791.1 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:102231636 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr13:102359163 C>G maps to NM_004791.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:52816057 C>A maps to NM_002215.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr3:52814364 C>A maps to NM_002215.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:52816081 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:52818396 C>T maps to NM_002215.2 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:52825614 G>T maps to NM_002215.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:52815975 C>A maps to NM_002215.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:52825804 C>T maps to NM_002215.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:52818318 G>T maps to NM_002215.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:52812519 C>A maps to NM_002215.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr3:52825827 G>A maps to NM_002215.2 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:52825632 C>T maps to NM_002215.2 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:7786919 C>T maps to NM_002216.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:7755191 G>A maps to NM_002216.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr10:7759699 C>A maps to NM_002216.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:7773946 C>T maps to NM_002216.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:7774361 C>A maps to NM_002216.2 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:7773793 C>A maps to NM_002216.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:7755206 T>G maps to NM_002216.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:7771948 T>A maps to NM_002216.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:52836351 C>T maps to NM_002217.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:52858332 T>G did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:7618422 C>T maps to ENST00000256861 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7614296 G>T maps to NM_001001851.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:7618493 C>A maps to ENST00000256861 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:7611658 G>T maps to ENST00000256861 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:7618974 C>A maps to ENST00000256861 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:7658062 T>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:7708825 C>A maps to ENST00000256861 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr10:7618932 G>A maps to ENST00000256861 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr10:7608071 C>T maps to ENST00000256861 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:7682811 A>T maps to ENST00000256861 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:7679320 G>A maps to ENST00000256861 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:7608353 T>C maps to ENST00000256861 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:7683903 G>A maps to ENST00000256861 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:7679398 G>T maps to ENST00000256861 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr10:7608296 C>T maps to ENST00000256861 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr10:7611747 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:7679257 C>T maps to ENST00000256861 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:7683888 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:7621836 G>A maps to ENST00000256861 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:54817332 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:54783878 G>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:54783870 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:54781459 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:54780085 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:54817492 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:54783841 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:54783838 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:54784368 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:54783744 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:54823427 T>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:54783436 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:54817377 A>G did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:54785034 C>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:54783876 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:54814954 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:54783847 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:54784518 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:54783746 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:54783889 T>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:54785021 G>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:54784217 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:54783792 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:54783922 G>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:54785080 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:54776400 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:54818408 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:54800518 C>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:54781506 G>T did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr23:54785154 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:54783459 G>C did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr23:54783793 G>A did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr23:54783698 G>T did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:54783621 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:54800581 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:54777567 G>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:54785243 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:54783637 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:54777683 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr23:54785264 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:54784413 G>C did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr5:156608053 T>C maps to NM_005546.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:156655368 T>A maps to NM_005546.3 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:156675974 C>A maps to NM_005546.3 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:156608056 C>T maps to NM_005546.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:160851745 C>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:160849121 G>T maps to NM_017625.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:160850417 G>A maps to NM_017625.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:160851994 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:160851994 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:160914947 T>C maps to NM_080878.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:160914953 C>T maps to NM_080878.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:160920405 C>T maps to NM_080878.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:78616924 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:78618572 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:78618571 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:78618509 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:78622625 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:78616852 G>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:78618447 G>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:78616642 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:78618149 G>C did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:78618124 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:78622628 C>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:78618172 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:48835305 C>T maps to NM_021999.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr13:48832950 C>T maps to NM_021999.4 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:93412787 C>A maps to NM_014216.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr14:93408112 C>A maps to NM_014216.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:93412781 G>A maps to NM_014216.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:41794613 C>T maps to NM_002220.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:226923449 G>T maps to NM_002221.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:226822506 C>A maps to NM_002221.3 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:226923662 C>G maps to NM_002221.3 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:41231330 T>G maps to NM_025194.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr3:4712559 G>A maps to ENST00000356617 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:4774904 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:4711403 G>T maps to ENST00000356617 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:4712517 C>T maps to ENST00000356617 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:4856129 G>T maps to ENST00000356617 E2527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr3:4712496 G>A maps to ENST00000356617 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:26775286 T>C maps to NM_002223.2 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:26636690 C>G maps to NM_002223.2 L1984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:26818886 G>A maps to NM_002223.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:26775202 C>T maps to NM_002223.2 Q1086Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:26809336 A>T maps to NM_002223.2 C779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:26553191 C>G did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr12:26835600 G>C maps to NM_002223.2 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:26493141 C>G maps to NM_002223.2 L2659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:26551832 G>A maps to NM_002223.2 L2558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr12:26810658 C>A maps to NM_002223.2 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:26784834 C>G maps to NM_002223.2 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:26775301 T>C maps to NM_002223.2 G1053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:33626577 C>T maps to ENST00000374316 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:33653452 C>G maps to ENST00000374316 S1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr6:33654856 C>G maps to ENST00000374316 L2017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:33638230 G>T maps to ENST00000374316 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:33650359 G>A maps to ENST00000374316 P1512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr6:33636798 C>T maps to ENST00000374316 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr6:33639881 C>G maps to ENST00000374316 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:33638116 C>T maps to ENST00000374316 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:33626604 C>T maps to ENST00000374316 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106075104 C>A maps to NM_033397.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:106074327 C>A maps to NM_033397.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr10:106074618 C>T maps to NM_033397.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:106075425 G>A maps to NM_033397.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:96993503 C>T maps to ENST00000420728 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:96993916 C>T maps to ENST00000420728 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr16:19126971 C>T maps to NM_001034841.3 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:35199147 G>T maps to NM_003024.2 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:35107375 A>C maps to NM_003024.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:35147372 G>A maps to NM_003024.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:35229037 A>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr21:35138244 C>T maps to NM_003024.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr21:35208838 G>A maps to NM_003024.2 E1188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:35186366 G>T maps to NM_003024.2 V906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:35183406 G>T maps to NM_003024.2 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr21:35147396 A>G maps to NM_003024.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr21:35229121 C>T maps to NM_003024.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr21:35124112 A>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr21:35122619 T>C maps to NM_003024.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:24533499 T>A maps to NM_006277.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr2:24533249 C>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:24494746 T>C maps to NM_006277.2 K715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr2:24498700 G>T maps to NM_006277.2 Y654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:24516555 C>G did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr15:40702869 G>T maps to NM_002225.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152883772 A>T maps to NM_005547.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:152883986 C>T maps to NM_005547.2 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr1:185278148 A>G maps to NM_006469.4 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:185270128 C>T maps to NM_006469.4 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:128252491 C>A maps to NM_017969.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:150690184 C>T maps to NM_203395.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr19:49246722 G>A maps to NM_182575.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:10644640 C>A maps to NM_000214.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr20:10622245 G>A maps to NM_000214.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr20:10632893 G>A maps to NM_000214.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:105614684 C>T maps to NM_002226.3 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr14:105609325 C>T maps to NM_002226.3 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:65323401 C>G maps to NM_002227.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:65323452 G>A maps to NM_002227.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:5029786 C>T maps to NM_004972.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:5126725 C>T maps to NM_004972.3 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr9:5080269 G>T maps to NM_004972.3 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr9:5054629 C>T maps to NM_004972.3 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:5072598 G>T maps to NM_004972.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr9:5081770 A>T maps to NM_004972.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:17937596 G>A maps to NM_000215.3 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:17945770 G>T maps to NM_000215.3 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:17954674 C>A maps to NM_000215.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:17949155 G>A maps to NM_000215.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:17937620 G>A maps to NM_000215.3 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:17947977 C>A maps to NM_000215.3 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:17942125 G>C maps to NM_000215.3 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:6086640 C>A maps to NM_001099433.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr4:6055779 G>C maps to NM_001099433.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:6042409 C>A maps to NM_001099433.1 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:6064086 C>T maps to NM_001099433.1 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:6082015 C>T maps to NM_001099433.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:6087217 G>T maps to NM_001099433.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr4:6114571 C>T maps to NM_001099433.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:146997551 C>T maps to NM_014790.3 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:147051254 G>A maps to NM_014790.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:146991889 T>C maps to NM_014790.3 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:147051333 G>A maps to NM_014790.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:147027965 G>T maps to NM_014790.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:147051273 G>A maps to NM_014790.3 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:147040726 G>T maps to NM_014790.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr5:147012310 A>G maps to NM_014790.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:147021328 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:133930852 G>C maps to NM_001105521.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr10:133948564 A>G maps to NM_001105521.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:133918386 C>T maps to NM_001105521.2 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:133930789 G>T maps to NM_001105521.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr21:27066140 G>A maps to NM_021219.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr11:134010582 G>T maps to NM_032801.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:134014887 T>A maps to NM_032801.3 L249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:15496898 G>A maps to NM_004973.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr6:15468782 G>C maps to NM_004973.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:27872595 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:139791671 G>T maps to NM_030647.1 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:139820321 G>T maps to NM_030647.1 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:59970756 A>T maps to ENST00000356057 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:59967907 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:64975021 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr10:64974625 C>T maps to NM_032776.1 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:64957293 C>A maps to NM_032776.1 G1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:64968212 G>C maps to NM_032776.1 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr10:64967072 G>A maps to NM_032776.1 T1452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:64950683 G>C maps to NM_032776.1 A2087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr10:64960396 G>T maps to NM_032776.1 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227922418 C>A maps to NM_023007.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr1:227921231 G>C maps to NM_023007.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr16:27221722 G>C maps to NM_001145348.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr17:74720118 T>C maps to NM_001081461.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:74720007 G>A maps to NM_001081461.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42127269 G>A maps to NM_005090.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr15:42126986 G>A maps to NM_005090.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr19:51010940 G>T maps to NM_138334.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:75227184 T>G maps to NM_020647.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr8:75227430 C>A maps to NM_020647.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr8:75156934 T>C maps to NM_020647.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr8:75227748 C>T maps to NM_020647.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:42744379 C>G maps to NM_020433.4 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:42747214 C>T maps to NM_020433.4 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:42788289 G>A maps to NM_020433.4 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:42747204 G>A maps to NM_020433.4 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:42744520 G>C maps to NM_020433.4 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr20:42788418 G>A maps to NM_020433.4 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:42788289 G>T maps to NM_020433.4 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:42788414 C>A maps to NM_020433.4 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr20:42814997 G>A maps to NM_020433.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr20:42788301 G>T maps to NM_020433.4 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr20:42815046 G>C maps to NM_020433.4 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:87677996 C>T maps to NM_020655.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:87678561 G>T maps to NM_020655.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr16:87723666 G>C maps to NM_020655.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:87678335 C>A maps to NM_020655.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:87678056 C>A maps to NM_020655.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:87637015 G>A maps to NM_020655.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr16:87678278 G>T maps to NM_020655.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:87678335 C>G maps to NM_020655.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:24040241 G>T maps to NM_032452.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:24040526 C>T maps to NM_032452.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:24041026 G>T maps to NM_032452.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:24041068 C>T maps to NM_032452.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:153949470 C>A maps to NM_006694.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:23450580 C>A maps to NM_032876.4 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:23450491 T>A maps to NM_032876.4 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:59248304 C>A maps to NM_002228.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:12902818 G>C maps to NM_002229.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr17:39912445 G>A maps to NM_021991.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:8503630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:8503727 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:8503683 C>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:8503717 G>A did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:8553413 C>G did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr23:8555902 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:8536380 C>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:8507734 G>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:8538723 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:124196145 C>T maps to NM_001024660.3 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:124351420 G>T maps to NM_001024660.3 R1777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:124438260 C>A maps to NM_001024660.3 R2969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:123813743 G>A maps to NM_001024660.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr3:124437977 G>T maps to NM_001024660.3 L2874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:124153185 G>T maps to NM_001024660.3 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:123987957 C>T maps to NM_001024660.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:124065999 G>A maps to NM_001024660.3 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:124153321 C>A maps to NM_001024660.3 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:124053293 G>C maps to NM_001024660.3 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:124378223 G>T maps to NM_001024660.3 E2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr3:124438298 G>T maps to NM_001024660.3 R2981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:124377364 G>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:124053287 G>A maps to NM_001024660.3 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr3:124193533 G>A maps to NM_001024660.3 K1350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:124048716 G>T maps to NM_001024660.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:124385986 G>A maps to NM_001024660.3 Q2219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:124393413 G>A maps to NM_001024660.3 A2382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:123988083 C>T maps to NM_001024660.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:124160830 A>T maps to NM_001024660.3 K1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:124196165 G>T maps to NM_001024660.3 A1390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:124351378 C>A maps to NM_001024660.3 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr3:124377300 G>A maps to NM_001024660.3 V2019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr3:124165678 G>T maps to NM_001024660.3 E1165*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-NJ-A4YF-01A-12D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:124378303 G>A maps to NM_001024660.3 K2071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:713020 C>G maps to NM_015158.2 S752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr9:730171 G>A maps to NM_015158.2 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr9:740897 C>T maps to NM_015158.2 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr9:711086 C>G maps to NM_015158.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr19:11303851 C>A maps to NM_015493.6 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:62739518 G>T maps to NM_181712.4 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:62728896 G>T maps to NM_181712.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr1:62739506 C>T maps to NM_181712.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:62703975 C>T maps to NM_181712.4 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:62713182 G>T maps to NM_181712.4 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:62734104 T>A maps to NM_181712.4 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:62718807 C>T maps to NM_181712.4 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:62728914 G>T maps to NM_181712.4 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:62734023 C>T maps to NM_181712.4 E722E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:62739725 C>G maps to NM_181712.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:62704014 G>T maps to NM_181712.4 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:62740091 G>T maps to NM_181712.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:75668120 C>A maps to NM_001130089.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:75665695 C>A maps to NM_001130089.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:40273004 T>A maps to NM_021078.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:40271405 G>A maps to NM_021078.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr3:20136891 C>T maps to NM_003884.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:20161126 C>A maps to NM_003884.4 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:20156407 C>T maps to NM_003884.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr11:65482335 C>G maps to NM_182710.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:65482088 C>A maps to NM_182710.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:65480859 G>A maps to NM_182710.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr6:149944337 G>A maps to NM_007044.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr13:30814602 T>C maps to NM_032116.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:44627235 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr16:57789823 G>A maps to NM_005886.2 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:15392291 G>A maps to NM_015209.2 *422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:14925522 C>T maps to NM_201628.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:15430523 C>A maps to NM_201628.2 Y629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:15440971 C>A maps to NM_201628.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:170366650 C>A maps to NM_006063.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:170367346 A>T maps to NM_006063.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:32910117 C>G maps to NM_015483.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:105924080 G>C maps to NM_198439.2 Y445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:41705438 T>C maps to NM_152903.4 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:41705564 T>A maps to NM_152903.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr13:41704874 C>T maps to NM_152903.4 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr13:41706311 C>A maps to NM_152903.4 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:67053804 A>G maps to NM_032505.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:67054222 C>T maps to NM_032505.2 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:5021977 C>A maps to NM_000217.2 C478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:5021668 C>A maps to NM_000217.2 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:5020925 G>T maps to NM_000217.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:5021827 C>T maps to NM_000217.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:5020915 G>A maps to NM_000217.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:5021551 G>T maps to NM_000217.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:111060305 C>T maps to NM_005549.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:111060704 C>T maps to NM_005549.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:111060233 T>A maps to NM_005549.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:111061073 C>A maps to NM_005549.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:111060224 A>G maps to NM_005549.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:111146102 G>A maps to NM_004974.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:111145925 G>C maps to NM_004974.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111146417 G>T maps to NM_004974.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:111146591 C>T maps to NM_004974.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:111146633 G>T maps to NM_004974.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:111146621 C>A maps to NM_004974.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:111216189 G>A maps to NM_002232.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:111216207 C>T maps to NM_002232.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111216069 G>T maps to NM_002232.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:111216141 G>A maps to NM_002232.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr1:111216621 C>A maps to NM_002232.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:111216474 G>A maps to NM_002232.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:30033016 G>T maps to NM_002233.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:30033076 G>T maps to NM_002233.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:30032811 T>A maps to NM_002233.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:30032875 T>C maps to NM_002233.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:30032965 G>A maps to NM_002233.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:30033102 C>A maps to NM_002233.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:30033103 C>A maps to NM_002233.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:30032821 G>T maps to NM_002233.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:30033663 C>A maps to NM_002233.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:30032335 C>T maps to NM_002233.2 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:30032902 G>T maps to NM_002233.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:30032584 C>A maps to NM_002233.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:30033835 C>T maps to NM_002233.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:30033973 C>T maps to NM_002233.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:30032404 G>A maps to NM_002233.2 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr11:30033985 C>A maps to NM_002233.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:5154950 G>T maps to NM_002234.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:5154194 C>T maps to NM_002234.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:5154821 C>A maps to NM_002234.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:5155088 C>T maps to NM_002234.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr12:5154153 C>T maps to NM_002234.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:5155109 C>A maps to NM_002234.2 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:5155013 G>T maps to NM_002234.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:5153657 G>T maps to NM_002234.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:5154974 G>C maps to NM_002234.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:5153876 G>T maps to NM_002234.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr12:5154560 C>T maps to NM_002234.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:5153822 C>G maps to NM_002234.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr12:5154968 C>A maps to NM_002234.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:4919848 C>T maps to NM_002235.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:4920248 C>A maps to NM_002235.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:4920769 A>T maps to NM_002235.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:4920463 A>T maps to NM_002235.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:4920340 G>T maps to NM_002235.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:4919561 G>T maps to NM_002235.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:4920436 G>A maps to NM_002235.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:4920656 C>T maps to NM_002235.3 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr12:4919524 G>T maps to NM_002235.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr12:4919344 T>C maps to NM_002235.3 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:4919407 C>A maps to NM_002235.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:156009857 G>T maps to NM_172159.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:155838621 C>A maps to NM_172160.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:155838504 C>A maps to NM_172160.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr3:156175288 C>G maps to NM_172159.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr3:156249198 G>A maps to NM_172159.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:155861078 C>T maps to NM_003471.3 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:156009857 G>T maps to NM_172159.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:156009788 T>C maps to NM_172159.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:6147571 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:6154458 G>C did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr1:6150512 G>T maps to NM_003636.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:7830684 G>A maps to NM_004732.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:7831099 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:7830693 C>T maps to NM_004732.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:47990217 G>T maps to NM_004975.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:48098459 C>A maps to NM_004975.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:47991189 G>A maps to NM_004975.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:47989795 G>T maps to NM_004975.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:47989977 C>A maps to NM_004975.2 G707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr20:47989744 C>T maps to NM_004975.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:47990290 G>T maps to NM_004975.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:48098894 C>T maps to NM_004975.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:48098842 T>A maps to NM_004975.2 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:73480015 C>A maps to NM_004770.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:73850035 T>C maps to NM_004770.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:73849101 C>A maps to NM_004770.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:73850046 A>C maps to NM_004770.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:73849191 T>C maps to NM_004770.2 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:73848768 A>T maps to NM_004770.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:73848717 C>A maps to NM_004770.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:73849038 C>T maps to NM_004770.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr8:73480034 A>G maps to NM_004770.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:73848561 G>C maps to NM_004770.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr8:73848225 C>A maps to NM_004770.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:73848447 C>A maps to NM_004770.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:73480145 G>A maps to NM_004770.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:73848882 G>A maps to NM_004770.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:17793918 C>T maps to NM_001112741.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:17793273 C>A maps to NM_001112741.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:17793474 C>A maps to NM_001112741.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:17793579 C>A maps to NM_001112741.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr11:17757662 G>A maps to NM_001112741.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:17758088 C>T maps to NM_001112741.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr11:17757770 C>T maps to NM_001112741.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:17793333 G>A maps to NM_001112741.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:17793516 G>A maps to NM_001112741.1 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:75601538 G>T maps to NM_139137.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:75444887 G>A maps to NM_139137.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:75444671 A>C maps to NM_139137.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:75444632 C>A maps to NM_139137.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:75601273 C>A maps to NM_139137.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:75444449 G>T maps to NM_139137.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr12:75601606 T>A maps to NM_139137.2 K53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:75444565 C>A maps to NM_139137.2 G407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr12:75601466 G>C maps to NM_139137.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:75437006 G>A maps to NM_139137.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:75601757 G>T maps to NM_139137.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr12:75601679 G>T maps to NM_139137.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:110768729 C>T maps to NM_004978.4 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:110766517 G>T maps to NM_004978.4 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:110766454 G>T maps to NM_004978.4 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:110754217 G>T maps to NM_004978.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:110766160 C>T maps to NM_004978.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:48822639 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:48825725 G>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:48820028 T>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:48822635 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:48825919 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:119915636 G>A maps to NM_012281.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:119915075 C>T maps to NM_012281.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:120373104 C>A maps to NM_012281.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr7:120373016 G>C maps to NM_012281.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:119915393 C>A maps to NM_012281.2 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr7:119914820 G>C maps to NM_012281.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:119915303 A>G maps to NM_012281.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:119915237 C>A maps to NM_012281.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:119915121 G>T maps to NM_012281.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:119915699 C>T maps to NM_012281.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:119915492 C>A maps to NM_012281.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:120387740 C>A maps to NM_012281.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:119915330 C>T maps to NM_012281.2 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr7:119915060 C>A maps to NM_012281.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr7:119915273 C>A maps to NM_012281.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:112525024 G>A maps to ENST00000315987 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:112524478 C>A maps to ENST00000315987 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:112524583 G>A maps to ENST00000315987 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:112525147 G>T maps to ENST00000315987 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:112524601 G>A maps to ENST00000315987 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:112524484 C>T maps to ENST00000315987 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:112524924 C>A maps to ENST00000315987 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:112525063 G>T maps to ENST00000315987 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:112525078 C>T maps to ENST00000315987 V90V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-97-7937-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr21:35821632 C>A maps to NM_000219.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:108867951 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:108867957 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:108868030 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:223917757 G>T maps to NM_080671.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:223917595 C>A maps to NM_080671.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:223918042 C>T maps to NM_080671.2 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:11053757 C>A maps to NM_002236.4 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:11052722 T>A maps to NM_002236.4 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr2:11053442 C>T maps to NM_002236.4 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:11053961 C>G maps to NM_002236.4 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr2:11053625 C>A maps to NM_002236.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:49626464 C>A maps to NM_002237.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr20:49620824 G>T maps to NM_002237.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626461 C>A maps to NM_002237.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:49626476 C>A maps to NM_002237.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:49620776 G>A maps to NM_002237.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr20:49626617 C>T maps to NM_002237.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:49620725 G>T maps to NM_002237.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:49626311 C>T maps to NM_002237.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:49626761 C>T maps to NM_002237.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:49621193 G>C maps to NM_002237.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr18:77659455 G>C maps to NM_012283.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr18:77659125 C>A maps to NM_012283.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:84256190 G>T maps to NM_172347.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:84270704 G>T maps to NM_172347.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84256461 G>T maps to NM_172347.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr16:84256089 G>A maps to NM_172347.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:211192226 G>A maps to NM_172362.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:211263911 G>T maps to NM_172362.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:211192454 C>T maps to NM_172362.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:211192568 G>T maps to NM_172362.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:210970994 G>T maps to NM_172362.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr1:210977508 C>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:211192292 G>C maps to NM_172362.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:211192255 G>A maps to NM_172362.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:210971015 C>A maps to NM_172362.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:210948701 G>A maps to NM_172362.2 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:211192439 G>A maps to NM_172362.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:211093085 G>T maps to NM_172362.2 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:211093213 G>T maps to NM_172362.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:210970943 G>C maps to NM_172362.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:150648008 C>A maps to NM_000238.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:150643982 G>T maps to NM_000238.2 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:150643994 G>T maps to NM_000238.2 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:49950227 G>A maps to NM_012284.1 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:49944095 C>T maps to NM_012284.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:49933243 G>A maps to NM_012284.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:40321503 G>A maps to NM_012285.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:40312059 A>T maps to NM_012285.2 *1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr17:40321563 C>A maps to NM_012285.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:40315735 G>A maps to NM_012285.2 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:63483637 C>A maps to NM_139318.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:63416869 C>G maps to NM_139318.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:63483589 T>A maps to NM_139318.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:63316463 T>C maps to NM_139318.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:63447715 C>T maps to NM_139318.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:63246541 G>T maps to NM_139318.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:63447816 T>A maps to NM_139318.3 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:63417142 C>T maps to NM_139318.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:63416959 C>G maps to NM_139318.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr14:63174540 C>A maps to NM_139318.3 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:63174516 A>T maps to NM_139318.3 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:63174776 C>A maps to NM_139318.3 G806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:63447965 G>T maps to NM_139318.3 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:63174903 C>A maps to NM_139318.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:63447705 C>A maps to NM_139318.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr14:63269074 G>T maps to NM_139318.3 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:61621388 G>T maps to NM_030779.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:61611611 C>G maps to NM_030779.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:61607485 C>A maps to NM_030779.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:61613224 A>T maps to NM_030779.2 K433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr17:61611299 C>T maps to NM_030779.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:61607587 G>C maps to NM_030779.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:61607737 A>T maps to NM_030779.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr17:61607560 C>T maps to NM_030779.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:163256900 G>C maps to NM_033272.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:163241387 C>T maps to NM_033272.2 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:163374375 C>A maps to NM_033272.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:163361084 A>T maps to NM_033272.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:163292065 G>T maps to NM_033272.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:163693087 G>T maps to NM_033272.2 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:163374549 T>C maps to NM_033272.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:163361033 T>C maps to NM_033272.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:163292017 G>A maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:163230090 G>T maps to NM_033272.2 Y1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr2:163302833 C>A maps to NM_033272.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:163360954 G>A maps to NM_033272.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:163241414 A>G maps to NM_033272.2 D915D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:163393573 A>G maps to NM_033272.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:163694974 G>A maps to NM_033272.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:163302908 C>T maps to NM_033272.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:163241411 G>T maps to NM_033272.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:19575002 C>T maps to NM_144633.2 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:19554548 G>T maps to NM_144633.2 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr3:19574961 C>T maps to NM_144633.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:19436594 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:19384092 A>T maps to NM_144633.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:19554469 C>T maps to NM_144633.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr3:19575177 C>T maps to NM_144633.2 Q971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:19498289 C>A maps to NM_144633.2 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:19295164 C>A maps to NM_144633.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr3:19554682 C>T maps to NM_144633.2 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr3:19575438 G>T maps to NM_144633.2 G1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:19559530 G>T maps to NM_144633.2 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:19575180 C>A maps to NM_144633.2 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:19479672 G>T maps to NM_144633.2 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:19295219 G>T maps to NM_144633.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:19492849 G>C maps to NM_144633.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:19389398 G>C maps to NM_144633.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:19295155 C>T maps to NM_144633.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:170145846 C>T maps to NM_001034837.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:96047360 C>T maps to NM_013434.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:96012781 C>A maps to NM_001034914.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:96040642 C>T maps to NM_013434.4 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr4:20852204 G>C maps to ENST00000382152 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:128709093 T>G maps to NM_000220.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:128712279 C>A maps to NM_000220.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:160011197 G>T maps to NM_002241.4 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:160012316 C>A maps to NM_002241.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:160011695 A>T maps to NM_002241.4 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:160012205 C>G maps to NM_002241.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:17409095 G>C maps to NM_000525.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr11:17408815 G>A maps to NM_000525.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:17409335 G>A maps to NM_000525.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr17:21319506 C>A maps to NM_021012.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:21318689 C>T maps to NM_021012.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:21318671 G>T maps to NM_021012.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:21318671 G>T maps to NM_021012.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:21319541 G>T maps to NM_021012.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr17:21319334 T>C maps to NM_021012.4 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:21319718 C>A maps to NM_021012.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:21319506 C>A maps to NM_021012.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:21318722 C>T maps to NM_021012.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:21319079 C>T maps to NM_021012.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:48967505 A>T maps to NM_170720.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr21:39671974 G>A maps to NM_170736.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128551 C>T maps to NM_018658.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128671 C>G maps to NM_018658.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128680 C>T maps to NM_018658.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68128950 C>G maps to NM_018658.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:68128481 G>A maps to NM_018658.1 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:68128470 T>A maps to NM_018658.1 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr17:68128524 T>C maps to NM_018658.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:68128794 T>G maps to NM_018658.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:68128428 C>T maps to NM_018658.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr17:68128494 C>A maps to NM_018658.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:68129280 C>A maps to NM_018658.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:68171770 C>T maps to NM_000891.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:68171861 C>A maps to NM_000891.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:68171797 C>A maps to NM_000891.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr17:68171197 C>A maps to NM_000891.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:68171722 C>A maps to NM_000891.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:68171490 G>A maps to NM_000891.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:68171366 G>T maps to NM_000891.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:155711581 T>C maps to NM_002239.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:155711557 C>T maps to NM_002239.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:155566146 C>A maps to NM_002239.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:155555400 G>T maps to NM_002239.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:155566152 C>T maps to NM_002239.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:155711421 C>A maps to NM_002239.2 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:155566331 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:155555775 C>A maps to NM_002239.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:155711658 C>G maps to NM_002239.2 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:155555913 C>A maps to NM_002239.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:155711818 C>T maps to NM_002239.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:155711506 T>C maps to NM_002239.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:155711686 C>T maps to NM_002239.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:155711377 C>A maps to NM_002239.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:155555739 C>A maps to NM_002239.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:155711599 C>A maps to NM_002239.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr22:38824023 C>T maps to NM_152868.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr22:38822910 C>T maps to NM_152868.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:38824041 G>A maps to NM_152868.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr22:38823006 C>A maps to NM_152868.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:38823369 C>A maps to NM_152868.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr22:38823150 G>A maps to NM_152868.1 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr22:38824098 G>T maps to NM_152868.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:128786319 C>A maps to NM_000890.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:128781305 C>T maps to NM_000890.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:128781479 C>T maps to NM_000890.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:128781776 C>A maps to NM_000890.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:128786490 G>A maps to NM_000890.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr21:39086535 T>C maps to NM_002240.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:21926523 C>T maps to NM_004982.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21926238 G>A maps to NM_004982.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr12:21919148 C>T maps to NM_004982.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:21919013 G>C maps to NM_004982.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr12:21919022 A>G maps to NM_004982.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:160054149 C>T maps to NM_004983.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:233802491 C>T maps to NM_002245.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:233802734 G>A maps to NM_002245.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:233802554 C>T maps to NM_002245.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:88658610 C>A maps to NM_138318.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:88652441 G>T maps to NM_138318.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:88729805 G>A maps to NM_138318.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr14:88729601 C>A maps to NM_138318.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:88651917 C>A maps to NM_138318.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr14:88729650 C>T maps to NM_138318.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr14:88729809 C>A maps to NM_138318.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:47748863 G>A maps to NM_022055.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:90651010 G>C maps to NM_022054.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr14:90650563 C>T maps to NM_022054.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:90651130 G>A maps to NM_022054.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr14:90650632 G>T maps to NM_022054.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:90651220 G>C maps to NM_022054.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:90650806 C>A maps to NM_022054.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr14:90650621 C>T maps to NM_022054.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:90650635 C>T maps to NM_022054.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr14:90651235 C>T maps to NM_022054.2 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:90650452 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:90651205 C>T maps to NM_022054.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:90651262 G>T maps to NM_022054.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr14:90650453 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:43379217 G>A maps to ENST00000372861 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:39286894 G>T maps to NM_032115.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:39284122 G>A maps to NM_032115.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr6:39284684 C>G maps to NM_032115.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:39278774 G>A maps to NM_031460.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:39271731 C>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:39271736 C>A maps to NM_031460.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:39267445 C>T maps to NM_031460.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:118969188 C>T maps to NM_181840.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:118960760 C>T maps to NM_181840.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:118969761 T>A maps to NM_181840.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:118969417 G>T maps to NM_181840.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr10:118969398 G>A maps to NM_181840.1 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr10:118969032 C>A maps to NM_181840.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:215259912 G>A maps to NM_001017425.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215259900 G>C maps to NM_001017425.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:215259841 A>T maps to NM_001017425.2 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:215259894 C>A maps to NM_001017425.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:215256770 G>T maps to NM_001017425.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:215259846 G>T maps to NM_001017425.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:215368368 C>A maps to NM_001017425.2 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:215342566 A>T maps to NM_001017425.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:215408280 C>T maps to NM_001017425.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:215345447 G>T maps to NM_001017425.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:215408400 C>A maps to NM_001017425.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:26951264 G>T maps to NM_002246.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:26951258 C>T maps to NM_002246.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr2:26950616 C>T maps to NM_002246.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:38817874 C>T maps to NM_004823.1 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:38817494 C>A maps to NM_004823.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:38817410 G>T maps to NM_004823.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:38817628 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:140630623 G>T maps to NM_016601.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr8:140630605 G>A maps to NM_016601.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:140630668 G>A maps to NM_016601.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:140630862 G>T maps to NM_016601.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:140630539 G>T maps to NM_016601.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:78771773 A>G maps to NM_001161352.1 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:78708917 G>T maps to NM_001161352.1 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:78669849 G>A maps to NM_001161352.1 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr10:78674703 G>A maps to NM_001161352.1 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:78708950 G>C maps to NM_001161352.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:78651441 C>G maps to NM_001161352.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:78651357 C>T maps to NM_001161352.1 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:78647149 C>A maps to NM_001161352.1 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr10:78647080 C>A maps to NM_001161352.1 R1218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr5:169805872 G>A maps to NM_004137.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:169805857 G>A maps to NM_004137.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr5:169812349 C>A maps to NM_004137.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:169805728 G>T maps to NM_004137.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:178560586 C>A maps to NM_005832.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr19:18096156 G>A maps to ENST00000222249 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:113698507 G>A maps to NM_021614.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:113831759 G>T maps to NM_021614.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr5:113831648 G>T maps to NM_021614.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:154842044 G>A maps to NM_002249.4 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:154841864 G>A maps to NM_002249.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:154744704 C>A maps to NM_002249.4 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:154744757 C>A maps to NM_002249.4 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:154680541 C>G maps to NM_002249.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:154744527 G>A maps to NM_002249.4 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:154680721 G>T maps to NM_002249.4 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:154841867 G>A maps to NM_002249.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:44273612 G>A maps to NM_002250.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:44271810 G>T maps to NM_002250.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:44273592 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:44280782 C>T maps to NM_002250.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr11:2592630 C>T maps to NM_000218.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr11:2591892 C>T maps to NM_000218.2 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:62073779 C>T maps to NM_172107.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:62046379 G>T maps to NM_172107.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046307 C>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62046309 G>T maps to NM_172107.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:62078121 G>T maps to NM_172107.2 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:62044882 G>C maps to NM_172107.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:62038383 C>A maps to NM_172107.2 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:62038173 C>A maps to NM_172107.2 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:133492608 G>A maps to NM_004519.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:133187729 C>T maps to NM_004519.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:133192463 C>A maps to NM_004519.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:133146535 C>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr8:133141655 C>A maps to NM_004519.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:41284240 C>T maps to NM_004700.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:41285913 G>A maps to NM_004700.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr6:73843263 C>A maps to NM_001160133.1 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:73904620 C>A maps to NM_001160133.1 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:50589842 T>C maps to NM_173605.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:99441528 C>A maps to NM_020697.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:99441274 G>A maps to NM_020697.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr8:99441376 T>A maps to NM_020697.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:99440815 C>A maps to NM_020697.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr8:99440332 C>A maps to NM_020697.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:99441238 C>A maps to NM_020697.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr8:99440314 G>A maps to NM_020697.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:99440677 C>T maps to NM_020697.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:99440548 C>T maps to NM_020697.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:18112295 C>T maps to NM_002252.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:18112325 C>A maps to NM_002252.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:18112662 G>T maps to NM_002252.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:18113189 G>A maps to NM_002252.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:18113213 A>G maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:138669215 G>A maps to ENST00000298480 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:138656984 A>T maps to ENST00000298480 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr9:138651665 C>G maps to ENST00000298480 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr9:138656974 C>T maps to ENST00000298480 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr9:138641991 C>G maps to ENST00000298480 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:138669353 C>T maps to ENST00000298480 N840N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:138670654 C>T maps to ENST00000298480 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:138651659 G>T maps to ENST00000298480 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:138660718 C>A maps to ENST00000298480 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:138678206 G>C maps to ENST00000298480 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr9:138678315 G>T maps to ENST00000298480 E1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:138671203 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:196227520 G>T maps to NM_198503.2 S1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:196309512 C>A maps to NM_198503.2 G581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:196309546 C>T maps to NM_198503.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:196227501 C>A maps to NM_198503.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr1:196205162 G>T maps to NM_198503.2 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:196302977 C>A maps to NM_198503.2 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:196395109 A>T maps to NM_198503.2 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:196227444 A>C maps to NM_198503.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:196395103 C>T maps to NM_198503.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:196438173 G>T maps to NM_198503.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:196434517 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:196438126 G>T maps to NM_198503.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:196227459 G>T maps to NM_198503.2 G1025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:196227383 C>A maps to NM_198503.2 E1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr1:196342360 C>A maps to NM_198503.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:196311312 T>C maps to NM_198503.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:196205147 A>T maps to NM_198503.2 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr1:196197421 C>A maps to NM_198503.2 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36671867 C>T maps to NM_001031836.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:36788632 C>A maps to NM_001031836.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:36763323 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:36671879 C>T maps to NM_001031836.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:36691146 A>C maps to NM_001031836.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:36641963 A>G maps to NM_001031836.2 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:36694373 G>T maps to NM_001031836.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr8:36766898 C>G maps to NM_001031836.2 S726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:36793065 G>A maps to NM_001031836.2 K1026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:36776408 G>T maps to NM_001031836.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr8:36663851 C>A maps to NM_001031836.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:36766950 T>A maps to NM_001031836.2 Y743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:36664968 G>T did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr8:36776395 C>T maps to NM_001031836.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:36698037 C>T maps to NM_001031836.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:110984553 C>A maps to NM_014379.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:110980757 G>T maps to NM_014379.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:110984679 G>A maps to NM_014379.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr8:110986566 G>A maps to NM_014379.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:110984780 C>A maps to NM_014379.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:110980454 G>T maps to NM_014379.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:2717918 C>T maps to NM_133497.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:2719073 C>A maps to NM_133497.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:2729456 C>A maps to NM_133497.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:2717771 G>A maps to NM_133497.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:24035814 C>T maps to NM_001142730.1 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:24039634 C>G maps to NM_001142730.1 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:109893982 C>G maps to NM_031954.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr12:109898545 C>A maps to NM_031954.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr17:7256608 C>T maps to NM_001002914.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:7256788 G>T maps to NM_001002914.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr13:77460025 G>A maps to NM_138444.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:77727788 C>A maps to NM_023930.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:77727719 G>A maps to NM_023930.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:34297899 G>T maps to ENST00000422820 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr19:34302441 G>T maps to ENST00000422820 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:34302444 C>G maps to ENST00000422820 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:143586459 G>T maps to NM_020768.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr5:143853424 C>T maps to NM_020768.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr5:143586714 C>T maps to NM_020768.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:143586313 C>T maps to NM_020768.3 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:143586837 G>T maps to NM_020768.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:67354629 T>C maps to NM_001100915.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr17:73059132 G>A maps to NM_015353.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr17:73055631 C>T maps to NM_015353.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:215760008 G>T maps to NM_016121.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:215759873 G>C maps to NM_016121.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:215792538 C>T maps to NM_016121.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:215793783 G>T maps to NM_016121.3 G758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:215752374 A>T maps to NM_016121.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:2752430 G>T maps to NM_018992.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:66103259 G>A maps to ENST00000451741 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:66098288 G>T maps to NM_153033.3 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:66104161 C>T maps to NM_153033.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr4:44177199 A>G maps to NM_198353.2 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:44177088 T>A maps to NM_198353.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr4:44177096 G>A maps to NM_198353.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr4:44177163 G>T maps to NM_198353.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr4:44176968 G>T maps to NM_198353.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:44450243 G>A maps to NM_198353.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:44177088 T>A maps to NM_198353.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr13:103443271 A>G maps to NM_024089.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:103436858 T>A maps to NM_024089.2 K499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:108348423 T>C maps to NM_153705.4 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:108357017 T>A maps to NM_153705.4 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr19:48887601 G>C maps to NM_006801.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:6505921 G>A maps to NM_006854.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:6502739 G>A maps to NM_001100603.1 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:23405645 G>A maps to NM_001009999.2 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:23405516 G>A maps to NM_001009999.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:18207729 A>G maps to ENST00000388870 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:18200801 G>T maps to ENST00000388870 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:67013472 A>T maps to NM_012308.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:67020927 G>A maps to NM_012308.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:66948815 G>T maps to NM_012308.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:67021878 C>G maps to NM_012308.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr11:67021836 C>T maps to NM_012308.2 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:121878957 G>A maps to ENST00000377071 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:121951130 C>A maps to ENST00000377071 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:121947690 G>T maps to ENST00000377071 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:122012499 T>C did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:121882327 T>A maps to ENST00000377071 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:86718114 C>T maps to NM_001146688.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:137759815 C>A maps to NM_016604.3 S1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:137759900 G>T maps to NM_016604.3 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:137754724 A>G maps to NM_016604.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:137753187 A>T maps to NM_016604.3 G1108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:137727660 G>C maps to NM_016604.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr5:137728896 G>A maps to NM_016604.3 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:137727579 G>T maps to NM_016604.3 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:44137188 C>A maps to NM_014663.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:5032933 C>T maps to NM_015015.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:6984405 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:6984339 A>G maps to NM_015061.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:6814717 A>T maps to NM_015061.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6893232 G>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:7174677 C>A maps to NM_015061.3 Y1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr9:6986620 C>A maps to NM_015061.3 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:6888032 A>G maps to NM_015061.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:7011842 C>T maps to NM_015061.3 H644H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr9:6986602 C>T maps to NM_015061.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr9:7049118 G>T maps to NM_015061.3 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:94731099 G>C maps to NM_018039.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:94731486 G>T maps to NM_018039.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:94759389 G>A maps to NM_001161630.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:94759533 C>T maps to NM_001161630.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:406209 G>A maps to NM_001042603.1 Q1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:404813 G>A maps to NM_001042603.1 D1460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr12:419115 C>A maps to NM_001042603.1 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:419076 C>T maps to NM_001042603.1 R1090R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:427405 G>A maps to NM_001042603.1 V921V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:202715448 T>A maps to ENST00000367264 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:202704716 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:202699082 C>A maps to ENST00000367264 E1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:202698302 T>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:53230769 G>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:53227963 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:53245283 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:53239922 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:53231147 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:53239737 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:53222384 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:53222184 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:53230826 C>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:53223698 G>C did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:53245267 G>C did not map to a codon.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr23:53228024 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:53246991 C>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:53222720 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:53230808 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:53243951 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:53226202 G>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:53244009 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:53225190 C>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:53245041 G>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:53225895 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:53228301 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:53245158 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:53222366 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr24:21894529 C>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr24:21869167 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr24:21870184 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr24:21871584 C>A did not map to a codon.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr24:21870789 C>G did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr24:21893665 C>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr24:21883060 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:44949009 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr23:44938571 C>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:44929566 A>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:44928906 C>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:44918510 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:44966736 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:44911045 A>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:44949025 A>G did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:44879871 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr23:44922914 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:44929404 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:44970626 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752587 G>C maps to NM_001080424.1 V994V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752683 G>A maps to NM_001080424.1 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7752914 G>C maps to NM_001080424.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr4:55972874 A>G maps to NM_002253.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:55964400 G>T maps to NM_002253.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:55961742 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:55979501 G>T maps to NM_002253.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55970999 G>T maps to NM_002253.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:55976849 G>T maps to NM_002253.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:55971026 A>T maps to NM_002253.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:55972943 A>T maps to NM_002253.2 C482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:55946211 C>A maps to NM_002253.2 E1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:55955876 C>G maps to NM_002253.2 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:55971997 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:55976615 G>T maps to NM_002253.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr4:55958873 T>C maps to NM_002253.2 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:55976588 C>A maps to NM_002253.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr4:55962477 G>T maps to NM_002253.2 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:55973986 C>G maps to NM_002253.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:60999135 T>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:10597494 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:10610573 G>A maps to NM_203500.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr19:10599865 A>T did not map to a codon.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr19:10610132 G>A maps to NM_203500.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:10602256 C>A maps to NM_203500.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:10599866 C>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:10610588 C>A maps to NM_203500.1 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:10602718 T>A maps to NM_203500.1 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:10599898 G>A maps to NM_203500.1 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:10610108 G>A maps to NM_203500.1 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:10610211 G>A maps to NM_203500.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr19:10602542 G>C maps to NM_203500.1 Y345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:142641807 C>A maps to NM_000420.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:142651422 C>A maps to NM_000420.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:142651327 C>T maps to NM_000420.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:142640390 G>A maps to NM_000420.2 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:142643377 G>A maps to NM_000420.2 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:142658953 A>T maps to NM_000420.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr7:142651423 C>A maps to NM_000420.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr7:142641792 G>A maps to NM_000420.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:142639610 G>A maps to NM_000420.2 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:142640583 A>T maps to NM_000420.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr12:91449622 G>A maps to NM_007035.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:91449758 T>A maps to NM_007035.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:91449194 G>A maps to NM_007035.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:91449754 G>A maps to NM_007035.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:73952132 G>A maps to ENST00000370385 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:73951299 G>T maps to ENST00000370384 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:32503441 T>A maps to NM_006559.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:62757845 T>A maps to NM_152688.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:62757887 C>A maps to NM_152688.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:62390882 G>T maps to NM_152688.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:62995787 C>A maps to NM_152688.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:136561008 A>C maps to NM_006558.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:136594171 G>T maps to NM_006558.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr8:136554895 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr14:24905376 C>T maps to NM_015299.2 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:24900868 G>T maps to NM_015299.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:6422414 C>T maps to NM_003685.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:6420439 C>A maps to NM_003685.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:2812305 T>C maps to NM_014878.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:2820098 C>A did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr9:2811462 C>A maps to NM_014878.4 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:2834128 T>C maps to NM_014878.4 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:19571463 C>T maps to NM_015047.1 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:19549905 G>C maps to NM_015047.1 S787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:26955576 C>A maps to NM_014680.2 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:26962060 C>T maps to NM_014680.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:26965368 G>A maps to NM_014680.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:26965112 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:26960961 C>A maps to NM_014680.2 V1071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:26961533 C>A did not map to a codon.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr17:26942150 C>A maps to NM_014680.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:26961559 G>A maps to NM_014680.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr15:64673549 G>A maps to NM_014736.4 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:141318257 C>T maps to NM_014773.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:48647873 C>G maps to NM_001080394.1 Y870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr8:48309165 A>T maps to NM_001080394.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:48309094 A>T maps to NM_001080394.1 K229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:48309123 T>A maps to NM_001080394.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:48614371 C>T maps to NM_001080394.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr8:48641527 G>A maps to NM_001080394.1 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:85695048 G>T maps to NM_014615.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr16:85694871 C>G maps to NM_014615.2 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:85689988 G>T maps to NM_014615.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:85690991 C>T maps to NM_014615.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr16:85667700 G>A maps to NM_014615.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr16:85690011 T>C maps to NM_014615.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:73487508 A>T maps to ENST00000375248 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:73487523 C>T maps to ENST00000375248 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:73489053 C>T maps to ENST00000375248 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:73485367 G>T maps to ENST00000375248 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr17:73492398 C>T maps to ENST00000375248 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr8:126091003 C>G maps to ENST00000377985 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:126051106 G>A maps to ENST00000377985 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:126090978 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:126056933 T>A maps to ENST00000377985 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr8:126056120 G>A maps to ENST00000377985 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:126085511 G>A maps to ENST00000377985 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:197402023 G>A maps to NM_014687.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:197428578 C>A maps to NM_014687.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:197427573 C>A maps to NM_014687.1 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:197430433 C>T maps to NM_014687.1 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:6860174 G>T maps to NM_014743.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:6863977 C>G maps to NM_014743.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:6863503 C>T maps to NM_014743.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:6865423 G>T maps to NM_014743.2 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr4:6863369 G>T maps to NM_014743.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:42832694 G>T maps to NM_015349.1 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:42796704 C>T maps to NM_015349.1 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr6:42797676 G>T maps to NM_015349.1 G536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:42796997 C>T maps to NM_015349.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:42797547 C>T maps to NM_015349.1 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:42797514 G>T maps to NM_015349.1 G482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:70170112 G>T maps to NM_014734.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:105350345 C>T maps to ENST00000453495 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr14:105356005 C>T maps to ENST00000453495 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:105350318 G>A maps to ENST00000453495 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:105353374 G>T maps to ENST00000453495 V934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:105353311 G>A maps to ENST00000453495 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:105353863 C>T maps to ENST00000453495 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:75150053 C>T maps to NM_001039479.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr14:75134249 C>G maps to NM_001039479.1 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr14:75142849 G>A maps to NM_001039479.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24596748 G>A maps to NM_014809.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr6:24582497 C>T maps to NM_014809.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:24596316 G>A maps to NM_014809.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:34832327 G>T maps to NM_014686.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:34838869 A>G maps to NM_014686.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:34818677 A>T maps to NM_014686.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:34824628 G>A maps to NM_014686.3 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:114151988 A>T maps to NM_001080398.1 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:114188021 C>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:114135594 C>A maps to NM_001080398.1 R1601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr9:114133963 T>C maps to NM_001080398.1 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr9:114128857 G>C maps to NM_001080398.1 L1899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:35739604 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:35592774 G>A maps to NM_014672.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:36611947 G>C maps to NM_014657.1 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:36641891 G>A maps to NM_014657.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:36634757 C>A maps to NM_014657.1 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:36640041 G>C maps to NM_014657.1 S726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr20:36641108 G>A maps to NM_014657.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr20:36627592 G>A maps to NM_014657.1 F930F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:36625250 G>A maps to NM_014657.1 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr20:36640337 T>G maps to NM_014657.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:36641191 C>A maps to NM_014657.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:127767819 A>G maps to NM_014702.4 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:4824629 G>A maps to ENST00000450194 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:4824651 C>T maps to ENST00000450194 Q1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:46197046 A>T maps to NM_001142397.1 K147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr18:46343674 C>T maps to NM_001142397.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:15703454 G>A maps to NM_014647.3 G1293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:15696061 T>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:15698212 G>A maps to NM_014647.3 R1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr16:15711301 G>C maps to NM_014647.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr16:15711343 C>A maps to NM_014647.3 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr16:15706554 C>G maps to NM_014647.3 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:43896737 G>T maps to NM_015284.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:43909129 T>C maps to NM_015284.2 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:43909090 C>T maps to NM_015284.2 F1957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:43893379 C>T maps to NM_015284.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:43896263 A>G maps to NM_015284.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:43906133 G>A maps to NM_015284.2 R1508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:43914142 C>A maps to NM_015284.2 I2420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:43898107 G>T maps to NM_015284.2 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:43891740 G>T maps to NM_015284.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:47173628 T>A maps to NM_014774.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:47144308 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:3662520 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:3662276 A>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:3662329 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:3662335 C>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:3662325 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:85116167 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:22624353 C>A maps to ENST00000446597 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:22606880 G>C maps to ENST00000446597 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:22676357 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:22623827 G>C maps to ENST00000446597 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:22624343 C>A maps to ENST00000446597 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:22609906 C>A maps to ENST00000446597 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:22610048 C>A maps to ENST00000446597 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:27751861 C>G maps to NM_015202.2 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:27786398 G>T maps to NM_015202.2 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:27640034 T>A maps to NM_015202.2 L65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:27585277 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:27777731 C>A maps to NM_015202.2 A1304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr16:27781321 G>T maps to NM_015202.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr16:27777673 G>A maps to NM_015202.2 W1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr16:27777779 G>A maps to NM_015202.2 E1320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr16:27789019 C>T maps to NM_015202.2 T1547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:27751436 G>T maps to NM_015202.2 G607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:27720168 G>A maps to NM_015202.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:27709763 A>G maps to NM_015202.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr16:27751672 T>A maps to NM_015202.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:3754083 C>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:3740026 C>A maps to NM_014704.3 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:42161646 C>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:42263516 T>A maps to NM_015058.1 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr13:42273407 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:58941425 G>T maps to ENST00000354386 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:58941419 A>G maps to ENST00000354386 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:58937329 G>C did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr14:58915179 A>G maps to ENST00000354386 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr14:58965517 G>T maps to ENST00000354386 V1389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:58897412 A>T maps to ENST00000354386 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:58955481 C>G maps to ENST00000354386 S1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:138376994 G>T maps to NM_014811.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:138377495 A>T maps to NM_014811.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:138379899 G>T maps to NM_014811.3 E1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:46686436 G>C maps to NM_001142673.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:46677780 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:2604049 C>A maps to NM_015229.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:2597327 G>A maps to NM_015229.3 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:55356792 G>A maps to NM_001098815.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:55357526 G>T maps to NM_001098815.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:55356412 G>A maps to NM_001098815.1 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:55356805 C>A maps to NM_001098815.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:6526309 C>A maps to NM_014804.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:6531764 C>T maps to NM_014804.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:6515397 C>A maps to NM_014804.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr1:39879983 G>T maps to NM_015038.1 V1349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:39876983 G>A maps to NM_015038.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr1:39877930 C>G maps to NM_015038.1 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:96997629 G>T maps to NM_015323.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:96988409 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:8824924 G>T maps to ENST00000456698 G1458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr18:8819247 C>T maps to ENST00000456698 R1368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:8796375 C>T maps to ENST00000456698 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:8825005 C>T maps to ENST00000456698 D1485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr18:8784096 G>T maps to ENST00000456698 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:8785984 G>T maps to ENST00000456698 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:8825212 C>T maps to ENST00000456698 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr18:8819031 C>T maps to ENST00000456698 P1296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19454665 C>T maps to NM_015329.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:19452186 C>T maps to NM_015329.3 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:19458138 T>C maps to NM_015329.3 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:19453456 G>A maps to NM_015329.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:19431730 G>T maps to NM_015329.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr7:36373543 G>T maps to NM_001100425.1 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr7:36429574 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:67214272 C>A maps to NM_001040715.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:75552465 A>T maps to NM_015037.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr10:75551940 G>A maps to NM_015037.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr10:75553645 G>A maps to NM_015037.2 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr10:75550012 C>T maps to NM_015037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:154548816 C>T maps to NM_001131007.1 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:154510156 C>T maps to NM_001131007.1 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr4:154547371 T>C maps to NM_001131007.1 N1373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:154525148 C>T maps to NM_001131007.1 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:5463460 G>A maps to NM_015325.1 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:5464766 C>T maps to NM_015325.1 Q1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:5461255 T>C maps to NM_015325.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:5463146 G>T maps to NM_015325.1 E1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:5462197 G>A maps to NM_015325.1 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:5463335 G>T maps to NM_015325.1 E1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:5462875 G>A maps to NM_015325.1 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:5486894 G>T maps to NM_015325.1 S2194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:5464363 G>A maps to NM_015325.1 L1639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:5463748 A>T maps to NM_015325.1 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr5:5464744 C>T maps to NM_015325.1 L1766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:5462381 G>T maps to NM_015325.1 G979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:5461237 A>G maps to NM_015325.1 E597E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:5460781 C>T maps to NM_015325.1 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:84865081 C>A maps to NM_014895.2 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:84904720 A>T maps to NM_014895.2 L303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:84904634 C>A maps to NM_014895.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr18:29437774 G>C maps to NM_014939.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr18:29454465 T>A maps to NM_014939.3 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:29451057 T>A maps to NM_014939.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr18:29447397 T>G maps to NM_014939.3 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr18:29451005 C>A maps to NM_014939.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr18:29453501 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr15:79749994 C>T maps to NM_015206.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:79749184 C>T maps to NM_015206.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr15:79750720 C>T maps to NM_015206.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr15:79749739 A>G maps to NM_015206.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr12:105538174 G>T maps to NM_015275.1 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr12:105509499 C>T maps to NM_015275.1 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:34971408 T>A maps to NM_015297.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:34976208 C>A maps to NM_015297.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr9:34971540 C>A maps to NM_015297.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:123264571 G>T maps to NM_015312.3 S4120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:123175387 A>G maps to NM_015312.3 L1987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:123192675 C>G maps to NM_015312.3 S2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:123192443 C>T maps to NM_015312.3 Q2589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr4:123192464 A>T maps to NM_015312.3 R2596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:123264574 A>T maps to NM_015312.3 G4121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:123192196 A>T maps to NM_015312.3 P2506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:123234841 G>T maps to NM_015312.3 E3438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:123271218 A>T maps to NM_015312.3 S4613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr4:123175475 A>T maps to NM_015312.3 R2017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:123107221 A>C maps to NM_015312.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:123147882 G>T maps to NM_015312.3 G939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:123192604 G>T maps to NM_015312.3 R2642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:123249263 A>T maps to NM_015312.3 P3667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:123275168 G>T maps to NM_015312.3 E4768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:123164213 C>G maps to NM_015312.3 S1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:123107276 C>T maps to NM_015312.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr4:123258168 A>T maps to NM_015312.3 R4048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:123193424 C>T maps to NM_015312.3 Q2771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr4:123264592 C>T maps to NM_015312.3 G4127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:123171515 G>C did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr4:123252501 A>G maps to NM_015312.3 A3757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:123164166 G>A maps to NM_015312.3 G1562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:123237903 A>T maps to NM_015312.3 R3519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:123113462 A>G maps to NM_015312.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:123171679 G>C maps to NM_015312.3 R1958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:141365038 G>A maps to NM_001080392.1 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:34372317 C>T maps to NM_020702.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr5:175782624 G>A maps to NM_020444.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:175774791 G>C maps to NM_020444.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:81171176 C>A maps to NM_018689.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:81229224 A>T maps to NM_018689.1 K1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:81201517 G>A maps to NM_018689.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr15:81224241 C>A maps to NM_018689.1 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:81171077 T>G maps to NM_018689.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:81188357 G>T maps to NM_018689.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:118221793 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:118284537 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:118284471 T>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:118220679 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:118220781 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:118221461 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:118222745 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:118221960 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:118223470 A>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:118284524 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:118223139 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:118220817 T>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:118220802 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:118221194 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:118222135 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:118223041 G>T did not map to a codon.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr23:118222521 C>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:118284405 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:118284534 G>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:118220735 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:118221402 A>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:118239096 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:118221890 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:118222822 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:118250487 G>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:118250552 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:118257544 C>A did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:118238955 T>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:118221719 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:118223079 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:118221650 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:118223025 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:118221391 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:118223006 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:57193888 C>T maps to NM_020722.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:57181644 C>G maps to NM_020722.1 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:57182421 G>A maps to NM_020722.1 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:57182100 G>T maps to NM_020722.1 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:57193885 C>A maps to NM_020722.1 A1206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:57164479 C>T maps to NM_020722.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:57182025 C>A maps to NM_020722.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:57181272 G>T maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr4:57181771 C>A maps to NM_020722.1 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:57181563 C>G maps to NM_020722.1 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:57182505 G>A maps to NM_020722.1 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:57173801 C>T maps to NM_020722.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:57181920 G>A maps to NM_020722.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr4:57181089 C>A maps to NM_020722.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:57181270 C>A maps to NM_020722.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:57182772 G>T maps to NM_020722.1 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:24833391 A>C maps to NM_019590.3 I1731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:24762578 A>G maps to NM_019590.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:24508696 G>T maps to NM_019590.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr10:24762917 C>T maps to NM_019590.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:24813539 C>T maps to NM_019590.3 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr10:24508696 G>A maps to NM_019590.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:24722074 C>T maps to NM_019590.3 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:24833115 G>A maps to NM_019590.3 R1639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:138584557 C>T maps to NM_020340.4 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:138629991 G>T maps to NM_020340.4 G1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:138610961 A>G maps to NM_020340.4 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr6:138618037 G>T maps to NM_020340.4 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:138584485 G>T maps to NM_020340.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr3:128696921 T>C maps to NM_020741.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:128697004 G>A maps to NM_020741.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr3:128706630 C>G maps to NM_020741.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:44249068 T>A maps to NM_015443.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:44117217 G>A maps to NM_015443.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:44249275 C>A maps to NM_015443.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr17:44248857 C>A maps to NM_015443.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:44108913 C>A maps to NM_015443.3 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr17:44116021 G>T maps to NM_015443.3 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:72285877 C>A maps to NM_014431.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72292513 C>A maps to NM_014431.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:72300941 C>T maps to NM_014431.2 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:72293677 G>T maps to NM_014431.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:72292489 G>C maps to NM_014431.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:72299376 C>A maps to NM_014431.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:72293751 C>T maps to NM_014431.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:72307195 C>G maps to NM_014431.2 Y752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:72292390 C>A maps to NM_014431.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:72298676 G>T maps to NM_014431.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:72326386 C>T maps to NM_014431.2 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:72300886 G>T maps to NM_014431.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr10:72307079 C>T maps to NM_014431.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:72307172 C>A maps to NM_014431.2 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:70776072 C>T maps to NM_015634.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:70775877 G>C maps to NM_015634.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:109740146 G>T maps to NM_020775.3 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:109740163 C>T maps to NM_020775.3 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:109743476 C>A maps to NM_020775.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:109734364 C>A maps to NM_020775.3 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr1:109743470 C>T maps to NM_020775.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:86544145 C>A maps to NM_001142749.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:86568130 T>C maps to NM_001142749.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:86548626 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:86556211 C>T maps to NM_001142749.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr18:34740210 T>A maps to NM_020776.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:34753035 C>T maps to NM_020776.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr15:52905959 T>A maps to NM_019600.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr15:52901304 C>T maps to NM_019600.2 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr11:101786026 G>A maps to NM_020802.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113724428 T>A maps to NM_020817.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:94088408 A>G maps to ENST00000393153 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:93962755 G>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:93963584 T>A maps to ENST00000393153 L284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:94156555 C>T maps to ENST00000393153 A2454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:94088192 C>A maps to ENST00000393153 I1560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr14:94044288 G>A maps to ENST00000393153 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:94007177 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94088825 C>A maps to ENST00000393153 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:94120108 G>T maps to ENST00000393153 A2096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr14:94046492 A>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr14:94046493 G>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr14:94088705 C>T maps to ENST00000393153 N1731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:94173126 G>A maps to ENST00000393153 P2617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:94089156 C>T maps to ENST00000393153 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:94060028 G>A maps to ENST00000393153 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:94007065 G>T maps to ENST00000393153 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:93962773 C>T maps to ENST00000393153 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr14:94008861 G>T maps to ENST00000393153 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr14:94084612 C>T maps to ENST00000393153 Q1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr14:94007149 G>T maps to ENST00000393153 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:94067066 G>A maps to ENST00000393153 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr14:94079308 G>T maps to ENST00000393153 T1329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:94044381 C>T maps to ENST00000393153 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:94120156 C>A maps to ENST00000393153 A2112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:94053227 C>A maps to ENST00000393153 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr14:94088588 C>G maps to ENST00000393153 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr14:94107578 G>T maps to ENST00000393153 T2024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:94063744 C>T maps to ENST00000393153 H1077H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr14:94107506 C>T maps to ENST00000393153 S2000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:94060040 C>A maps to ENST00000393153 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr14:94079308 G>T maps to ENST00000393153 T1329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr14:94063706 G>T maps to ENST00000393153 E1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:94083514 G>A maps to ENST00000393153 V1385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:95508629 C>A maps to NM_015496.3 E1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:95539313 T>A maps to NM_015496.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:95503859 C>A maps to NM_015496.3 G1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr8:95508681 G>A maps to NM_015496.3 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr8:95507123 T>A maps to NM_015496.3 P1535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95524281 G>C maps to NM_015496.3 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:95539139 C>A maps to NM_015496.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:95541570 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:95523748 C>A maps to NM_015496.3 T1018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:5754899 G>A maps to ENST00000414202 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:5765718 C>T maps to ENST00000414202 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:5689957 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr9:5763243 G>C maps to ENST00000414202 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:5743004 A>C maps to ENST00000414202 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:5772979 C>T maps to ENST00000414202 Q1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr10:30315635 G>T maps to NM_020848.2 G1147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:30336462 C>A maps to NM_020848.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:30317993 C>T maps to NM_020848.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:30317503 G>A maps to NM_020848.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:30336558 C>G maps to NM_020848.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:30316109 G>C maps to NM_020848.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:30316681 G>T maps to NM_020848.2 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:30336468 C>T maps to NM_020848.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:13232873 C>G maps to NM_020853.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:13208569 G>A maps to NM_020853.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:13215866 C>T maps to NM_020853.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:59942666 T>A maps to NM_020854.3 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr18:59855221 G>T maps to NM_020854.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:59912038 G>T maps to NM_020854.3 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr18:59854908 A>T maps to NM_020854.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:226446930 C>T maps to NM_020864.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:226378245 A>G maps to NM_020864.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:226447455 C>T maps to NM_020864.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr2:226446721 C>T maps to NM_020864.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:226446721 C>A maps to NM_020864.1 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:226447662 G>A maps to NM_020864.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:226446729 G>C maps to NM_020864.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:226446777 T>C maps to NM_020864.1 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:33235818 C>T maps to NM_020888.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr1:33236885 C>G maps to NM_020888.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:33234320 G>A maps to NM_020888.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:33233511 G>A maps to NM_020888.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:33236707 C>G maps to NM_020888.2 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:108278851 C>A maps to NM_020890.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr3:108300276 C>G maps to NM_020890.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:108308150 C>G maps to NM_020890.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:100056342 C>T maps to ENST00000375206 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:100082425 T>C maps to ENST00000375206 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:100126311 C>G maps to ENST00000375206 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr9:100105800 A>G maps to ENST00000375206 E1001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:100092614 A>T maps to ENST00000375206 K797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:1345537 A>T maps to NM_020894.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:1347163 C>G maps to NM_020894.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr4:1346873 C>T maps to NM_020894.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:1369227 G>T maps to NM_020894.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:1373846 G>A maps to NM_020894.2 Q527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr9:35107818 G>A maps to NM_025182.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr9:35105220 G>C maps to NM_025182.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:7671670 G>T maps to NM_001080429.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:7676947 C>A maps to NM_001080429.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:138536985 C>A maps to NM_001164665.1 P1759P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z026-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:138522651 C>T maps to ENST00000413208 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:138555916 T>A maps to NM_001164665.1 K1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:138556068 G>C maps to NM_001164665.1 S1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:138545902 C>A maps to NM_001164665.1 T1743T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5930-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:138601521 T>C maps to NM_001164665.1 T950T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:138579243 C>A maps to NM_001164665.1 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:138554408 T>C maps to NM_001164665.1 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:138602484 T>A maps to NM_001164665.1 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:138579144 G>A maps to NM_001164665.1 R1325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:118719675 G>A maps to NM_001127211.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:118689513 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:118699990 G>A maps to NM_001127211.1 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr16:84520564 C>G maps to NM_020947.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:180905360 C>T maps to NM_020950.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:180905606 C>A maps to NM_020950.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:180905600 C>G maps to NM_020950.1 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:43497740 G>A maps to NM_020964.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr18:43497768 A>G maps to NM_020964.2 C1038C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr18:43462410 C>G maps to NM_020964.2 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:43483968 G>T maps to NM_020964.2 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr18:43514916 C>A maps to NM_020964.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr18:43523983 C>A maps to NM_020964.2 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr18:43514840 C>A maps to NM_020964.2 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr22:44692598 C>A maps to NM_001099294.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr19:18375844 C>T maps to NM_001145304.1 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr19:18375895 C>T maps to NM_001145304.1 Q818Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:18376263 G>A maps to NM_001145304.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr19:18368830 C>T maps to NM_001145304.1 W1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:175237374 A>C maps to NM_001145314.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:1920389 C>G maps to ENST00000434971 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:1919948 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:36841716 A>T maps to NM_001029864.1 P1110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:36851965 T>A maps to NM_001029864.1 K748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:36851984 A>T maps to NM_001029864.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:36869725 C>T maps to NM_001029864.1 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:36870090 C>A maps to NM_001029864.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:36870262 G>T maps to NM_001029864.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr20:36841845 G>T maps to NM_001029864.1 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:36848064 G>A maps to NM_001029864.1 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:36870199 G>A maps to NM_001029864.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:36841991 G>A maps to NM_001029864.1 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:36856551 G>A maps to NM_001029864.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr20:36856569 G>A maps to NM_001029864.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:36874462 G>T maps to NM_001029864.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:20912887 G>A maps to NM_017794.3 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr9:20946797 G>T maps to NM_017794.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:20820324 G>T maps to NM_017794.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr9:20929592 C>G maps to NM_017794.3 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:20912902 A>G maps to NM_017794.3 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:233497908 G>T maps to NM_032435.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:233511713 A>G maps to NM_032435.2 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:233518099 C>T maps to NM_032435.2 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:233514941 G>T maps to NM_032435.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:233514968 C>T maps to NM_032435.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:233518217 C>T maps to NM_032435.2 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:233507806 C>T maps to NM_032435.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:233464508 G>C maps to NM_032435.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:61304154 G>T maps to NM_001129993.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:61319700 G>T maps to NM_001129993.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr6:111587202 G>C maps to NM_153369.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:30647007 C>A maps to NM_133471.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:30653750 G>T maps to NM_133471.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:115337205 G>A maps to NM_133465.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:115422297 C>T maps to NM_133465.2 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr8:22472989 C>T maps to NM_021174.5 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr9:139697162 G>A maps to NM_001039374.4 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr9:139697159 C>T maps to NM_001039374.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:11985481 G>A maps to ENST00000376576 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:11985903 G>A maps to ENST00000376576 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:113376754 C>T maps to NM_001009899.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:113375009 G>C maps to NM_001009899.2 S1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:113377383 G>A maps to NM_001009899.2 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:113378521 C>T maps to NM_001009899.2 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:113389015 C>T maps to NM_001009899.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:113378248 A>T maps to NM_001009899.2 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr3:113378653 T>C maps to NM_001009899.2 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:113379547 G>A maps to NM_001009899.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:113388994 C>T maps to NM_001009899.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:113380123 A>C maps to NM_001009899.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:113375044 G>A maps to NM_001009899.2 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:73960672 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:73960673 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:73959986 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:73962483 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:73961079 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:73962118 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:73963898 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:73960664 G>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:73963451 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:73964217 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:73962656 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:73962890 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:73960536 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:73961649 A>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:73961403 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:73963751 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:73960591 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:73961411 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:73963422 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:73961229 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:73963749 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:73964290 G>C did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:73960757 G>C did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:73960981 T>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:73962505 T>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:73963379 A>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:73961183 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:73960274 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:73961381 T>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:73961444 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:73963349 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:73962408 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:73959996 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:73962861 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:73963689 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:73962056 C>A did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:73963136 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:73960133 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:73962850 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:73963406 T>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:73963196 C>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:73960292 G>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:73962795 G>C did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:73961330 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:73963342 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:73963489 G>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:73960666 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:73961114 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:73960837 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:5968613 C>T maps to NM_001017969.2 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:5922998 G>A maps to NM_001017969.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:5921210 T>C maps to NM_001017969.2 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:5922046 G>A maps to NM_001017969.2 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:5920562 C>A maps to NM_001017969.2 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:5921792 A>G maps to NM_001017969.2 I1401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr9:5929151 C>T maps to NM_001017969.2 W797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr9:5988523 C>T maps to NM_001017969.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:5923223 C>T maps to NM_001017969.2 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:8930076 G>A maps to NM_020738.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:8888085 G>T maps to NM_020738.2 G1153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:8926113 G>A maps to NM_020738.2 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr2:8946490 G>A maps to NM_020738.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:8919883 G>A maps to NM_020738.2 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr2:8919860 G>A maps to NM_020738.2 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:8872021 C>A maps to NM_020738.2 E1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:8919173 C>G maps to NM_020738.2 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:8940622 C>A maps to NM_020738.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:94393440 T>C maps to NM_004523.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr9:116859703 G>A maps to ENST00000259410 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:116858337 C>G maps to ENST00000259410 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr6:17817464 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:17764657 C>A maps to NM_022113.4 E1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr6:17764466 T>C maps to NM_022113.4 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:17834251 C>T maps to NM_022113.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr6:17805798 T>A maps to NM_022113.4 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:17817339 G>C maps to NM_022113.4 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr6:17804714 A>G maps to NM_022113.4 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:28998002 G>A maps to NM_015254.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:28981625 C>T maps to NM_015254.3 E1089E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:28998071 G>C maps to NM_015254.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:29120524 C>A maps to NM_015254.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:28976450 C>A maps to NM_015254.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:28976416 C>A maps to NM_015254.3 E1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:200534576 A>G maps to NM_014875.2 D1294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:200522785 A>G maps to NM_014875.2 Y1559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:200574419 G>T maps to NM_014875.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:200529852 G>T maps to NM_014875.2 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr1:200559400 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:200571186 T>C maps to NM_014875.2 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:200567483 T>C maps to NM_014875.2 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:44869001 G>T maps to NM_020242.2 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:44841921 G>C maps to NM_020242.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:16316588 C>T maps to NM_024704.4 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:16253909 G>A maps to NM_024704.4 H1314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:16355029 C>A maps to NM_024704.4 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr20:16493526 G>A maps to NM_024704.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr20:16506808 G>C maps to NM_024704.4 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:16359916 C>T maps to NM_024704.4 Q910Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:16407824 C>G maps to NM_024704.4 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:21009181 C>A maps to NM_020816.2 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:21036153 G>A maps to NM_020816.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:21039952 C>T maps to NM_020816.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:21014375 G>A maps to NM_020816.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:21031392 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:28058002 T>A maps to NM_031217.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:28116281 C>A maps to NM_031217.3 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr11:28090928 A>G maps to NM_031217.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:43005457 C>A maps to ENST00000438933 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:43013480 C>A maps to ENST00000438933 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43004446 C>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:72345450 G>T maps to NM_153209.3 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:72348398 G>T maps to NM_153209.3 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:72341015 G>T maps to NM_153209.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:72324565 G>A maps to NM_153209.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:72350346 C>A maps to NM_153209.3 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:72346568 G>T maps to NM_153209.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:72345424 G>T maps to NM_153209.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr17:72348160 G>C maps to NM_153209.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:72351373 C>A maps to NM_153209.3 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:72346893 G>A maps to NM_153209.3 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr17:72345399 C>A maps to NM_153209.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:241727623 C>A maps to ENST00000373308 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:241715307 G>A maps to ENST00000373308 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:241685264 C>A maps to ENST00000373308 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:241727524 G>T maps to ENST00000373308 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:241697883 G>A maps to ENST00000373308 Y825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:241712630 G>T maps to ENST00000373308 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:241656810 G>T maps to ENST00000373308 S1790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:241724428 C>A maps to ENST00000373308 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:241700762 C>A maps to ENST00000373308 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:241700233 C>G maps to ENST00000373308 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:241724410 C>A maps to ENST00000373308 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:241700756 C>T maps to ENST00000373308 W718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr2:241710411 G>A maps to ENST00000373308 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:241666332 C>A maps to ENST00000373308 A1352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:10407884 G>A maps to ENST00000377086 Q1288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:10407885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:10338103 C>T maps to ENST00000377086 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:10435100 G>A maps to ENST00000377086 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:10423340 G>T maps to ENST00000377086 S1435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:10425555 C>T maps to ENST00000377086 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:10383940 G>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:10336454 G>A maps to ENST00000377086 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:10327559 G>A maps to ENST00000377086 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:10327514 T>C maps to ENST00000377086 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:4927271 A>G maps to NM_006612.5 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:4905403 A>C maps to NM_006612.5 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:137519014 G>C maps to NM_005733.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:137522937 C>T maps to NM_005733.2 Q837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:137519249 C>G maps to NM_005733.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr5:137521325 C>T maps to NM_005733.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:91522498 A>T maps to ENST00000416354 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:91498222 C>T maps to ENST00000416354 Q1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:91477353 T>C maps to ENST00000416354 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:91497558 G>T maps to ENST00000416354 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:91497635 C>G maps to ENST00000416354 S1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:39750631 A>G did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:39761734 C>A maps to ENST00000395670 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:39726098 C>A maps to ENST00000395670 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:39701508 C>A maps to ENST00000395670 G1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:39703568 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr12:39763915 G>A maps to ENST00000395670 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:39761690 T>C maps to ENST00000395670 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:39751209 C>T maps to ENST00000395670 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:200972737 C>T maps to NM_017596.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:200971447 C>A maps to NM_017596.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:200967545 T>A maps to NM_017596.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:200960256 C>A maps to NM_017596.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:200960045 G>T maps to NM_017596.2 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:200969555 C>T maps to NM_017596.2 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:200948840 G>A maps to NM_017596.2 R1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:200959319 G>A maps to NM_017596.2 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:200960055 G>T maps to NM_017596.2 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:200977968 G>T maps to NM_017596.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:200948799 G>T maps to NM_017596.2 I1328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:200959709 G>T maps to NM_017596.2 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:200965359 C>T maps to NM_017596.2 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr1:200945902 C>G did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:200950097 T>A maps to NM_017596.2 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:200968554 C>A maps to NM_017596.2 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:200959156 G>C maps to NM_017596.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:200946362 G>T maps to NM_017596.2 A1421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr16:29816618 T>C maps to NM_007317.1 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr16:29816491 G>A maps to NM_007317.1 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:34255857 T>C maps to NM_194313.2 E1249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:34257576 G>T maps to NM_194313.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr9:34297037 T>A maps to NM_194313.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:168430276 C>G maps to NM_030615.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:104643063 G>T maps to NM_015656.1 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:104643534 C>T maps to NM_015656.1 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr14:104641578 C>T maps to NM_015656.1 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:104640601 G>T maps to NM_015656.1 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:104640562 G>T maps to NM_015656.1 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr14:104642349 C>T maps to NM_015656.1 I1075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:245848963 G>A maps to NM_018012.3 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:245849617 C>A maps to NM_018012.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:245848894 C>A maps to NM_018012.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:245530404 G>A maps to NM_018012.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:245851057 G>A maps to NM_018012.3 R1591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:245582879 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:86452348 G>C maps to NM_017576.1 S1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:86498853 G>C maps to NM_017576.1 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:51901062 C>G maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:51901062 C>T maps to NM_032559.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr17:51901863 T>A maps to NM_032559.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:51901578 T>C maps to NM_032559.4 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:51902346 T>A maps to NM_032559.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:51901176 C>T maps to NM_032559.4 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:51901011 G>T maps to NM_032559.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:51902404 A>T maps to NM_032559.4 K671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:51900627 G>A maps to NM_032559.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:51901296 C>A maps to NM_032559.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:51901792 G>T maps to NM_032559.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr17:51901329 C>T maps to NM_032559.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:51901605 G>T maps to NM_032559.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:51900966 C>A maps to NM_032559.4 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:51902313 G>T maps to NM_032559.4 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:51900705 G>T maps to NM_032559.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr17:51900597 C>A maps to NM_032559.4 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:51900999 G>A maps to NM_032559.4 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:51902199 C>A maps to NM_032559.4 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:51901353 G>T maps to NM_032559.4 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:51900475 G>T maps to NM_032559.4 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:51900891 G>T maps to NM_032559.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr17:51902370 G>C maps to NM_032559.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr17:51900903 C>A maps to NM_032559.4 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:51900544 A>C maps to NM_032559.4 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:51900438 C>A maps to NM_032559.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:45232524 G>T maps to NM_006845.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:45223724 G>T maps to NM_006845.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:45221599 G>T did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:132051568 G>T maps to ENST00000403231 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:132051608 C>T maps to ENST00000403231 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:30898857 G>T maps to NM_004798.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr20:30898036 C>T maps to NM_004798.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr20:30898134 G>A maps to NM_004798.3 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:26203667 C>T maps to NM_002254.6 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:26204591 A>G maps to NM_002254.6 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr2:26151930 A>G maps to NM_002254.6 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:69521900 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:69640089 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:69595966 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:69563563 G>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:69550031 T>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:69637838 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:69516869 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:69623845 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:69622418 T>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:69516980 C>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:69640064 A>C did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:69521844 T>C did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:69595169 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:69624659 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:69637806 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:69622522 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:69595092 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:69623834 C>A did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr23:69563591 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr23:69623831 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:69640089 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:154395644 A>T maps to NM_001099293.1 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:154395248 T>C maps to NM_001099293.1 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr5:154396898 C>G maps to NM_001099293.1 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:154396289 A>G maps to NM_001099293.1 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:154394126 G>T maps to NM_001099293.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr5:154396338 C>A maps to NM_001099293.1 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr5:154394276 G>T maps to NM_001099293.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:154395530 G>T maps to NM_001099293.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:154396481 C>T maps to NM_001099293.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:154394240 C>T maps to NM_001099293.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:154394957 T>A maps to NM_001099293.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr5:154393469 C>A maps to NM_001099293.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:154394945 C>T maps to NM_001099293.1 D509D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:57970089 C>A maps to NM_004984.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:57957262 G>A maps to NM_004984.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:57960937 G>T maps to NM_004984.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:57960916 T>A maps to NM_004984.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:57962810 A>C maps to NM_004984.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:57963139 C>T maps to NM_004984.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:57975351 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:57968991 G>A maps to NM_004984.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:57972079 C>A maps to NM_004984.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:57970637 G>T maps to NM_004984.2 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr12:57971860 A>T maps to NM_004984.2 K811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:32307276 G>C maps to NM_004521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:149799275 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:149840213 C>T maps to NM_004522.1 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:149851027 G>T maps to NM_004522.1 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr2:149837993 C>A maps to NM_004522.1 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:149857287 G>T maps to NM_004522.1 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:149847595 G>T maps to NM_004522.1 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:149679791 C>T maps to NM_004522.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:39512385 T>C maps to NM_145027.4 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:39328217 G>A maps to NM_145027.4 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:39563848 G>C maps to NM_145027.4 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7816-01A-11D-2167-08 chr6:39693059 G>A maps to NM_145027.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:39607384 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:39387721 A>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:39513403 A>C maps to NM_145027.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr6:39325069 T>C maps to NM_145027.4 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:39512396 C>A maps to NM_145027.4 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:90188651 C>A maps to NM_198525.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:90176116 C>A maps to NM_198525.2 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:47305840 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:47289506 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:47288922 C>T maps to NM_182902.3 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr3:47286387 G>A maps to NM_182902.3 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr3:47286909 C>G did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:169947324 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:169941688 G>A maps to NM_014970.2 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:169953738 T>A maps to NM_014970.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:169890870 G>T maps to NM_014970.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:169953792 A>T maps to NM_014970.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:169993678 C>T maps to NM_014970.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:170004650 C>T maps to NM_014970.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:33372727 C>A maps to NM_002263.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:33374367 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:33374259 C>T maps to NM_002263.3 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:33372690 G>T maps to NM_002263.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:33372691 C>T maps to NM_002263.3 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:33373020 A>G maps to NM_002263.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr8:145694126 C>T maps to NM_145754.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:145695011 A>G maps to NM_145754.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr8:145693758 C>G maps to NM_145754.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr16:57803855 G>T maps to NM_005550.3 Y317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:7804420 T>A maps to NM_012311.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:7801864 G>A maps to NM_012311.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:7801873 T>A maps to NM_012311.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:7801894 G>A maps to NM_012311.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:7805720 C>A maps to NM_012311.2 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:7805721 C>A maps to NM_012311.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr10:7820938 C>T maps to NM_012311.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:55294935 A>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:55294936 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:55281319 C>A maps to ENST00000291633 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:55290113 G>T maps to ENST00000291633 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:55263201 A>T maps to NM_015868.2 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:55250024 C>G maps to NM_015868.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:55341633 C>A maps to NM_013289.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:55331432 A>T maps to ENST00000355608 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:55341714 T>A maps to NM_013289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55330025 C>A maps to ENST00000355608 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:55333047 C>A maps to ENST00000355608 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:55331208 C>T maps to ENST00000355608 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:55341567 A>G maps to NM_013289.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:55331450 G>A maps to ENST00000355608 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr19:55341577 G>T maps to NM_013289.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55377867 G>T maps to ENST00000355608 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:55377284 G>C maps to ENST00000355608 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:55246762 C>A maps to NM_153443.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158064100 A>G did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:158057873 G>A maps to ENST00000368173 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:158059419 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158046020 G>C maps to ENST00000368173 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158058244 G>C did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:158064492 A>G maps to ENST00000368173 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:158064143 C>T maps to ENST00000368173 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:158058183 C>T maps to ENST00000368173 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:36350478 C>A maps to NM_199180.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:36352121 G>T maps to NM_199180.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:36350468 C>T maps to NM_199180.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:36357306 G>T maps to NM_199180.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36349666 T>A maps to NM_199180.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:36351519 C>T maps to NM_199180.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr19:36357372 G>A maps to NM_199180.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:36348265 G>T maps to NM_199180.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:126306856 G>A maps to NM_032531.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:126316710 G>T maps to NM_032531.3 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:126396517 C>G maps to NM_032531.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:126319003 G>T maps to NM_032531.3 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:55561879 C>T maps to NM_000222.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr4:55564661 C>T maps to NM_000222.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:55564657 C>G maps to NM_000222.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:55602662 G>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:88900915 T>C did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr12:88912644 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:33635063 G>A maps to NM_004795.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:33629296 C>T maps to NM_004795.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr13:33628215 C>T maps to NM_004795.3 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:39436087 G>T maps to NM_175737.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:39408721 T>A maps to NM_175737.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:39448618 G>A maps to NM_175737.3 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:104145827 C>T maps to ENST00000445352 Y704Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:104123945 C>T maps to ENST00000445352 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr14:104129246 C>T maps to ENST00000445352 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:66031146 A>T maps to NM_022822.2 K257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:66033335 C>T maps to NM_022822.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:45851262 G>A maps to NM_177417.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:43030662 G>T maps to NM_201523.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:43030854 G>A maps to NM_201523.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:12995806 G>T maps to NM_006563.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:103664247 A>G maps to NM_005655.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr8:103663608 G>A maps to NM_005655.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:10188396 G>T maps to NM_003597.4 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:10187791 C>T maps to NM_003597.4 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr13:74387410 G>A maps to NM_007249.4 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr13:74420039 T>G maps to NM_007249.4 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:126071102 C>T maps to NM_014079.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:44584644 G>C maps to NM_173484.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr1:44595557 C>A maps to NM_173484.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:38690330 A>T maps to NM_016531.5 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:38690564 G>T maps to NM_016531.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:110249615 G>C maps to NM_004235.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:3821781 C>T maps to NM_001300.5 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:207988803 C>A maps to NM_003709.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:56291840 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:56291789 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:56310867 C>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:56296678 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:56291996 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:50246942 C>T maps to NM_014315.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:42986280 G>T maps to NM_057161.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:42987062 T>A maps to NM_057161.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr6:42986280 G>C maps to NM_057161.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr16:87743081 C>A maps to NM_017566.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr16:87744894 G>A maps to NM_017566.3 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:87743096 C>A maps to NM_017566.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:27933610 C>T maps to NM_020782.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:18809214 G>T maps to NM_152375.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:18808308 G>T maps to NM_152375.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:18808833 G>T maps to NM_152375.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:18809712 G>A maps to NM_152375.2 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr22:50987959 C>A maps to NM_138433.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr22:50988041 C>A maps to NM_138433.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:70456618 T>A maps to NM_020866.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr13:70681537 T>A maps to NM_020866.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:70293520 C>A maps to NM_020866.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:70681449 C>A maps to NM_020866.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:70681380 C>A maps to NM_020866.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:70371026 G>T maps to NM_020866.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:70681366 A>G maps to NM_020866.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr13:70681813 T>A maps to NM_020866.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:70371065 C>A maps to NM_020866.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr13:70314559 G>T maps to NM_020866.2 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:70535440 T>G maps to NM_020866.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr13:70293594 C>A maps to NM_020866.2 G641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr13:70413106 C>G did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr13:70681460 G>T maps to NM_020866.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr13:70535455 G>T maps to NM_020866.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:70681444 C>A maps to NM_020866.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:70681663 C>A maps to NM_020866.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr13:70456626 C>A maps to NM_020866.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr13:70456627 C>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr17:40004381 G>A maps to NM_152467.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:40001919 G>A maps to NM_152467.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:40021371 C>T maps to NM_018143.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:202878153 C>T maps to NM_021633.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:202863731 C>T maps to NM_021633.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:202887328 C>A maps to NM_021633.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:117043467 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:117033334 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:117043454 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:117079538 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:117079443 G>T did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:117079538 C>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:117043380 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:117079467 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:117043546 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:117033332 T>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:117033282 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:117043359 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:117033101 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:117043633 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:30260370 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:30267169 G>T maps to NM_020805.1 R396R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-53-A4EZ-01A-12D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr18:30257293 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:24006318 T>C did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:24006483 G>A did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:24006106 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:24006585 C>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:24024447 G>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:898277 G>A maps to NM_198317.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:898495 G>T maps to NM_198317.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr1:900405 C>T maps to NM_198317.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr3:47364147 C>T maps to NM_025010.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:47371575 G>T maps to NM_025010.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:166160027 C>T maps to NM_001161521.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:166231703 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:166235211 A>T maps to NM_001161521.1 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr1:173703049 G>A maps to NM_014458.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:173735413 C>T maps to NM_014458.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:173703133 A>T maps to NM_014458.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:173703134 G>T maps to NM_014458.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:173703193 G>T maps to NM_014458.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:6655583 C>A maps to NM_014851.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:20819221 C>A maps to NM_032775.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr22:20819797 G>A maps to NM_032775.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:20825747 G>A maps to NM_032775.3 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:170592411 A>T maps to NM_144711.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:170606184 G>C maps to NM_144711.5 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183396890 T>A maps to NM_017644.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:183368275 A>T maps to NM_017644.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:183390118 A>T maps to NM_017644.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:86312942 C>T maps to NM_022480.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:86312159 G>T maps to NM_022480.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:86311277 G>A maps to NM_022480.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:18779361 C>T maps to NM_018316.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:45400638 C>A maps to ENST00000355081 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:45414260 T>A maps to ENST00000355081 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr14:45414806 G>A maps to ENST00000355081 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr14:45415020 G>A maps to ENST00000355081 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:136964067 C>A maps to NM_017415.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:137045460 G>A maps to NM_017415.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:136969801 G>A maps to NM_017415.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:137013242 T>G maps to NM_017415.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:136961544 C>A maps to NM_017415.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr5:137034053 G>A maps to NM_017415.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr2:239056487 C>T maps to NM_198582.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:239057732 C>T maps to NM_198582.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:239059671 G>A maps to NM_198582.3 W568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:53519983 T>C maps to NM_001003760.4 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:53519728 A>G maps to NM_001003760.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:53518929 G>A maps to NM_001003760.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:97561768 G>T maps to NM_052904.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:97533168 G>A maps to NM_052904.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:21674112 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:21674275 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:21675498 G>C did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:21675801 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:21674056 C>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:21675116 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:21674704 C>T did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:21675702 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:21675866 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:21675156 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:21674823 C>A did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr23:21675837 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:21674330 C>A did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:21674751 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:21674660 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:21674178 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:21674669 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:84690869 G>T maps to NM_024731.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:84690790 G>T maps to NM_024731.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr16:84693367 G>T maps to NM_024731.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:84690772 G>T maps to NM_024731.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:84691177 G>T maps to NM_024731.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:84695240 C>G maps to NM_024731.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:124663934 C>T maps to NM_001081675.2 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:124658089 G>A maps to NM_001081675.2 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:124665151 T>C maps to NM_001081675.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr8:124664254 C>G maps to NM_001081675.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:124658212 A>T maps to NM_001081675.2 C504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:124664209 C>A maps to NM_001081675.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr8:124664962 C>A maps to NM_001081675.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:86888895 T>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:86773014 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:86877363 A>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:86877377 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:86869503 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:86877245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:86887307 G>C did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:86868946 C>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:86890731 C>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:86773223 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:86880729 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr23:86924388 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:86921486 A>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:86872998 G>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:86888883 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:86880771 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:86868948 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:86772934 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:86888889 G>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:86888866 G>A did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:86877259 C>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:86869440 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:86868906 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:86921525 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr23:86869525 G>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:86919908 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:86888890 T>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:86773108 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:86880702 G>T did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:86773269 A>G did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:86773169 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:86880683 G>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:86773042 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:86877410 A>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:86887406 C>G did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:86887274 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:86880718 T>C did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:86773138 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:86869562 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:86872976 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:86773043 G>C did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr4:39077640 C>G maps to NM_015990.4 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:39082721 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:39105075 C>T maps to NM_015990.4 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:39077582 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:39105131 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:183217605 C>A maps to NM_130446.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr3:183273318 G>T maps to NM_130446.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:183210492 G>T maps to NM_130446.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr3:183211923 G>T maps to NM_130446.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:23205403 G>T maps to NM_001031710.2 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr4:88106792 G>A maps to NM_020803.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:21334729 A>G maps to NM_018847.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:21334825 G>A maps to NM_018847.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:51323214 C>T maps to NM_002257.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:51323186 C>A maps to NM_002257.2 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr19:51520451 G>A maps to NM_001077500.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:51527937 G>A maps to NM_144947.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:51527499 T>A maps to NM_144947.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:51532653 C>A maps to NM_019598.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr19:51559890 G>A maps to NM_015596.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:51559974 C>A maps to NM_015596.1 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51330320 G>A maps to NM_017509.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:51380291 G>T maps to NM_001002231.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:51379988 C>A maps to NM_005551.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:51379745 G>A maps to NM_005551.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:51363277 G>A maps to NM_001648.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:51361539 C>A maps to NM_001648.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:51361823 C>T maps to NM_001648.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr19:51361317 G>T maps to NM_001648.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:51359577 C>T maps to NM_001648.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:51359526 G>T maps to NM_001648.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51412524 G>T maps to NM_004917.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:51411734 C>A maps to NM_004917.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:51411999 G>T maps to NM_004917.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:51410330 C>G maps to NM_004917.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:51410273 C>A maps to NM_004917.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51451955 C>G maps to NM_012427.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:51446940 C>A maps to NM_012427.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:51465017 G>T maps to NM_001012964.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:51466591 G>A maps to NM_001012964.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:51466620 C>A maps to NM_001012964.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:51480935 C>A maps to NM_005046.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51483571 G>A maps to NM_005046.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:51503810 C>A maps to NM_144505.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:51503888 G>A maps to NM_144505.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr19:51499389 G>A maps to NM_144505.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:51507025 G>T maps to NM_012315.1 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr19:51507040 G>C maps to NM_012315.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:187178396 C>T maps to ENST00000511608 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:187172426 T>C maps to ENST00000511608 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr4:187175750 G>T maps to ENST00000511608 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:48738496 A>T maps to NM_001135629.2 K735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:48688330 C>G maps to NM_001135629.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:48687257 G>T maps to NM_001135629.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:48687232 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:9751093 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:9754097 T>A maps to NM_002258.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:10599198 G>C maps to NM_213658.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10588480 T>C maps to NM_002260.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:10583757 C>T maps to NM_002260.3 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573031 G>A maps to NM_007333.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr12:10573044 T>C maps to NM_007333.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:10462273 A>T maps to ENST00000381908 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:9997029 G>T maps to NM_016523.1 G202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:9985930 G>T maps to NM_016523.1 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:9995032 G>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:9162083 C>G maps to NM_005810.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:139164444 C>G maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:10531200 A>T maps to NM_007360.3 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:241725626 G>T maps to NM_003679.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:241753532 G>T maps to NM_003679.3 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:241729873 C>T maps to NM_003679.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:241714304 A>T maps to NM_003679.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:47014886 G>T maps to ENST00000481882 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:135027498 C>A maps to ENST00000368572 S1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:135020831 G>A maps to ENST00000368572 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:135012103 G>T maps to ENST00000368572 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:134997464 C>A maps to ENST00000368572 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:135000109 C>T maps to ENST00000368572 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:186450462 G>A maps to NM_001102416.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:186459573 T>C maps to NM_001102416.2 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr12:123067517 A>G maps to NM_014708.4 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr12:123087421 G>A maps to NM_014708.4 S1624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:123087621 A>T maps to NM_014708.4 K1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:123072256 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:122215282 C>T did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr3:122168503 G>A maps to NM_002264.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr13:50276608 C>T maps to NM_002267.3 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:160243896 T>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:160239565 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:117053461 A>G maps to NM_002269.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:117053312 G>T maps to NM_002269.2 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr6:117023207 T>C maps to NM_002269.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr6:117019961 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:32626213 A>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:32623005 G>A maps to NM_012316.4 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:32627616 A>T maps to NM_012316.4 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:45734224 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:45748180 C>T maps to NM_002265.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:152733140 G>A maps to NM_001025231.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:152733251 G>A maps to NM_001025231.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:152733725 G>C maps to NM_001025231.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:152733200 C>G maps to NM_001025231.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:152732099 G>T maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:152733151 G>A maps to NM_001025231.1 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:152732402 C>A maps to NM_001025231.1 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:152732370 C>T maps to NM_001025231.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:152732972 C>G maps to NM_001025231.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr1:152733005 T>A maps to NM_001025231.1 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:152732909 C>A maps to NM_001025231.1 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:47986461 C>T maps to NM_007059.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:25380195 T>A maps to NM_033360.2 K88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:149427527 C>T maps to NM_032534.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr7:149427527 C>T maps to NM_032534.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:149428769 C>T maps to NM_032534.2 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:88327781 G>A maps to NM_016618.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr22:29521312 C>T maps to NM_032045.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr16:3014591 C>A maps to NM_172229.1 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr16:3016182 G>A maps to NM_172229.1 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr19:10668511 C>A maps to NM_023008.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:10670524 C>T maps to NM_023008.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:10665776 T>G maps to NM_023008.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:91870325 A>T maps to NM_194456.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr7:91851242 C>T maps to NM_194456.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:91842526 G>A maps to NM_194456.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr12:75900383 T>C maps to NM_007043.6 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53070111 G>T maps to NM_006121.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:53071141 G>T maps to NM_006121.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:53074042 C>T maps to NM_006121.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:53071970 C>T maps to NM_006121.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:53072008 T>C did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr12:53073745 A>G maps to NM_006121.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:53069372 A>G maps to NM_006121.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:38978714 G>T maps to NM_000421.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:38978438 A>G maps to NM_000421.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr17:39021132 C>A maps to NM_000223.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:39661352 C>A maps to NM_153490.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr17:39658971 G>T maps to NM_153490.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:39661463 G>A maps to NM_153490.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:39661386 C>T maps to NM_153490.2 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:39740107 G>T maps to NM_000526.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:39739907 C>T maps to NM_000526.4 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr17:39739886 C>T maps to NM_000526.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:39767201 G>T maps to NM_005557.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr17:39767598 C>A maps to NM_005557.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr17:39768576 G>A maps to NM_005557.3 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr12:53345994 A>C maps to NM_000224.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:39681166 G>C maps to NM_002276.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:39680182 G>A maps to NM_002276.4 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr17:39681199 G>C maps to NM_002276.4 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:39684412 G>A maps to NM_002276.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:53045522 A>T maps to NM_000423.2 L135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:53044262 G>T maps to NM_000423.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:53045386 C>T maps to NM_000423.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:53040626 A>G maps to NM_000423.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:39034617 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:39034572 G>A maps to NM_019010.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:39041260 G>T maps to NM_019010.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:39038821 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:39036943 G>T maps to NM_019010.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr17:39092846 G>A maps to NM_015515.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:39092708 C>T maps to NM_015515.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:39092762 A>G maps to NM_015515.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:39092741 C>A maps to NM_015515.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:39092801 G>A maps to NM_015515.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:39092647 C>A maps to NM_015515.3 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:38856533 C>A maps to NM_019016.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:38859774 G>A maps to NM_019016.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:38855798 C>A maps to NM_019016.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:38907457 C>A maps to NM_181534.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:38911182 C>T maps to NM_181534.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:38907524 G>A maps to NM_181534.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:38910702 G>A maps to NM_181534.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:38907312 G>A maps to NM_181534.3 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:38910714 G>A maps to NM_181534.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:38907491 C>A maps to NM_181534.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:38926017 G>A maps to NM_181539.4 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:38926576 A>T maps to NM_181539.4 C203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:38922841 G>A maps to NM_181539.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:38935858 C>T maps to NM_181537.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:38953455 C>A maps to NM_181535.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:38955965 G>A maps to NM_181535.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:38953258 G>C maps to NM_181535.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:38953281 C>A maps to NM_181535.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:53189643 G>C maps to ENST00000309505 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:53188082 C>T maps to ENST00000309505 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:53189277 G>T maps to ENST00000309505 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:53189301 G>T maps to ENST00000309505 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:53186141 G>A maps to ENST00000309505 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:39551496 C>T maps to ENST00000393998 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr17:39552824 G>A maps to ENST00000393998 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:39551739 C>A maps to ENST00000393998 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:39551869 G>T maps to ENST00000393998 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:39551719 G>T maps to ENST00000393998 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:39553641 G>C maps to ENST00000393998 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:39553556 G>T maps to ENST00000393998 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr17:39553698 C>A maps to ENST00000393998 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:39553677 G>A maps to ENST00000393998 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:39619224 G>T maps to NM_002278.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:39619140 C>A maps to NM_002278.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39506805 C>A maps to NM_004138.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:39502725 C>T maps to NM_004138.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39521736 C>T maps to ENST00000394004 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:39521462 A>G maps to ENST00000394004 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr17:39520198 G>T maps to ENST00000394004 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39521115 C>A maps to ENST00000394004 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:39525759 G>A maps to ENST00000394004 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr17:39525924 G>A maps to ENST00000394004 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:39522853 C>A maps to ENST00000394004 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:39521468 T>C maps to ENST00000394004 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:39538047 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:39535824 C>A maps to NM_021013.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:39538477 C>A maps to NM_021013.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39535401 C>T maps to NM_021013.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:39538480 G>T maps to NM_021013.3 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:39538414 G>A maps to NM_021013.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:39644972 G>A maps to NM_003771.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:39646023 G>A maps to NM_003771.4 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:39644572 G>T maps to NM_003771.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:39580622 G>A maps to NM_003770.4 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr17:39578656 C>A maps to NM_003770.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr17:39579082 G>A maps to NM_003770.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:39578640 C>A maps to NM_003770.4 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:39594555 G>A maps to NM_006771.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:39594373 G>T maps to NM_006771.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:39595501 C>A maps to NM_006771.3 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:39597104 G>C maps to NM_006771.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr17:39596462 C>A maps to NM_006771.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:39597002 C>A maps to NM_006771.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr17:39597092 G>T maps to NM_006771.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:39118698 G>T maps to NM_213656.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53202128 G>A maps to NM_002272.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr12:53205731 G>T maps to NM_002272.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:53201034 C>A did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:53201582 G>T maps to NM_002272.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:53203199 G>A maps to NM_002272.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:39139300 G>C maps to NM_182497.3 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:39138575 T>A maps to NM_182497.3 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:39138654 C>G maps to NM_182497.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:39140303 C>A maps to NM_182497.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr17:39135198 G>A maps to NM_182497.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:52910539 C>T maps to NM_000424.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:52911460 C>A maps to NM_000424.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52913792 G>T maps to NM_000424.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:52910578 A>G maps to NM_000424.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:52913993 G>T maps to NM_000424.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:52911460 C>A maps to NM_000424.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:52886966 G>T maps to NM_005554.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr12:52885322 C>T maps to NM_005554.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:52885385 C>A maps to NM_005554.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:52885424 C>A maps to NM_005554.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr12:52882329 G>A maps to NM_005554.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:52886531 G>A maps to NM_005554.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:52845378 C>A maps to NM_005555.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:52841599 G>A maps to NM_005555.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:52845721 C>A maps to NM_005555.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:52843417 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:52844257 C>T maps to NM_005555.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:52845358 C>T maps to NM_005555.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr12:52843282 C>T maps to NM_005555.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:52842747 C>A maps to NM_005555.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:52841081 G>A maps to NM_005555.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:52841736 C>A maps to NM_005555.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr12:52865968 C>T maps to NM_173086.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:52865454 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:52867506 G>A maps to NM_173086.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:52867404 G>T maps to NM_173086.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:52862851 C>T maps to NM_173086.4 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr12:52863674 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:52863628 C>A maps to NM_173086.4 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr12:52635263 A>T maps to NM_005556.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:52946606 G>T maps to NM_033448.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr12:52946690 G>T maps to NM_033448.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:52992866 C>A maps to NM_080747.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:52985301 G>A maps to NM_080747.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:52981413 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:52980763 C>T maps to NM_080747.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:52994867 G>T maps to NM_080747.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:52979951 G>A maps to NM_080747.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:52984642 C>A maps to NM_080747.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:53012170 C>G maps to NM_175068.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:53009974 C>A maps to NM_175068.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:53002213 G>T maps to NM_175068.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:53012077 C>A maps to NM_175068.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:53002075 C>A maps to NM_175068.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:53007600 C>G maps to NM_175068.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:53010125 G>A maps to NM_175068.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:53008437 C>A maps to NM_175068.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:53011876 G>T maps to NM_175068.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:53012211 G>A maps to NM_175068.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr12:53007534 A>G maps to NM_175068.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:52967150 G>T maps to NM_175053.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr12:52962143 G>A maps to NM_175053.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:52961995 C>A maps to NM_175053.3 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:52967129 G>T maps to NM_175053.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:52964527 G>T maps to NM_175053.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:52962031 G>A maps to NM_175053.3 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:52966241 C>T maps to NM_175053.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr12:52967354 C>A maps to NM_175053.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:52824462 G>T maps to ENST00000252245 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:52827728 G>T maps to ENST00000252245 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:52826901 C>T maps to ENST00000252245 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:52824402 G>A maps to ENST00000252245 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:52822500 G>T maps to ENST00000252245 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:52827668 G>T maps to ENST00000252245 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr12:53169353 C>T maps to NM_015848.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:53086371 G>T maps to NM_175078.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:53090180 G>A maps to NM_175078.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:53096690 G>A maps to NM_175078.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:53086628 T>C maps to NM_175078.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:53091650 C>A maps to NM_175078.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:53096951 C>T maps to NM_175078.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53215787 C>A maps to NM_175834.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:53225305 G>T maps to NM_175834.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:53216828 G>T maps to NM_175834.2 Y446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:52565270 G>A maps to NM_182507.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:52574326 G>A maps to NM_182507.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:52685240 G>T maps to NM_002281.3 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:52799788 G>A maps to NM_033033.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:52797657 C>T maps to NM_033033.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:52799946 G>T maps to NM_033033.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr12:52797630 C>T maps to NM_033033.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:52799697 C>A maps to NM_033033.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:52789932 C>A maps to NM_033033.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:52797533 C>A maps to NM_033033.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:52788851 G>T maps to NM_033033.3 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr12:52788814 G>T maps to NM_033033.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:52714927 G>A maps to NM_002282.3 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:52715050 G>A maps to NM_002282.3 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:52777467 G>A maps to NM_033045.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:52776826 G>T maps to NM_033045.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:52778862 G>A maps to NM_033045.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:52778901 G>C maps to NM_033045.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:52778967 G>T maps to NM_033045.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr12:52775273 C>T maps to NM_033045.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:52776280 G>A maps to NM_033045.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:52756685 G>A maps to NM_002283.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:52761087 G>A maps to NM_002283.3 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:52758744 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:52695777 C>A maps to NM_002284.3 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:39197229 G>T maps to NM_030967.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr17:39190710 G>A maps to NM_030966.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:39183047 G>T maps to NM_031957.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:39183194 G>A maps to NM_031957.1 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:39182936 G>T maps to NM_031957.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:45959613 G>A maps to NM_198691.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr21:46057393 C>T maps to NM_181688.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr21:46057936 C>G maps to NM_181688.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr21:46067214 C>A maps to NM_198692.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr21:46067169 C>A maps to NM_198692.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr21:46067127 G>A maps to NM_198692.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr21:46067010 C>T maps to NM_198692.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:46117154 C>T maps to NM_198699.1 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr21:45971329 G>A maps to NM_198693.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr21:45970969 A>G maps to NM_198693.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr21:45970595 G>C maps to NM_198693.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr21:45971116 G>A maps to NM_198693.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:45994747 C>A maps to NM_198687.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:45994432 C>A maps to NM_198687.1 C266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr21:46000422 G>A maps to NM_198694.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr21:45999882 G>C maps to NM_198694.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:46000335 G>A maps to NM_198694.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr21:46011807 G>T maps to NM_198688.2 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr21:46011945 G>A maps to NM_198688.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr21:46011438 G>A maps to NM_198688.2 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr21:46011576 G>A maps to NM_198688.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr21:46021135 C>A maps to ENST00000380102 C205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr21:46020562 C>T maps to ENST00000380102 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr21:46032169 C>T maps to NM_198695.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr21:46032334 G>A maps to NM_198695.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:46047093 C>G maps to NM_198690.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr21:46047396 C>G maps to NM_198690.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr21:32253684 C>T maps to NM_175858.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:32253372 G>T maps to NM_175858.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr21:32253549 A>G maps to NM_175858.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:32253684 C>A maps to NM_175858.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr21:32253723 G>T maps to NM_175858.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr21:32253353 A>T maps to NM_175858.2 *164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:32253393 C>A maps to NM_175858.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:32253438 T>A maps to NM_175858.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:32253636 G>T maps to NM_175858.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr21:46101810 G>T maps to NM_181686.1 C76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr21:46074507 C>A maps to NM_198698.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:31768823 G>T maps to NM_181599.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr21:31768820 C>A maps to NM_181599.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31768508 C>T maps to NM_181599.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr21:31744327 C>G maps to NM_181621.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:31744159 G>T maps to NM_181621.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr21:31744267 G>A maps to NM_181621.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr21:31744438 G>T maps to NM_181621.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr21:31797798 G>T maps to NM_181622.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr21:31797993 G>T maps to NM_181622.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr21:31798083 A>T maps to NM_181622.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr21:31797876 G>A maps to NM_181622.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31802903 C>A maps to NM_181600.1 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr21:31802688 C>T maps to NM_181600.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr21:31812800 G>A maps to NM_181623.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr21:31812809 C>G maps to NM_181623.1 Y55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr21:31812737 C>T maps to NM_181623.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:39471644 G>T maps to NM_031964.1 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:39471860 C>T maps to NM_031964.1 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr21:31852533 G>T maps to NM_181607.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr21:31859600 C>A maps to NM_181608.1 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr21:31859622 C>T maps to NM_181608.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:31864088 C>A maps to ENST00000433652 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr21:31869295 C>A maps to ENST00000433652 G45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:31869265 C>A maps to NM_181610.1 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:31914062 G>T maps to ENST00000437381 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:31914062 G>T maps to ENST00000437381 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:31933542 G>A maps to ENST00000437381 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:31933419 A>G maps to NM_181614.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:32127564 G>T maps to NM_181619.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr21:32127494 G>T maps to NM_181619.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr21:32127504 G>T maps to NM_181619.1 Y64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:32127579 G>C maps to NM_181619.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:32119310 G>C maps to NM_181617.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr21:32119348 C>A maps to NM_181617.1 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:32119421 G>T maps to NM_181617.1 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:31973474 C>T maps to NM_181620.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr21:31720768 G>T maps to NM_181624.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr21:31654686 G>T maps to NM_001085455.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:31655172 G>T maps to NM_001085455.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr21:31655010 G>T maps to NM_001085455.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr21:31655175 A>G maps to NM_001085455.1 Y25Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr21:31655070 G>T maps to NM_001085455.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr21:31692092 G>T maps to NM_203405.1 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr21:31691903 G>A maps to NM_203405.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr21:31692173 G>A maps to NM_203405.1 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr21:31692203 G>A maps to NM_203405.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:39165299 G>A maps to NM_031958.1 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:39155964 G>A maps to NM_031959.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:39150304 A>C maps to NM_033185.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr17:39340689 G>T maps to ENST00000458321 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:39274378 G>T maps to NM_033059.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:39274126 G>T maps to NM_033059.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:39280109 G>A maps to NM_031854.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:39334242 G>T maps to ENST00000458321 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:39324028 G>T maps to NM_033187.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:39316799 G>A maps to NM_032524.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:39316622 C>T maps to NM_032524.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39316514 G>T maps to NM_032524.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:39305587 G>A maps to NM_033188.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr17:39240559 T>C maps to ENST00000377731 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:39240793 C>A maps to ENST00000377731 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39254036 G>A maps to NM_031960.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:39254150 G>T maps to NM_031960.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr17:39254135 G>T maps to NM_031960.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:39262140 C>A maps to ENST00000377731 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr11:1606209 G>A maps to NM_001005922.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:1606149 G>A maps to NM_001005922.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:1606011 G>A maps to NM_001005922.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:71293439 G>A maps to ENST00000376535 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:71293436 G>T maps to ENST00000376535 P149P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-3918-01A-01D-1105-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-55-8506-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:1629390 C>G maps to ENST00000359229 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr11:1629045 G>A maps to ENST00000359229 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:1643059 C>T maps to ENST00000359229 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:1643083 G>T maps to ENST00000359229 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:1643104 G>T maps to ENST00000359229 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:1642657 C>A maps to NM_001012709.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:1643302 A>G maps to ENST00000359229 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:1651702 C>A maps to NM_001001480.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:1651150 C>T maps to NM_001001480.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:1651408 G>T maps to NM_001001480.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:1651687 A>T maps to NM_001001480.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:1718519 G>T maps to NM_001012416.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr11:71238381 C>T maps to ENST00000422553 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:71259801 C>A maps to NM_005553.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:71259972 A>T maps to NM_005553.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:31986076 A>G maps to NM_181602.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:31971136 T>A maps to NM_181604.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:31964925 G>T maps to ENST00000399871 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr21:31965081 T>C maps to NM_181605.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:31964946 G>A maps to ENST00000399871 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr21:32185364 C>A maps to NM_175857.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr21:32185471 G>A maps to NM_175857.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr21:32185424 C>T maps to NM_175857.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:39383274 C>G maps to NM_031961.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:39383100 C>G maps to NM_031961.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr17:39383274 C>A maps to NM_031961.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:39383163 C>A maps to NM_031961.2 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:39388902 T>G maps to NM_031962.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39406097 C>A maps to ENST00000431129 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:39406208 C>A maps to NM_033191.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:39406070 C>T maps to ENST00000431129 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:39394428 C>T maps to NM_031963.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:39394359 G>A maps to NM_031963.2 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:39394380 C>A maps to NM_031963.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:39394413 C>A maps to NM_031963.2 C37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:39394395 C>T maps to NM_031963.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:39394317 T>C maps to NM_031963.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:39394531 C>T maps to NM_031963.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:155145211 A>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:27665542 C>T maps to NM_001168364.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:25932627 G>T maps to ENST00000268763 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:25948959 A>T maps to ENST00000319524 *801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr17:25936344 C>T maps to ENST00000268763 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:117968783 C>G maps to ENST00000339824 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:117922264 C>G maps to ENST00000339824 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:117968768 C>A maps to ENST00000339824 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:117992972 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:118198877 C>A maps to ENST00000339824 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr1:52499286 G>A maps to NM_138417.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:52498520 C>A maps to NM_138417.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:52499067 C>T maps to NM_138417.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:134338107 C>G did not map to a codon.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr3:134329158 C>T maps to NM_178554.4 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:134362164 G>A maps to NM_178554.4 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:143676235 T>G maps to NM_003937.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:143718264 C>T maps to NM_003937.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:143742744 C>T maps to NM_003937.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:143798073 G>A maps to NM_003937.2 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:143685269 A>G maps to NM_003937.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr2:143799695 C>G maps to NM_003937.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:143790830 G>T maps to NM_003937.2 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:143742716 G>A maps to NM_003937.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:143676238 C>T maps to NM_003937.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:143715263 C>A maps to NM_003937.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:143713798 C>T maps to NM_003937.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:153130871 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153128311 A>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153130447 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153132928 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153136380 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:153137769 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:153134359 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:153132827 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:153141231 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:153137772 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:153135305 T>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:153130578 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:153132120 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:153132924 T>C did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:153131204 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:153135081 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:153130792 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:153137717 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:153135651 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:153134080 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:153135920 A>C did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:153128981 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:153133825 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:153128301 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153129864 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153129865 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:153133882 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:153141221 C>G did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:153133493 T>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153136376 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153136377 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:153128179 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:153129775 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:153129776 C>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr23:153132163 C>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:153130417 G>A did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:153134105 C>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:153129861 G>T did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr23:153136267 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:153136580 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:153130293 C>G did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:153132859 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:153133299 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:153133865 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:153136565 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:153130401 C>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:153136407 C>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:153135386 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr23:153138061 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:153132120 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:62672825 G>T maps to NM_019079.4 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:50735894 C>A maps to NM_024884.2 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:50760886 C>A maps to NM_024884.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:50760874 C>T maps to NM_024884.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:50750751 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:42158946 G>T maps to NM_032107.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:42162014 G>T maps to NM_032107.4 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:42164824 G>T maps to NM_032107.4 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:42164886 G>A maps to NM_032107.4 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:130378623 G>T maps to NM_032438.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr6:130399765 T>C maps to NM_032438.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:130378626 G>A maps to NM_032438.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130372451 G>T maps to NM_032438.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:130381179 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr18:6301946 C>A maps to NM_173464.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr18:6046751 C>A maps to NM_173464.3 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr18:6241404 G>A maps to NM_173464.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:5956347 C>A maps to NM_173464.3 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr6:108843558 C>T maps to NM_145315.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr6:108843516 C>G maps to NM_145315.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:108616294 C>G maps to NM_145315.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:108616315 G>T maps to NM_145315.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:71553274 T>G maps to NM_016027.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:71581331 G>A maps to NM_016027.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr8:71570007 A>C maps to NM_016027.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:201352444 C>A maps to NM_005558.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr1:201355987 T>C maps to NM_005558.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:201355870 C>A maps to NM_005558.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:201356086 G>C maps to NM_005558.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:153707109 C>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:54867008 C>A maps to NM_002287.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:54872583 G>T maps to NM_002287.3 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:54867866 C>A maps to NM_002287.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:54868181 G>C maps to NM_002287.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:55019256 G>T maps to NM_002288.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:55021736 G>A maps to NM_002288.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr19:55019244 T>C maps to NM_002288.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:48962358 G>A maps to NM_002289.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr12:48963776 C>T maps to NM_002289.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:6961755 G>T maps to NM_005559.2 P2485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:7079971 A>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:7008578 T>A maps to NM_005559.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:7016520 G>A maps to NM_005559.2 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:7050761 G>T maps to NM_005559.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr18:6958504 G>A maps to NM_005559.2 G2645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr18:7017303 C>A maps to NM_005559.2 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr18:7080333 G>T maps to NM_005559.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr18:6943236 T>C maps to NM_005559.2 P3003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:7040235 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr18:6986171 C>T maps to NM_005559.2 L1781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr18:6956685 C>T maps to NM_005559.2 L2681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:6948534 G>A maps to NM_005559.2 A2859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:6975017 C>A maps to NM_005559.2 V2169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr18:6943278 G>A maps to NM_005559.2 I2989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr18:6956679 G>A maps to NM_005559.2 P2683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:6950864 G>T maps to NM_005559.2 G2771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr18:7050845 C>G maps to NM_005559.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:6986273 T>C maps to NM_005559.2 K1747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr18:6980544 G>T maps to NM_005559.2 L1994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:6942085 C>A maps to NM_005559.2 E3074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr18:6992566 C>A maps to NM_005559.2 E1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:6985288 G>A maps to NM_005559.2 Y1869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:129762060 C>T maps to NM_000426.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129571288 C>A maps to NM_000426.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:129833583 G>A maps to NM_000426.3 L2978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:129785588 C>A maps to NM_000426.3 R2383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:129802475 A>G maps to NM_000426.3 G2547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:129785485 T>A maps to NM_000426.3 Y2348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129618939 T>C maps to NM_000426.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:129802527 T>C maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:129511366 A>T maps to NM_000426.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:129649484 C>G maps to NM_000426.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:129714271 C>A maps to NM_000426.3 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:129609189 G>T maps to NM_000426.3 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr6:129636647 C>T maps to NM_000426.3 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:129498914 C>A maps to NM_000426.3 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:129635807 G>T maps to NM_000426.3 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr6:129468150 C>A maps to NM_000426.3 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:129802490 G>A maps to NM_000426.3 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:129786363 C>A maps to NM_000426.3 S2410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:129785584 C>A maps to NM_000426.3 A2381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:129371168 C>G maps to NM_000426.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:129468114 G>T maps to NM_000426.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:129826416 A>T maps to NM_000426.3 K2874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:129498923 C>G maps to NM_000426.3 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:129635885 C>A maps to NM_000426.3 C1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:129762066 C>A maps to NM_000426.3 G2064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:129634130 C>G maps to NM_000426.3 Y1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:129618856 A>C maps to NM_000426.3 R962R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:129762042 A>G maps to NM_000426.3 T2056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr6:129759896 T>A maps to NM_000426.3 A2025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr6:129823817 A>T maps to NM_000426.3 A2753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:129419544 C>T maps to NM_000426.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:129826415 C>A maps to NM_000426.3 P2873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:129674434 T>C maps to NM_000426.3 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:129725053 G>T maps to NM_000426.3 E1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:129823802 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:21508617 A>C maps to ENST00000416669 G2777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:21453130 C>G maps to NM_000227.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:21441623 G>A maps to ENST00000416669 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr18:21513859 T>A maps to ENST00000416669 S2943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:21526202 C>T maps to ENST00000416669 I3104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr18:21483061 G>A maps to ENST00000416669 A2099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:21338377 G>A maps to ENST00000416669 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr18:21485526 G>T maps to ENST00000416669 L2221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr18:21479328 G>T maps to ENST00000416669 E1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:112463319 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:112463443 C>A maps to NM_001105206.1 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:112460429 G>T maps to NM_001105206.1 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:112471781 G>A maps to NM_001105206.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:112471752 T>C maps to NM_001105206.1 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:112457323 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:112466085 C>A maps to NM_001105206.1 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:112513052 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:112435333 G>T maps to NM_001105206.1 P1757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr6:112450150 G>T maps to NM_001105206.1 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:112461006 G>T maps to NM_001105206.1 Y1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:112457440 G>A maps to NM_001105206.1 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:112451148 G>A maps to NM_001105206.1 Y1354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:112462120 C>A maps to NM_001105206.1 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:112476085 G>A maps to NM_001105206.1 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:112466013 G>T maps to NM_001105206.1 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:60892795 C>A maps to NM_005560.3 L2426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:60889673 G>A maps to NM_005560.3 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:60885532 G>A maps to NM_005560.3 I3514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:60886056 G>C maps to NM_005560.3 L3394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr20:60907448 G>A maps to NM_005560.3 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:60885293 G>A maps to NM_005560.3 I3558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:60897352 G>C maps to NM_005560.3 Y2106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:60913345 G>A maps to NM_005560.3 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:60891002 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:60913644 T>A maps to NM_005560.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:60885061 G>A maps to NM_005560.3 Q3604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:60889691 G>C maps to NM_005560.3 L2762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:60892741 C>A maps to NM_005560.3 L2444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:60907677 C>A maps to NM_005560.3 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:60889908 G>A maps to NM_005560.3 A2714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:60904862 C>T maps to NM_005560.3 V1363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr20:60904065 G>C maps to NM_005560.3 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:60927003 G>A maps to NM_005560.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:107642143 G>T maps to NM_002291.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:107575874 T>C maps to NM_002291.2 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:107642163 G>A maps to NM_002291.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:107580555 G>T maps to NM_002291.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:107591680 C>A maps to NM_002291.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:107621256 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:107592471 G>A maps to NM_002291.2 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:107642017 G>T maps to NM_002291.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr7:107580786 G>T maps to NM_002291.2 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:107600229 G>A maps to NM_002291.2 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:107601719 C>G maps to NM_002291.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:107602081 G>A maps to NM_002291.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:107605038 C>A maps to NM_002291.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:49168415 G>C maps to NM_002292.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:49162899 C>A maps to NM_002292.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:49163400 C>T maps to NM_002292.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr1:209788687 T>A maps to NM_000228.2 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr1:209797335 G>C maps to NM_000228.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr1:209807938 G>A maps to NM_000228.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:209790825 G>A maps to NM_000228.2 Q1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:209800793 G>T maps to NM_000228.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr1:209797323 C>T maps to NM_000228.2 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:209790913 C>A maps to NM_000228.2 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:107752391 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:107692542 C>A maps to NM_007356.2 A1305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:107688430 C>A maps to NM_007356.2 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:107720069 G>T maps to NM_007356.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:107752254 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr7:107696312 A>G maps to NM_007356.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:107756606 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr7:107745022 C>G maps to NM_007356.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:107696228 A>G maps to NM_007356.2 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:107677873 T>C maps to NM_007356.2 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:107756450 C>A maps to NM_007356.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107696156 A>T maps to NM_007356.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107718761 C>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:107703284 G>T maps to NM_007356.2 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:107696318 A>T maps to NM_007356.2 T1171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:183086516 G>T maps to NM_002293.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:183072670 C>T maps to NM_002293.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:183093763 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:183096489 G>A maps to NM_002293.3 W1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:183079767 G>T maps to NM_002293.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:183106962 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:183177097 C>G maps to NM_005562.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:183189968 A>G maps to NM_005562.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:133962939 G>C maps to ENST00000355048 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:133951286 C>T maps to ENST00000355048 Y1188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:133914605 G>T maps to ENST00000355048 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:133942512 C>A maps to ENST00000355048 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr9:133942410 C>A maps to ENST00000355048 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr9:133948699 C>A maps to ENST00000355048 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:133942392 G>A maps to ENST00000355048 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr9:133932493 C>T maps to ENST00000355048 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr9:133920909 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:133961004 G>A maps to ENST00000355048 K1387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:133911561 C>A maps to ENST00000355048 C273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:133960986 C>A maps to ENST00000355048 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:133943615 G>T maps to ENST00000355048 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr13:113974700 G>A maps to NM_005561.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr13:113975948 G>T maps to NM_005561.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:119575733 T>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:119589314 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:119582866 G>C did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:119573052 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:119575691 T>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:119576489 C>G did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:55467748 G>C maps to NM_018697.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:37518780 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:37515062 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:37514996 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:37526708 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:37518837 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:37526533 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:37526534 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:17597047 C>T maps to NM_015907.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:17590483 C>T maps to NM_015907.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr8:98863680 G>A maps to ENST00000378722 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:31230535 G>A maps to NM_006762.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr22:34046643 G>A maps to NM_133642.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:33733748 C>T maps to NM_133642.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:34046549 C>A maps to NM_133642.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr22:33777943 G>A maps to NM_133642.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:34046466 G>A maps to NM_133642.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr22:34046370 C>A maps to NM_133642.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr22:34157356 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:33733702 C>A maps to NM_133642.3 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr22:33733756 G>T maps to NM_133642.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr22:33960891 C>A maps to NM_133642.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr5:154172334 C>T maps to ENST00000377643 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:154182848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:50867904 A>G maps to ENST00000429001 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:50867319 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:50822839 G>T maps to ENST00000429001 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr12:50867788 C>T maps to ENST00000429001 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr12:50867253 C>T maps to ENST00000429001 C540C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:50834245 G>T maps to ENST00000429001 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:909731 G>A maps to NM_015155.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:910207 T>A maps to NM_015155.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:909760 C>A maps to NM_015155.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:71124813 C>T maps to NM_018357.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:71124585 G>T maps to NM_018357.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:71128756 C>T maps to NM_018357.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:71125074 C>T maps to NM_018357.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr15:71124471 G>T maps to NM_018357.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr15:71125455 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:113578471 G>T maps to ENST00000509061 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:145551511 C>A maps to NM_020117.9 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:145537166 G>A maps to NM_020117.9 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:145537025 T>A maps to NM_020117.9 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:45565505 C>T maps to NM_015340.3 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:64738058 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:64738295 G>C did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:64749664 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:64754485 G>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:64749693 C>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:64744854 T>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:64734729 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:64738200 T>G did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:64738074 C>T did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:37034382 A>G maps to NM_006148.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:37074946 G>A maps to NM_006148.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:37074910 C>T maps to NM_006148.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:37074985 C>T maps to NM_006148.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:18989735 C>T maps to NM_198207.2 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:150938987 G>A maps to NM_181746.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:100942988 C>A maps to ENST00000394113 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:100996235 C>A maps to ENST00000394113 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:8320763 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:8321906 G>A maps to NM_024552.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:8320498 G>A maps to NM_024552.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:50529759 G>A maps to NM_147190.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:169547563 G>C maps to ENST00000392687 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:73635037 C>T maps to NM_032464.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:149982924 C>A maps to NM_004690.2 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:150001332 C>A maps to NM_004690.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr6:149983375 T>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:21557765 C>A maps to NM_014572.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr13:21549419 G>A maps to NM_014572.2 C952C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr13:21565414 G>A maps to NM_014572.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:203740012 C>A maps to NM_017773.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:203743031 G>A maps to NM_017773.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:203743668 C>T maps to NM_017773.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:111420459 G>T maps to ENST00000375615 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:111420387 G>T maps to ENST00000375615 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:36993348 G>T maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr20:36999437 G>T maps to NM_004139.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:225594528 C>A maps to NM_194442.1 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:225609924 T>A maps to NM_194442.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr1:225592187 T>C maps to NM_194442.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:80196774 T>G maps to NM_181714.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr6:80197407 A>T maps to NM_181714.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr21:40792769 C>G did not map to a codon.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr21:40781903 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-91-6836-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:40777864 C>T maps to ENST00000415847 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr16:67976478 C>A maps to NM_000229.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:152800070 T>C maps to NM_178348.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:152799983 C>A maps to NM_178348.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:152800118 G>T maps to NM_178348.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:152784984 T>A maps to NM_178349.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:152777924 G>A maps to NM_178351.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:152777924 G>T maps to NM_178351.3 C10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:152777654 C>G maps to NM_178351.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:152770362 T>G maps to NM_178352.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:152759840 C>T maps to NM_178353.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:152749164 C>T maps to NM_178354.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:152748871 C>T maps to ENST00000417924 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:152748894 C>A maps to ENST00000417924 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:152748918 C>A maps to ENST00000417924 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:152749116 C>G maps to NM_178354.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:152671550 C>A maps to NM_178428.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:152659577 C>T maps to NM_014357.4 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:152648742 C>A maps to NM_178429.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:152648700 C>A maps to NM_178429.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:152648532 C>G maps to NM_178429.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:152636661 G>A maps to NM_178430.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr1:152636889 C>T maps to NM_178430.2 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:152636901 G>T maps to NM_178430.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152595537 G>T maps to NM_178431.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:152595327 A>G maps to NM_178431.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:152595432 C>G maps to NM_178431.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:152586354 A>G maps to NM_178433.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:152586432 T>A maps to NM_178433.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:152552268 G>T maps to NM_032563.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552358 T>G maps to NM_032563.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152552406 G>T maps to NM_032563.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:152552370 G>T maps to NM_032563.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:152538489 G>T maps to NM_178435.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152681592 C>A maps to NM_178356.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:152681700 C>A maps to NM_178356.2 C50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:152681628 C>T maps to NM_178356.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:32745302 A>C maps to ENST00000373562 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:32745314 G>A maps to ENST00000373562 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:32740034 G>T maps to ENST00000373562 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:32740622 G>T maps to ENST00000373562 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr2:30863131 G>T maps to NM_182551.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:30785158 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr2:30748530 G>T maps to NM_182551.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:25175933 G>C maps to ENST00000380963 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:25175975 C>T maps to ENST00000380963 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr15:43622120 C>G maps to NM_014793.4 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr15:43621187 A>C maps to NM_014793.4 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:43622381 C>A maps to NM_014793.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr15:43621285 T>A maps to NM_014793.4 K468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr9:138413351 C>G maps to NM_002297.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:139847405 G>A maps to NM_178536.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr9:130912525 A>T maps to ENST00000373013 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:46708385 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:46726969 C>A maps to NM_002298.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:169714975 C>G maps to NM_005565.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:169701311 G>T maps to NM_005565.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:169702355 C>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:169685156 A>C maps to NM_005565.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:136594655 G>A maps to NM_002299.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136569959 G>T maps to NM_002299.2 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:136575240 C>A maps to NM_002299.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:136552260 G>C maps to NM_002299.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:136562351 G>A maps to NM_002299.2 A1483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:136562354 G>A maps to NM_002299.2 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr2:136570241 G>C maps to NM_002299.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:136567174 G>T maps to NM_002299.2 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr2:136562357 C>A maps to NM_002299.2 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:136567156 G>A maps to NM_002299.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:136567372 G>T maps to NM_002299.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:136575321 A>G maps to NM_002299.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:66853626 C>T maps to NM_207338.2 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr15:66850174 G>A maps to NM_207338.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:66855910 G>T maps to NM_207338.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:66857163 G>T maps to NM_207338.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:66850108 G>T maps to NM_207338.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:103869186 G>C maps to NM_001113407.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:103870878 G>A maps to NM_001113407.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:103870647 C>G maps to NM_001113407.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:16899976 C>T maps to NM_001290.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr4:16504267 A>C maps to NM_001290.3 *374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:16590419 G>T maps to NM_001290.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr4:16760781 G>C maps to NM_001290.3 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:16504378 C>A maps to NM_001290.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:88476272 C>A maps to NM_001171610.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:88441311 C>T maps to NM_001171610.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:88441335 C>T maps to NM_001171610.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:88477867 G>A maps to NM_001171610.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:88476444 T>A maps to NM_001171610.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:88476423 G>T maps to NM_001171610.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr10:88446861 G>A maps to NM_001171610.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:88441551 C>A maps to NM_001171610.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:88466389 G>A maps to NM_007078.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:18427046 C>G maps to NM_001165414.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:18425353 G>T maps to NM_001165414.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:18418442 C>A maps to NM_001165414.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:18422548 C>G maps to NM_001165414.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:18497988 T>C maps to NM_144972.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr15:59499267 C>A maps to NM_033195.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:59499435 T>C maps to NM_033195.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:21788508 C>T maps to NM_002300.6 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:21788498 G>A maps to NM_002300.6 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:18436750 C>G maps to NM_017448.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:18472598 G>A maps to NM_017448.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr16:75148832 G>A maps to NM_153486.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:11213427 G>A maps to NM_000527.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:11200277 G>C maps to NM_000527.4 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:22138962 C>T maps to NM_001013693.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36248824 G>T maps to NM_174902.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:36103328 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:36103257 T>C maps to NM_174902.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr11:36057734 C>T maps to NM_174902.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:36248959 C>T maps to NM_174902.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:25880542 G>A maps to NM_015627.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:140270798 G>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:140270932 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:140270994 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:140271040 T>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:140271176 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:140271182 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr22:44893103 C>A maps to NM_032287.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr13:53307451 G>A maps to NM_007015.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr13:53286962 A>T maps to NM_007015.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:53313267 C>T maps to NM_007015.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr13:53307473 G>T maps to NM_007015.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr13:53313201 G>T maps to NM_007015.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:109084819 G>T maps to NM_016269.4 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:109000649 G>A maps to NM_016269.4 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:226076565 G>A maps to NM_020997.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:226075724 G>T maps to ENST00000419724 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr1:226127628 C>T maps to NM_003240.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr3:156746007 A>G maps to NM_001004316.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:153177370 C>A maps to NM_001010857.1 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:153177224 T>C maps to NM_001010857.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:153177225 G>T maps to NM_001010857.1 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:153177401 C>G maps to NM_001010857.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:153177437 C>G maps to NM_001010857.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:205389622 G>A maps to ENST00000367153 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:65639479 C>T maps to NM_014319.4 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:54969280 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:54967271 G>C maps to ENST00000431846 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:54967575 C>T maps to ENST00000431846 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:127892139 C>T maps to NM_000230.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:127894614 G>A maps to NM_000230.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:127892121 C>T maps to NM_000230.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:66058459 C>G maps to NM_002303.5 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:66036390 G>T maps to NM_002303.5 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:66102602 A>T maps to NM_002303.5 K1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:66102547 C>A maps to NM_002303.5 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:66083706 G>A maps to NM_002303.5 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:66067535 C>T maps to NM_002303.5 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr1:66098833 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:66058390 G>A maps to NM_002303.5 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:66064344 T>C maps to NM_002303.5 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:66085627 G>T maps to NM_002303.5 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:66102071 C>T maps to NM_002303.5 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:43215956 G>A maps to NM_022356.3 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:43220834 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:43215926 C>T maps to NM_022356.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:189681779 C>A maps to NM_018192.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:189838136 G>A maps to NM_018192.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:189711924 C>A maps to NM_018192.3 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:189713231 C>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:6946681 G>A maps to NM_014262.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:65897499 C>T maps to NM_017526.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:29963353 C>T maps to NM_015344.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:1823940 C>T maps to NM_012318.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:38258378 A>T maps to ENST00000379957 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:38257830 A>T maps to ENST00000379957 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr12:51451897 C>T maps to ENST00000448283 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:63283067 T>C maps to NM_001142535.1 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:40095950 G>T maps to NM_013268.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40095886 C>T maps to NM_013268.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40197259 C>A maps to NM_203471.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:40199883 G>T maps to NM_203471.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr22:37966317 C>T maps to NM_006498.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr22:37966364 C>A maps to NM_006498.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:76968605 T>A maps to NM_005567.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr17:76968020 T>C maps to NM_005567.3 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:39303123 G>C maps to NM_006149.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:25969280 C>A maps to NM_009587.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:25974144 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:25974418 G>A maps to NM_009587.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:25974358 G>A maps to NM_009587.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:25975921 G>T maps to NM_009587.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:25972375 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:20358693 G>C maps to ENST00000324290 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr17:20354811 G>T maps to ENST00000324290 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:95557397 G>A maps to NM_005097.2 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:95556800 C>G maps to NM_005097.2 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:95557472 C>T maps to NM_005097.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:95517963 T>C maps to NM_005097.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr10:95549921 A>T maps to NM_005097.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25014121 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:25014017 G>A maps to NM_018176.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:25005129 G>A maps to NM_018176.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22005800 C>A maps to NM_139278.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:22009053 G>A maps to NM_139278.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:22005822 T>C maps to NM_139278.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:35617781 G>T maps to NM_139284.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr19:35617311 G>T maps to NM_139284.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:35616111 G>T maps to NM_139284.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr14:93182533 C>T maps to NM_005606.6 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr14:93172872 G>A maps to NM_005606.6 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr14:93185137 C>A maps to NM_005606.6 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:93171049 G>A maps to NM_005606.6 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:27390069 T>A maps to NM_018490.2 K734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:27393195 A>G maps to NM_018490.2 H515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71978258 C>T maps to NM_003667.2 F823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:71974056 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:71978096 C>T maps to NM_003667.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:71960643 C>A maps to NM_003667.2 S341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71977970 C>T maps to NM_003667.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:71918218 C>A maps to NM_003667.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:71946858 G>T maps to NM_003667.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr12:71833871 C>A maps to NM_003667.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:71977997 C>T maps to NM_003667.2 C736C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr12:71977981 T>A maps to NM_003667.2 L731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:71974078 T>A maps to NM_003667.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:71977946 G>A maps to NM_003667.2 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:71977916 C>A maps to NM_003667.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:71977580 G>T maps to NM_003667.2 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:71978234 C>G maps to NM_003667.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:202245514 C>T maps to NM_001017403.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:202245541 C>A maps to NM_001017403.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:202287920 C>T maps to NM_001017403.1 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:202275998 C>T maps to NM_001017403.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:202287278 C>A maps to NM_001017403.1 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:202163290 C>A maps to NM_001017403.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:63990183 A>T maps to NM_016571.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:63990807 G>T maps to NM_016571.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr6:63995566 G>T maps to NM_016571.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:206767040 G>T maps to NM_006893.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:206772943 C>A maps to NM_006893.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:49519333 G>C maps to NM_000894.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:48915564 G>T maps to NM_000233.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:48915894 T>C maps to NM_000233.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:48915777 T>C maps to NM_000233.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:40175065 G>A maps to NM_005780.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:111874651 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:111914405 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:111914412 C>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:111914365 T>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:111903859 T>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:111874738 C>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:111874684 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:111903858 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:111914459 A>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:111914477 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:104377164 G>A maps to NM_199000.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr7:103969568 C>A maps to NM_199000.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:103969247 T>C maps to NM_199000.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr7:103969337 C>A maps to NM_199000.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:104377161 C>A maps to NM_199000.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:103969352 C>T maps to NM_199000.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:103969334 C>T maps to NM_199000.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:35773815 G>T maps to NM_182548.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:35773572 C>T maps to NM_182548.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:35773659 C>T maps to NM_182548.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:35773494 C>A maps to NM_182548.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:35298036 G>T maps to NM_005568.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:35300289 G>T maps to NM_005568.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr17:35297910 C>G maps to NM_005568.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:35300421 G>T maps to NM_005568.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:35300202 G>T maps to NM_005568.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:126794862 C>A maps to NM_004789.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:126794958 A>G maps to NM_004789.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr9:126777715 C>A maps to NM_004789.3 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:126794715 C>A maps to NM_004789.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr9:139091647 C>T maps to NM_014564.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:180243318 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:180243353 T>C maps to NM_033343.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:113909174 G>A maps to NM_022363.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:113907083 G>A maps to NM_022363.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:113907095 C>A maps to NM_022363.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:124971943 G>T maps to NM_014368.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:124979410 C>T maps to NM_014368.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:124976560 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:124979356 G>T maps to NM_014368.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:124976255 G>T maps to NM_014368.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:75626523 G>T maps to NM_001001933.1 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:75608901 C>A maps to NM_001001933.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75602867 C>T maps to NM_001001933.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:75606692 C>A maps to NM_001001933.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:75608952 G>T maps to NM_001001933.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:75622663 C>A maps to NM_001001933.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:75609564 G>T maps to NM_001001933.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:75622762 T>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:75622603 C>G maps to NM_001001933.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr1:75614327 A>G maps to NM_001001933.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:75602876 C>A maps to NM_001001933.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:75602801 G>C maps to NM_001001933.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:197890481 C>A maps to NM_020204.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:197886997 C>T maps to NM_020204.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:197896829 C>T maps to NM_020204.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:197898253 C>T maps to NM_020204.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:197889241 C>T maps to NM_020204.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:39478733 A>T maps to NM_006859.2 *373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:30639729 C>A maps to NM_002309.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:38496682 A>G maps to NM_002310.5 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:38506049 C>A maps to NM_002310.5 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:48665537 C>A maps to NM_000234.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:48620930 G>A maps to NM_000234.1 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr19:48653098 C>A did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr19:48653360 C>G maps to NM_000234.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:48620981 G>A maps to NM_000234.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:33319596 G>A maps to NM_013975.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:108862283 C>A maps to NM_001098268.1 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:108861584 G>A maps to NM_001098268.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:108863580 A>T maps to NM_001098268.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr13:108861555 A>C maps to NM_001098268.1 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr13:108863172 T>A maps to NM_001098268.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr13:108862092 A>G maps to NM_001098268.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr13:108862287 T>C maps to NM_001098268.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55106733 G>T maps to NM_006863.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:55107392 G>C maps to NM_006863.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:55107720 G>T maps to NM_006863.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:55106661 C>G maps to NM_006863.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:55105927 C>A maps to NM_006863.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:55107690 G>A maps to NM_006863.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:55107242 G>A maps to NM_006863.1 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:55107260 C>A maps to NM_006863.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:55106319 C>T maps to NM_006863.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:55112230 G>T maps to NM_006863.1 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:55105732 G>T maps to NM_006863.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:55107954 A>G maps to NM_006863.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:55087568 G>T maps to NM_001130917.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:55086240 G>C maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:55086240 G>A maps to NM_001130917.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:55087388 C>A maps to NM_001130917.1 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:55087493 G>T maps to NM_001130917.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:55085801 A>T maps to NM_001130917.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:55086270 G>A maps to NM_001130917.1 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:55098701 G>A maps to NM_001130917.1 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:55098702 G>T maps to NM_001130917.1 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:55087349 G>C maps to NM_001130917.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:55086396 C>A maps to NM_001130917.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:55098803 C>A maps to NM_001130917.1 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:55085978 G>T maps to NM_001130917.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:54803139 C>A maps to ENST00000251375 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:54801975 G>A maps to ENST00000251375 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:54802621 G>T maps to ENST00000251375 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:54804155 C>A maps to ENST00000251375 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr19:54802516 C>T maps to ENST00000251375 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:54801942 C>A maps to ENST00000251375 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:54850355 G>T maps to NM_012276.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:54849818 G>T maps to NM_012276.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:54849249 G>T maps to NM_012276.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:54849399 C>T maps to NM_012276.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:54848800 C>G maps to NM_012276.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:54850148 G>T maps to NM_012276.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:54849341 C>A maps to NM_012276.3 G174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:54848129 G>A maps to NM_012276.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:54848794 G>A maps to NM_012276.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:54848313 G>A maps to NM_012276.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:54818757 C>A maps to NM_021250.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:54744953 G>T maps to ENST00000245620 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:54744953 G>T maps to ENST00000245620 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:55142737 C>A maps to ENST00000427581 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:55146211 C>A maps to ENST00000427581 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:55143410 A>T maps to ENST00000427581 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:55145101 C>A maps to ENST00000427581 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55143932 C>A maps to ENST00000427581 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55144092 C>A maps to ENST00000427581 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:55143392 C>G maps to ENST00000427581 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr19:55146110 G>T maps to ENST00000427581 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr19:55143593 G>A maps to ENST00000427581 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:55144056 C>A maps to ENST00000427581 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:55144176 G>C maps to ENST00000427581 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr19:55144615 A>C maps to ENST00000427581 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:55144062 C>T maps to ENST00000427581 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:55144083 C>G maps to ENST00000427581 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55143452 C>A maps to ENST00000427581 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr19:55146164 C>A maps to ENST00000427581 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55143584 C>T maps to ENST00000427581 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:55144590 G>T maps to ENST00000427581 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr19:55143041 G>A maps to ENST00000427581 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:54782198 C>A maps to ENST00000391747 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54778670 C>A maps to ENST00000391747 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:54783925 G>T maps to ENST00000391747 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:54783420 G>T maps to ENST00000391747 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr19:54780766 C>A maps to ENST00000391747 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr19:54781434 G>T maps to ENST00000391747 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:54782416 C>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr19:54780706 G>A maps to ENST00000391747 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:54721090 G>C maps to NM_001081450.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:54725718 G>C maps to NM_001081450.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:55179178 C>T maps to ENST00000391733 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:55179364 G>A maps to ENST00000391733 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:55177760 G>A maps to ENST00000391733 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:55175212 G>T maps to ENST00000391733 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:55175786 C>A maps to ENST00000391733 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:55175721 G>A maps to ENST00000391733 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:55174999 G>T maps to ENST00000391733 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:55175230 C>A maps to ENST00000391733 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr19:55179237 C>T maps to ENST00000391733 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:54754667 G>A maps to NM_001081442.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:54758730 A>T maps to NM_001081442.1 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:54760089 C>T maps to NM_001081442.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:54759299 A>T maps to NM_001081442.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr19:54758819 G>A maps to NM_001081442.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr19:54760436 A>G maps to NM_001081442.1 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:54760173 C>A maps to NM_001081442.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr19:54759182 C>A maps to NM_001081442.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:54758763 G>T maps to NM_001081442.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:54760610 C>T maps to NM_001081442.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr19:54760502 G>T maps to NM_001081442.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:54758763 G>C maps to NM_001081442.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:54759272 G>T maps to NM_001081442.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:51883798 G>A maps to NM_030657.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:51890460 G>T maps to NM_030657.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:51885673 G>C maps to NM_030657.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:51885705 C>A maps to NM_030657.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:50589611 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr12:50598412 G>T maps to NM_001113546.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:41687769 A>T maps to NM_014988.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:41615568 C>T maps to NM_014988.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:45637519 C>G maps to NM_014240.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:45714994 G>T maps to NM_014240.2 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr3:45677726 C>T maps to NM_014240.2 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:61776058 G>T maps to NM_030576.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:73520556 C>A maps to NM_002314.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr7:73535280 C>G maps to NM_002314.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr7:73513499 C>T maps to NM_002314.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:73521483 G>T maps to NM_002314.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:31661988 G>C maps to NM_001031801.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr22:31663871 G>A maps to NM_001031801.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr2:109292447 C>T maps to NM_001193484.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:128415048 C>A maps to NM_017980.4 G57G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-86-8073-01A-11D-2238-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-8073-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr14:74665652 C>T maps to NM_001024674.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr12:81239531 G>A maps to NM_004664.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:49619581 C>T maps to NM_022165.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:27521052 T>C maps to NM_018362.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:27528278 G>T maps to NM_018362.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:27528283 C>A maps to NM_018362.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr11:27520275 G>A maps to NM_018362.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:77907656 G>A maps to NM_032808.5 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr15:77907882 C>A maps to NM_032808.5 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:77906790 G>A maps to NM_032808.5 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr15:77908158 C>T maps to NM_032808.5 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:27949429 C>A maps to NM_152570.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:27948890 C>A maps to NM_152570.1 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr9:27948880 C>A maps to NM_152570.1 G597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr9:27949217 G>T maps to NM_152570.1 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:151774292 G>T maps to NM_001004432.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:151774556 G>C maps to NM_001004432.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:151773521 C>T maps to NM_001004432.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:151773695 C>T maps to NM_001004432.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:101109666 G>A maps to NM_001040616.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr15:101109583 T>C maps to NM_001040616.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr15:101120466 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:91007375 G>C maps to NM_000235.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:58834024 C>G maps to NM_000236.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:58840560 C>T maps to NM_000236.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:42909603 G>T maps to NM_005357.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:42912145 G>A maps to NM_005357.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:90438200 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:47108729 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:47107813 G>T maps to NM_006033.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr18:47107848 G>T maps to NM_006033.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:185245368 G>C maps to NM_139248.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr21:15561681 A>G maps to NM_198996.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:15537619 A>T maps to NM_198996.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:15561487 A>T maps to NM_198996.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr21:15554082 G>T maps to NM_198996.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr21:15561402 G>A maps to NM_198996.2 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:90492044 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr10:90537932 C>T maps to NM_001102469.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:90537954 C>A maps to NM_001102469.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:90521182 A>T maps to NM_001102469.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:96430679 G>T maps to NM_153234.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:145487436 G>T maps to NM_153713.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr17:18135838 C>T maps to NM_004140.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:18145250 G>C maps to NM_004140.3 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:18138448 G>T maps to NM_004140.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:73569270 C>T maps to NM_001031803.1 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:73539527 A>T maps to NM_001031803.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr17:73566507 C>T maps to NM_001031803.1 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:73559174 G>A maps to NM_001031803.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:73539530 G>T maps to NM_001031803.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:73566088 G>T maps to NM_001031803.1 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:75116744 G>T maps to NM_021819.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:75115995 C>A maps to NM_021819.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:75114168 G>T did not map to a codon.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr15:75111614 T>A maps to ENST00000379709 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:176765533 C>A maps to NM_006816.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr5:176778293 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:97377717 G>A maps to NM_001142292.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:97405753 A>T maps to NM_001142292.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:97373073 C>G maps to NM_001142292.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:156518510 G>A maps to ENST00000354505 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:156554847 G>A maps to ENST00000354505 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:49491725 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:70386116 G>T maps to NM_018368.3 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:70386410 T>G maps to NM_018368.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr5:36136535 C>A maps to NM_001007527.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:36111360 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr3:8590450 C>T maps to NM_014583.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr16:929611 C>A maps to ENST00000262301 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:961034 G>A maps to ENST00000262301 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:197687286 G>T maps to NM_001136049.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:197707306 C>T maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr3:197751541 C>T maps to NM_001136049.2 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:197765465 G>T maps to NM_001136049.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:156100422 G>A maps to NM_170707.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:156084744 C>T maps to NM_170707.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:126161781 A>T maps to NM_005573.3 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:126168412 A>T maps to NM_005573.3 K547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2438178 C>T maps to NM_032737.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:2434012 C>A maps to NM_032737.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:2444430 C>T maps to NM_032737.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr11:33886308 G>A maps to NM_005574.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:87797877 C>A maps to NM_006769.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:87805251 C>A maps to NM_006769.3 C90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr13:76397901 C>T maps to ENST00000357063 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:76382300 A>C maps to ENST00000357063 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr13:76429422 C>G maps to ENST00000357063 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:201869258 C>T maps to NM_012134.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:201869654 C>A maps to NM_012134.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:201869372 T>C maps to NM_012134.2 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:123302839 C>A maps to NM_207163.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:123302794 T>A maps to NM_207163.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:123302674 G>A maps to NM_207163.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:123303144 C>G maps to NM_207163.1 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:123302770 C>A maps to NM_207163.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:123302407 A>T maps to NM_207163.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:123302236 T>A maps to NM_207163.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:69171324 A>T maps to NM_198271.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:69168980 G>T maps to NM_198271.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:97823188 G>T maps to NM_014916.3 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:97821046 C>T maps to NM_014916.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:97821534 G>C maps to NM_014916.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr7:97821987 C>T maps to NM_014916.3 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:165173230 G>A maps to NM_177398.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:165218774 G>T maps to NM_177398.3 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:165182943 G>T maps to NM_177398.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:165173116 T>C maps to NM_177398.3 *383W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:165218683 C>A maps to NM_177398.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:165177306 C>T maps to NM_177398.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:165324790 C>A maps to NM_177398.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:165322349 G>T maps to NM_177398.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8648-01A-11D-2393-08 chr1:165175206 G>T maps to NM_177398.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:165182937 T>C maps to NM_177398.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:165322395 C>A maps to NM_177398.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:165179964 G>A maps to NM_177398.3 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:165218684 C>T maps to NM_177398.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr9:129453246 C>T maps to NM_001174147.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:129453231 G>T maps to NM_001174147.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:96315553 C>T maps to NM_005575.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:96315307 A>T maps to NM_005575.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:96350768 G>T maps to NM_005575.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:54347884 A>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:54362195 C>G maps to NM_001126328.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:54364993 G>A maps to NM_001126328.1 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr13:28143300 A>G maps to NM_153371.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr13:28155639 A>G maps to NM_153371.3 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:207508986 G>T maps to NM_001102659.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:40172729 T>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:193794 G>T maps to NM_145651.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr16:20838514 G>A maps to NM_030941.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:20851771 T>C maps to NM_030941.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:5705940 G>A maps to NM_004793.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:5711935 G>C maps to NM_004793.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:5705925 G>C maps to NM_004793.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:48304126 G>T maps to NM_031490.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr8:12595581 T>C maps to NM_152271.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:100900819 G>A maps to NM_198461.3 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:118151595 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:118123382 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:118145780 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:118147001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:118123450 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:118147137 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:118108864 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:118109400 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:118140176 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:118124488 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:118147112 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:118109307 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:118112366 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:118109182 C>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:118109471 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:118123527 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:118112340 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:118109534 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:118147028 G>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:121413407 G>A maps to NM_002317.5 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:121412655 C>A maps to NM_002317.5 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:121406284 C>G did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:121405864 T>A did not map to a codon.
Alternatively spliced codon TCGA-97-A4LX-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-97-A4LX-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:74763215 C>T maps to NM_032603.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:74762798 G>A maps to NM_032603.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:74763973 A>T maps to NM_032603.2 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:160953583 G>A maps to NM_005577.2 A1980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:161027593 C>T maps to NM_005577.2 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:161022111 G>A maps to NM_005577.2 Y988Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:161011991 C>A maps to NM_005577.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:160968970 T>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:161007592 G>A maps to NM_005577.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr6:160969684 C>T maps to NM_005577.2 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr6:160999591 C>T maps to NM_005577.2 V1478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:160962168 C>T maps to NM_005577.2 W1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:161007517 C>A maps to NM_005577.2 V1364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr6:161071368 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:161027690 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:160969552 C>A maps to NM_005577.2 P1704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:161006105 G>T maps to NM_005577.2 R1421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:161010583 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr9:113704145 C>A maps to NM_057159.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr9:113704289 T>C maps to NM_057159.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:85331431 G>A maps to NM_012152.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr1:85279570 A>G maps to NM_012152.2 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:78010478 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:78010953 C>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:78010374 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:78011381 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:78010953 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:78010544 C>A did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr23:78010492 G>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:78010847 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:78011207 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:78011191 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:78011435 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:78011274 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:78010444 G>T did not map to a codon.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr23:78011030 C>G did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:78011360 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr23:78011468 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:78010522 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:78010783 A>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:48986493 G>T maps to NM_005767.5 C22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:55613022 G>C maps to NM_017839.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:55565830 A>T maps to NM_017839.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr16:55562496 C>T maps to NM_017839.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:55568377 A>G maps to NM_017839.4 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr12:7086585 G>A maps to NM_005768.5 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:7087519 G>A maps to NM_005768.5 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:34652347 G>T maps to NM_153613.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:34657814 G>A maps to NM_153613.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:211966498 G>C maps to NM_014873.2 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:82456309 C>G maps to ENST00000370717 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:82409231 C>A maps to ENST00000370717 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:82456357 A>T maps to ENST00000370717 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:82409388 C>A maps to ENST00000370717 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:82432280 G>T maps to ENST00000370717 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:82447617 G>A maps to ENST00000370717 Q1091Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:82417711 T>C maps to ENST00000370717 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:82421637 A>G maps to ENST00000370717 Q633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:82437595 T>C maps to ENST00000370717 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:82456780 A>T maps to ENST00000370717 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:82409208 C>T maps to ENST00000370717 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:82431853 G>A maps to ENST00000370717 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:82445623 T>C maps to ENST00000370717 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:82434974 A>G maps to ENST00000370717 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:82456487 G>T maps to ENST00000370717 G1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:82416771 T>C maps to ENST00000370717 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:82417738 G>A maps to ENST00000370717 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:82416125 G>A maps to ENST00000370717 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:82417742 G>T maps to ENST00000370717 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:82450265 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:82415957 C>T maps to ENST00000370717 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:82450395 G>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:82408842 C>A maps to ENST00000370717 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:82431847 C>G maps to ENST00000370717 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:62775372 G>T maps to ENST00000506720 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:62542616 A>T maps to ENST00000506720 K183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:62935914 C>T maps to ENST00000506720 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:62453098 T>A maps to ENST00000506720 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:62903540 T>A maps to ENST00000506720 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:62778448 G>T maps to ENST00000506720 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:62758578 C>T maps to ENST00000506720 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:62910168 A>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:62910169 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62862035 C>T maps to ENST00000506720 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:62894600 T>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:62598883 G>A maps to ENST00000506720 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:62758596 T>G maps to ENST00000506720 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:62758491 G>C maps to ENST00000506720 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:62800634 G>A maps to ENST00000506720 Q730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:62849168 G>T maps to ENST00000506720 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:62812686 G>C maps to ENST00000506720 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:62845294 C>A maps to ENST00000506720 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:62845390 G>T maps to ENST00000506720 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:62897171 A>T maps to ENST00000506720 I1145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr4:62599250 G>T maps to ENST00000506720 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:62679578 C>T maps to ENST00000506720 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:62845291 G>T maps to ENST00000506720 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:62935830 G>T maps to ENST00000506720 G1316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:62849322 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr4:62453108 G>T maps to ENST00000506720 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:62849273 G>T maps to ENST00000506720 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:11964913 G>T maps to ENST00000396099 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr2:11945255 C>A maps to ENST00000396099 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr2:11925194 C>T maps to ENST00000396099 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:2922154 G>T maps to NM_014646.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr18:2922112 G>A maps to NM_014646.2 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:39984670 G>A maps to NM_022896.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr20:39977392 G>A maps to NM_022896.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:39974574 G>T maps to NM_022896.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr20:39987101 G>A maps to NM_022896.1 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:19805736 C>A maps to NM_000237.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr8:19805712 C>A maps to NM_000237.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:19818411 G>T maps to NM_000237.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:56343593 C>T maps to NM_006151.2 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr17:56342294 C>T maps to NM_006151.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:56332322 C>A maps to NM_006151.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr17:56344884 G>T maps to NM_006151.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:188327237 C>G maps to NM_005578.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:188583986 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:188326965 A>T maps to NM_005578.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:104071592 A>T maps to NM_017753.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:11473280 C>T maps to NM_001170635.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:814457 G>A maps to NM_024888.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:812943 G>A maps to NM_024888.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:815827 G>A maps to NM_024888.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr19:813106 G>A maps to NM_024888.1 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:814445 G>T maps to NM_024888.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:99772454 C>A maps to NM_014839.4 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:99771305 C>A maps to NM_014839.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:99753595 G>T maps to NM_014839.4 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:99753706 G>C did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:99753636 T>A maps to NM_014839.4 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:99771932 T>C maps to NM_014839.4 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:99772037 C>A maps to NM_014839.4 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:99771893 T>A maps to NM_014839.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:99771696 A>T maps to NM_014839.4 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:99753633 C>A maps to NM_014839.4 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:99771715 C>A maps to NM_014839.4 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:99418781 A>T maps to NM_001037317.1 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:99470068 G>T maps to NM_001037317.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:99470220 G>A maps to NM_001037317.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:99470068 G>T maps to NM_001037317.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:99470155 C>T maps to NM_001037317.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:99418877 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:99470014 C>T maps to NM_001037317.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:58317463 G>A maps to NM_004811.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:58318699 T>G maps to NM_004811.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:58338124 T>A maps to NM_004811.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:151773297 T>A maps to NM_006726.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:151829937 C>T maps to NM_006726.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:151749750 G>A maps to NM_006726.3 S1584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr4:151388913 G>A maps to NM_006726.3 Q2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:151511865 G>A maps to NM_006726.3 A2075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:151520207 A>C maps to NM_006726.3 P1999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:151203600 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:151850103 G>C maps to NM_006726.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr13:47286679 A>C maps to NM_001164211.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:114422811 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:114398285 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:114400180 T>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:114357642 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:114357724 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:114357725 C>A did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:114357659 T>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:197598237 G>T maps to ENST00000425562 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:197579472 A>T maps to ENST00000425562 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:100176406 G>A maps to NM_002319.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100174740 C>A maps to NM_002319.3 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:39805952 C>A maps to NM_020862.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:39805628 C>A maps to NM_020862.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:39798956 G>A maps to NM_020862.1 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:39799010 C>A maps to NM_020862.1 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:39798580 G>T maps to NM_020862.1 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:40360440 G>A maps to NM_020737.1 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:40399610 G>A maps to NM_020737.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:40399543 G>A maps to NM_020737.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:40400624 C>A maps to NM_020737.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:40359792 C>G maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:40400435 G>T maps to NM_020737.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:40400489 C>A maps to NM_020737.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:40399865 C>A maps to NM_020737.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:40400491 G>T maps to NM_020737.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr6:40399871 G>A maps to NM_020737.1 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr6:40360551 C>G maps to NM_020737.1 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:40399694 G>T maps to NM_020737.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:40400489 C>A maps to NM_020737.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:36430710 C>T maps to NM_024509.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:36435503 G>A maps to NM_024509.1 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:36431076 C>T maps to NM_024509.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr19:36430830 C>T maps to NM_024509.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr19:36430422 C>A maps to NM_024509.1 C32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr11:66625658 G>A maps to NM_024036.4 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:42356778 A>T maps to NM_152447.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:42356875 A>T maps to NM_152447.3 K350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:42356853 T>A maps to NM_152447.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr14:42356304 A>G maps to NM_152447.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:42360758 C>A maps to NM_152447.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:42360585 C>T maps to NM_152447.3 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:42360866 C>A maps to NM_152447.3 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr14:42357035 C>A maps to NM_152447.3 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:42360650 C>G maps to NM_152447.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:42356334 G>A maps to NM_152447.3 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:42355848 T>A maps to NM_152447.3 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:42357020 C>A maps to NM_152447.3 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr14:42356637 T>A maps to NM_152447.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:42356449 C>T maps to NM_152447.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:42356094 T>C maps to NM_152447.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:42356283 G>T maps to NM_152447.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:133932381 A>T maps to NM_144648.1 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:133868524 A>T maps to NM_144648.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:133881854 G>T maps to NM_144648.1 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:133812254 C>T maps to NM_144648.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr7:133824233 C>T maps to NM_144648.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:66502040 C>A maps to NM_015541.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:66431235 A>G maps to NM_015541.2 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:66465369 T>G maps to NM_015541.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:66434529 C>T maps to NM_015541.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr1:113637317 G>C maps to NM_014813.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:59271634 C>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr12:59277357 G>A maps to NM_153377.3 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:59274657 C>T maps to NM_153377.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:59270272 G>A maps to NM_153377.3 V883V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:59282682 G>A maps to NM_153377.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:59272720 G>C maps to NM_153377.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:85993874 G>T maps to NM_015613.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr10:85992333 A>T maps to NM_015613.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:85992381 G>T maps to NM_015613.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:85992168 G>T maps to NM_015613.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr10:85997411 G>T maps to NM_015613.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:85985201 C>A maps to NM_001017924.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:85984515 G>T maps to NM_001017924.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:85982088 C>A maps to NM_001017924.2 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:85984200 G>T maps to NM_001017924.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:85984611 G>A maps to NM_001017924.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:85984329 G>A maps to NM_001017924.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:85984320 G>A maps to NM_001017924.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:57594925 G>A maps to NM_002332.2 E3445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:57588381 T>C maps to NM_002332.2 P2697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:57556761 C>T maps to NM_002332.2 C842C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr12:57602923 C>T maps to NM_002332.2 V4068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:57552239 G>T maps to NM_002332.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:57603848 C>G maps to NM_002332.2 L4159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr12:57578911 A>T maps to NM_002332.2 T2129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:57599407 C>T maps to NM_002332.2 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:57559723 C>T maps to NM_002332.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:57591139 C>T maps to NM_002332.2 D3045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr12:57594274 C>T maps to NM_002332.2 T3355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr12:57567572 C>T maps to NM_002332.2 I1119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:57556191 C>G maps to NM_002332.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr12:57605789 C>T maps to NM_002332.2 R4447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:57588393 C>T maps to NM_002332.2 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr12:57569387 C>G maps to NM_002332.2 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr12:57584590 C>T maps to NM_002332.2 L2345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:57599437 G>A maps to NM_002332.2 T3856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:57559723 C>G maps to NM_002332.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:57548024 C>T maps to NM_002332.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:57570822 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr14:23345404 G>A maps to NM_014045.3 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:105503206 T>C maps to NM_013437.4 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr8:105509339 G>A maps to NM_013437.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:105510239 T>C maps to NM_013437.4 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr8:105511742 G>A maps to NM_013437.4 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:141812829 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:141299534 T>A maps to NM_018557.2 I2400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:141473548 C>A maps to NM_018557.2 E2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141680575 G>T maps to NM_018557.2 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:141777507 C>A maps to NM_018557.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:141747098 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:141609220 C>A maps to NM_018557.2 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:141528457 G>T maps to NM_018557.2 S1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:141625750 G>T maps to NM_018557.2 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:141027815 C>T maps to NM_018557.2 V4414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:141460099 C>A maps to NM_018557.2 G2016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:141607710 A>T maps to NM_018557.2 A1633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:141081473 T>A maps to NM_018557.2 K4168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:141819715 G>T maps to NM_018557.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:141259432 G>T maps to NM_018557.2 C2891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:141259287 G>A maps to NM_018557.2 Q2940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:141113971 T>A maps to NM_018557.2 T3823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:141083399 C>A maps to NM_018557.2 E4091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:141707802 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:141665494 G>T maps to NM_018557.2 C1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:141135855 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:141607773 G>A maps to NM_018557.2 D1612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr2:141215175 C>A maps to NM_018557.2 E3224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:141267566 G>T maps to NM_018557.2 P2776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:141819817 C>G maps to NM_018557.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:141214101 G>T maps to NM_018557.2 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:141299375 G>T maps to NM_018557.2 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:141751665 C>A maps to NM_018557.2 G848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:141812829 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:142012103 C>A maps to NM_018557.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:141294159 C>A maps to NM_018557.2 L2544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:141116458 G>A maps to NM_018557.2 L3730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr2:141598491 G>T maps to NM_018557.2 V1703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:141625675 T>A maps to NM_018557.2 T1442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:141115560 T>C maps to NM_018557.2 Q3794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:141641531 T>A maps to NM_018557.2 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:141773357 A>G maps to NM_018557.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:141625342 A>T maps to NM_018557.2 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:141122262 C>A maps to NM_018557.2 G3700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:141707939 C>A maps to NM_018557.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:141092094 G>A maps to NM_018557.2 S4050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:141093206 A>T maps to NM_018557.2 A4031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:140992363 T>A maps to NM_018557.2 L4550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:140995719 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:141093287 C>T maps to NM_018557.2 L4004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:141625315 A>T maps to NM_018557.2 A1474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:141641552 C>A maps to NM_018557.2 L1334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:141571370 T>A maps to NM_018557.2 L1738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr2:141680546 G>T maps to NM_018557.2 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:141242912 C>A maps to NM_018557.2 G3142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:141260666 G>T maps to NM_018557.2 R2843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:141093242 G>T maps to NM_018557.2 T4019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:141243075 C>T maps to NM_018557.2 A3087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:141274512 G>T maps to NM_018557.2 T2698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:141665548 G>T maps to NM_018557.2 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:141359035 G>T maps to NM_018557.2 A2324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr2:141665467 G>A maps to NM_018557.2 G1166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:141032054 C>T maps to NM_018557.2 K4360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr2:141643727 C>A maps to NM_018557.2 G1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr2:141643728 C>T maps to NM_018557.2 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:141474385 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:141528564 G>A maps to NM_018557.2 S1837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:141762960 G>T maps to NM_018557.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:141806768 G>A maps to NM_018557.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:141202177 A>T maps to NM_018557.2 C3376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr2:141819774 G>A maps to NM_018557.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:141457844 C>T maps to NM_018557.2 W2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:141200192 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:141245233 G>T maps to NM_018557.2 P3065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:141004718 G>A maps to NM_018557.2 N4420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:141641432 T>A maps to NM_018557.2 A1374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:141474374 G>T maps to NM_018557.2 T1923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr2:140992399 C>T maps to NM_018557.2 P4538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr2:141093377 A>G maps to NM_018557.2 I3974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:141643782 G>A maps to NM_018557.2 H1296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:140992360 A>C maps to NM_018557.2 T4551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:141773447 T>G maps to NM_018557.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr2:141299351 A>G maps to NM_018557.2 N2461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr2:141299475 C>T maps to NM_018557.2 W2420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:141108557 A>T maps to NM_018557.2 G3900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:141242970 A>G maps to NM_018557.2 T3122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:141459304 G>T maps to NM_018557.2 R2138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:141459777 C>A maps to NM_018557.2 V2078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:142012210 C>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:141055419 G>T maps to NM_018557.2 Y4308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:141571229 G>T maps to NM_018557.2 I1785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr2:141135787 C>T maps to NM_018557.2 W3533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:141081581 C>A maps to NM_018557.2 G4132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:141771217 G>A maps to NM_018557.2 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:170002407 G>A maps to NM_004525.2 I4279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:170090059 G>A maps to NM_004525.2 D1653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:170009460 G>A maps to NM_004525.2 Y4103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:170042167 C>A maps to NM_004525.2 V3230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:170063224 G>T maps to NM_004525.2 P2335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:170059449 G>A maps to NM_004525.2 C2675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:170042415 G>T maps to NM_004525.2 R3148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:170097558 C>A maps to NM_004525.2 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:170042428 G>T maps to NM_004525.2 L3143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:170150673 A>G maps to NM_004525.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr2:170101362 G>A maps to NM_004525.2 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:170077067 C>T maps to NM_004525.2 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr2:170002320 C>T maps to NM_004525.2 T4308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr2:170058243 G>A maps to NM_004525.2 A2782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:170103488 G>A maps to NM_004525.2 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:170027085 C>T maps to NM_004525.2 G3785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:170044615 C>T maps to NM_004525.2 L3064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:170148850 G>A maps to NM_004525.2 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:170072849 G>C maps to NM_004525.2 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:170112702 C>A maps to NM_004525.2 E895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:170044657 G>A maps to NM_004525.2 V3050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr2:170177287 G>A maps to NM_004525.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:170055392 T>G maps to NM_004525.2 T2827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:170112652 C>T maps to NM_004525.2 E911E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:46917794 A>T maps to ENST00000256991 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:46894954 G>T maps to ENST00000256991 P1518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr11:46907941 G>A maps to ENST00000256991 H831H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:46897369 G>A maps to ENST00000256991 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:46893081 G>A maps to ENST00000256991 L1607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:46886045 G>A maps to ENST00000256991 L1777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:46880824 G>A maps to ENST00000256991 I1854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:46916242 G>A maps to ENST00000256991 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:46898189 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:46916281 G>A maps to ENST00000256991 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:68171003 G>A maps to NM_002335.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:68181229 C>G maps to NM_002335.2 Y859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:68183796 G>A maps to NM_002335.2 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:68153796 G>A maps to NM_002335.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:68179088 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:68193605 C>T maps to NM_002335.2 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:25755957 G>A maps to NM_001135772.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:12274344 T>C maps to NM_002336.2 P1519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:12315347 G>A maps to NM_002336.2 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:12279760 A>G maps to NM_002336.2 F1392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:53728115 A>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr4:3526661 C>T maps to NM_002337.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:3521897 C>T maps to NM_002337.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:44204191 C>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:44204415 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:44201882 C>A maps to NM_133259.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:44201893 G>A maps to NM_133259.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:53785558 G>T maps to NM_018214.4 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:70004027 C>A maps to NM_201550.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:70004183 G>T maps to NM_201550.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr12:70004096 G>A maps to NM_201550.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:194951 G>A maps to NM_001080478.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:191673 C>T maps to NM_001080478.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:194081493 C>A maps to NM_001135057.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194080143 G>T maps to NM_001135057.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:194080632 G>C maps to NM_001135057.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:194080146 G>T maps to NM_001135057.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:194081121 A>G maps to NM_001135057.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:194080365 G>A maps to NM_001135057.2 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:25450200 C>T maps to NM_017640.5 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:25551169 G>A maps to NM_017640.5 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr6:25529039 A>T maps to NM_017640.5 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr6:25466177 T>G did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:24538409 C>T maps to NM_138360.3 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24528927 A>C maps to NM_138360.3 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr7:102584657 C>A maps to NM_001031692.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:102574464 G>T maps to NM_001031692.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr10:50121501 T>C maps to NM_001006939.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:50121480 C>G maps to NM_001006939.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:50121486 G>C maps to NM_001006939.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:50121435 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:46574295 A>G maps to NM_024512.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:72061135 C>A maps to NM_207119.1 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:7021986 C>T maps to NM_201650.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:7016569 C>G maps to NM_201650.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:7014863 G>T maps to NM_201650.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr8:145749503 C>T maps to NM_001024678.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:18507650 C>A maps to NM_145256.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:134174992 G>A maps to NM_030626.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr10:134161560 G>A maps to NM_030626.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr10:134179055 T>G did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:99828100 G>T maps to NM_144598.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr15:99901705 C>T maps to NM_144598.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr21:45876766 G>A maps to NM_030891.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:7231727 C>T maps to NM_001105581.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:7231798 C>A maps to NM_001105581.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:7231609 C>A maps to NM_001105581.1 C158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr18:7231273 G>C maps to NM_001105581.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr18:7231579 G>A maps to NM_001105581.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:7231612 C>T maps to NM_001105581.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:7231810 G>T maps to NM_001105581.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr18:7231663 G>T maps to NM_001105581.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:169574169 C>T maps to NM_024727.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:169557829 T>C maps to NM_024727.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:76372212 C>A maps to NM_001128922.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:76376989 G>T maps to NM_001128922.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76370953 G>T maps to NM_001128922.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:76372201 C>T maps to NM_001128922.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:76371442 C>G maps to NM_001128922.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:76372261 G>A maps to NM_001128922.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:76372110 C>A maps to NM_001128922.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr11:76372306 C>T maps to NM_001128922.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr3:196386666 G>T maps to NM_198565.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:196387776 C>G maps to NM_198565.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:196387755 C>A maps to NM_198565.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:196388191 C>T maps to NM_198565.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:196387011 G>A maps to NM_198565.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:196387080 G>A maps to NM_198565.1 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr3:196387428 C>T maps to NM_198565.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:196386877 G>T maps to NM_198565.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:196386987 G>T maps to NM_198565.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:196387299 G>T maps to NM_198565.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr16:67409313 C>T maps to NM_018296.5 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:44626162 C>T maps to NM_001006607.2 Q1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:62856867 T>A maps to NM_199340.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:62865264 G>A maps to NM_199340.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:62856184 G>T maps to NM_199340.2 S1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:62856234 C>T maps to NM_199340.2 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:30377038 A>G maps to ENST00000327564 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:30376181 G>C maps to ENST00000327564 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:30377080 G>T maps to ENST00000327564 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr3:26751339 T>G maps to NM_052953.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:26751756 T>C maps to NM_052953.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:127670305 G>A maps to NM_022143.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:127670541 G>T maps to NM_022143.4 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:127670198 G>T maps to NM_022143.4 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr7:127669961 G>A maps to NM_022143.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:127670417 G>A maps to NM_022143.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:70618155 C>A maps to NM_017768.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:70611485 A>C maps to NM_017768.4 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46746158 C>T maps to ENST00000254454 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:46746149 C>A maps to ENST00000254454 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:46745194 C>T maps to ENST00000254454 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:46752035 G>T maps to ENST00000254454 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:54427705 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:54418023 C>T maps to NM_052940.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:122684750 C>T maps to NM_001098519.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:79982203 C>T maps to NM_144999.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:3699301 C>A maps to NM_020710.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:3701698 G>T maps to NM_020710.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:3703871 C>A maps to NM_020710.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:17891327 G>T maps to NM_031294.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:71196914 C>T maps to NM_017691.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:51022251 G>T maps to NM_001080457.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:51022504 C>T maps to NM_001080457.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:51051825 G>C maps to NM_001080457.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:51021451 C>T maps to NM_001080457.1 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:51051797 C>G did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:51051855 G>T maps to NM_001080457.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:51021619 C>A maps to NM_001080457.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:51022087 G>A maps to NM_001080457.1 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:51021235 G>A maps to NM_001080457.1 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr19:51021867 C>A maps to NM_001080457.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:51021091 G>C maps to NM_001080457.1 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:40136678 A>G maps to NM_020929.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:40137251 G>C maps to NM_020929.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:40136612 C>A maps to NM_020929.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:40137749 C>T maps to NM_020929.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:40137278 G>T maps to NM_020929.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:40136098 C>A maps to NM_020929.1 E582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:40137637 C>A maps to NM_020929.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:40136543 C>A maps to NM_020929.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:40136624 G>T maps to NM_020929.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:40137191 C>G maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr11:40136375 C>T maps to NM_020929.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:40137020 C>A maps to NM_020929.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:40137464 G>T maps to NM_020929.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:40136343 G>T maps to NM_020929.1 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:40136877 G>T maps to NM_020929.1 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:40137470 C>T maps to NM_020929.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:40136102 G>T maps to NM_020929.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:40137254 C>A maps to NM_020929.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:84199427 T>A maps to NM_178452.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:84203520 G>T maps to NM_178452.4 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:165532901 G>T maps to NM_001005214.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:165532868 C>A maps to NM_001005214.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:165532799 G>A maps to NM_001005214.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:165514003 C>T maps to NM_001005214.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr1:165513895 C>T maps to NM_001005214.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:56954807 C>T maps to NM_001005210.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:56949879 G>A maps to NM_001005210.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:552667 C>A maps to NM_198075.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:549997 G>A maps to NM_198075.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:120053874 C>T maps to NM_001099678.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr17:48470102 G>C maps to NM_018509.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:133644984 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:133650266 G>A maps to ENST00000250173 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:133650260 C>A maps to ENST00000250173 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:133673704 C>A did not map to a codon.
Alternatively spliced codon TCGA-55-7994-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr8:133650266 G>A maps to ENST00000250173 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr8:133673712 C>T maps to ENST00000250173 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133637537 C>T maps to ENST00000250173 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:52861975 C>G maps to NM_001024611.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:52861507 G>T maps to NM_001024611.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:52861920 C>A maps to NM_001024611.1 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:52863951 C>T maps to NM_001024611.1 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:52860544 T>G maps to NM_001024611.1 *881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:52861528 C>A maps to NM_001024611.1 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:52860730 C>A maps to NM_001024611.1 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:52861432 T>A maps to NM_001024611.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr4:52861971 G>A maps to NM_001024611.1 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:52861366 C>A maps to NM_001024611.1 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:52860964 C>A maps to NM_001024611.1 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:52861909 G>T maps to NM_001024611.1 Y426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr4:52861216 T>C maps to NM_001024611.1 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr4:52861891 C>A maps to NM_001024611.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr8:67923042 G>A maps to ENST00000421742 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:70505073 G>T maps to NM_020794.2 G1151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:70477609 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:70587566 C>A maps to NM_020794.2 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:70446072 G>C maps to NM_020794.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:70478655 G>C did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:70478697 C>A maps to NM_020794.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:70505178 G>A maps to NM_020794.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:70541827 G>A maps to NM_020794.2 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:70587495 G>T maps to NM_020794.2 E1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:70503867 C>A maps to NM_020794.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:70505160 A>G maps to NM_020794.2 Q1180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:70505430 G>A maps to NM_020794.2 W1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:70504867 G>T maps to NM_020794.2 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:70504323 C>A maps to NM_020794.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:70460310 T>A maps to NM_020794.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:70504159 A>T maps to NM_020794.2 R847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:70300461 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:70504554 C>T maps to NM_020794.2 H978H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:70504740 G>T maps to NM_020794.2 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:70504741 G>T maps to NM_020794.2 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr1:70505429 G>A maps to NM_020794.2 W1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:70518716 C>A maps to NM_020794.2 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr1:70541965 T>C maps to NM_020794.2 D1441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:70504407 A>G maps to NM_020794.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:70446060 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:70502241 G>T maps to NM_020794.2 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:70291429 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:70541764 C>A maps to NM_020794.2 G1374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:70291428 A>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:70478694 C>A maps to NM_020794.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:70509695 A>T maps to NM_020794.2 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr1:70477603 A>T maps to NM_020794.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:70482217 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:70489038 C>A maps to NM_020794.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:70541813 C>A maps to NM_020794.2 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:70503923 G>A maps to NM_020794.2 W768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:131669875 A>T maps to NM_001127244.1 K145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131678376 C>T maps to NM_001127244.1 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:131670204 G>T maps to NM_001127244.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:131670678 G>C maps to NM_001127244.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr1:90049438 G>T maps to NM_015350.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:90049088 C>T maps to NM_015350.2 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:90048427 G>A maps to NM_015350.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:90179619 C>T maps to NM_032270.4 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:90180270 A>T maps to NM_032270.4 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:90399290 G>T maps to NM_001134479.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:90399986 G>T maps to NM_001134479.1 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr1:90399790 C>T maps to NM_001134479.1 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:90400576 C>T maps to NM_001134479.1 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:90400996 C>G maps to NM_001134479.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:7964660 G>A maps to NM_025061.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:7965608 G>A maps to NM_025061.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr19:7965113 G>A maps to NM_025061.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:7964675 C>G maps to NM_025061.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:86027780 C>T maps to NM_033402.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr8:86025215 A>G maps to NM_033402.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:86027440 G>T maps to NM_033402.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:86022347 A>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:86039055 C>T maps to NM_033402.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:238672083 C>T maps to NM_001137552.1 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:238643908 A>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:238642442 G>A maps to ENST00000391999 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:37100391 G>A maps to NM_006309.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:37170576 C>A maps to NM_006309.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr12:85459114 C>T maps to NM_001079910.1 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:85518289 G>T maps to NM_001079910.1 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:85449966 A>T maps to NM_001079910.1 K466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:85449836 A>T maps to NM_001079910.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr12:85531677 G>A maps to NM_001079910.1 E1420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:85546921 A>T maps to NM_001079910.1 R1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:85438562 A>G maps to NM_001079910.1 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:85515610 C>T maps to NM_001079910.1 R1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr12:85449855 G>T maps to NM_001079910.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:85517925 A>G maps to NM_001079910.1 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:85466739 C>T maps to NM_001079910.1 H917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:85446026 G>T maps to NM_001079910.1 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr12:85450463 A>G maps to NM_001079910.1 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:74507413 C>A maps to NM_001105659.1 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:74575190 C>A maps to NM_001105659.1 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:74507408 C>A maps to NM_001105659.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:74506912 C>A maps to NM_001105659.1 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:74507408 C>G maps to NM_001105659.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:74507087 G>T maps to NM_001105659.1 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:74575205 C>A maps to NM_001105659.1 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr3:169540677 T>A maps to NM_001080460.1 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:169540005 G>A maps to NM_001080460.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:169540380 C>A maps to NM_001080460.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:101567856 C>T maps to NM_024652.3 Y847Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr15:101597146 C>A maps to NM_024652.3 A1473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr15:101606940 G>T maps to NM_024652.3 P1955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:101523839 A>T maps to NM_024652.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:101595211 G>T maps to NM_024652.3 S1372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr15:101464887 G>C maps to NM_024652.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr15:101605813 C>T maps to NM_024652.3 C1724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:101605804 G>A maps to NM_024652.3 L1721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:101606266 C>T maps to NM_024652.3 C1875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr15:101550912 A>G maps to NM_024652.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr15:101555607 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr15:101605870 T>C maps to NM_024652.3 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr12:40692295 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr12:40672042 G>T maps to NM_198578.3 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:40672060 C>T maps to NM_198578.3 Q747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:40697791 A>T maps to NM_198578.3 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:40745366 A>G maps to NM_198578.3 E2136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:40716277 C>T maps to NM_198578.3 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr12:40653347 G>A maps to NM_198578.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr12:40728852 G>T maps to NM_198578.3 E1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:40681165 A>G maps to NM_198578.3 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:3887743 A>T maps to NM_020873.5 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:3887995 G>T maps to NM_020873.5 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:204587526 G>T maps to NM_201630.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:204588511 G>T maps to NM_201630.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:204588910 G>C maps to NM_201630.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:204588189 C>A maps to NM_201630.1 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:204588136 G>C maps to NM_201630.1 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:110763691 G>A maps to NM_018334.4 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:110763979 C>A maps to NM_018334.4 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:110763520 C>A maps to NM_018334.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:110763421 T>C maps to NM_018334.4 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr7:110762845 C>A maps to NM_018334.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:6022726 G>A maps to NM_152611.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:62455962 G>A maps to NM_203422.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:80530200 C>G maps to NM_178839.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:80529444 G>T maps to NM_178839.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:80530119 C>A maps to NM_178839.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr2:80530239 C>A maps to NM_178839.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:80530455 G>A maps to NM_178839.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:80529462 C>A maps to NM_178839.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:80529804 G>A maps to NM_178839.4 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:80529618 C>T maps to NM_178839.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:80530539 G>T maps to NM_178839.4 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:80529978 C>G maps to NM_178839.4 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:138208767 G>A maps to NM_015564.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:138209400 G>T maps to NM_015564.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:68687142 C>A maps to NM_178011.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr10:68857482 G>T maps to NM_178011.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr10:68687360 C>G maps to NM_178011.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:68687789 C>G maps to NM_178011.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr10:68688211 T>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:68687429 G>A maps to NM_178011.3 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:68688095 C>A maps to NM_178011.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:77746568 G>T maps to NM_001134745.1 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:77745713 G>T maps to NM_001134745.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:77745830 G>A maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr2:77746184 C>T maps to NM_001134745.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:77746574 G>C maps to NM_001134745.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:77745476 G>A maps to NM_001134745.1 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:77746067 A>T maps to NM_001134745.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:77745497 C>A maps to NM_001134745.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:77745959 G>A maps to NM_001134745.1 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:76975979 G>T maps to NM_001134745.1 C538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:77745748 C>A maps to NM_001134745.1 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:77746949 C>A maps to NM_001134745.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:76975877 G>T maps to NM_001134745.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:77746370 C>T maps to NM_001134745.1 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:77745779 G>C maps to NM_001134745.1 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:77745842 G>A maps to NM_001134745.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:77746673 C>A maps to NM_001134745.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr9:130216817 C>T maps to NM_001005374.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:54958982 C>A maps to NM_020678.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:54952836 G>T maps to NM_020678.2 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:54959163 G>C maps to NM_020678.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr3:54952686 C>A maps to NM_020678.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:54959210 G>T maps to NM_020678.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:54952668 G>A maps to NM_020678.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:1943778 C>T maps to NM_001163926.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:1940100 G>A maps to NM_001163926.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr12:1943634 G>A maps to NM_001163926.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:1940362 C>A maps to NM_001163926.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:102108634 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:102110021 G>A maps to NM_152892.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:102108573 G>T maps to NM_152892.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:115560788 G>T maps to NM_002338.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:115805311 G>T maps to NM_002338.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:115805318 C>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:115560779 C>T maps to NM_002338.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:115805270 G>A maps to NM_002338.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:115738359 A>T did not map to a codon.
Alternatively spliced codon TCGA-73-4658-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:115560691 T>A maps to NM_002338.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:115561342 C>T maps to NM_002338.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:194386358 G>A maps to NM_018385.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr3:194392801 A>T maps to NM_018385.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:157182270 G>T maps to NM_173491.2 *361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr19:34706140 T>C maps to NM_001114093.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr6:31765614 G>A maps to NM_021177.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:31773870 C>A maps to NM_021177.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:32529941 C>A maps to NM_012322.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:2324189 C>A maps to NM_016199.2 G35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:7760051 G>C maps to NM_032356.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:1908757 G>T maps to ENST00000381758 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:1905190 C>A maps to ENST00000381758 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:35749959 C>T maps to NM_205834.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:35752836 C>G maps to NM_205834.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr21:47642572 T>A maps to NM_002340.5 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47647499 C>G maps to NM_002340.5 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr21:47611872 C>T maps to NM_002340.5 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr21:47636392 G>T maps to NM_002340.5 C231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr21:47647529 C>T maps to NM_002340.5 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:21207543 T>G maps to ENST00000381541 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:21242931 T>C maps to ENST00000381541 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:21201839 G>T maps to ENST00000381541 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:21242856 C>A maps to ENST00000381541 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr12:21229491 C>A maps to ENST00000381541 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr6:31541367 G>A maps to NM_000595.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:24785582 G>A maps to NM_181657.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr14:24785513 C>A maps to NM_181657.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr14:24785492 C>T maps to NM_181657.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr14:24785063 C>G maps to NM_181657.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr14:24780784 G>T maps to ENST00000336557 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:33585789 C>A maps to ENST00000354476 S1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:33525617 G>A maps to ENST00000354476 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:33567971 C>A maps to ENST00000354476 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:33484661 T>A maps to ENST00000354476 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33505173 C>T maps to ENST00000354476 Q1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:33500928 G>T maps to ENST00000354476 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr2:33246129 C>A maps to ENST00000354476 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:33589304 C>T maps to ENST00000354476 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:33526643 T>A maps to ENST00000354476 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr2:33572461 G>C maps to ENST00000354476 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:33588553 G>T maps to ENST00000354476 T1457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:33518225 G>C did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:33572577 G>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:33411921 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:33413809 C>G maps to ENST00000354476 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:33335696 C>G maps to ENST00000354476 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:33482358 A>T maps to ENST00000354476 K726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:33623605 G>T maps to ENST00000354476 L1721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:33412022 C>A maps to ENST00000354476 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:33534499 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:33477849 C>A maps to ENST00000354476 C702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:74999204 A>T maps to NM_000428.2 C637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr14:74976010 C>A maps to NM_000428.2 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr14:74975650 C>T maps to NM_000428.2 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr14:75078523 T>A maps to NM_000428.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:74976539 C>A maps to NM_000428.2 R1058R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr14:75022275 C>A maps to NM_000428.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:75078230 C>A maps to NM_000428.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:41111392 C>T maps to ENST00000308370 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr19:41115742 C>T maps to ENST00000308370 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr19:41133697 C>A maps to ENST00000308370 P1551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr19:41105432 A>G maps to ENST00000308370 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:6494498 C>T maps to NM_002342.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:179221116 C>A maps to NM_145867.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:46480870 G>A maps to NM_002343.3 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:46490395 G>T maps to NM_002343.3 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:46491362 G>T maps to NM_002343.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:46496867 C>T maps to NM_002343.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:46497382 G>T maps to NM_002343.3 C134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:91502283 A>T maps to NM_002345.3 L158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:91502246 C>T maps to NM_002345.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:91502038 C>A maps to NM_002345.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:24927593 G>T maps to NM_001009909.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:25098930 A>C maps to NM_001009909.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:24759848 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:25004826 G>T maps to NM_001009909.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:25004778 G>C maps to NM_001009909.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:25004765 C>G maps to NM_001009909.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:24936019 A>T did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr11:24998150 T>A maps to NM_001009909.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:24784844 C>A maps to NM_001009909.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:24998156 G>T maps to NM_001009909.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:114541030 G>C did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:114541016 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:114540963 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:114536682 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:114540825 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:114537983 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:114540907 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:114540879 C>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:143867035 G>T maps to NM_003695.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:143867038 C>T maps to NM_003695.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:31648051 C>T maps to NM_025262.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr8:144239831 T>C maps to NM_001130478.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:144239672 C>T maps to NM_001130478.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:143784659 A>G maps to ENST00000292430 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:143784548 C>T maps to ENST00000292430 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:160728992 C>A maps to NM_001198759.1 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:160735148 A>G maps to NM_001198759.1 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:160661620 G>A maps to NM_002349.3 F1701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:160673340 T>C maps to NM_001198759.1 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr2:160673442 T>A maps to NM_001198759.1 A1418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:160742943 G>A maps to NM_001198759.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:6654823 C>A maps to NM_004271.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:160771578 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:160786462 C>T maps to ENST00000263285 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:160789136 C>T maps to ENST00000263285 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:160769810 C>A maps to ENST00000263285 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:160797584 T>A maps to ENST00000263285 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:160783651 C>A maps to ENST00000263285 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:74941232 G>T maps to NM_015364.4 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:4276495 C>A maps to NM_017816.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:4285409 C>T maps to NM_017816.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:4283516 C>T maps to NM_017816.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:99907837 G>A maps to NM_174898.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr19:13211507 C>T maps to NM_005583.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:143846157 C>A maps to NM_023946.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:143856770 G>A maps to NM_177457.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:143846487 C>T maps to NM_023946.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:133403779 G>A maps to ENST00000409034 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr8:143832526 G>T maps to NM_205545.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:43965970 C>A maps to NM_014400.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:43965823 C>A maps to NM_014400.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:42341303 C>T maps to NM_173506.4 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:42342204 G>A maps to NM_173506.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:150327361 T>C maps to NM_194317.3 *172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:150061877 C>A maps to NM_177964.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:150061871 A>G maps to NM_177964.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:24121029 C>G maps to NM_007260.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:219347246 G>C maps to NM_138794.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr6:90348408 C>T maps to NM_020466.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:90348408 C>A maps to NM_020466.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:25357144 C>T maps to NM_001001660.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr1:151134228 C>T maps to NM_212551.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr15:52017210 T>C maps to NM_153374.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:52017074 C>A maps to NM_153374.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:89815302 T>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:100271392 C>T maps to NM_152449.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:235840793 T>A maps to NM_000081.2 I3642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:235918831 A>T maps to NM_000081.2 L2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:235918892 T>A maps to NM_000081.2 K2372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr1:235950597 G>A maps to NM_000081.2 L1588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:235860530 G>A maps to NM_000081.2 Y3472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:235971798 C>G maps to NM_000081.2 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:235866046 C>G maps to NM_000081.2 P3458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:235914597 T>A maps to NM_000081.2 A2564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:235993606 C>A maps to NM_000081.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:235955263 C>T maps to NM_000081.2 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr1:235937219 T>C maps to NM_000081.2 V1902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:235929519 T>A maps to NM_000081.2 K1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:235972422 G>A maps to NM_000081.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:30915807 G>A maps to NM_183058.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:30915075 C>A maps to NM_183058.2 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:30918541 G>T maps to NM_183058.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:30918550 A>G maps to NM_183058.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:42448643 C>A maps to NM_144634.2 G34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:34263781 G>A maps to NM_020426.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:34264777 G>A maps to NM_020426.1 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:21343119 T>C maps to NM_006767.3 S184S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-38-4631-01A-01D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr22:21344733 G>T maps to NM_006767.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr22:21340174 C>T maps to NM_006767.3 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr22:21336851 G>T maps to NM_006767.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr22:21336743 G>T maps to NM_006767.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr8:20110420 C>A maps to NM_021020.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr8:20110357 T>A maps to NM_021020.2 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:20110568 G>A maps to NM_021020.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr10:102763814 G>T maps to NM_032429.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:102763280 G>A maps to NM_032429.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr10:102763433 C>G maps to NM_032429.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:102763688 C>T maps to NM_032429.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr10:102762639 A>C maps to NM_032429.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr13:36049543 C>A maps to NM_005584.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr13:36049915 G>T maps to NM_005584.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr13:36049840 G>A maps to NM_005584.4 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:36049777 G>T maps to NM_005584.4 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr13:36049333 C>A maps to NM_005584.4 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:151505110 C>A maps to NM_006439.4 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:151504237 C>G maps to NM_006439.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:151504264 C>A maps to NM_006439.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr4:151504342 C>T maps to NM_006439.4 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:151504189 C>A maps to NM_006439.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:20198441 G>A maps to NM_182762.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:20198816 T>C maps to NM_182762.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:20198852 G>A maps to NM_182762.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr7:20180569 T>C maps to NM_182762.3 *853W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:20180729 C>A maps to NM_182762.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:39888556 G>A maps to ENST00000361689 Q3316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:39844178 A>G maps to ENST00000361689 G2358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:39750084 A>G maps to ENST00000361689 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:39782999 C>T maps to ENST00000361689 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:39844974 C>A maps to ENST00000361689 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:39549928 A>T maps to ENST00000361689 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:39910444 C>T maps to ENST00000361689 Q4456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:39549967 C>A maps to ENST00000361689 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:39801547 G>T maps to ENST00000289893 G1536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:39893129 A>G maps to ENST00000361689 Q3378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr1:39768594 G>C did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:39785346 A>G maps to ENST00000361689 A1324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr1:39853046 C>T maps to ENST00000361689 Q2783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:39919443 C>T maps to ENST00000361689 V4877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:39888077 G>A maps to ENST00000361689 Q3221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:39910338 C>G maps to ENST00000361689 L4420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:39851374 G>C maps to ENST00000361689 L2644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:39852908 C>T maps to ENST00000361689 Q2737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:39816642 G>T maps to ENST00000361689 E1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:63767230 G>T maps to NM_014067.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr20:13983011 C>G maps to ENST00000310348 S42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr20:16030515 A>T maps to ENST00000310348 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:2252890 C>A maps to NM_003550.2 L314L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-64-5775-01A-01D-1625-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2108972 G>A maps to NM_003550.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr6:43604259 T>C maps to NM_001003690.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43607849 C>T maps to NM_001003690.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:11734864 A>G maps to ENST00000376669 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:11740466 G>T maps to ENST00000376669 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:11736106 G>A maps to ENST00000376669 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:47307000 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:47317081 A>T maps to NM_003682.3 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr11:47345826 G>A maps to NM_003682.3 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:47307013 G>T maps to NM_003682.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:47330185 A>T maps to NM_003682.3 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr11:47311439 G>T maps to NM_003682.3 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:1309327 C>T maps to ENST00000505177 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:166959053 C>T maps to NM_032858.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:166973414 A>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:166990372 G>T maps to NM_032858.1 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:166973513 A>T maps to NM_032858.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:166990947 C>T maps to NM_032858.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:166987186 G>T maps to NM_032858.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:79633526 G>A maps to NM_005360.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr20:39317310 G>A maps to NM_005461.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:39316632 C>A maps to NM_005461.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:35804347 G>T maps to NM_002361.3 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:35790539 G>T maps to NM_002361.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:35791224 C>A maps to NM_002361.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:35786759 G>C maps to NM_002361.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:35791290 G>T maps to NM_002361.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr19:35801011 C>A maps to NM_002361.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:35786759 G>C maps to NM_002361.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:152482653 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:152482310 C>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:152482451 G>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:152482691 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:152482538 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:151303237 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:151303179 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:151303999 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:151303500 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:151303811 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:151303812 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:151304021 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:151302987 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:151303880 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:151303294 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:151303052 G>T did not map to a codon.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr23:151304024 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:151303803 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:151303838 T>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:151304085 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:151303179 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:151303309 G>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:151303998 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:151303776 C>G did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:151303720 T>C did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:151303681 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:151303512 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:151303630 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:148797639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:148798326 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:148797450 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:148797985 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:148797986 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:148796182 A>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:148798267 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:148797682 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:148798361 G>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:148798205 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:148798189 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:148798281 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:148797296 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:148797833 G>C did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:148796169 C>A did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr23:148798376 C>T did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:148796187 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:148797769 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:148798205 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:151899892 G>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:151900188 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:151900541 A>G did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:151900356 A>G did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:151900431 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr23:151900215 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:151900478 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:151900600 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:151900503 A>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:151900414 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:151900579 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:151900013 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:151900059 G>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:151900060 G>A did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr23:151899929 G>C did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:151899993 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:151900673 A>C did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:151900385 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:151935452 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:151935331 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:151935721 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:151935267 G>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:151935512 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:151935686 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:151935328 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:151935924 C>A did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr23:151935913 C>G did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:151935428 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:151935696 G>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:151092767 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:151092879 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:151092780 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:151092220 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:151092250 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:151093074 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:151093079 A>T did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:151092423 A>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:151092387 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:151092362 T>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:151092808 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:151092681 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:151093031 G>A did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr23:151092401 G>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:151092657 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:151092785 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:151092208 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:151283668 T>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:151283819 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:151283686 A>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:151283869 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:151283845 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:151283808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:151869754 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:151869624 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:151869625 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:151869834 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:151869822 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:151869938 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:151870188 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:151870084 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:151870198 C>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:151870218 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:151869775 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:151869628 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:151869541 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:151869910 T>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:151869652 A>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:151869559 T>G did not map to a codon.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr23:151869807 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:151869765 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:151869583 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:151870059 C>G did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:149013193 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:149013594 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:149013507 C>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:149013857 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:149013288 C>G did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:149013829 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:149013497 C>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:149013680 T>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:149013305 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:149013293 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:149013263 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:149013937 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:149013936 T>C did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:149013558 A>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:149013097 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:30268768 T>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:30269223 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:30269347 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:30269286 T>G did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:30269435 G>C did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:30269403 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:30269324 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:30268783 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:30269549 A>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:30268914 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:30269187 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:30269392 C>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:30268910 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:30268939 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:30268894 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:30269347 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:30268897 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:30269466 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:27839828 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:27840393 C>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:27839659 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:27839902 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:27840146 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:27839474 G>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:27840204 A>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:27839859 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:27840431 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:27839624 C>A did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:35820817 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:35820656 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:35820779 T>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:35820399 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:35821059 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:35820907 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:35820855 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:35821114 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:35821106 T>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:35820647 C>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:35821062 C>G did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:35820673 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:35820878 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr23:35820366 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:35820686 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:35820409 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:35820798 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:35820937 G>T did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr23:26157196 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:26157431 A>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:26158063 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:26157898 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:26157297 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:26157546 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:26157779 G>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:26158056 G>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:26157439 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:26157880 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:26157881 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:26157197 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:26158043 C>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:26157178 G>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:26157185 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:26157160 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:26157553 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:26157192 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:26157348 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:26157898 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:30237291 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:30237504 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:30237131 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:30236731 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:30237421 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:30237050 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:30237250 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:30237128 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:30237383 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:30237274 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:30237512 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:30237050 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:30254365 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:30254709 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:30254064 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:30254105 C>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:30254297 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:30254959 T>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:30254960 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:30254904 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:30254135 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:30254209 A>C did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:30254546 A>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:30254095 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:30254524 G>T did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:30254628 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:30260300 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:30261233 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:30261046 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:30260838 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:30261204 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:30260997 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:30260472 C>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:30260504 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:30260329 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:30260716 T>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:30260349 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:30260541 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:30260720 C>G did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:30260933 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:30261170 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:30260942 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:30260294 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:30260574 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:30260393 G>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:30260946 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:30261204 G>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:30261110 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:26213126 A>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:26212995 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:26212157 G>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:26211970 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:26212606 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:26212409 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:26212381 A>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:26211991 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:26212019 T>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:26212555 A>C did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:26212098 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:26212808 G>C did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:26212173 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:26212697 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:26212970 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:26212775 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:26212995 C>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:26212722 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:26212835 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:26212564 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr23:26212441 G>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:26212218 G>T did not map to a codon.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:26212752 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:26212835 C>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:26213003 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:26212383 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:140995492 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:140995905 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:140994910 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:140993252 T>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:140996175 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:140994077 G>C did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:140994372 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:140993693 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:140995521 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:140996308 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:140996385 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:140993844 G>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:140995952 C>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:140996476 C>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:140995524 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:140993802 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:140993472 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:140995948 T>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:140996455 C>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:140993917 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:140993918 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:140993217 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:140994984 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:140996471 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:140994297 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:140995284 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:140994416 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:140995861 T>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:140996383 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:140994334 C>G did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr23:140995627 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:140995913 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:140995914 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:140994801 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:140995889 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:140995441 C>T did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:140995416 C>A did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:140993297 G>A did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:140993707 C>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:140996369 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:140994392 G>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:140995383 C>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:140994192 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:140996386 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:140994822 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:140994324 C>G did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:140996288 G>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:140995206 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:140995409 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:140995479 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:140995162 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:140995295 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:140995614 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:140992862 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:140996098 C>A did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:140993223 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:140995103 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:140994658 C>A did not map to a codon.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:140995830 T>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:140993277 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:140995409 C>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:140995287 G>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:140993866 A>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:140994076 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:140996506 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:140993204 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:140995239 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:140995517 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:140996535 G>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:140994581 G>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:140995220 G>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:140996286 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:140996189 G>C did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:140995100 A>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:140994193 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:140996596 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:140996281 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:141291235 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:141290889 G>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:141290890 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:141290724 G>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:141291283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:141291493 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:141291191 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:141291483 T>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:141290863 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:141291519 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:141291678 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:141291698 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:141290893 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:141291381 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:141291382 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:141291724 G>T did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:141291160 A>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:141291039 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:141291185 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:141290745 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:141291431 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:141291416 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:141291002 C>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:141291757 C>A did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:141291446 C>G did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:141291099 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:141290685 C>A did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:141290802 G>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:141291590 C>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:141291175 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:141291279 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:141291121 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:141291649 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:140967166 C>A did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:140984613 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:140985461 A>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr23:140969492 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:140983192 G>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:140985529 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:140985491 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:140984512 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:140926217 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:140983094 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:140983190 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:140983191 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:140953328 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:140953364 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:140985168 G>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:140985256 G>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:140984474 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:140969217 A>G did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:140984543 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:140969363 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:140985548 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:140969329 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:140985420 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:140984909 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:140985236 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:140969465 A>G did not map to a codon.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr23:140953387 C>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:140985060 A>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:140969260 C>G did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:140969200 C>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:140984970 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:140983303 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:140984491 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:140984516 G>C did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:140969368 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:140985370 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:140984986 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:140984899 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:140984796 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:140985086 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:140985303 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:140969492 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:140953351 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:140984731 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:51641288 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:51641677 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr23:51645009 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:51639759 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:51640680 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:51639711 C>A did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr23:51644714 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:51637833 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:51638237 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:51638352 A>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:51639803 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:51639632 G>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:51637415 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:51638313 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:51640672 C>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:54837314 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:54841722 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:54839945 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:54839586 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:54841755 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:54838628 C>A did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr23:54837296 G>A did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:54837359 G>A did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:54841755 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:54838684 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:75649134 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:75649076 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:75649283 C>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:75649782 C>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:75649783 C>A did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr23:75648899 G>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:75648397 G>T did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:75650134 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:75649491 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:75649327 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:75649194 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:75649048 G>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:75650018 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:75649312 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:75650313 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:75649517 G>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:75648362 C>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:75648965 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:75650065 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:75003458 G>C did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:75003938 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:75003399 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:75004228 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:75004592 G>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:75004249 G>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:75004308 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:75003735 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:75004433 A>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:75003414 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:75003877 G>T did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:75004326 A>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:75003785 A>T did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr23:75004085 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:75003850 C>A did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:75004054 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:75004217 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:55479418 G>C did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:55479157 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:55479279 A>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:55479392 G>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:55478883 A>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:23889628 A>G maps to NM_019066.4 Y1087Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:23889964 G>T maps to NM_019066.4 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr15:23889140 T>C maps to NM_019066.4 *1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:23890519 G>A maps to NM_019066.4 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:23889430 A>T maps to NM_019066.4 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:23890798 G>T maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:23889460 G>C maps to NM_019066.4 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr15:23890792 G>T maps to NM_019066.4 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr15:23889219 C>A maps to NM_019066.4 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:23889610 C>A maps to NM_019066.4 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:66023764 C>A maps to NM_001033057.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:65342807 C>G did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:65367573 C>T maps to NM_001033057.1 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:65367576 C>A maps to NM_001033057.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:65456113 A>T maps to NM_001033057.1 L268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:65456114 A>G maps to NM_001033057.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr3:65438996 T>C maps to NM_001033057.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:65342343 G>A maps to NM_001033057.1 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:77789354 A>T maps to NM_012301.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:77764362 G>A maps to NM_012301.3 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:78150962 C>A did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr7:77764448 G>T maps to NM_012301.3 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr7:77764518 C>A maps to NM_012301.3 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:79082587 C>A maps to NM_012301.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:77797302 G>T maps to NM_012301.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:79082429 C>G maps to NM_012301.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:77789516 G>T maps to NM_012301.3 Y890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:114226574 G>A maps to NM_001142782.1 W1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:114215272 C>A maps to NM_001142782.1 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:114225727 G>T maps to NM_001142782.1 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:114157247 A>T maps to NM_001142782.1 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:114128102 A>C maps to NM_001142782.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr1:114224870 C>T maps to ENST00000369617 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:49022560 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:49022528 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:49022559 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:49021365 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr23:49021097 C>G did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:77150819 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:77086362 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:77126339 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:77112881 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:77112245 C>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:77112342 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:77109423 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:77126322 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:77112935 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:77112882 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:10764812 G>T maps to NM_005906.3 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr6:10796245 G>A maps to NM_005906.3 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:95715323 A>G did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:95691560 G>A maps to NM_002371.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:95713807 C>A maps to NM_002371.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr8:120252493 C>T maps to ENST00000276681 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:56363624 C>G maps to NM_006785.2 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr18:56414821 A>T maps to NM_006785.2 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr18:56348549 C>T maps to NM_006785.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:56377242 C>G maps to NM_006785.2 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr18:56409232 G>A maps to NM_006785.2 W580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr9:72833382 T>A maps to NM_153267.4 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:72783655 T>C maps to NM_153267.4 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:179192955 A>G maps to NM_014757.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:179192658 G>T maps to NM_014757.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:179192989 C>T maps to NM_014757.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:179201688 G>T maps to NM_014757.4 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:95724743 C>T maps to NM_032427.1 Q761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:95825223 T>C maps to NM_032427.1 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:95826240 C>A maps to NM_032427.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:141074130 G>A maps to ENST00000509479 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr4:140641169 C>G maps to ENST00000509479 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:140640517 C>A maps to ENST00000509479 E1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:141074180 C>A maps to ENST00000509479 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr4:140641355 C>A maps to ENST00000509479 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149638183 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149638522 G>C did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149638600 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149638621 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149638633 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:149639225 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:149639222 C>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:149638792 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:149638911 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:149639108 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:149639244 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:149638774 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:149639336 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:149638270 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:149631067 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:149639101 G>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:149639427 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:149639650 A>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:149638354 G>T did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:149638349 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:149671597 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:149638403 C>G did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:149671614 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:149639149 C>A did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:149638204 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:149638376 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:149638281 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:149639080 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:149642050 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:119669821 C>A maps to NM_005907.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:119670137 C>A maps to NM_005907.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr6:119670167 C>A maps to NM_005907.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:117948253 C>T maps to NM_006699.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:118065452 G>A maps to NM_006699.3 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:139994316 C>T maps to NM_016219.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:109117173 G>C maps to NM_002372.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr5:109124721 T>G maps to NM_002372.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:109153045 A>T maps to NM_002372.2 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:109120442 A>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:109181675 T>G maps to NM_002372.2 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:109181593 T>A maps to NM_002372.2 L910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:91450650 C>T maps to NM_006122.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:91452641 C>T maps to NM_006122.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr15:91447493 C>T maps to NM_006122.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:12758268 G>C maps to NM_000528.3 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:12768895 G>A maps to NM_000528.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:12760785 C>A maps to NM_000528.3 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr19:12760824 G>A maps to NM_000528.3 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr4:6580190 G>C maps to NM_015274.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:6611596 G>T maps to NM_015274.1 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:6577071 G>C maps to NM_015274.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr15:75652054 C>T maps to NM_006715.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr15:75648463 G>A maps to NM_006715.2 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:103557060 A>G maps to NM_005908.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr4:103644165 C>T maps to NM_005908.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:103579012 C>A maps to NM_005908.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:103560924 C>A maps to NM_005908.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:96053764 C>A maps to NM_024641.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr1:38265670 G>A maps to NM_001113482.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr1:38260315 C>G maps to NM_001113482.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:38265343 C>G maps to NM_001113482.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:12491435 G>A maps to NM_018050.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:43590551 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:43592025 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:43515602 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:43599970 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:43603415 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:43652682 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:43640773 T>C did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:43626801 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:43626796 G>C did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:43626787 A>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:43662544 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:43821528 C>A maps to ENST00000382031 R2858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:43814039 G>A maps to ENST00000382031 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr15:43817873 G>A maps to ENST00000382031 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:43818392 G>A maps to ENST00000382031 E1812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr15:43819214 G>A maps to ENST00000382031 K2086K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr15:43814036 C>T maps to ENST00000382031 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr15:43815986 A>G maps to ENST00000382031 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:71490201 C>T maps to NM_005909.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:71490030 C>A maps to NM_005909.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:71493792 C>A maps to NM_005909.3 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr5:71493279 T>C maps to NM_005909.3 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:71490075 C>A maps to NM_005909.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:71492127 T>A maps to NM_005909.3 A982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:71495655 C>A maps to NM_005909.3 T2158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:71495530 G>T maps to NM_005909.3 E2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:71495083 G>T maps to NM_005909.3 E1968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:71491581 C>A maps to NM_005909.3 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:71495082 C>T maps to NM_005909.3 P1967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr5:71490840 T>C maps to NM_005909.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr5:71494365 C>T maps to NM_005909.3 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr5:71492073 G>A maps to NM_005909.3 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:71479621 C>A maps to NM_005909.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr5:71492535 C>T maps to NM_005909.3 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:172926241 C>T maps to NM_199227.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:172942560 A>C maps to NM_199227.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:242161852 G>A maps to NM_001004343.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:242159523 C>A maps to NM_001004343.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:242161880 C>A maps to NM_001004343.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:242159548 G>T maps to NM_001004343.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:242161835 G>A maps to NM_001004343.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:242159554 G>T maps to NM_001004343.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:242162077 C>T maps to NM_001004343.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:242161820 G>T maps to NM_001004343.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:17838466 G>T maps to NM_018174.4 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:17838799 C>T maps to NM_018174.4 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:17837846 A>T maps to NM_018174.4 K552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:210557841 C>T maps to NM_002374.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:210574773 C>T maps to NM_002374.3 P1623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:210557722 G>T maps to NM_002374.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:210574779 C>A maps to NM_002374.3 T1625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:210574908 A>T maps to NM_002374.3 P1668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:210518020 C>T maps to NM_002374.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:210561472 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:210559332 A>T maps to NM_002374.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:210574869 G>C maps to NM_002374.3 A1655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:210560640 C>G maps to NM_002374.3 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:66737041 A>T maps to NM_002755.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:21206508 G>T maps to NM_145109.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:21207865 G>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:21201776 C>G maps to NM_145109.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:21201791 G>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:21201776 C>A maps to NM_145109.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:21201776 C>A maps to NM_145109.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr17:21208418 C>G maps to NM_145109.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:12032560 G>T maps to ENST00000415385 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:12028609 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:12028688 G>C did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:12016548 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:68065080 A>G maps to NM_145160.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr15:67885299 A>T maps to NM_145160.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:67532288 C>A maps to NM_002758.3 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:67522850 G>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr17:67521064 C>G maps to NM_002758.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:7976016 G>C maps to ENST00000425613 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr19:7975183 G>T maps to ENST00000425613 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:56160758 C>T maps to NM_005921.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:40710445 C>T maps to NM_002446.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:40704285 G>T maps to NM_002446.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr19:40710442 G>A maps to NM_002446.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:40710508 G>T maps to NM_002446.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:65365944 C>A maps to NM_002419.3 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53876413 G>T maps to NM_001193511.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:53876153 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:53876885 G>A maps to NM_001193511.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:53877415 C>A maps to NM_001193511.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:53876678 G>C maps to NM_001193511.1 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr12:53879206 T>A maps to NM_001193511.1 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:53875979 C>G maps to NM_001193511.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:185198314 G>T maps to NM_004721.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:185191545 G>A maps to NM_004721.3 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:185146648 G>T maps to NM_004721.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr3:185161272 G>T maps to NM_004721.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr3:185181372 G>A maps to NM_004721.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:43368042 G>C maps to ENST00000344686 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:43364127 G>A maps to ENST00000344686 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:19389160 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:19389462 G>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:19444421 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:19398321 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:19392631 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:19392722 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:19389564 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:19443725 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:19387327 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:19443708 T>C did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:19410150 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:19379643 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:19387334 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:19507054 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:19389508 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128072408 C>A maps to NM_006609.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr2:128066327 G>T maps to NM_006609.3 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:61744397 C>T maps to NM_203351.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:61766974 C>T maps to NM_203351.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:61771007 C>T maps to NM_203351.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:161508850 C>T maps to NM_005922.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:161527736 G>T maps to NM_005922.2 G1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr6:161522922 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:161530848 G>T maps to NM_005922.2 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:136926373 C>A maps to NM_005923.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:136904769 T>A maps to NM_005923.3 K1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr6:136913357 C>A maps to NM_005923.3 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:137019811 A>G maps to NM_005923.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:27687468 C>A maps to NM_004672.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:91257067 C>A maps to NM_145331.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:30747104 G>A maps to NM_005204.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:30740625 C>T maps to NM_005204.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748248 G>C maps to NM_005204.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:30748320 G>C maps to NM_005204.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:71206861 C>A maps to NM_033141.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:71205043 C>A maps to NM_033141.2 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:71197237 C>T maps to NM_033141.2 G1072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:71197333 T>A maps to NM_033141.2 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr14:71209066 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:47957469 G>C maps to ENST00000426837 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr3:47960229 C>A maps to ENST00000426837 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:47951343 C>A maps to ENST00000426837 G1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:47956429 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr3:47950807 G>A maps to ENST00000426837 V1718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:39103296 C>A maps to NM_001042600.1 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:39086174 G>A maps to NM_001042600.1 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:39103261 C>G maps to NM_001042600.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr19:39103252 G>A maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:39090577 G>C maps to NM_001042600.1 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:39086639 C>T maps to NM_001042600.1 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:39101765 A>T maps to NM_001042600.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr19:39090622 G>C maps to NM_001042600.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:39104542 G>A maps to NM_001042600.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:64564480 G>A maps to NM_004579.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:64564574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:39514069 G>A maps to NM_003618.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:39487786 C>A maps to NM_003618.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr2:39542449 C>A did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr2:39481641 C>T maps to NM_003618.2 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:39487870 C>A maps to NM_003618.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr2:39515341 G>C maps to NM_003618.2 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:39485693 T>C maps to NM_003618.2 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:102314936 T>C maps to NM_145686.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:75379384 G>T maps to NM_033063.1 C10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:136693703 G>A maps to NM_001198609.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:136681911 C>A maps to NM_001198609.1 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:36640514 C>T maps to NM_018067.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:20062498 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:20030536 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:20074797 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:20082922 C>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr23:20031730 T>G did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:20034373 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:20033339 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:20062530 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:20081687 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:20043821 C>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:20043196 C>G did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:20029093 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr23:20028992 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:20043801 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:20033361 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:20071026 G>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:135314285 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:135303095 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:135301624 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:135314149 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:135323325 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:135303036 T>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:135328239 T>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:135326889 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:135312578 C>T did not map to a codon.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr23:135308163 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:135322607 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:135323318 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:135314095 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr4:156273848 T>A maps to NM_001039580.1 K574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr22:22142564 G>A maps to NM_138957.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:86988934 T>A maps to NM_138982.2 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:87019675 C>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr4:87028498 C>A maps to NM_138982.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr22:50693761 C>T maps to NM_002969.3 A296A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-NJ-A4YQ-01A-11D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:36106175 C>T maps to NM_002754.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:36099122 C>T maps to NM_002754.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:36106755 T>C maps to NM_002754.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:36075267 C>G maps to NM_139012.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:36041824 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr6:36043627 C>T maps to NM_139012.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr6:36075337 T>C maps to NM_139012.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:30129041 G>T maps to NM_002746.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:30129406 C>A maps to NM_002746.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:30129732 G>A maps to NM_002746.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:48256145 C>T maps to NM_002747.3 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:48255620 G>C maps to NM_002747.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr18:48255740 C>A maps to NM_002747.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:48248366 G>T maps to NM_002747.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:48252468 G>T maps to NM_002747.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:19284395 G>T maps to NM_139034.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr10:49634456 G>T maps to NM_139049.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:49628331 G>A maps to NM_139049.1 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:49634456 G>T maps to NM_139049.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:45924190 C>T maps to NM_005456.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:45925560 C>T maps to NM_005456.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:45924235 G>T maps to NM_005456.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:51043817 C>T maps to ENST00000329492 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:1797082 C>T maps to NM_015133.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:1818200 C>A maps to NM_015133.3 A1187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:1797136 C>T maps to NM_015133.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:1798332 C>T maps to NM_015133.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:179663482 C>A maps to NM_002752.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:179688754 T>A maps to NM_002752.4 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:179668156 T>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr9:128206872 G>A maps to NM_001006617.1 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:206905048 T>C maps to NM_032960.2 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr3:50684207 C>T maps to NM_004635.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:50677798 C>T maps to NM_004635.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:112326314 G>A maps to NM_139078.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:112323738 G>T maps to NM_139078.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:42108777 G>A maps to NM_001128608.1 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr15:42109165 G>T maps to NM_001128608.1 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr15:42092019 G>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr2:27248598 C>T maps to NM_012326.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:44060625 C>T maps to NM_001123066.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr17:44073921 C>A maps to NM_001123066.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:44060874 C>G maps to NM_001123066.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:44060901 G>T maps to NM_001123066.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:44101404 G>A maps to NM_001123066.3 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:164449920 G>T maps to ENST00000514618 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:164534584 G>A maps to NM_017923.3 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:164506996 G>T maps to ENST00000514618 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:164534470 G>A maps to ENST00000514618 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:164534584 G>C maps to NM_017923.3 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:164507068 G>A maps to ENST00000514618 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr4:164507068 G>A maps to ENST00000514618 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:164534584 G>T maps to NM_017923.3 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:164506982 C>T maps to ENST00000514618 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60821889 C>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:60814343 G>A maps to NM_152598.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:60814268 C>G maps to NM_152598.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:60821815 C>T maps to NM_152598.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:60821830 T>C maps to NM_152598.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:60799893 A>G maps to NM_152598.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:16067612 C>A maps to NM_001102562.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:16067807 G>T maps to NM_001102562.1 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:16067902 C>G did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:16067855 G>T maps to NM_001102562.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:16067867 T>C maps to NM_001102562.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr5:16091094 G>A maps to NM_001102562.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:16177990 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:16177927 C>T maps to NM_001102562.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:16067785 G>T maps to NM_001102562.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:16177987 A>T maps to NM_001102562.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:217124199 G>T maps to NM_020814.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:217124301 G>A maps to NM_020814.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:217142539 G>C maps to NM_020814.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:217124169 G>A maps to NM_020814.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:217142434 G>T maps to NM_020814.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:217124066 G>T maps to NM_020814.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:10423936 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:10415777 C>T maps to NM_005885.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:10417473 G>A maps to NM_005885.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:160602443 A>T maps to NM_022826.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:45953763 C>A maps to NM_145021.4 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:45953769 C>A maps to NM_145021.4 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr10:45954694 C>A maps to NM_145021.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:45959699 G>A maps to NM_145021.4 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:119731984 C>T maps to NM_006770.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:119699918 G>T maps to NM_006770.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:119727849 C>A maps to NM_006770.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:119750740 C>T maps to NM_006770.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:220805568 C>T maps to NM_018650.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:220752847 G>A maps to NM_018650.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:220808734 G>C maps to NM_018650.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:220825453 G>C maps to NM_018650.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:220835439 C>T maps to NM_018650.3 R774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:220835210 G>T maps to NM_018650.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:220752823 C>T maps to NM_018650.3 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:220791807 G>T maps to NM_018650.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:220791830 C>T maps to NM_018650.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr1:220835283 C>T maps to NM_018650.3 R722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:220835230 G>A maps to NM_018650.3 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:63670187 A>T maps to NM_001039469.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:63666129 G>T maps to NM_001039469.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:63676621 C>T maps to NM_001039469.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr11:63668528 C>G maps to NM_001039469.2 Y363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr11:63668050 G>A maps to NM_001039469.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:103932327 T>G maps to ENST00000335102 L289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:103969273 C>T maps to ENST00000335102 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:45783903 A>T maps to NM_031417.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:45781215 G>T maps to NM_031417.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:57910303 A>G maps to NM_004990.2 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:198570479 C>G maps to NM_138395.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:198570929 G>T maps to NM_138395.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:198571773 G>T maps to NM_138395.3 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr2:198570446 G>T maps to NM_138395.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:198570233 T>C maps to NM_138395.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:198571469 T>A maps to NM_138395.3 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:198571569 C>A maps to NM_138395.3 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:198571794 C>T maps to NM_138395.3 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:198570149 C>T maps to NM_138395.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:71663284 G>A maps to NM_001017967.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr16:71668339 C>G maps to NM_052858.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:71663395 A>G maps to NM_001017967.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:160328730 C>A maps to NM_002377.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:29455568 C>T maps to NM_052967.1 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr6:29455256 G>T maps to NM_052967.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:186961389 T>A maps to NM_139125.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:186943139 G>A maps to NM_001879.5 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:186978604 G>T maps to NM_139125.3 C157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:186937995 T>A maps to NM_001879.5 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:186953827 G>T maps to NM_139125.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:186954341 G>T maps to NM_139125.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:186974547 G>T maps to NM_139125.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:186980340 G>T maps to NM_139125.3 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr3:186954191 C>A maps to NM_139125.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:186944246 C>A maps to NM_001879.5 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr3:186947572 C>T maps to NM_001879.5 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:11097865 G>A maps to NM_006610.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr1:11103419 G>C maps to NM_006610.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:12963014 C>A maps to NM_014975.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:12976613 C>T maps to NM_014975.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:12981643 G>T maps to NM_014975.2 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr19:12958666 T>A maps to NM_014975.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:12976218 C>A maps to NM_014975.2 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:46487707 C>G maps to NM_015112.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:46500534 T>A maps to NM_015112.2 R1398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:46500345 C>A maps to NM_015112.2 R1335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:66460706 G>A maps to NM_001164664.1 R1900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:66462833 G>T maps to NM_001164664.1 R2609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:66462215 G>A maps to NM_001164664.1 A2403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:66462680 G>T maps to NM_001164664.1 G2558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:66055637 G>C maps to NM_001164664.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr5:66400348 C>T maps to NM_001164664.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:66405957 A>G maps to NM_001164664.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr5:66462785 C>T maps to NM_001164664.1 R2593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:66426036 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:27475432 C>T maps to NM_001172303.1 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:82045297 T>A maps to NM_000429.2 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:82036221 G>T maps to NM_000429.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr10:82049158 G>T maps to NM_000429.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr10:82049167 C>T maps to NM_000429.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:85769040 A>T maps to NM_005911.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:85766469 C>T maps to NM_005911.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:3785123 G>T maps to NM_139355.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:3783218 T>C did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:3779572 G>A maps to NM_002378.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:3779790 G>T maps to NM_002378.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:3778544 C>A maps to NM_002378.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:3779010 C>A maps to NM_002378.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:31194359 G>T maps to NM_002379.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:31188924 G>C maps to NM_002379.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:31188897 C>A maps to NM_002379.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:99015916 G>A maps to ENST00000254898 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:98943568 G>T maps to ENST00000254898 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:98954083 C>T maps to ENST00000254898 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:99047913 C>T maps to ENST00000254898 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:98943359 G>T maps to ENST00000254898 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr8:98943316 C>T maps to ENST00000254898 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr20:43933170 C>A maps to ENST00000372754 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr20:43926891 G>A maps to ENST00000372754 N489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr20:43927089 C>T maps to ENST00000372754 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:138643961 G>A maps to ENST00000394800 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:3835372 C>G maps to NM_020746.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:3842152 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:65550993 C>T maps to NM_145114.1 L65L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-6594-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:65560455 C>A maps to NM_002382.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:65544681 G>A maps to NM_002382.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr14:65544711 G>A maps to NM_002382.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr14:65544712 G>A maps to NM_002382.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr16:29821464 A>G maps to NM_002383.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:47799765 C>A maps to ENST00000424334 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr18:47800234 T>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:47796067 G>C maps to NM_015845.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:51686215 T>C maps to NM_003927.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr18:51750539 C>T maps to NM_003927.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:1578485 C>T maps to NM_003926.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr19:8953770 C>T maps to NM_145208.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:129158649 C>G maps to NM_003925.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:149227674 G>T maps to ENST00000404807 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:149247112 G>T maps to ENST00000404807 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:149247497 G>T maps to ENST00000404807 E1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:149247151 C>T maps to ENST00000404807 S1317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:149220166 T>C maps to ENST00000404807 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:149227561 G>T maps to ENST00000404807 G684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:149247400 C>T maps to ENST00000404807 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr12:57919410 C>T maps to NM_052897.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr14:36785916 T>C maps to NM_016586.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:54527922 G>A maps to NM_000242.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:54529049 T>G maps to NM_000242.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr10:54528268 C>T maps to NM_000242.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:54529058 C>A maps to NM_000242.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:54528148 G>T maps to NM_000242.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr10:54527929 G>T maps to NM_000242.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:99725359 C>T maps to NM_203397.1 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:89756989 C>A maps to NM_203406.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:152150693 A>T maps to NM_021038.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:97999158 C>T maps to ENST00000376673 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:131573491 G>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:131518704 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:131540321 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:131524888 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:131526361 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:131540342 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr23:131573567 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:131540290 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr6:20113208 G>A maps to NM_001080480.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr6:20124654 G>C maps to NM_001080480.1 Y297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:54682525 C>A maps to NM_024298.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:74778253 C>A maps to NM_001025101.1 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr18:74696829 T>A maps to NM_001025101.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:74701953 C>A maps to NM_001025101.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr17:49280152 A>G maps to ENST00000389496 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:49280557 A>C maps to ENST00000389496 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr16:84124547 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:21887654 G>A did not map to a codon.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr23:21896703 C>G did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:21900703 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:21861373 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:21887671 A>G did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:21887737 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:21871550 A>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:21896618 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:21900606 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:21863481 G>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:21861317 G>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr16:89986022 C>T maps to ENST00000304984 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr16:89986055 C>T maps to ENST00000304984 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:89986364 G>A maps to ENST00000304984 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:13885376 C>T maps to NM_000529.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr18:13884794 C>T maps to NM_000529.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr18:13884625 A>T maps to NM_000529.2 *298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr18:13884722 G>T maps to NM_000529.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:13884809 C>T maps to NM_000529.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr18:13884722 G>T maps to NM_000529.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr18:13885088 G>T maps to NM_000529.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr18:13885061 C>T maps to NM_000529.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:13884887 G>A maps to NM_000529.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr18:13885435 C>A maps to NM_000529.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:13884959 C>A maps to NM_000529.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:54824868 T>C maps to ENST00000371389 *361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:54824387 C>T maps to ENST00000371389 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:54824717 C>A maps to ENST00000371389 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:54824345 G>T maps to ENST00000371389 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:54824012 C>A maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr20:54823931 G>A maps to ENST00000371389 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:54824513 C>A maps to ENST00000371389 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:54824138 G>A maps to ENST00000371389 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:58039570 G>A maps to NM_005912.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:58039135 A>G maps to NM_005912.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:58039474 A>T maps to NM_005912.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr18:58039198 C>T maps to NM_005912.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr18:13826432 C>G maps to NM_005913.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr18:13826013 C>T maps to NM_005913.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:13825904 T>G maps to NM_005913.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr18:13825811 C>A maps to NM_005913.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:13826378 C>G maps to NM_005913.2 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr18:13826336 C>A maps to NM_005913.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr18:13826519 C>A maps to NM_005913.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr18:13826730 A>T maps to NM_005913.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr18:13825920 G>T maps to NM_005913.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:13826138 C>G maps to NM_005913.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:119183320 C>A maps to NM_006500.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:119185741 C>T maps to NM_006500.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr18:29340104 G>A maps to NM_001034172.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:29340602 C>A maps to NM_001034172.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:103349435 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:103349077 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:103349149 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:103349076 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:103349496 T>G did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:103349838 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:112437458 C>A maps to NM_001085377.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:112676325 C>A maps to NM_001085377.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:112720710 C>A maps to NM_001085377.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:112458518 C>A maps to NM_001085377.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:112406906 T>C maps to NM_001085377.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:112421000 C>A maps to NM_001085377.1 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:182812356 T>A maps to NM_020166.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:182810277 C>A maps to NM_020166.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:182733249 T>C maps to NM_020166.3 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:182759538 C>A did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr3:182743551 A>G maps to NM_020166.3 Y574Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:138687137 A>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:138667242 T>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:138708866 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr23:138698556 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:138708795 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:138680576 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:138728981 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:138689897 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:138708451 A>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:138714569 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:138714570 G>T did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr23:138729001 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:138670543 C>A did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:138671998 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:138697091 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:138698514 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:138672049 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:138689895 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:138697086 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:138672049 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:138708395 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:138713552 C>A did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:138699759 C>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:138701770 A>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:138684575 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:138679701 A>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:138708384 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr13:113728837 C>T maps to NM_001112732.1 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:113740514 G>A maps to NM_001112732.1 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr13:113714935 C>T maps to NM_001112732.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr13:113719371 G>T maps to NM_001112732.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:182947467 G>T maps to NM_015078.2 Y677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:183059374 G>T maps to NM_015078.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:183056659 A>T maps to NM_015078.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:183035951 C>A maps to NM_015078.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr3:183006943 C>A maps to NM_015078.2 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr22:41075733 G>A maps to NM_005297.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr22:41077313 C>A maps to NM_005297.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:100395738 T>A maps to NM_032503.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:100395639 G>A maps to NM_032503.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr6:100395746 G>A maps to NM_032503.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:100368953 G>A maps to NM_032503.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:150550956 C>G maps to NM_021960.4 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr1:150551664 C>A maps to NM_021960.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:150551691 C>A maps to NM_021960.4 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr1:150549904 C>A maps to NM_021960.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:13228162 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:13233304 A>T maps to NM_182751.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:13239663 T>C maps to NM_182751.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:127336222 G>C maps to NM_004526.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:127339965 C>G maps to NM_004526.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr3:127325632 C>T maps to NM_004526.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:127339569 G>T maps to NM_004526.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:127327829 C>A maps to NM_004526.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:52147592 G>T maps to ENST00000419835 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr6:52141251 C>A maps to ENST00000419835 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:47660845 C>A maps to NM_003906.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr21:47663460 C>T maps to NM_003906.3 E1738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:47655301 C>T maps to NM_003906.3 A1941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr21:47705110 T>A maps to NM_003906.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr21:47697525 G>C maps to NM_003906.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr21:47678950 G>A maps to NM_003906.3 V1212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:48883389 C>A maps to NM_182746.1 S585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:48883390 G>A maps to NM_182746.1 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:35802718 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:35802586 C>T maps to NM_006739.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr22:35817406 C>T maps to NM_006739.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr22:35817362 C>T maps to NM_006739.3 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr22:35806851 C>T maps to NM_006739.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr22:35809930 A>T maps to NM_006739.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:136609034 C>A maps to NM_005915.4 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:136630274 C>T maps to NM_005915.4 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:136605725 C>T maps to NM_005915.4 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:99696338 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:99697244 T>A maps to NM_005916.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:5958577 C>T maps to NM_032485.4 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:5966773 A>T maps to NM_032485.4 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr20:5932735 G>A maps to NM_032485.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:5939245 A>G maps to NM_032485.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:5974338 C>T maps to NM_032485.4 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:5948642 G>T maps to NM_032485.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:7589949 C>G maps to NM_020533.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:7593513 G>T maps to NM_020533.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:7598407 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:7591410 C>G maps to NM_020533.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:7591449 G>A maps to NM_020533.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:85403455 T>C maps to NM_153259.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:85403488 A>G maps to NM_153259.2 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:85397143 C>G maps to NM_153259.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:85506694 G>A maps to NM_018298.9 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:85499835 T>A maps to NM_018298.9 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:6302907 G>T maps to NM_024596.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:6302376 G>A maps to NM_024596.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:6272335 C>T maps to NM_024596.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:49958271 G>T maps to NM_001012300.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49959861 G>T maps to NM_001012300.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:94248657 T>A maps to NM_024717.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:94207046 C>A maps to NM_024717.4 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:94253648 C>T maps to NM_024717.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:94417131 T>A maps to NM_001002796.2 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:94050519 G>A maps to NM_024717.4 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:94927251 G>T maps to NM_018349.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr15:94841679 C>T maps to NM_018349.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr15:94983436 A>G maps to NM_018349.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:119739398 T>C did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr23:119739376 A>G did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:119746107 A>C did not map to a codon.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr23:119739989 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:119746094 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:30672203 G>A maps to NM_014641.2 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:30672753 C>T maps to NM_014641.2 K1402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:30676134 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:30681751 C>G maps to NM_014641.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:30675937 C>A maps to NM_014641.2 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:41621100 C>T maps to NM_005586.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:41621192 C>A maps to NM_005586.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:114655760 C>T maps to NM_199072.4 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:37612387 G>C maps to ENST00000297153 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:37620024 G>A maps to ENST00000297153 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:37605235 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:37618146 G>T maps to ENST00000297153 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:37619859 G>T maps to ENST00000297153 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:37614115 C>A maps to ENST00000297153 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:37611711 G>A maps to ENST00000297153 Y806Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:47504502 T>A maps to NM_001113498.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:47426713 A>T maps to NM_001113498.2 L651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:47601037 C>T maps to NM_001113498.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:47530707 C>T maps to NM_001113498.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:47601034 G>T maps to NM_001113498.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:47530667 C>A maps to NM_001113498.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr14:47351349 A>T maps to NM_001113498.2 Y771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:47600917 T>A maps to NM_001113498.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:47346707 A>C maps to NM_001113498.2 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr14:47342757 A>T maps to NM_001113498.2 L877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:47566195 A>T maps to NM_001113498.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:47504235 G>T maps to NM_001113498.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:47311160 G>T maps to NM_001113498.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr14:47566204 G>A maps to NM_001113498.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr14:47343382 C>A maps to NM_001113498.2 E820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr14:47343355 G>A maps to NM_001113498.2 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:47342681 A>T maps to NM_001113498.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:63832412 G>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:207621749 G>A maps to NM_001039845.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:207621659 C>T maps to NM_001039845.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:207619826 G>A maps to NM_001039845.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:75692873 C>T maps to NM_005918.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:75693727 G>T maps to NM_005918.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:68708777 T>C maps to NM_017440.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:68720478 C>A maps to NM_017440.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:69218141 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:204513694 A>T maps to NM_002393.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:90468062 C>A maps to NM_014611.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:90402560 G>A maps to NM_014611.1 A3396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:90382347 G>C maps to NM_014611.1 L4516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:90428641 A>T maps to NM_014611.1 C2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:90354757 A>C maps to NM_014611.1 V5526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:90458989 C>T maps to NM_014611.1 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:90449993 G>A maps to NM_014611.1 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:90499591 T>A maps to NM_014611.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:90424409 T>A maps to NM_014611.1 G2307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:90472077 G>A maps to NM_014611.1 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:90453324 C>T maps to NM_014611.1 L1429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:90466039 C>T maps to NM_014611.1 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:90388456 C>G maps to NM_014611.1 V4091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr6:90365609 C>G maps to NM_014611.1 L5121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:90421911 C>G maps to NM_014611.1 L2498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:90460091 C>T maps to NM_014611.1 G1129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:84025048 G>A maps to NM_002395.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:84117592 G>A maps to NM_002395.4 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:84108162 C>T maps to NM_002395.4 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr18:48458656 A>G maps to NM_002396.4 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:37975082 G>A maps to NM_022756.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr3:168833634 T>A maps to NM_004991.3 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:169099028 C>T maps to NM_004991.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:153297885 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:153297825 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:153297829 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:153297808 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:153296369 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:153363092 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:153363093 C>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:153296253 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:153296437 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:153295920 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr17:37566051 G>A maps to NM_004774.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:37565296 G>C maps to NM_004774.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:37563814 A>G maps to NM_004774.3 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr17:37584014 G>C maps to NM_004774.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:37566427 C>A maps to NM_004774.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:37566259 G>A maps to NM_004774.3 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:37571362 G>C maps to NM_004774.3 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr17:37596725 C>A maps to NM_004774.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:4635146 T>G maps to NM_001001683.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:70345278 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:70345899 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:70342989 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:70347237 G>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:70348170 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:70347241 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:70354969 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:70342078 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:70340929 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:70356804 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:70354596 G>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:70356266 A>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:70345264 G>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:70349020 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:70347270 T>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:70341001 G>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:70339601 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:70339602 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:70345559 T>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:70343027 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:70345906 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:70352292 G>C did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:70343053 G>C did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:70343073 G>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:70342951 C>G did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:70357729 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:70345918 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:70356418 C>A did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:70344992 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:70360512 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:70345276 G>C did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:70357792 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:70357793 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:70360627 A>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:70347743 G>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:70341630 C>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:70348449 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:70340945 G>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:70346924 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:70343475 G>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:70340904 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:70340905 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:70348216 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:70356319 C>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:70342100 G>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:70357596 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:70341557 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:70352233 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:70352314 G>T did not map to a codon.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr23:70343060 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:70349189 C>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:70342141 T>C did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:70352356 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:70341626 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:70349189 C>A did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:70348240 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:151134201 C>T maps to NM_053002.4 Q2099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:151083775 A>G maps to NM_053002.4 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:151105803 G>T maps to NM_053002.4 L1730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr3:150881711 G>T maps to NM_053002.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:151105632 G>T maps to NM_053002.4 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:151101921 G>A maps to NM_053002.4 T1579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151102897 C>T maps to NM_053002.4 V1634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr3:150876564 C>A maps to NM_053002.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:151101948 C>A maps to NM_053002.4 S1588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:150881801 G>T maps to NM_053002.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:151134111 C>T maps to NM_053002.4 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:151078260 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:151105893 C>T maps to NM_053002.4 T1760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:150840727 A>T maps to NM_053002.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:151102936 A>G maps to NM_053002.4 K1647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:151127029 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60059766 T>C maps to NM_005121.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:60024296 G>A maps to NM_005121.2 Q2125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:60040304 G>T maps to NM_005121.2 I1624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:60043925 T>G maps to NM_005121.2 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr17:60042680 C>A maps to NM_005121.2 A1510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr17:60043907 T>C maps to NM_005121.2 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:60088524 T>C maps to NM_005121.2 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:116428864 C>A maps to NM_015335.4 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:116434321 C>A maps to NM_015335.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:116424271 C>G maps to NM_015335.4 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:116422113 C>A maps to NM_015335.4 G1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr12:116399154 C>A maps to NM_015335.4 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:116422078 A>T maps to NM_015335.4 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:116424068 A>T did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr12:116446312 A>G maps to NM_015335.4 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:40569229 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:40572199 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:40562804 T>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:40523720 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:40534477 G>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:40568707 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:40531113 T>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:40531143 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:40513716 T>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:20937231 A>T maps to NM_001003891.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:20939287 C>T maps to NM_001003891.1 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:872019 C>T maps to NM_005481.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:881703 T>C maps to NM_005481.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41874857 G>A maps to NM_004275.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:41877045 C>A maps to NM_004275.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:41884591 C>A maps to NM_004275.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:131943068 A>T maps to ENST00000403834 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:131937142 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:131943062 T>A maps to ENST00000403834 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:131917225 C>A maps to ENST00000403834 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:131917231 G>C maps to ENST00000403834 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr6:131944568 A>G maps to ENST00000403834 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr6:131924231 G>A maps to ENST00000403834 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr6:131948537 G>A maps to ENST00000403834 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:131944586 G>A maps to ENST00000403834 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:38188961 C>A maps to NM_014815.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:38179413 G>A maps to NM_014815.3 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:50332241 G>T maps to NM_030973.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:134889751 G>A maps to NM_004269.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:134738473 C>T maps to NM_004269.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr4:17616276 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:118533168 G>T maps to NM_080651.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr17:6547881 G>A maps to NM_016060.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:71058047 G>A maps to ENST00000430055 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr5:156566061 T>A maps to NM_004270.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:156565908 T>C maps to NM_004270.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:43851673 T>C maps to NM_052877.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:100230590 A>T maps to ENST00000338042 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:156446947 C>A maps to NM_005920.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:3304164 C>A maps to NM_000243.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:3304665 C>T maps to NM_000243.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:3294566 A>G maps to NM_000243.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr16:3306344 C>A maps to NM_000243.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:3293509 A>T maps to NM_000243.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:3294474 G>C maps to NM_000243.2 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:3304278 T>A maps to NM_000243.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr16:3304701 G>A maps to NM_000243.2 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:126674905 C>A maps to NM_032446.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:126732431 G>A maps to NM_032446.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126754828 C>G maps to NM_032446.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:126792949 C>T maps to NM_032446.2 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126734442 G>T maps to NM_032446.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:126771051 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:126738320 G>T maps to NM_032446.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:126792829 G>T maps to NM_032446.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:126774200 C>T maps to NM_032446.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:126769091 G>A maps to NM_032446.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr5:126755778 A>G maps to NM_032446.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:126792895 G>A maps to NM_032446.2 K1103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:126755841 C>T maps to NM_032446.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:126738284 C>T maps to NM_032446.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:126738320 G>T maps to NM_032446.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:126746104 G>T maps to NM_032446.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:126705632 C>T maps to NM_032446.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:126776494 C>T maps to NM_032446.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:3511959 G>A maps to ENST00000452816 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr1:3428234 G>A maps to ENST00000452816 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:3424436 G>A maps to ENST00000452816 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:42856542 C>T maps to ENST00000251268 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:42839470 G>T maps to ENST00000251268 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:42863308 G>T maps to ENST00000251268 G1801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:42860569 G>T maps to ENST00000251268 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr19:42856389 C>T maps to ENST00000251268 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:42873082 C>T maps to ENST00000251268 N2190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr19:42861132 G>A maps to ENST00000251268 K1610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:42855447 C>T maps to ENST00000251268 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:42864987 G>A maps to ENST00000251268 G1850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:123367658 C>A maps to ENST00000426959 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:123367491 C>T maps to ENST00000426959 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:123370268 A>G maps to ENST00000426959 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr9:123476276 G>A maps to ENST00000426959 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr22:42099415 C>T maps to NM_152513.3 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr22:42180618 C>A maps to NM_152513.3 I1059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr22:42174742 C>A maps to NM_152513.3 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr2:66670113 C>T maps to ENST00000407092 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:66670039 G>T maps to ENST00000407092 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:66667698 C>T maps to ENST00000407092 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:66667692 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr2:66739371 C>T maps to ENST00000407092 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:37184517 T>A maps to NM_170675.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:37242562 C>G maps to NM_170675.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr15:37184625 C>T maps to NM_170675.2 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr15:37390205 G>C maps to NM_170675.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:37390310 G>A maps to NM_170675.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:37188827 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:47910196 C>T maps to NM_020160.1 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:47918038 G>T maps to NM_020160.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:36633106 A>T maps to NM_014791.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:36669320 C>T maps to NM_014791.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:32145865 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:64574663 C>A maps to NM_130804.2 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:41738662 G>T maps to NM_004527.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:41738725 G>T maps to NM_004527.3 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:41738785 C>T maps to NM_004527.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr17:41738629 G>A maps to NM_004527.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:41720924 G>T maps to NM_004527.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:15725982 C>T maps to NM_005924.4 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:15652161 C>A maps to NM_005924.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:15725580 G>T maps to NM_005924.4 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:15666538 G>C maps to NM_005924.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr7:15666508 G>A maps to NM_005924.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:15725718 C>A maps to NM_005924.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:15652017 G>A maps to NM_005924.4 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:15666475 G>T maps to NM_005924.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr7:15652112 G>A maps to NM_005924.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:46794187 G>A maps to NM_005588.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:46806779 C>A maps to NM_005588.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:46777205 C>T maps to NM_005588.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:46801129 G>A maps to NM_005588.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:29784169 C>A maps to NM_005925.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:100028993 C>T maps to NM_019606.5 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:100028624 G>A maps to NM_019606.5 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:88766961 A>T maps to ENST00000395102 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr4:88766955 T>C maps to ENST00000395102 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr4:88766514 G>A maps to ENST00000395102 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:88766515 G>T maps to ENST00000395102 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:88766835 T>A maps to ENST00000395102 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:88766568 T>C maps to ENST00000395102 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:112740431 A>T maps to NM_006343.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:112767570 A>T maps to NM_006343.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:112786011 C>G maps to NM_006343.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:112786077 G>A maps to NM_006343.2 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:112754933 G>T maps to NM_006343.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:112766011 C>A maps to NM_006343.2 C640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:112779951 G>T maps to NM_006343.2 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:112686860 G>T maps to NM_006343.2 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:81295658 G>T maps to NM_022566.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:90319995 G>A maps to NM_001039958.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:90319944 G>T maps to NM_001039958.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:130140722 C>T maps to NM_002402.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:116397813 A>T maps to NM_001127500.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:116339632 G>A maps to NM_001127500.1 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr7:116412044 T>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:116412043 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:116403322 G>T did not map to a codon.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr7:116339263 G>A maps to NM_001127500.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:116339806 A>G maps to NM_001127500.1 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:116412044 T>C did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr7:116412023 C>G maps to NM_001127500.1 Y1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr7:116411901 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:116411685 G>A maps to NM_001127500.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr7:116412043 G>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:116371798 C>T maps to NM_001127500.1 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:99960597 G>A maps to NM_015143.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:81052031 C>T maps to NM_001004431.1 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr14:21461275 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:21462765 A>G maps to NM_001029991.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:28318425 A>G maps to NM_001113528.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:58162891 C>A maps to ENST00000408972 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr12:58165039 G>A maps to ENST00000408972 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:126477721 C>A maps to NM_212554.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:132397703 C>T maps to NM_014064.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:132396448 G>A maps to NM_014064.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:62434206 C>G maps to NM_001043229.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:62434477 C>T maps to NM_001043229.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:171753361 C>T maps to NM_015935.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:171759641 G>T maps to NM_015935.4 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:171752882 C>T maps to NM_015935.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:171753467 G>T maps to NM_015935.4 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:171763662 T>C maps to NM_015935.4 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:60518051 A>G maps to NM_181725.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:128138161 C>A maps to NM_018396.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:128116824 C>T maps to NM_018396.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21969066 G>C maps to NM_019852.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:21971721 T>C did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:2566939 C>G maps to NM_022840.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:2539037 C>T maps to NM_022840.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:51319243 G>A maps to NM_014033.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:51318913 A>T maps to NM_014033.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:172195852 C>T maps to NM_024770.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:172195975 C>T maps to NM_024770.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:21636436 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:21611104 G>A maps to NM_016025.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:82336838 C>T maps to NM_032246.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:82337974 C>A maps to NM_032246.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:1555341 T>C maps to NM_001174118.1 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:1556668 C>G maps to NM_001174118.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:44097384 C>T maps to NM_005926.2 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:153433098 G>T maps to NM_005927.4 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:170913131 G>A maps to NM_021647.6 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:170912687 T>A maps to NM_021647.6 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:170912945 C>T maps to NM_021647.6 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:170912531 G>C maps to NM_021647.6 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:170913200 G>A maps to NM_021647.6 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19288710 G>T maps to NM_001198695.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:8813494 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:8813494 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:8814676 C>G maps to NM_003480.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:8814694 C>A maps to NM_003480.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:228205012 A>T maps to NM_020194.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:89442733 G>T maps to NM_005928.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:89449994 C>A maps to NM_005928.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr8:8748914 G>A maps to NM_004225.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:8749295 G>A maps to NM_004225.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:8654981 G>C maps to NM_004225.2 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:196733535 G>A maps to NM_005929.5 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:196748343 T>C did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:196735713 G>A maps to NM_005929.5 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr3:179085232 A>T maps to NM_033540.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:179085888 G>T maps to NM_033540.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:12061526 C>T maps to NM_014874.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:12066592 A>G did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr1:12069781 A>C maps to NM_014874.3 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:119215662 G>T maps to NM_031433.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:119217189 C>A maps to NM_031433.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:119215632 C>A maps to NM_031433.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr3:158531836 C>T maps to NM_022736.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:158527040 C>T maps to NM_022736.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:74738049 G>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:74772620 C>T maps to NM_024311.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:74740467 C>T maps to NM_024311.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:74734526 G>A maps to NM_024311.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:40434039 C>T maps to NM_001136493.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:40432480 A>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:40434080 C>T maps to NM_001136493.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr1:40434238 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:40432831 G>T maps to NM_001136493.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:24246991 C>T maps to ENST00000338315 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:24240373 C>T maps to ENST00000338315 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:145736022 C>T maps to NM_138431.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:145736016 C>T maps to NM_138431.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:53647660 C>T maps to NM_001170790.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr2:191334510 T>C maps to NM_017694.3 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:8701313 A>G maps to NM_152599.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr17:8700983 G>T maps to NM_152599.3 P485P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8089-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:678303 C>A maps to ENST00000404286 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:678310 G>C maps to ENST00000404286 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:128865084 T>C maps to NM_152778.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:128870976 T>A maps to NM_152778.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr4:128861024 C>T maps to NM_152778.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:128842777 G>A maps to NM_152778.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:103343411 C>A maps to NM_032718.3 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:103340369 T>C did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:103335610 G>T maps to NM_032718.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:103335115 C>A maps to NM_032718.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:42042587 A>G maps to ENST00000219905 A2310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr15:41991272 A>T maps to ENST00000219905 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr15:42040833 G>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:42052640 G>T maps to ENST00000219905 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr15:41988516 G>T maps to ENST00000219905 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:42042147 G>T maps to ENST00000219905 E2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:42021491 C>A maps to ENST00000219905 S1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr15:42003302 C>G maps to ENST00000219905 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:42052654 C>G maps to ENST00000219905 L2491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:42005480 C>T maps to ENST00000219905 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr15:42041490 C>T maps to ENST00000219905 Q1945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:42000360 G>T maps to ENST00000219905 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr15:41961655 A>G maps to ENST00000219905 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:42042357 A>T maps to ENST00000219905 K2234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr15:42003402 A>G maps to ENST00000219905 Q980Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:42028380 A>T maps to ENST00000219905 K1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr15:42005390 C>T maps to ENST00000219905 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr15:42032401 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:42058760 C>T maps to ENST00000219905 L2876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr15:41988855 C>T maps to ENST00000219905 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:41988780 G>T maps to ENST00000219905 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr15:42003310 C>T maps to ENST00000219905 Q950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:41989077 A>T maps to ENST00000219905 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:41989079 G>A maps to ENST00000219905 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr15:42042522 G>T maps to ENST00000219905 E2289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr15:41988960 A>T maps to ENST00000219905 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:141722154 G>T maps to ENST00000475668 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:141730528 C>G maps to ENST00000475668 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr7:141750532 A>T maps to ENST00000475668 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141734529 G>T maps to ENST00000475668 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:141765176 C>A maps to ENST00000475668 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:141727024 G>T maps to ENST00000475668 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:141763342 A>T maps to ENST00000475668 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:141740553 C>A maps to ENST00000475668 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:141756708 G>C maps to ENST00000475668 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:141758010 C>A maps to ENST00000475668 G1234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:141730438 A>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr7:141758100 T>C maps to ENST00000475668 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:141756636 G>A maps to ENST00000475668 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:141738390 C>A maps to ENST00000475668 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:141795483 C>A maps to ENST00000475668 G2527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:141708453 G>A maps to ENST00000475668 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:141708480 C>A maps to ENST00000475668 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:141803202 C>T maps to ENST00000475668 V2717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:180219535 C>A maps to NM_001114617.1 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:50088219 G>T maps to NM_002408.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr22:39884032 G>A maps to NM_001098270.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr22:39884212 C>A maps to NM_001098270.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:39884737 G>T maps to NM_001098270.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:39883361 A>T maps to NM_001098270.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr22:39884101 G>T maps to NM_001098270.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr22:39884101 G>T maps to NM_001098270.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:86373509 C>A maps to ENST00000393205 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr12:86373687 C>T maps to ENST00000393205 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr12:86373771 T>A maps to ENST00000393205 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:86383240 G>A maps to ENST00000393205 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:86373963 T>A maps to ENST00000393205 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:86373366 A>G maps to ENST00000393205 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:135076303 C>T maps to NM_002410.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:135076255 C>T maps to NM_002410.3 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:74936812 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:74900416 C>T maps to NM_198955.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:74922711 G>A maps to NM_198955.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:74901390 G>T maps to NM_198955.1 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr17:74878336 G>T maps to NM_198955.1 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:74921062 G>A maps to NM_198955.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88423496 A>T maps to NM_152706.2 *254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:88424009 C>A maps to NM_152706.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:43245924 T>C maps to NM_153361.2 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr5:43245937 C>A maps to NM_153361.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:43277258 C>A maps to NM_153361.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:43280084 G>T maps to NM_153361.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:43245912 G>T maps to NM_153361.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:43277384 C>T maps to NM_153361.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:43280486 G>T maps to NM_153361.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:22532983 G>A maps to ENST00000441815 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:22533416 A>G maps to ENST00000441815 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr3:127439933 G>A maps to NM_007283.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:131557533 C>T maps to NM_002412.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr10:131557475 C>A maps to NM_002412.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:131557571 G>T maps to NM_002412.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4715112 G>T maps to NM_015246.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4727536 C>G maps to NM_015246.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:4731567 A>C maps to NM_015246.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:140624669 T>A maps to NM_002413.3 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:41281459 C>T maps to NM_006533.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr14:39717247 T>C maps to NM_054024.3 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:39709791 A>T maps to NM_054024.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr14:39722409 T>A maps to NM_054024.3 L641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:39721950 G>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:222800921 G>T maps to NM_198551.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:222801654 C>T maps to NM_198551.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr1:222802407 G>T maps to NM_198551.2 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:222833603 G>A maps to NM_198551.2 V1687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:222805591 G>A maps to NM_198551.2 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:222827591 G>T maps to NM_198551.2 R1443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:19399575 C>T maps to NM_020774.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr18:19345791 C>T maps to NM_020774.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:19348712 G>A maps to NM_020774.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr18:19353596 C>T maps to NM_020774.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:1565067 C>T maps to NM_080875.2 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:1560536 C>T maps to NM_080875.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:1558936 G>T maps to NM_080875.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:1565852 C>G maps to NM_080875.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:109771183 C>G maps to NM_022765.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:109771520 C>A maps to NM_022765.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:109767561 T>A maps to NM_022765.3 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:12247750 G>T maps to NM_014632.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:12262606 A>T maps to NM_014632.2 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:12183737 G>T maps to NM_014632.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr22:18300617 G>A maps to NM_015241.2 S1603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr22:18301211 C>A maps to NM_015241.2 R1405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:18273593 C>A maps to NM_015241.2 V1971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:18300137 G>A maps to NM_015241.2 T1763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr22:18301082 C>T maps to NM_015241.2 S1448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr22:18300358 C>A maps to NM_015241.2 E1690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr22:18324715 G>T maps to NM_015241.2 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:12345532 G>A maps to NM_032867.2 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr22:38320697 G>A maps to NM_033386.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr7:1482020 C>A maps to NM_182924.3 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:1482020 C>T maps to NM_182924.3 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr7:1478551 C>T maps to NM_182924.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr6:31475189 G>A maps to NM_005931.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:10535286 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:10535313 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:10427695 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:10535194 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:10450569 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:10417701 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:10423045 C>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:10442752 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:10423041 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:10535353 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:10535480 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:10535482 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:10535314 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:10417749 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:10423064 G>C did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:38664294 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:38664361 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:107084309 T>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107169510 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:107084576 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:107084006 G>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:107169958 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:107170201 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:107160842 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:107084432 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:107159296 A>C did not map to a codon.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr23:107084256 G>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:107167714 T>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:107169376 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:107084477 T>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:107084258 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:313533 C>G maps to NM_017550.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73263868 G>T maps to NM_020679.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:12089846 G>T maps to NM_021933.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:97686194 G>A maps to NM_153182.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:97677915 C>A maps to NM_153182.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr17:4789856 G>A maps to NM_153827.4 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:7636006 C>T maps to NM_019005.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:7612757 C>T maps to NM_019005.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr7:7613239 G>T maps to NM_019005.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:56848061 G>T maps to NM_012064.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr13:24449046 G>T maps to NM_005932.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:24415542 C>A maps to NM_005932.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:24453493 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:37838829 G>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:37754521 G>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:99797426 C>G maps to NM_138798.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:70014047 G>T maps to ENST00000448226 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:70014209 G>C maps to ENST00000448226 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr3:69990418 A>G maps to ENST00000448226 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:70014354 C>A maps to ENST00000448226 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr3:69987130 G>T maps to ENST00000448226 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr3:69986995 C>T maps to ENST00000448226 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:129902900 G>A maps to NM_002417.4 N2401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:129902309 C>A maps to NM_002417.4 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:129903224 T>C maps to NM_002417.4 P2293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr10:129905292 G>C maps to NM_002417.4 S1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:129907465 C>A maps to NM_002417.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr10:129899920 T>C maps to NM_002417.4 E3102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:129897488 T>G maps to NM_002417.4 R3246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:129906515 C>T maps to NM_002417.4 Q1196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr10:129901396 T>A maps to NM_002417.4 R2903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:129903115 T>A maps to NM_002417.4 K2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr10:129905597 G>A maps to NM_002417.4 D1502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:129905762 A>G maps to NM_002417.4 S1447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:129913971 C>A maps to NM_002417.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:129906386 T>C maps to NM_002417.4 E1239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr10:129902507 G>T maps to NM_002417.4 I2532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:129904625 G>A maps to NM_002417.4 A1826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:129913426 T>C maps to NM_002417.4 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:129901457 C>T maps to NM_002417.4 T2882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:122486105 G>A maps to NM_032390.4 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:10393427 A>G maps to NM_170784.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr20:10389283 C>A maps to NM_170784.1 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:40819641 G>A maps to NM_020831.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr22:40814545 G>A maps to NM_020831.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr22:40816867 G>A maps to NM_020831.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:14345717 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr16:14352004 C>A maps to NM_014048.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14340373 G>T maps to NM_014048.3 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:14345840 G>T maps to NM_014048.3 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr16:14346238 A>T maps to NM_014048.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr16:14341060 C>T maps to NM_014048.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:131113904 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:47037777 C>G maps to NM_003684.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:47037738 G>C maps to NM_003684.4 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:2039644 C>T maps to NM_199054.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:140159582 A>G maps to NM_013446.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:140158962 G>A maps to NM_013446.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:140159033 C>A did not map to a codon.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr7:140156558 G>A maps to NM_013446.3 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:23811384 G>T maps to NM_005664.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:23811792 C>T maps to NM_005664.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:23812140 G>A maps to NM_005664.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:23811027 C>T maps to NM_005664.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:23811834 T>G maps to NM_005664.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr15:23811369 G>A maps to NM_005664.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:23811042 C>A maps to NM_005664.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:23811207 C>A maps to NM_005664.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:23812449 G>T maps to NM_005664.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:56291139 G>A maps to NM_017777.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr17:56295992 G>A maps to NM_017777.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:27964307 C>T maps to NM_173576.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr22:50523301 C>A maps to NM_015166.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:50515284 G>T maps to NM_015166.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr22:50521572 C>A maps to NM_015166.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr12:121131924 G>A maps to NM_014730.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:158322895 C>T maps to NM_001195432.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr3:158310300 C>T maps to NM_001195432.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:185623262 G>A maps to NM_024629.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:37067447 G>A maps to NM_000249.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr3:37081767 C>G maps to NM_000249.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:37053548 C>T maps to NM_000249.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75515140 C>T maps to NM_001040108.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr14:75515968 C>A maps to NM_001040108.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:75514921 T>C maps to NM_001040108.1 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:74716670 T>C maps to NM_152649.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:118376836 A>G maps to NM_001197104.1 P3410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118359360 C>T maps to NM_001197104.1 F1455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr11:118352427 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:118375888 C>G maps to NM_001197104.1 L3094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:118374109 C>G maps to NM_001197104.1 P2501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:118376563 A>T maps to NM_001197104.1 T3319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:49437155 G>C maps to NM_003482.3 A1841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:49438021 G>A maps to NM_003482.3 Q1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:49437166 C>A maps to NM_003482.3 E1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:49444340 C>T maps to NM_003482.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr12:49442513 C>T maps to NM_003482.3 E1353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:49420193 G>A maps to NM_003482.3 F5185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:49445463 C>A maps to NM_003482.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:49438016 C>A maps to NM_003482.3 A1718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:49428008 C>A maps to NM_003482.3 V3527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr12:49436375 T>A maps to NM_003482.3 P1945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:49440207 C>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:49425026 G>A maps to NM_003482.3 I4487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr12:49447386 C>T maps to NM_003482.3 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr12:49445941 T>C maps to NM_003482.3 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:49445139 C>A maps to NM_003482.3 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:49439941 G>T maps to NM_003482.3 G1533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:49444043 G>A maps to NM_003482.3 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:49434559 C>A maps to NM_003482.3 L2331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr12:49425895 G>A maps to NM_003482.3 R4198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:49446091 C>G maps to NM_003482.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:49420766 C>A maps to NM_003482.3 L4994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr12:49444939 C>G maps to NM_003482.3 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151932900 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:151945259 T>C maps to ENST00000355193 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:151970871 A>T maps to ENST00000355193 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:151945106 A>T maps to ENST00000355193 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:151850039 C>G did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr7:151874410 G>A maps to ENST00000355193 V2709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:151945169 G>C maps to ENST00000355193 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:151878269 T>A maps to ENST00000355193 P2225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:151945169 G>A maps to ENST00000355193 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:151859669 G>A maps to ENST00000355193 V3664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:151874167 T>C maps to ENST00000355193 V2790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:151970865 T>A maps to ENST00000355193 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:151962208 A>C maps to ENST00000355193 Y366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr7:151902287 C>A maps to ENST00000355193 R1288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr7:151879336 G>A maps to ENST00000355193 Q1870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:151891313 C>A maps to ENST00000355193 E1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr7:151877212 T>G did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:151932916 A>G maps to ENST00000355193 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr7:151927016 G>A maps to ENST00000355193 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr7:151877858 T>A maps to ENST00000355193 S2362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:151873491 G>A maps to ENST00000355193 Q3016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:151878314 T>C maps to ENST00000355193 P2210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr7:151945601 G>A maps to ENST00000355193 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:36228978 C>T maps to NM_014727.1 R2587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36211922 G>A maps to NM_014727.1 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:36221469 G>C maps to NM_014727.1 L1743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36212498 C>T maps to NM_014727.1 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:36214651 G>T maps to NM_014727.1 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:36227813 G>T maps to NM_014727.1 G2433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:104742406 T>C maps to NM_182931.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr7:104681416 A>T maps to NM_182931.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:104749672 A>G maps to NM_182931.2 Q1251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:104749462 C>G maps to NM_182931.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:21959418 G>A maps to NM_004641.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:22021900 G>A maps to NM_004641.3 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:22015198 C>T maps to NM_004641.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:21962688 G>T maps to NM_004641.3 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:22002776 C>T maps to NM_004641.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr10:21959511 T>C maps to NM_004641.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:20414141 C>T maps to NM_004529.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168352254 G>T maps to ENST00000400822 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:168281112 A>T maps to ENST00000400822 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:36873841 T>G maps to NM_005937.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36863737 G>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:36874165 C>T maps to NM_005937.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:36876111 C>T maps to NM_005937.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr17:36868999 C>T maps to NM_005937.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:36868119 C>T maps to NM_005937.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:36874192 G>A maps to NM_005937.3 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:36872845 G>A maps to NM_005937.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:36873052 T>G maps to NM_005937.3 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr13:49795192 G>A maps to NM_001507.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:49796398 C>A maps to NM_001507.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr2:238462216 G>T maps to NM_024101.5 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:238419634 C>A maps to NM_024101.5 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:2256184 C>T maps to NM_022372.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:122614648 C>T maps to NM_014938.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:122625580 G>T maps to NM_014938.3 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:122622811 C>T maps to NM_014938.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:122615451 C>T maps to NM_014938.3 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:73010569 C>T maps to NM_032951.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:73020021 G>A maps to NM_032951.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:146576325 G>T maps to NM_172250.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:110002928 G>A maps to NM_052845.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr2:150427648 G>A maps to NM_015702.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:53471757 C>A maps to NM_012329.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:4947149 C>A maps to NM_001100600.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:4959884 G>T maps to NM_001100600.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr7:4965099 G>T maps to NM_001100600.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:154861314 G>A maps to NM_007289.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:154884700 C>A maps to NM_007289.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:154802042 C>A maps to NM_007289.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:154862149 C>T maps to NM_007289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:154860024 G>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:154886335 A>T maps to NM_007289.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:154855958 C>T maps to NM_007289.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:154855907 G>A maps to NM_007289.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:154859917 T>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:2537710 C>T maps to NM_033467.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:2537762 G>C maps to NM_033467.3 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:2524403 G>T maps to NM_033467.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:2525343 G>T maps to NM_033467.3 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2535349 C>T maps to NM_033467.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:2541154 G>A maps to NM_033467.3 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:135047289 C>A did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr11:102661455 A>T maps to NM_002421.3 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:102668045 C>G maps to NM_002421.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:102649992 G>T maps to NM_002425.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:102646041 G>A maps to NM_002425.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:102643669 C>T maps to NM_002425.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:24122620 C>T maps to NM_005940.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr22:24123439 G>T maps to NM_005940.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:102745612 G>A maps to ENST00000326227 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102743680 G>A maps to ENST00000326227 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:102743719 C>A maps to ENST00000326227 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:102819850 C>A maps to NM_002427.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:102824900 C>T maps to NM_002427.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:102825982 G>T maps to NM_002427.3 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:102815024 G>T maps to NM_002427.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:102819819 C>A maps to NM_002427.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr14:23306130 C>T maps to NM_004995.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:58075662 C>T maps to NM_002428.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:89179913 T>C maps to NM_005941.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:89179958 A>G maps to NM_005941.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:89180005 C>A maps to NM_005941.4 G201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:89053847 C>A maps to NM_005941.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:89209475 G>A maps to NM_005941.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:89198709 A>T maps to NM_005941.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:89128819 G>T maps to NM_005941.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:89209481 C>T maps to NM_005941.4 V62V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5941-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:89209451 G>T maps to NM_005941.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:89339375 C>A maps to NM_005941.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:89180113 G>A maps to NM_005941.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:89198706 G>T maps to NM_005941.4 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:89131042 C>A maps to NM_005941.4 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr8:89209502 C>A maps to NM_005941.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:132323256 C>A maps to NM_016155.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:132325240 C>A maps to NM_016155.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr12:132334398 C>T maps to NM_016155.4 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr12:132334345 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:56233400 G>T maps to NM_002429.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:56231059 G>T maps to NM_002429.4 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:56234592 C>A maps to NM_002429.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:55525858 G>T maps to NM_004530.4 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:55530858 G>A maps to NM_004530.4 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:55532289 C>T maps to NM_004530.4 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:55522584 G>A maps to NM_004530.4 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:55519645 C>A maps to NM_004530.4 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:55516993 C>T maps to NM_004530.4 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:55513492 C>T maps to NM_004530.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:55516876 G>A maps to NM_004530.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:55532221 C>A maps to NM_004530.4 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr16:55523569 C>T maps to NM_004530.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:102482489 A>G maps to NM_004771.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:3107614 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:3100497 C>T maps to NM_022468.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr16:3108218 G>A maps to NM_022468.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:3108180 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:3100389 C>T maps to NM_022468.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr16:3100308 C>T maps to NM_022468.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:5009449 C>G maps to NM_021801.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:5011950 C>T maps to NM_021801.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:5011854 G>A maps to NM_021801.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:5013209 G>C maps to NM_021801.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:5010966 G>A maps to NM_021801.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:5011056 G>A maps to NM_021801.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:102573541 C>A maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:102573849 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:102562550 G>A maps to NM_022122.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565709 G>A maps to NM_022122.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:102565800 G>A maps to NM_022122.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:102575397 C>A maps to NM_022122.2 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:102709382 G>A maps to NM_002422.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:102712963 G>T maps to NM_002422.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr11:102710879 A>C maps to NM_002422.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:102711238 G>A maps to NM_002422.3 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:102394102 C>A maps to NM_002423.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:102395787 C>A maps to NM_002423.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:102395736 C>T maps to NM_002423.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr11:102595532 G>T maps to NM_002424.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:102586168 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr20:44641099 C>T maps to NM_004994.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr20:44641963 C>G maps to NM_004994.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44641126 C>A maps to NM_004994.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:44640872 C>A maps to NM_004994.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr20:44640803 G>T maps to NM_004994.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:44640210 A>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr20:44641105 C>T maps to NM_004994.2 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr20:44639908 G>T maps to NM_004994.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:90857617 A>G maps to NM_007351.2 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:90874328 C>A maps to NM_007351.2 Y1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:90856531 G>A maps to NM_007351.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:90872783 G>T maps to NM_007351.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:90816484 T>A maps to NM_007351.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:90816178 G>T maps to NM_007351.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr4:90856621 C>T maps to NM_007351.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:90816329 G>T maps to NM_007351.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:90874232 C>A maps to NM_007351.2 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:90816677 C>A maps to NM_007351.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:90874331 C>T maps to NM_007351.2 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:90844394 G>A maps to NM_007351.2 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:90816138 T>A maps to NM_007351.2 L6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:88702980 C>A maps to NM_024756.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:28193498 C>A maps to NM_002430.2 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:28196354 C>A maps to NM_002430.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:28192874 C>A maps to NM_002430.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:61201637 A>T maps to NM_002431.3 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:154318394 G>T maps to NM_032117.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158815571 T>C maps to NM_002432.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:158813833 C>A maps to NM_002432.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:158817646 C>T maps to NM_002432.1 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:158812023 C>A maps to NM_002432.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:158815600 C>A maps to NM_002432.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:158815390 G>A maps to NM_002432.1 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr1:158819003 G>T maps to NM_002432.1 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr15:56726470 A>T maps to NM_018365.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr17:2297372 A>G maps to NM_020310.2 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:93649945 T>G maps to NM_022151.4 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:93649560 G>A maps to NM_022151.4 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:1492548 C>A maps to NM_001172223.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:71840983 G>T maps to ENST00000396051 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:71844960 G>T maps to ENST00000396051 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:2078214 C>G maps to NM_130807.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr9:27455458 C>A maps to NM_024761.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr9:27359198 T>A maps to NM_024761.3 K152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr18:33779984 G>A maps to NM_017947.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr18:33778702 G>T maps to NM_017947.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:39883914 C>A maps to ENST00000425303 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr5:52403031 G>A maps to NM_176806.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:49576692 A>G maps to NM_014484.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:49576221 G>A maps to NM_014484.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:29627267 T>C maps to NM_002433.4 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:29627381 C>T maps to NM_002433.4 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:29627267 T>C maps to NM_002433.4 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:29627219 C>A maps to NM_002433.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:223554069 G>C maps to NM_058165.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:223574453 G>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:223559871 G>T maps to NM_058165.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:75439834 G>T maps to NM_025098.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:75438610 T>A maps to NM_025098.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:100839573 G>T maps to NM_178176.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:100839370 G>T maps to NM_178176.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:100841638 A>G maps to NM_178176.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:100839310 G>T maps to NM_178176.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:74690084 T>G maps to NM_006302.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:74689622 G>A maps to NM_006302.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:74689727 G>A maps to NM_006302.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr16:77225495 G>T maps to NM_014940.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:77227492 G>A maps to NM_014940.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:62938754 A>T maps to ENST00000393630 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:62936947 G>A maps to ENST00000393630 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:62861047 T>C maps to ENST00000393630 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:62929425 C>T maps to ENST00000393630 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:108778675 T>C maps to NM_014429.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:108819262 C>G did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:108819310 C>A maps to NM_014429.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr3:108780902 C>A maps to NM_014429.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:108719442 C>T maps to NM_014429.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:108723720 A>T maps to NM_014429.3 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr3:108836878 G>T maps to NM_014429.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:108746722 C>A maps to NM_014429.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:108723662 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31342402 C>A maps to ENST00000397641 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr22:31328533 G>C maps to ENST00000397641 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:31328731 C>A maps to ENST00000397641 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr21:37741630 T>A maps to ENST00000290384 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr21:37713754 G>T maps to ENST00000290384 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:37744772 A>T maps to ENST00000290384 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr21:37741748 C>T maps to ENST00000290384 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr21:37741460 G>T maps to ENST00000290384 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr21:37741774 A>G maps to ENST00000290384 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:106219856 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:106221359 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:106228324 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:106186355 C>G did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:106185872 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:106185960 C>G did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr23:106198241 C>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:106186009 G>C did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:106224170 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:106186364 G>C did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:106201565 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:106228378 A>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:79186408 G>T maps to NM_206839.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:79183908 G>T maps to NM_206839.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:102931675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:102931490 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:102931731 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:102931157 A>G did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:102931355 G>C did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:102931111 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:102931252 T>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:2317244 C>A did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr1:2268206 C>T maps to NM_024848.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:57026313 C>T maps to NM_005372.1 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:57025677 G>C maps to NM_005372.1 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:57025797 C>T maps to NM_005372.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr8:57026127 G>T maps to NM_005372.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:57026478 C>T maps to NM_005372.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:220970053 G>T maps to NM_022746.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220935099 G>T maps to NM_017898.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:220928438 C>G maps to NM_017898.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:134025543 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:134030922 T>C did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:134033371 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:14932623 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:14934406 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:14915214 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:14910923 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:14915339 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:14934423 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:14933884 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:14933885 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:14915306 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:14933850 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:100212488 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr7:100211253 G>T maps to NM_023948.4 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:50580511 T>C maps to NM_018995.2 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr22:50547204 A>T maps to NM_018995.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr22:50553670 G>T maps to NM_018995.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:50572450 G>T maps to NM_018995.2 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr22:50547227 C>A maps to NM_018995.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:132695847 G>T maps to NM_015529.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr6:132693761 C>T maps to NM_015529.2 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr6:132722337 G>T maps to NM_015529.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:132618312 C>A maps to NM_015529.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:13162688 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13119527 G>A maps to ENST00000319217 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:13125263 C>T maps to ENST00000319217 Q1586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:13109985 C>A maps to ENST00000319217 G1969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:13216852 C>A maps to ENST00000319217 G404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr9:13121877 C>T maps to ENST00000319217 L1697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr9:13247786 G>A maps to ENST00000319217 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr9:13168518 G>A maps to ENST00000319217 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:58979597 G>C maps to NM_001039396.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:58979597 G>T maps to NM_001039396.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr11:58979535 G>T maps to NM_001039396.1 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:82182359 C>T maps to NM_005792.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:82182335 T>A maps to NM_005792.2 *161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:20235959 C>T maps to ENST00000414242 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:123694638 G>A maps to NM_022782.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:123694649 C>A maps to NM_022782.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr12:123687367 G>A maps to NM_022782.2 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:75185533 G>A maps to NM_002435.1 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr15:75189908 C>T maps to NM_002435.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43812250 G>C maps to NM_005373.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:43804243 C>T maps to NM_005373.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:43805735 C>A maps to NM_005373.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:43812538 G>A maps to NM_005373.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:56350205 C>T maps to ENST00000340482 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:56355386 G>A maps to ENST00000340482 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:56355305 C>A maps to ENST00000340482 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:56355398 G>A maps to ENST00000340482 N363N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:56348199 C>T maps to ENST00000340482 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:56349149 C>T maps to ENST00000340482 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr17:56350976 C>T maps to ENST00000340482 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr17:56356989 G>A maps to ENST00000340482 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:56357806 C>T maps to ENST00000340482 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:56358092 G>A maps to ENST00000340482 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:154007497 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:154007555 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:154014615 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:154007589 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:154018235 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:154020487 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:154007574 G>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:154013433 T>C did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:41958158 C>A maps to NM_005374.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:41955345 C>T maps to NM_005374.3 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr17:41955175 C>A maps to NM_005374.3 *553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:41891568 C>G maps to ENST00000398393 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:41898261 G>T maps to ENST00000398393 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:202547585 C>A maps to NM_033066.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:202550694 C>A maps to NM_033066.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:202545595 G>A maps to NM_033066.2 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:28378645 C>A maps to NM_173496.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr10:28348646 C>T maps to NM_173496.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr18:11885719 G>A maps to ENST00000344987 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr22:43870649 A>T maps to NM_001044370.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:43870646 C>T maps to NM_001044370.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr22:43831028 G>T maps to NM_001044370.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr22:43870628 C>G maps to NM_001044370.1 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:30516970 G>A maps to NM_001584.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:30435855 T>A maps to NM_001584.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:30433116 G>A maps to NM_001584.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr11:30433050 T>G maps to NM_001584.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:30439176 G>T maps to NM_001584.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:30433025 G>A maps to NM_001584.2 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:17076054 G>C maps to NM_015134.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:17062135 G>T maps to NM_015134.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr17:17078656 G>A maps to NM_015134.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:17053522 G>A maps to NM_015134.2 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:17053523 A>T maps to NM_015134.2 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:167757139 G>T maps to NM_003953.5 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:33684057 C>A maps to ENST00000445271 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:33671311 A>T maps to ENST00000445271 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:84772654 G>A maps to NM_138409.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr6:84765087 T>A maps to NM_138409.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:84765060 T>A maps to NM_138409.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:84772675 G>T maps to NM_138409.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:84765080 C>A maps to NM_138409.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr6:84765132 A>T maps to NM_138409.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr3:138121071 G>T maps to NM_001085049.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr10:18122661 G>T maps to NM_002438.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:60741987 G>T maps to NM_006039.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:60744808 C>T maps to NM_006039.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:60744813 G>A maps to NM_006039.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:60765738 C>T maps to NM_006039.3 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:60754844 A>T maps to NM_006039.3 K684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:60758260 C>G maps to NM_006039.3 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:60754765 G>T maps to NM_006039.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:60749476 G>C maps to NM_006039.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:60758179 C>T maps to NM_006039.3 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:60749181 C>G maps to NM_006039.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:94212875 C>A maps to NM_005591.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:6710990 C>T maps to NM_203462.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:68747858 C>G maps to NM_198923.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr11:68747744 C>T maps to NM_198923.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:3249690 G>T maps to ENST00000328215 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr11:3249720 G>A maps to ENST00000328215 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:3249660 C>A maps to ENST00000328215 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:68777349 C>T maps to NM_145015.4 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:68773567 G>C maps to NM_145015.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:68777348 C>T maps to NM_145015.4 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:68773089 G>T maps to NM_145015.4 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:18955898 G>A maps to NM_147199.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:18955986 G>A maps to NM_147199.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:18955515 G>A maps to NM_147199.3 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:18955701 C>A maps to NM_147199.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:18955911 C>A maps to NM_147199.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:19077786 G>A maps to NM_054030.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:19077039 G>A maps to NM_054030.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:19077388 A>T maps to NM_054030.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:19077262 C>A maps to NM_054030.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:18159366 C>A maps to NM_054031.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18159296 G>A maps to NM_054031.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:18159486 G>A maps to NM_054031.3 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:18159717 A>T maps to NM_054031.3 *323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:18159384 C>T maps to NM_054031.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:18195147 C>G maps to NM_054032.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:18194907 C>A maps to NM_054032.3 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:18194988 C>A maps to NM_054032.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:18195489 C>A maps to NM_054032.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:18195009 C>A maps to NM_054032.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:13883023 G>T maps to NM_001031727.2 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:34964760 A>G maps to NM_024864.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr18:48325736 C>T maps to NM_001127176.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr18:48331522 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:78830508 C>T maps to NM_020236.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:78830456 A>G maps to NM_020236.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:45904480 C>G maps to NM_145255.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:45904123 A>G maps to NM_145255.3 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:66206174 G>A maps to NM_016050.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:121437551 T>A maps to NM_014078.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:44081946 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr8:55060068 C>G maps to NM_014175.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:59573867 G>T maps to NM_017840.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr11:59577326 C>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:160218466 C>T maps to NM_014161.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:160212137 C>T maps to NM_014161.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:154320678 G>T maps to NM_014180.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:1972197 G>T maps to NM_021134.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:419157 C>T maps to NM_006428.4 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:131208915 T>A maps to ENST00000425847 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:131221616 G>A maps to ENST00000425847 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:131206584 C>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:42972002 G>T maps to NM_031903.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:27997374 T>A maps to NM_004891.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:86433235 A>T maps to NM_016622.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:86437739 C>T maps to NM_016622.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:54675728 C>T maps to NM_016491.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:54666260 G>A maps to NM_016491.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:73900722 C>A maps to NM_032478.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr17:73895712 C>T maps to NM_032478.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr21:26976214 G>A maps to NM_080794.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr21:26979748 G>C maps to NM_080794.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr21:26979757 C>A maps to NM_080794.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr19:10369341 C>T maps to NM_146387.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:93881409 T>C maps to NM_172177.2 T119T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-53-A4EZ-01A-12D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr10:102746901 G>A maps to NM_176794.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:224822339 C>T maps to NM_022915.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:36478393 G>T maps to NM_032351.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr17:36455434 G>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr17:36455402 C>A maps to NM_032351.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:36478457 C>T maps to NM_032351.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:179306783 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:64893329 G>T maps to NM_004927.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr9:104153116 T>C maps to NM_019051.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:104160868 C>A maps to NM_019051.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:74699246 C>T maps to NM_053050.3 *113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:74699359 A>T maps to NM_053050.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:151732527 A>T maps to NM_031420.2 *268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:36923550 A>T maps to NM_031280.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr10:75010726 C>A maps to NM_016065.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr10:75011590 G>C maps to NM_016065.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:56022735 C>T maps to ENST00000426595 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr6:43648834 C>T maps to ENST00000372118 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:30585656 A>G maps to NM_014046.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:30587584 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr6:30587513 C>T maps to NM_014046.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr4:84377238 T>C maps to NM_016067.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:138395819 G>T maps to NM_016034.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:43906429 C>A maps to NM_032014.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr20:3027120 G>T maps to NM_030811.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr20:3028484 G>C maps to NM_030811.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr5:71616012 C>A maps to ENST00000513900 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:44815241 C>T maps to NM_016640.3 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr5:44809471 G>C maps to NM_016640.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:44812015 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:44809663 C>T maps to NM_016640.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr5:44815045 T>G maps to NM_016640.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:41345257 G>C maps to NM_005830.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr16:1822356 A>T maps to ENST00000432952 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:27888438 A>T maps to NM_021821.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:27908111 A>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:68522175 A>G maps to NM_033281.5 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr21:35514758 G>C maps to NM_032476.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr21:35514759 G>T maps to NM_032476.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr2:105705440 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:125047484 G>T maps to NM_138777.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:125075535 G>T maps to NM_138777.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:24423245 G>T maps to NM_020662.2 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr6:24412542 C>T maps to NM_020662.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:24403333 G>A maps to NM_020662.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr6:24418413 T>C maps to NM_020662.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:19584404 G>T maps to NM_016183.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19582446 G>T maps to NM_016183.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:10648124 G>T maps to NM_001098579.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:60231793 G>T maps to NM_152866.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:60233576 G>T maps to NM_152866.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:60233392 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr11:60561458 G>T maps to NM_206893.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:60557888 C>G maps to NM_206893.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:60563026 G>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:60268516 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:60268519 G>C maps to NM_017716.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:60285610 G>T maps to NM_001012417.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:60296835 A>G did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:60296932 G>A maps to NM_001012417.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:60164177 A>T maps to NM_032597.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60164086 C>T maps to NM_032597.3 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:60164095 T>A maps to NM_032597.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:60165335 C>T maps to NM_032597.3 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:60183866 G>T maps to NM_032597.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:60170395 C>T maps to NM_032597.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:60182929 G>T maps to NM_032597.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:60531431 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:60541371 G>T maps to NM_001098835.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:60538783 C>A maps to NM_001098835.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:59861505 G>T maps to NM_000139.4 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:59860290 T>A maps to NM_000139.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:59828638 C>T maps to NM_006138.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:59834500 A>T maps to NM_006138.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:59830041 C>T maps to NM_006138.4 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:59834461 A>T maps to NM_006138.4 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:59834551 G>A maps to NM_006138.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:59837058 C>T maps to NM_006138.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59828747 G>T maps to NM_006138.4 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:59834452 C>T maps to NM_006138.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:60070117 T>C maps to NM_148975.1 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:60064674 G>T maps to NM_148975.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr11:60059734 G>T maps to NM_148975.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:60048189 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:60215126 T>A maps to NM_023945.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:60215230 G>T maps to NM_023945.2 *201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:60215195 C>T maps to NM_023945.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:59947339 C>A maps to NM_152852.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:59949101 C>A maps to NM_152852.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:59949119 G>A maps to NM_152852.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:59947357 G>C maps to NM_152852.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:60102421 C>A maps to NM_139249.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:60152571 C>A maps to NM_206939.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:60161283 C>T maps to NM_206939.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60156903 T>C maps to NM_206939.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:60156888 A>T maps to NM_206939.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:60150751 C>A maps to NM_206939.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:60150733 G>T maps to NM_206939.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr11:60468331 G>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:72754982 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:72754931 A>T maps to NM_005098.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:72754952 C>A maps to NM_005098.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:72754967 C>T maps to NM_005098.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:72756271 C>A maps to NM_005098.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:17998015 G>T maps to NM_001105569.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:17997961 T>A maps to NM_001105569.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:47690291 T>C maps to NM_000251.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:47690167 A>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:47637442 C>T maps to NM_000251.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:47630473 G>A maps to NM_000251.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:47637472 G>T maps to NM_000251.1 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:80040323 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:80074608 G>T maps to NM_002439.3 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:80168938 A>T maps to NM_002439.3 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:80171578 C>G maps to NM_002439.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:76313919 C>T maps to NM_002440.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:76349376 G>T maps to NM_002440.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:76363722 T>G maps to NM_002440.2 Y829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:76262882 C>T maps to NM_002440.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:76313960 G>T maps to NM_002440.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:76346999 G>T maps to NM_002440.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:76343981 G>T maps to NM_002440.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:76356385 A>T maps to NM_002440.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:76349312 A>T maps to NM_002440.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:76349324 T>C maps to NM_002440.2 D642D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:76345769 A>G maps to NM_002440.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:76288232 C>T maps to NM_002440.2 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:76282202 G>T maps to NM_002440.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:31711738 C>T maps to ENST00000375742 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:48027171 C>T maps to NM_000179.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr2:48033415 A>G maps to NM_000179.2 K1240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:48026795 G>T maps to NM_000179.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:120800881 C>A maps to NM_002442.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:120800893 C>T maps to NM_002442.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:55709161 G>T maps to NM_170721.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:55478804 A>C maps to NM_138962.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr17:55478816 C>T maps to NM_138962.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr17:55693445 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:55729472 G>A maps to NM_138962.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:135871275 T>A maps to NM_018133.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:135913853 G>C maps to NM_018133.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:135871361 C>A maps to NM_018133.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:11790813 C>G did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr23:11783604 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:11790300 C>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:11790777 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:11790314 G>A did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:11790365 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:11781089 C>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:11778597 A>C did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr23:11793129 C>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:11778577 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:11778535 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:11778536 A>G did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr2:234775526 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:234775668 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:234775345 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:816887 G>T maps to NM_013404.4 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:815524 A>T did not map to a codon.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr16:816149 G>A maps to NM_013404.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:823009 C>A maps to NM_001025190.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:824873 G>T maps to NM_001025190.1 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr16:830153 G>A maps to NM_001025190.1 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:830601 C>T maps to NM_001025190.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr16:830592 G>A maps to NM_001025190.1 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:822937 C>T maps to NM_001025190.1 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr16:823188 G>T maps to NM_001025190.1 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:51555831 C>A maps to NM_002443.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr10:51562319 A>T maps to NM_002443.2 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr10:51556789 C>A maps to NM_002443.2 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:35753748 C>T maps to NM_001044264.1 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr23:64959736 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:64958392 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:64959653 C>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:64958874 T>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:64958954 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:64955188 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:64949299 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:64955187 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:15998537 A>G maps to NM_002445.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:16026152 A>C maps to ENST00000445506 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:16035464 C>T maps to ENST00000445506 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:16032707 C>A maps to ENST00000445506 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:16032809 C>G did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:16021572 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:10177493 C>T maps to NM_012331.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:10177391 G>A did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr8:9912115 C>T maps to NM_012331.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:23409754 C>T maps to ENST00000277598 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:23393071 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:23408278 G>T maps to ENST00000277598 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:65762786 C>A maps to NM_001031679.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:49724891 G>A maps to NM_020998.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:49723311 C>A maps to NM_020998.3 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:49725031 C>A maps to NM_020998.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:49927403 C>T maps to NM_002447.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:49928031 G>A maps to NM_002447.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:49935560 C>A maps to NM_002447.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:49940624 G>A maps to NM_002447.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr3:49934038 C>T maps to NM_002447.2 Q791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:49936630 G>A maps to NM_002447.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:49927460 C>A maps to NM_002447.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:131202583 C>G did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:131188766 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:131197484 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:131202483 G>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:131206386 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:131188888 G>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:131202310 C>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:131197495 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:131202554 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:131202252 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:155582962 G>T maps to NM_018116.2 G408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:4864773 C>A maps to NM_002448.3 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:4861964 G>T maps to NM_002448.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:4864599 G>A maps to NM_002448.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:56701236 G>A maps to ENST00000379811 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr16:56667669 C>T maps to NM_176870.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:56667690 T>A maps to NM_176870.2 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:56716475 G>A maps to NM_005952.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:56599069 T>A maps to NM_032935.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr14:105911819 C>T maps to NM_004689.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr14:105927154 C>A maps to NM_004689.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr14:105911753 G>C did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:105929518 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr14:105916636 G>A maps to NM_004689.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr14:105931078 C>T maps to NM_004689.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:42836679 C>G maps to ENST00000405094 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42883391 A>T maps to ENST00000405094 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:42909653 A>T maps to ENST00000405094 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr2:42909572 C>T maps to ENST00000405094 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:21837987 G>A maps to NM_002451.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr9:21854736 C>T maps to NM_002451.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:21818189 G>A maps to NM_002451.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:121531008 C>T maps to NM_022045.3 F854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr8:121535539 G>T maps to NM_022045.3 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:121534920 G>T maps to NM_022045.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:36938180 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:36946278 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:154293942 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:154293985 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:154292294 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:154290187 C>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:98656865 G>C maps to NM_178812.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr7:91503059 G>T maps to NM_006980.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr7:91503719 G>A maps to NM_006980.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:97270788 G>A maps to NM_015942.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:97269309 G>A maps to NM_015942.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:97256191 G>A maps to NM_015942.3 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:97270749 C>A maps to NM_015942.3 G57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:242036734 G>A maps to NM_182501.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:107371700 C>T maps to NM_025198.3 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:107371382 T>C maps to NM_025198.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:38281086 C>T maps to NM_005955.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:93602422 C>T maps to NM_007358.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:65308839 A>G maps to NM_139242.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:135233638 G>T maps to NM_138384.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:135209676 C>G maps to NM_138384.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr10:135209734 C>T maps to NM_138384.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr10:135213067 C>G maps to NM_138384.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:151209071 C>T maps to NM_015440.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:151247408 G>T maps to NM_015440.3 G412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr6:151358098 A>G did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr6:151277194 C>T maps to NM_015440.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:151239762 G>T maps to NM_015440.3 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:151331057 G>T maps to NM_015440.3 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:75066998 A>G maps to NM_001144978.1 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:11852385 T>C maps to ENST00000376585 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:11861278 G>A maps to ENST00000376585 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:86582140 C>A maps to NM_001159377.1 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:86565715 G>A maps to NM_001159377.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:55481788 C>A did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr2:55463885 G>A maps to NM_002453.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:55481267 G>A maps to NM_002453.2 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr13:28014489 T>A maps to NM_152912.4 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr13:28014555 T>C maps to NM_152912.4 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:68480779 G>T maps to NM_004923.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:68478346 G>A maps to NM_004923.3 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:149783136 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:149807450 C>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:149839951 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:149832037 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:149828152 A>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:149787522 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:149761085 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:149809818 G>C did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:149809740 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:149809741 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:149826500 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:149905221 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:149901076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:149898999 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:149899010 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:149899013 C>A did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr23:149901146 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:149924336 G>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:149919241 C>T did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr23:149901146 C>A did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:149905078 G>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:149901130 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:149887135 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:149895726 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr15:31233849 G>A maps to NM_017762.2 N719N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr15:31234218 G>A maps to NM_017762.2 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:149906416 C>A maps to NM_001145862.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:149905395 C>G maps to NM_001145862.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:149901550 C>T maps to NM_001145862.1 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr5:32229892 C>T maps to NM_001040446.1 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:32270927 T>A maps to NM_001040446.1 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:32230131 C>A maps to NM_001040446.1 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:32229898 G>A maps to NM_001040446.1 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:32263286 C>A maps to NM_001040446.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:32230381 T>C maps to NM_001040446.1 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:9730436 G>A maps to NM_001077525.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:9704013 G>T maps to NM_001077525.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:31222753 C>T maps to NM_014967.4 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr15:31197996 G>T maps to NM_014967.4 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr15:31222870 T>C maps to NM_014967.4 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:31197636 C>T maps to NM_014967.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:31212783 C>T maps to NM_014967.4 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:31218080 G>T maps to NM_014967.4 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr22:30387537 A>G maps to NM_021090.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:56572925 C>A maps to NM_004687.4 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr17:56573569 C>A maps to NM_004687.4 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:56589852 C>A maps to NM_004687.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25840040 T>C maps to NM_004685.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr13:25823504 G>A maps to NM_004685.3 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:17228695 G>A maps to NM_004686.4 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:17157478 G>C maps to NM_004686.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr8:17169137 G>C maps to NM_004686.4 S328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:63490884 A>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:63490910 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:63557209 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:63488885 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:63565050 C>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:63488493 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:63488882 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:63488737 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:63579328 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:63569936 T>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:63569931 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:63574714 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:63488606 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:63551457 T>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:63569930 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:63557223 C>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:11177237 C>T maps to NM_015458.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:187455304 G>T maps to NM_005958.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:187455010 G>T maps to NM_005958.3 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr4:187455379 C>T maps to NM_005958.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:187455292 G>T maps to NM_005958.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:92715247 G>T maps to NM_005959.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:92715237 C>A maps to NM_005959.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:92715441 C>A maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:92703025 G>C maps to NM_005959.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:92714982 C>A maps to NM_005959.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:92715174 C>A maps to NM_005959.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:92715179 G>A maps to NM_005959.3 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:74176131 G>T did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:74207495 A>G maps to NM_001123226.1 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:74183110 G>T maps to NM_001123226.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:11313973 G>T maps to NM_004958.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:11319409 C>A maps to NM_004958.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr1:11270917 G>A maps to NM_004958.3 R1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:11227549 C>G maps to NM_004958.3 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:11297962 C>A maps to NM_004958.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:11300432 C>A maps to NM_004958.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:11288727 C>A maps to NM_004958.3 R1009R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:11181320 C>T maps to NM_004958.3 L2305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:11217212 C>A maps to NM_004958.3 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:11199667 C>A maps to NM_004958.3 R1640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:30602882 T>C maps to ENST00000358107 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr10:30615548 G>A maps to ENST00000358107 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:30615417 C>A maps to ENST00000358107 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:135614760 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:237024422 A>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:237052595 G>C maps to NM_000254.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237057838 G>A maps to NM_000254.2 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:237058850 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:236995356 C>A maps to NM_000254.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:237057699 C>G maps to NM_000254.2 S1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:236966852 C>T maps to NM_000254.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:41814394 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr5:7895959 A>G maps to NM_024010.2 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:7892875 C>T maps to NM_024010.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:125603416 C>A maps to NM_014751.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr8:125577907 G>C maps to NM_014751.4 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:125565304 C>T maps to NM_014751.4 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:125580617 A>G did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr4:100534104 C>T maps to ENST00000511045 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr4:100521875 C>T maps to ENST00000511045 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:100522816 C>A maps to ENST00000511045 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr4:100512480 G>T maps to ENST00000511045 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:17542024 G>A maps to NM_001001924.2 R884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:17612581 T>C maps to NM_001001924.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr8:17579392 T>A maps to NM_001001931.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr8:17512105 C>A maps to NM_001001924.2 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr13:29855913 C>T maps to NM_001033602.2 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr13:29599884 G>C maps to NM_001033602.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr13:30066846 G>C maps to NM_001033602.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:30075295 C>G maps to NM_001033602.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:29598828 G>C maps to NM_001033602.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr13:30077255 G>C maps to NM_001033602.2 P1351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr13:29598882 G>T maps to NM_001033602.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:29598870 C>T maps to NM_001033602.2 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr13:29600250 C>T maps to NM_001033602.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr13:29599233 G>T maps to NM_001033602.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr13:29608080 C>G maps to NM_001033602.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr13:29600968 G>T maps to NM_001033602.2 G722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr13:29600082 A>T maps to NM_001033602.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr13:29600022 C>G maps to NM_001033602.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:29600748 G>A maps to NM_001033602.2 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr13:29600400 C>A maps to NM_001033602.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:177193076 C>G maps to NM_006554.4 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:79285041 G>C maps to ENST00000512528 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:26584731 A>G maps to NM_001135091.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr11:26584812 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:26582725 C>A maps to NM_001135091.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:26586886 T>G maps to NM_001135091.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:26586718 G>T maps to NM_001135091.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:26586849 C>A maps to NM_001135091.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:9065902 T>A maps to NM_024690.2 T7181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:9047973 G>T maps to NM_024690.2 T11219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:9048897 G>T maps to NM_024690.2 T10911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:9057666 G>A maps to NM_024690.2 Q9927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:9091785 G>T maps to NM_024690.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:9082766 G>T maps to NM_024690.2 L3016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:8996402 C>A maps to NM_024690.2 L13723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9049863 A>G maps to NM_024690.2 S10589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:9059266 T>A maps to NM_024690.2 P9393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:9089858 A>G maps to NM_024690.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:9024901 C>T maps to NM_024690.2 W12320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9072491 G>T maps to NM_024690.2 S4985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:8996372 A>G maps to NM_024690.2 N13733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:9010702 G>T maps to NM_024690.2 T12986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:9089918 T>G maps to NM_024690.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:9083753 G>T maps to NM_024690.2 T2687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:9000567 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:9045756 A>G maps to NM_024690.2 H11958H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:9067654 C>T maps to NM_024690.2 V6597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9072067 G>T maps to NM_024690.2 T5126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:9088055 G>T maps to NM_024690.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9002504 G>T maps to NM_024690.2 V13437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9064621 A>T maps to NM_024690.2 S7608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:9070918 A>C maps to NM_024690.2 S5509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:9003350 A>G maps to NM_024690.2 L13362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:9011387 G>A maps to NM_024690.2 Q12949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:9063442 C>A maps to NM_024690.2 V8001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:9046506 A>G maps to NM_024690.2 F11708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:9077692 G>T maps to NM_024690.2 A3251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:9047920 G>T maps to NM_024690.2 S11237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:9076465 T>C maps to NM_024690.2 E3660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9064315 G>T maps to NM_024690.2 I7710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:9084425 C>A maps to NM_024690.2 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9012893 A>T maps to NM_024690.2 A12850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:9071875 A>G maps to NM_024690.2 P5190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:9088130 T>A maps to NM_024690.2 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9083144 C>T maps to NM_024690.2 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:9086903 C>T maps to NM_024690.2 G1637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:9082424 G>T maps to NM_024690.2 P3130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr19:9065056 T>C maps to NM_024690.2 E7463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:9013854 G>T maps to NM_024690.2 P12845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:9065837 G>C maps to NM_024690.2 S7203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9066577 G>C maps to NM_024690.2 T6956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:9077713 T>C maps to NM_024690.2 P3244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:9068782 G>T maps to NM_024690.2 L6221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:9072997 T>G maps to NM_024690.2 A4816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:9090538 C>A maps to NM_024690.2 G426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:9049764 T>C maps to NM_024690.2 L10622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9064858 A>T maps to NM_024690.2 T7529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:9065530 G>C maps to NM_024690.2 T7305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:9059704 T>G maps to NM_024690.2 T9247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:9091775 G>T maps to NM_024690.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:9070909 G>T maps to NM_024690.2 P5512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:9071028 G>A maps to NM_024690.2 Q5473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr19:9047454 T>A maps to NM_024690.2 P11392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:9061795 C>T maps to NM_024690.2 P8550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr19:9069682 C>T maps to NM_024690.2 V5921V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:9060334 T>A maps to NM_024690.2 T9037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:9002549 G>T maps to NM_024690.2 I13422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:9049155 G>T maps to NM_024690.2 V10825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:9075688 A>C maps to NM_024690.2 T3919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:9046228 G>T maps to NM_024690.2 S11801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:9056319 A>G maps to NM_024690.2 L10376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:9014571 C>A maps to NM_024690.2 L12801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:9017385 C>A maps to NM_024690.2 L12646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:9019278 G>C maps to NM_024690.2 P12536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:9056248 G>C maps to NM_024690.2 T10399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:9075070 C>T maps to NM_024690.2 T4125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:9090478 C>A maps to NM_024690.2 G446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:9063685 A>G maps to NM_024690.2 S7920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:9003571 C>T maps to NM_024690.2 Q13356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:9048741 A>T maps to NM_024690.2 P10963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:9060122 G>T maps to NM_024690.2 S9108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:9088249 G>T maps to NM_024690.2 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:9069916 G>T maps to NM_024690.2 T5843T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:9061381 G>T maps to NM_024690.2 S8688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:9084641 G>T maps to NM_024690.2 I2391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:8966816 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:9062524 G>A maps to NM_024690.2 T8307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:9049833 C>T maps to NM_024690.2 W10599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:9076552 G>T maps to NM_024690.2 P3631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:9072072 C>A maps to NM_024690.2 E5125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9046893 A>G maps to NM_024690.2 T11579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:9063967 A>C maps to NM_024690.2 A7826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:9060458 G>T maps to NM_024690.2 S8996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:9071389 G>T maps to NM_024690.2 S5352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:9089802 G>C maps to NM_024690.2 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:9000510 C>A maps to NM_024690.2 R13491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:9026255 C>A maps to NM_024690.2 E12244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:9028326 G>T maps to NM_024690.2 L12155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:9061254 C>A maps to NM_024690.2 G8731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:9056230 A>C maps to NM_024690.2 V10405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:9087446 G>A maps to NM_024690.2 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr19:9011469 A>C maps to NM_024690.2 T12921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:9064675 A>G maps to NM_024690.2 P7590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:9073700 G>T maps to NM_024690.2 S4582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:8997116 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:9070226 G>C maps to NM_024690.2 S5740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr19:9065218 G>C maps to NM_024690.2 S7409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:9009599 G>T maps to NM_024690.2 V13042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:9082873 C>A maps to NM_024690.2 G2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr19:9061354 A>T maps to NM_024690.2 T8697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr19:9069179 G>C maps to NM_024690.2 S6089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:9060013 G>T maps to NM_024690.2 A9144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:9067729 C>T maps to NM_024690.2 K6572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr19:9057031 G>A maps to NM_024690.2 S10138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:9082973 G>T maps to NM_024690.2 A2947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr19:9090467 G>T maps to NM_024690.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:9021068 C>T maps to NM_024690.2 R12418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:9087335 G>T maps to NM_024690.2 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:9077020 G>T maps to NM_024690.2 T3475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:9087989 A>T maps to NM_024690.2 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:9091424 C>T maps to NM_024690.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr19:9056590 G>T maps to NM_024690.2 A10285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:9056417 G>T maps to NM_024690.2 S10343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:9069688 G>T maps to NM_024690.2 P5919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:9088964 C>T maps to NM_024690.2 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:9088934 A>T maps to NM_024690.2 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr19:9089300 G>A maps to NM_024690.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:9073567 A>C maps to NM_024690.2 S4626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9017373 G>T maps to NM_024690.2 T12650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:9089318 T>A maps to NM_024690.2 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:9070270 G>T maps to NM_024690.2 T5725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:9048195 T>A maps to NM_024690.2 S11145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:9090896 G>T maps to NM_024690.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:9085553 C>T maps to NM_024690.2 T2087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:9090221 G>T maps to NM_024690.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:9077353 T>C maps to NM_024690.2 T3364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:8994194 G>A maps to NM_024690.2 F13830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:9049134 G>A maps to NM_024690.2 S10832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:9014601 C>G maps to NM_024690.2 L12791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:9008335 C>T maps to NM_024690.2 K13072K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:8976585 G>A maps to NM_024690.2 S14130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:9017344 C>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:9091523 G>A maps to NM_024690.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr19:8997161 G>T maps to NM_024690.2 T13678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr19:9076272 G>A maps to NM_024690.2 L3725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:9061926 C>A maps to NM_024690.2 E8507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:9077808 C>A maps to NM_024690.2 E3213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:9062707 G>A maps to NM_024690.2 S8246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:8987248 G>C maps to NM_024690.2 S13946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:9056554 G>T maps to NM_024690.2 A10297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:9070669 C>A maps to NM_024690.2 G5592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:9047615 C>A maps to NM_024690.2 E11339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:8976392 G>T maps to NM_024690.2 T14145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:9074638 G>T maps to NM_024690.2 S4269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:9084071 G>T maps to NM_024690.2 P2581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr19:9067666 T>A maps to NM_024690.2 A6593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr19:8999023 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:9084563 T>A maps to NM_024690.2 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr19:9077500 G>A maps to NM_024690.2 S3315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:9069055 G>T maps to NM_024690.2 S6130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:9075907 T>C maps to NM_024690.2 P3846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:9075312 T>A maps to NM_024690.2 K4045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:9087200 G>A maps to NM_024690.2 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr19:9065768 G>C maps to NM_024690.2 S7226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:9076852 G>A maps to NM_024690.2 T3531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:8976588 G>T maps to NM_024690.2 I14129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr19:9045879 G>T maps to NM_024690.2 S11917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:100685328 C>A maps to NM_001040105.1 S3544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100681104 T>A maps to NM_001040105.1 S2136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:100675477 G>T maps to NM_001040105.1 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100676088 G>A maps to NM_001040105.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100676861 C>A maps to NM_001040105.1 S722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:100696651 G>A maps to NM_001040105.1 W4433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:100681800 T>A maps to NM_001040105.1 P2368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:100677756 C>A maps to NM_001040105.1 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr7:100685799 C>G maps to NM_001040105.1 V3701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:100680894 A>C maps to NM_001040105.1 T2066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100680393 C>A maps to NM_001040105.1 T1899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:100684468 G>T maps to NM_001040105.1 E3258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:100677981 T>A maps to NM_001040105.1 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:100683156 G>T maps to NM_001040105.1 T2820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:100682118 C>A maps to NM_001040105.1 G2474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100680747 C>T maps to NM_001040105.1 T2017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100684016 T>A maps to NM_001040105.1 L3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:100682805 G>A maps to NM_001040105.1 L2703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100681896 A>C maps to NM_001040105.1 T2400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr7:100679316 C>G maps to NM_001040105.1 V1540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:100683642 T>C maps to NM_001040105.1 P2982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:100679895 T>G maps to NM_001040105.1 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:100677954 T>C maps to NM_001040105.1 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:100680570 C>A maps to NM_001040105.1 T1958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:100681295 C>A maps to NM_001040105.1 S2200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:100676133 C>T maps to NM_001040105.1 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:100674948 T>C maps to NM_001040105.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:100676538 T>A maps to NM_001040105.1 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:100684575 G>T maps to NM_001040105.1 V3293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100678560 G>T maps to NM_001040105.1 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:100678180 T>C maps to NM_001040105.1 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:100682520 T>A maps to NM_001040105.1 S2608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:100693916 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:100676469 A>C maps to NM_001040105.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:100680372 T>A maps to NM_001040105.1 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr7:100679100 C>T maps to NM_001040105.1 A1468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:100681470 T>G maps to NM_001040105.1 T2258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:100677570 T>A maps to NM_001040105.1 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:100676877 C>A maps to NM_001040105.1 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr7:100675542 C>A maps to NM_001040105.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:100684737 C>T maps to NM_001040105.1 F3347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:100696347 G>A maps to NM_001040105.1 V4395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:100683729 T>C maps to NM_001040105.1 P3011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:100692123 A>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:100679184 T>G maps to NM_001040105.1 P1496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr7:100675989 C>T maps to NM_001040105.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr7:100680858 G>T maps to NM_001040105.1 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:100676817 C>A maps to NM_001040105.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:100679319 C>T maps to NM_001040105.1 T1541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:100675086 C>A maps to NM_001040105.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:100682445 C>A maps to NM_001040105.1 T2583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:100677444 C>T maps to NM_001040105.1 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:1102475 C>A maps to ENST00000441003 A2620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:1101127 G>T maps to ENST00000441003 T2509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:1099770 G>T maps to ENST00000441003 V2456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:1093565 C>A maps to ENST00000441003 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:1100992 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:1093934 T>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:1087977 C>T maps to ENST00000441003 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:1083841 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:1090897 C>T maps to ENST00000441003 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:1081647 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:1104127 C>T maps to ENST00000441003 S2773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr11:1096454 C>T maps to ENST00000441003 I2160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:1087464 C>A maps to ENST00000441003 Y1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr3:195453012 C>T maps to ENST00000447234 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:30955046 C>A maps to NM_001010909.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:30955256 C>A maps to NM_001010909.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:195477784 C>A maps to NM_018406.5 G5282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:195475819 A>G maps to NM_018406.5 C5329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:195498652 G>C maps to NM_018406.5 S4371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr3:195538661 G>C maps to NM_018406.5 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:195474199 C>T maps to NM_018406.5 L5362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr3:195492165 G>A maps to NM_018406.5 D4591D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:1273699 G>A maps to ENST00000447027 P5000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:1267037 C>A maps to ENST00000447027 A2979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:1247869 G>A maps to ENST00000447027 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1262981 C>A maps to ENST00000447027 T1627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1279597 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:1246914 C>T maps to ENST00000447027 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:1272806 C>T maps to ENST00000447027 T4902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:1264139 C>T maps to ENST00000447027 P2013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:1275484 C>A maps to ENST00000447027 A5130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:1271324 T>A maps to ENST00000447027 T4408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr11:1275511 C>G maps to ENST00000447027 L5139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:1268478 C>A maps to ENST00000447027 R3460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:1271090 C>G maps to ENST00000447027 P4330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:1271042 G>A maps to ENST00000447027 L4314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:1272833 G>C maps to ENST00000447027 V4911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr11:1272611 C>G maps to ENST00000447027 S4837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:1270337 C>G maps to ENST00000447027 T4079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:1274100 C>A maps to ENST00000447027 V5039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr11:1269188 C>T maps to ENST00000447027 L3696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:1264034 C>A maps to ENST00000447027 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:1265879 C>G maps to ENST00000447027 T2593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:1278884 C>T maps to ENST00000447027 F5468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:1247899 C>A maps to ENST00000447027 Y85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:1265810 C>A maps to ENST00000447027 P2570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:1272653 C>T maps to ENST00000447027 L4851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:1271063 C>A maps to ENST00000447027 S4321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr11:1263476 G>A maps to ENST00000447027 E1792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:1263423 T>C maps to ENST00000447027 L1775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:1266116 G>A maps to ENST00000447027 V2672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr11:1263122 G>A maps to ENST00000447027 T1674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:1026436 G>T maps to NM_005961.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:1026472 G>A maps to NM_005961.2 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1025313 G>T maps to NM_005961.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:1015780 T>C maps to NM_005961.2 T2340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:1025346 C>T maps to NM_005961.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:1028697 G>T maps to NM_005961.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr11:1018717 G>A maps to NM_005961.2 G1361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:1013996 G>T maps to NM_005961.2 V2348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:1017652 G>T maps to NM_005961.2 P1716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr4:71346521 G>T maps to NM_152291.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:71347309 C>A maps to NM_152291.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:71346871 C>A maps to NM_152291.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:57749650 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:57741543 C>T maps to ENST00000431972 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:20827839 G>A maps to NM_024544.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:1362246 A>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:105449920 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:105450165 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:105450835 T>C did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:105449934 A>G did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:105449931 A>G did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:105449724 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:105449858 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:105450160 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:105449797 C>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:105450146 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:105449716 A>G did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:105450999 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:105451270 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:103340820 G>C maps to NM_001018116.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:103348394 G>T maps to NM_001018116.1 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:103348399 G>A maps to NM_001018116.1 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:113496624 C>A maps to ENST00000189978 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr9:113562895 C>T maps to ENST00000189978 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr9:113563054 C>A maps to ENST00000189978 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:113530297 G>A maps to ENST00000189978 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr9:113496655 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:49415405 T>G maps to NM_000255.3 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:49425721 G>A maps to NM_000255.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:49403210 C>T maps to NM_000255.3 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:49426987 C>A maps to NM_000255.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:49403170 G>A maps to NM_000255.3 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:49409662 T>A maps to NM_000255.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:49419393 C>A maps to NM_000255.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:49427044 G>A maps to NM_000255.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr6:49403167 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:8041434 C>A maps to NM_201280.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:45798842 C>A did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:45798604 G>T maps to NM_001128425.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:88723850 G>A maps to NM_002461.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:110034366 C>T maps to NM_001114185.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:110029113 G>A maps to NM_001114185.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:29842280 C>T maps to NM_017458.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:29845346 C>T maps to NM_017458.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr21:42830501 C>T maps to NM_001144925.1 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr21:42811705 G>T maps to NM_001144925.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr21:42808969 G>A maps to NM_001144925.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr21:42762540 T>A maps to NM_002463.1 L261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr21:42771257 C>T maps to NM_002463.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:42778786 G>A maps to NM_002463.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr21:42748970 T>C maps to NM_002463.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr21:42748937 A>G maps to NM_002463.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:70164437 G>A maps to NM_002357.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr10:111967664 C>A maps to NM_130439.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:3228222 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:3238800 C>A did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr23:3240768 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:3228240 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:3261776 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:3242082 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:3242296 C>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:3248371 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:3235263 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:3235986 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:3228255 C>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:3242604 T>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:3235433 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:3242455 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:3261745 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:3235286 G>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:3229354 G>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:3238058 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr23:3228089 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:3229247 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:3241143 G>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:3241358 T>G did not map to a codon.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr23:3238064 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:3229154 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:3242301 C>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:3242839 G>C did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:3240107 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:3240857 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:3240238 G>A did not map to a codon.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr23:3235706 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:3228003 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:3240047 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:3240385 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:3241315 A>C did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr23:3241385 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:3229471 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:3261794 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:3235640 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:3248299 G>T did not map to a codon.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr23:3229172 C>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:3241186 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:3228211 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:3240551 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:3235858 A>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:3240142 G>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:3238913 T>C did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:3235810 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:3228871 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:3239783 T>A did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr23:3238682 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:3228905 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:3228352 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:3238387 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:3228007 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:3229499 C>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:3235677 G>A did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr23:3235827 C>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:3239344 C>G did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:3227794 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:3228024 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:3229374 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:3229375 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:3242050 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:3238164 T>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:3242413 C>G did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:3238831 A>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:3240762 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:3228469 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:3238843 T>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:3235693 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:3235694 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:3242958 C>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:3241896 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:3228498 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:3240327 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:3241505 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:3242156 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:3239347 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:3241884 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:3228246 T>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:3248431 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:3229559 A>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:3235450 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:3238376 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:3228408 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:3238245 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:3241310 A>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:3239234 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:3235847 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:3248398 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:3238187 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:3242200 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:3239832 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:3248709 G>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:3228147 C>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:3239968 A>T did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:3235281 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:3238889 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:3241626 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:3235646 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:3242242 C>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:3261705 C>G did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:3240967 G>C did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:3242277 C>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:3238246 C>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:3235274 C>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:3241305 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:3240312 G>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:3242066 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:3238885 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr23:3248361 G>A did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:3239241 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:3229390 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:3239277 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:3241974 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:3228469 G>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:3238939 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:3240147 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:3240148 A>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:3227871 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:3228019 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:3228256 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:3241048 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr23:3235196 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:3228222 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:3241715 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:3235841 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:3240524 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:3242136 C>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:3228415 C>A did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr1:1290365 C>G maps to NM_032348.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:1290158 G>C maps to NM_032348.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr19:54377403 G>T maps to NM_001020818.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:54377031 C>T maps to NM_001020818.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:54377019 C>A maps to NM_001020818.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:135520131 T>A maps to NM_001130173.1 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:135521438 C>T maps to NM_001130173.1 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:135511329 G>T maps to NM_001130173.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr6:135515582 A>T maps to NM_001130173.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:4446342 G>A maps to NM_001105538.1 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:4453603 C>A maps to NM_001105538.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr8:67492484 C>T maps to NM_001080416.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:42315706 A>G maps to NM_002466.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:42331359 C>T maps to NM_002466.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr20:42331446 C>T maps to NM_002466.2 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:42341661 G>A maps to NM_002466.2 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:102036301 C>G maps to NM_002465.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:102023251 C>A maps to NM_002465.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:102061561 C>A maps to NM_002465.2 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:50957558 G>T maps to NM_004533.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:50944202 G>A maps to NM_004533.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:50958470 C>A maps to NM_004533.3 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:50939885 G>T maps to NM_004533.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50945489 C>A maps to NM_004533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:50940737 C>T maps to NM_004533.3 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:50944253 C>G maps to NM_004533.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:47360128 C>A maps to ENST00000399249 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:47363609 C>T maps to ENST00000399249 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:47363651 G>A maps to ENST00000399249 D560D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:47356683 G>T maps to ENST00000399249 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:203138422 G>T maps to NM_004997.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr13:77755943 A>G maps to NM_015057.4 D1611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr13:77671868 G>C maps to NM_015057.4 T3140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:77662999 T>A maps to NM_015057.4 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr13:77847654 G>A maps to NM_015057.4 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr13:77656070 G>C maps to NM_015057.4 V3698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:77713444 C>T maps to NM_015057.4 L2515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:77699603 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:77754432 C>A maps to NM_015057.4 G1654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr13:77799690 T>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:48600955 A>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr17:48586034 C>T maps to NM_032133.4 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:48594811 C>A maps to NM_032133.4 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr17:48603495 T>C maps to NM_032133.4 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:48598507 C>T maps to NM_032133.4 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:48593970 A>T maps to NM_032133.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:16082253 C>A maps to NM_005378.4 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:16085777 G>T maps to NM_005378.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:16082269 C>T maps to NM_005378.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:16082269 C>T maps to NM_005378.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:153043127 C>T maps to NM_025107.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:153043386 G>T maps to NM_025107.2 *236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:38182677 C>T maps to NM_001172567.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:48444430 C>A maps to NM_016132.3 G380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr15:48446076 G>A maps to NM_016132.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:48451077 G>A maps to NM_016132.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:69063508 C>T maps to NM_138768.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:241069408 G>A maps to NM_138336.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr2:241066015 C>T maps to NM_138336.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:241066155 C>A maps to NM_138336.1 G195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr12:81112713 G>T maps to NM_005593.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:81111007 C>A maps to NM_005593.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:81112162 C>A maps to NM_005593.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:81110974 G>T maps to NM_005593.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:81111174 G>T maps to NM_005593.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:81110964 G>A maps to NM_005593.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:81111333 T>A maps to NM_005593.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:81101698 C>A maps to NM_002469.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:81101729 C>T maps to NM_002469.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:81101563 G>T maps to NM_002469.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:81102717 G>A maps to NM_002469.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:10403990 G>A maps to NM_005963.3 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:10397670 C>T maps to NM_005963.3 A1889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:10419598 C>A maps to NM_005963.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:10412920 G>A maps to NM_005963.3 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:10402374 T>A maps to NM_005963.3 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10417173 G>A maps to NM_005963.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr17:10399400 C>A maps to NM_005963.3 E1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10400384 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:10402040 T>C maps to NM_005963.3 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:10419767 G>C maps to NM_005963.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr17:10415290 C>A maps to NM_005963.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:10398274 C>T maps to NM_005963.3 K1813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:10399346 C>A maps to NM_005963.3 E1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr17:10415800 C>A maps to NM_005963.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:10409237 C>A maps to NM_005963.3 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:10403999 G>A maps to NM_005963.3 Q1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:10419288 G>T maps to NM_005963.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:10399749 C>T maps to NM_005963.3 K1591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:10409226 A>T maps to NM_005963.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10401160 C>A maps to NM_005963.3 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr17:10409223 G>T maps to NM_005963.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10417164 G>T maps to NM_005963.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:10402066 C>A maps to NM_005963.3 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:10401190 C>A maps to NM_005963.3 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:10419568 C>A maps to NM_005963.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr17:10404774 C>A maps to NM_005963.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:10411686 C>T maps to NM_005963.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:10395747 G>A maps to NM_005963.3 I1935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:10404774 C>A maps to NM_005963.3 R1130R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MP-A4T8-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:10404446 C>A maps to NM_005963.3 E1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:8455462 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:8408031 C>T maps to ENST00000360416 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:8384695 G>A maps to ENST00000360416 H1736H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:8480656 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:15839063 G>T maps to NM_001040114.1 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:15818777 C>T maps to NM_001040114.1 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:15831438 C>A maps to NM_001040114.1 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:15797964 G>T maps to NM_001040114.1 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:15811106 C>G maps to NM_001040114.1 R1805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr16:15826435 A>T maps to NM_001040114.1 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:15851830 G>T maps to NM_001040114.1 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:15841518 G>T maps to NM_001040114.1 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:15808818 C>T maps to NM_001040114.1 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:15844069 C>A maps to NM_001040114.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr16:15865510 G>A maps to NM_001040114.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:15878554 G>T maps to NM_001040114.1 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr16:15815293 A>G maps to NM_001040114.1 D1528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:15832533 G>T maps to NM_001040114.1 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr16:15844060 C>T maps to NM_001040114.1 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr16:15809105 G>T maps to NM_001040114.1 S1850*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-NJ-A4YF-01A-12D-A25L-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-NJ-A4YF-01A-12D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:15850334 C>A maps to NM_001040114.1 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:10243656 C>A maps to NM_003802.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:10210315 C>A maps to NM_003802.2 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:10222286 G>T maps to NM_003802.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:10222424 G>T maps to NM_003802.2 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:10209811 C>T maps to NM_003802.2 K1810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:10206755 C>T maps to NM_003802.2 K1842K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:10253942 C>T maps to NM_003802.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr17:10248921 C>T maps to NM_003802.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:10206727 T>A maps to NM_003802.2 K1852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:10265754 G>A maps to NM_003802.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr17:10258047 T>A maps to NM_003802.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:10231253 G>T maps to NM_003802.2 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr17:10212754 C>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:10265444 G>A maps to NM_003802.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:10265474 G>T maps to NM_003802.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:10265706 G>A maps to NM_003802.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:10219324 C>A maps to NM_003802.2 T1252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:10231407 G>A maps to NM_003802.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:10206530 C>T maps to NM_003802.2 K1883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:10214473 C>T maps to NM_003802.2 K1534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:10250077 A>T maps to NM_003802.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:10213108 C>A maps to NM_003802.2 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr17:10247285 A>T maps to NM_003802.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr17:10267667 G>C maps to NM_003802.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:10253902 C>A maps to NM_003802.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr17:10224995 T>A maps to NM_003802.2 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:10258268 C>A maps to NM_003802.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:50735302 G>T maps to NM_001145809.1 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:50804967 G>A maps to NM_001145809.1 K1840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:50781446 G>A maps to NM_001145809.1 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:50764740 C>T maps to NM_001145809.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:50766619 G>T maps to NM_001145809.1 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:108189604 G>T maps to NM_014981.1 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:108107872 C>A maps to NM_014981.1 E1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:108220686 C>A maps to NM_014981.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:108135676 C>T maps to NM_014981.1 Q1330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:108112925 C>A maps to NM_014981.1 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:108175614 T>C maps to NM_014981.1 Q732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr3:108211362 T>C maps to NM_014981.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:108127252 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:108189546 C>A maps to NM_014981.1 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:108174687 T>A maps to NM_014981.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr3:108218986 G>A maps to NM_014981.1 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:108219046 G>A maps to NM_014981.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr3:108110645 C>G maps to NM_014981.1 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:108179194 C>T maps to NM_014981.1 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr3:108139992 C>T maps to NM_014981.1 K1277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10440586 T>A maps to NM_017534.5 L620L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4410-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10432237 C>T maps to NM_017534.5 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:10432342 G>T maps to NM_017534.5 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr17:10432553 G>A maps to NM_017534.5 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:10448801 G>A maps to NM_017534.5 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:10428088 G>C maps to NM_017534.5 T1652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:10433042 T>C maps to NM_017534.5 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:10430274 G>A maps to NM_017534.5 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:10439864 T>G maps to NM_017534.5 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10448684 G>A maps to NM_017534.5 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr17:10436695 G>A maps to NM_017534.5 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:10429959 G>T maps to NM_017534.5 Y1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr17:10447063 G>A maps to NM_017534.5 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:10428933 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:10431125 C>T maps to NM_017534.5 E1270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:10428076 G>T maps to NM_017534.5 L1656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:10438681 C>A maps to NM_017534.5 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr17:10450850 G>A maps to NM_017534.5 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:10436735 G>C maps to NM_017534.5 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10426899 G>T maps to NM_017534.5 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:10432522 G>A maps to NM_017534.5 Q1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:10428109 G>A maps to NM_017534.5 A1645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:10443933 G>A maps to NM_017534.5 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:10426461 A>T maps to NM_017534.5 L1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:10424659 G>T maps to NM_017534.5 S1921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr17:10439903 G>T maps to NM_017534.5 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:10426672 G>C maps to NM_017534.5 V1843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:10424631 G>T maps to NM_017534.5 R1931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:10432949 C>T maps to NM_017534.5 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:10547772 C>T maps to NM_002470.2 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:10558330 G>A maps to NM_002470.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:10533200 C>A maps to NM_002470.2 L1872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr17:10542451 T>A maps to NM_002470.2 K1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:10541665 G>T maps to NM_002470.2 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:10543657 C>G maps to NM_002470.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:10535948 G>A maps to NM_002470.2 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr17:10538772 C>T maps to NM_002470.2 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:10541662 C>T maps to NM_002470.2 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:10533024 G>C maps to NM_002470.2 T1895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:10535230 C>A maps to NM_002470.2 E1687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:10535935 C>A maps to NM_002470.2 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr17:10541608 C>G maps to NM_002470.2 T1160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:10533166 C>A maps to NM_002470.2 E1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:10538315 T>C maps to NM_002470.2 Q1399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:10551905 T>A maps to NM_002470.2 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:10535213 A>G maps to NM_002470.2 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:10544689 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr17:10538841 G>C maps to NM_002470.2 R1338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10360869 G>T maps to NM_017533.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:10356998 C>A maps to NM_017533.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:10360770 A>T maps to NM_017533.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:10362639 C>T maps to NM_017533.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:10356615 A>T maps to NM_017533.2 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:10352022 G>C maps to NM_017533.2 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr17:10360812 A>T maps to NM_017533.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:10346843 C>A maps to NM_017533.2 E1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:10369628 C>T maps to NM_017533.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:10354165 C>T maps to NM_017533.2 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:10358328 G>A maps to NM_017533.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:10363310 G>T maps to NM_017533.2 Y458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:10366944 G>A maps to NM_017533.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr17:10362582 G>A maps to NM_017533.2 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:10354108 T>C maps to NM_017533.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:10356488 G>A maps to NM_017533.2 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr17:10366241 G>T maps to NM_017533.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:10351985 C>A maps to NM_017533.2 E1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:10367812 C>T maps to NM_017533.2 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr17:10366909 G>A maps to NM_017533.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr17:10363355 G>A maps to NM_017533.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr17:10358536 T>C maps to NM_017533.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:10355749 T>A maps to NM_017533.2 K1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:10355768 A>T maps to NM_017533.2 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:10368003 A>T maps to NM_017533.2 L176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:10367996 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:10368005 G>T maps to NM_017533.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:10348295 G>T maps to NM_017533.2 A1821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:10358512 G>T maps to NM_017533.2 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:23872969 G>T maps to NM_002471.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr14:23853923 G>T maps to NM_002471.3 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:23851756 G>A maps to NM_002471.3 N1892N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:23858084 C>T maps to NM_002471.3 E1386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:23859649 G>C maps to NM_002471.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:23871691 C>A maps to NM_002471.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:23876423 A>G maps to NM_002471.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:23872644 C>T maps to NM_002471.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:23863102 G>T maps to NM_002471.3 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:23871703 C>T maps to NM_002471.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:23861782 C>G maps to NM_002471.3 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:23852436 C>T maps to NM_002471.3 E1886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:23855253 C>A maps to NM_002471.3 L1682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:23874573 G>T maps to NM_002471.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr14:23851720 C>T maps to NM_002471.3 E1904E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23866763 C>A maps to NM_002471.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:23855700 C>A maps to NM_002471.3 R1594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:23872557 C>A maps to NM_002471.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:23874012 C>A maps to NM_002471.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr14:23873946 G>T maps to NM_002471.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:23871911 G>T maps to NM_002471.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:23868096 G>A maps to NM_002471.3 H577H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr14:23862217 G>T maps to NM_002471.3 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:23872001 C>T maps to NM_002471.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:23894912 G>A maps to NM_000257.2 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:23887539 C>A maps to NM_000257.2 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:23883230 G>C maps to NM_000257.2 R1880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:23893160 C>G maps to NM_000257.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:23898509 C>G maps to NM_000257.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:23885421 C>A maps to NM_000257.2 E1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr14:23886427 T>A maps to NM_000257.2 K1485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr14:23886428 G>A maps to NM_000257.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr14:23885029 A>G maps to NM_000257.2 I1655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr14:23884588 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr14:23887489 C>T maps to NM_000257.2 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23886821 C>A maps to NM_000257.2 E1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:23886822 C>A maps to NM_000257.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:23884425 C>A maps to NM_000257.2 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:23884427 G>A maps to NM_000257.2 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr14:23884615 C>A maps to NM_000257.2 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr14:23887557 G>T maps to NM_000257.2 R1344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr14:23895276 G>A maps to NM_000257.2 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:23891510 C>T maps to NM_000257.2 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:23884887 C>A maps to NM_000257.2 E1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr20:33570261 C>T maps to NM_020884.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:33568394 C>T maps to NM_020884.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:33578867 C>A maps to NM_020884.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:10298620 C>A maps to NM_002472.2 V1597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:10309715 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:10299914 G>A maps to NM_002472.2 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:10301945 G>T maps to NM_002472.2 A1331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:10304650 C>A maps to NM_002472.2 E1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:10322314 A>T maps to NM_002472.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr17:10296303 A>G maps to NM_002472.2 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:10304096 C>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr17:10317240 T>C maps to NM_002472.2 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:10315770 G>T maps to NM_002472.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:10319002 C>T maps to NM_002472.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr17:10299897 C>G maps to NM_002472.2 T1500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:10302104 G>A maps to NM_002472.2 Q1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:10312899 C>A maps to NM_002472.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr17:10300290 G>T maps to NM_002472.2 A1397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:10317595 G>T maps to NM_002472.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36691696 G>T maps to NM_002473.4 I1113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr22:36708173 G>A maps to NM_002473.4 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr22:36723528 T>A maps to NM_002473.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:36684362 C>A maps to NM_002473.4 E1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:36684363 C>A maps to NM_002473.4 L1622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:101256814 G>A maps to NM_138403.4 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:101265450 C>A maps to NM_138403.4 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr7:101265409 C>A maps to NM_138403.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:111352023 A>T maps to NM_000432.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:111352080 C>A maps to NM_000432.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:45299180 G>T maps to NM_002476.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:44179169 T>A maps to ENST00000434895 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:44180570 C>A maps to ENST00000457314 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:16145360 C>G maps to NM_013262.3 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:16143377 C>T maps to NM_013262.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:16145421 G>A maps to NM_013262.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:123452993 C>A maps to NM_053025.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:123512523 C>A maps to NM_053025.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr3:123452801 C>T maps to NM_053025.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:123418891 G>A maps to NM_053025.3 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:123419622 G>A maps to NM_053025.3 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:123456293 C>A maps to NM_053025.3 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:123337558 G>T maps to NM_053025.3 P1809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:123357039 C>T maps to NM_053025.3 E1613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:123458824 G>A maps to NM_053025.3 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:123383051 G>A maps to NM_053025.3 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:30408010 G>C maps to NM_033118.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr20:30418881 G>A maps to NM_033118.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:30408220 G>A maps to NM_033118.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:30408289 A>T maps to NM_033118.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:46781865 C>A maps to NM_182493.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:46781730 G>A maps to NM_182493.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:46766386 C>A maps to NM_182493.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr16:46771657 G>A maps to NM_182493.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr16:46755045 C>A maps to NM_182493.2 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:46761279 C>G maps to NM_182493.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:2749381 A>G maps to NM_001012418.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:2679628 C>A maps to NM_001012418.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:2679575 C>G maps to NM_001012418.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:2685594 G>A maps to NM_001012418.3 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr6:2680455 T>A maps to NM_001012418.3 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:2685800 G>A maps to NM_001012418.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr16:30387756 G>A maps to NM_013292.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr5:16701569 C>T maps to NM_012334.2 E978E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:16685845 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:16711276 G>C maps to NM_012334.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:16699586 C>T maps to NM_012334.2 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:16877804 G>A maps to NM_012334.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:16680172 G>A maps to NM_012334.2 Y1475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:16672931 C>T maps to NM_012334.2 V1725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:16672829 G>A maps to NM_012334.2 T1759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:16680115 G>A maps to NM_012334.2 N1494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:16694688 G>A maps to NM_012334.2 C1197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:16701709 C>A maps to NM_012334.2 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:16682001 C>T maps to NM_012334.2 E1389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:16694541 C>T maps to NM_012334.2 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr5:16670831 C>A maps to NM_012334.2 G1896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:16769189 G>A maps to NM_012334.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr5:16674978 G>C maps to NM_012334.2 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:16668541 C>T maps to NM_012334.2 L1973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:16694646 C>T maps to NM_012334.2 Q1211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:16666851 C>T maps to NM_012334.2 K2042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:16671036 G>T maps to NM_012334.2 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:16701631 C>A maps to NM_012334.2 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:18023557 C>T maps to ENST00000205890 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:18023154 G>A maps to ENST00000205890 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:18058424 C>A maps to ENST00000205890 A2742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:18022482 C>T maps to ENST00000205890 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:18024000 G>A maps to ENST00000205890 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr17:18043892 C>T maps to ENST00000205890 S1758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr17:18023016 G>A maps to ENST00000205890 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr17:18023034 C>T maps to ENST00000205890 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr17:18025525 C>T maps to ENST00000205890 Q1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr17:18052077 G>A maps to ENST00000205890 G2256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:18051507 C>T maps to ENST00000205890 D2225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr17:18059601 G>C maps to ENST00000205890 A2851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:18052869 C>T maps to ENST00000205890 D2396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:109610050 C>A maps to NM_015011.1 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr13:109507807 T>C maps to NM_015011.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:109817396 C>A maps to NM_015011.1 S1749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:109672171 G>T maps to NM_015011.1 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr13:109540773 C>T maps to NM_015011.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr13:109459024 A>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr13:109707854 C>T maps to NM_015011.1 Q1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr13:109518568 G>A maps to NM_015011.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr13:109475581 C>A maps to NM_015011.1 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:109793317 C>T maps to NM_015011.1 S1564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr13:109779779 C>T maps to NM_015011.1 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:109318300 C>A maps to NM_015011.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:109779719 C>G maps to NM_015011.1 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr13:109610080 T>G maps to NM_015011.1 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:27448160 G>A maps to NM_078471.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:27417863 G>A maps to NM_078471.3 N1756N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:27493466 C>A maps to NM_078471.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27425146 A>T maps to NM_078471.3 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:27425125 C>A maps to NM_078471.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr22:26351203 G>A maps to ENST00000407587 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr22:26400767 T>C maps to ENST00000407587 T2141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:26164761 G>T maps to ENST00000407587 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26177726 G>T maps to ENST00000407587 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:26239789 G>T maps to ENST00000407587 T1101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr22:26343715 G>T maps to ENST00000407587 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr22:26423043 G>T maps to ENST00000407587 P2370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:26298649 C>T maps to ENST00000407587 Q1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr22:26193996 C>T maps to ENST00000407587 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:26317264 A>G maps to ENST00000407587 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr22:26423256 G>T maps to ENST00000407587 V2441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:26168353 C>T maps to ENST00000407587 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr22:26423475 C>T maps to ENST00000407587 S2514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:26224871 T>C maps to ENST00000407587 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:26423001 C>T maps to ENST00000407587 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr22:26173680 C>A maps to ENST00000407587 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr22:26165076 C>A maps to ENST00000407587 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr22:26165077 C>T maps to ENST00000407587 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:26422692 G>T maps to ENST00000407587 S2253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr22:26422575 C>T maps to ENST00000407587 A2214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr22:26422707 G>C maps to ENST00000407587 G2258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr22:26422428 G>C maps to ENST00000407587 G2165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr22:26164179 T>A maps to ENST00000407587 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:34864955 T>C maps to NM_001163735.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:34883450 G>A maps to NM_001163735.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:34859854 C>A maps to NM_001163735.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr17:34881082 G>A maps to NM_001163735.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:34862944 G>A maps to NM_001163735.1 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr12:57424943 T>C maps to NM_005379.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:57422607 T>A maps to NM_005379.2 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:57435269 C>A maps to NM_005379.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:57432272 C>A maps to NM_005379.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:57437122 C>T maps to NM_005379.2 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:57442098 G>T maps to NM_005379.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:192194696 A>T maps to NM_001130158.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:192273772 C>T maps to NM_001130158.1 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:192261174 G>A maps to NM_001130158.1 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:192252059 C>T maps to NM_001130158.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:1384167 C>A maps to NM_001080779.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:1369046 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:1386343 C>A maps to NM_001080779.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:1371351 G>A maps to NM_001080779.1 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:31075975 G>A maps to NM_015194.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:31087343 T>C maps to NM_015194.1 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:30932129 C>A maps to NM_015194.1 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:31094725 G>A maps to NM_015194.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:31105501 C>A maps to NM_015194.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:31107651 C>T maps to NM_015194.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:30821872 C>T maps to NM_015194.1 K975K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:59494606 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:59480398 C>A maps to NM_004998.2 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:59494581 C>G maps to NM_004998.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:59553678 G>A maps to NM_004998.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:59494581 C>G maps to NM_004998.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:59523933 G>A maps to NM_004998.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:8601437 T>G maps to NM_012335.3 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:8592262 C>T maps to NM_012335.3 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr19:8595412 A>G maps to NM_012335.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:8587291 G>A maps to NM_012335.3 N1063N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:8601851 G>T maps to NM_012335.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:8590438 C>A maps to NM_012335.3 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr7:45010483 T>A maps to NM_033054.2 K341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr7:45004681 C>A maps to NM_033054.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:109853403 G>T maps to NM_001101421.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:109877483 C>T maps to NM_001101421.3 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:109835535 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr10:26436438 C>T maps to NM_017433.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:26432510 C>T maps to NM_017433.4 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:26446270 G>T maps to NM_017433.4 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:26465715 G>C maps to NM_017433.4 L1460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:26417318 G>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr10:26377322 C>A maps to NM_017433.4 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:26436360 C>T maps to NM_017433.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:26465694 G>A maps to NM_017433.4 Q1453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr10:26446297 C>T maps to NM_017433.4 C951C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr10:26310430 G>A did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr10:26432415 G>T maps to NM_017433.4 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr10:26463125 C>T maps to NM_017433.4 T1311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr10:26463096 G>T maps to NM_017433.4 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:171258114 C>T maps to NM_138995.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:171239650 C>A maps to NM_138995.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:171070932 C>G maps to NM_138995.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:171262115 C>A maps to NM_138995.3 C831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:171400484 C>A maps to NM_138995.3 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:171070899 G>T maps to NM_138995.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:171260905 G>T maps to NM_138995.3 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:171240281 A>T maps to NM_138995.3 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:171238571 G>T maps to NM_138995.3 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:52646196 C>T maps to ENST00000358212 K1146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:52645804 G>C maps to ENST00000358212 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr15:52700337 C>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:52611477 C>T maps to ENST00000358212 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:52664515 C>A maps to ENST00000358212 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52646176 G>C maps to ENST00000358212 S1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr15:52622588 T>A maps to ENST00000358212 K1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:52635342 C>A maps to ENST00000358212 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:52613628 C>T maps to ENST00000358212 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr15:52672055 C>A maps to ENST00000358212 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:47375946 C>T maps to NM_001080467.2 Q1435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr18:47432934 C>A maps to NM_001080467.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr18:47518663 G>A maps to NM_001080467.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr18:47462674 C>G maps to NM_001080467.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:47527633 G>A maps to NM_001080467.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:52517701 C>A maps to NM_018728.3 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:52539166 C>A maps to NM_018728.3 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:52571808 C>A maps to NM_018728.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr15:52527959 T>A maps to NM_018728.3 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:52564028 G>A maps to NM_018728.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:52562006 C>A maps to NM_018728.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr6:76599836 G>T maps to ENST00000428345 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:76602275 G>A maps to ENST00000428345 Q992Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:76602279 G>T maps to ENST00000428345 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:76558186 G>C maps to ENST00000428345 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:76916515 G>A maps to NM_000260.3 E1830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:76900499 C>T maps to NM_000260.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76872032 G>T maps to NM_000260.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76910852 C>T maps to NM_000260.3 N1614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr11:76853807 C>A maps to NM_000260.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:76872054 A>T maps to NM_000260.3 K413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:76867813 C>T maps to NM_000260.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:76885841 C>A maps to NM_000260.3 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:76919799 G>T maps to NM_000260.3 T2001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:76873996 C>T maps to NM_000260.3 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:76886495 A>T maps to NM_000260.3 K725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:128347794 G>A maps to ENST00000389524 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:128381780 C>T maps to ENST00000389524 F1285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128347776 C>A maps to ENST00000389524 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:128389268 G>T maps to ENST00000389524 P1705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr2:128331591 G>A maps to ENST00000389524 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:128367542 G>T maps to ENST00000389524 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:128380775 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:128346069 A>G maps to ENST00000389524 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:128354110 C>T maps to ENST00000389524 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:128341822 C>A maps to ENST00000389524 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr2:128384579 C>T maps to ENST00000389524 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:128339540 C>T maps to ENST00000389524 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:128391815 G>A maps to ENST00000389524 Q1834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:128393796 C>A maps to ENST00000389524 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:128324228 C>T maps to ENST00000389524 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:128380916 G>T maps to ENST00000389524 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:128341834 C>T maps to ENST00000389524 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:128341855 C>T maps to ENST00000389524 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:128324280 G>T maps to ENST00000389524 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:128393856 C>T maps to ENST00000389524 I2002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:128367239 C>A maps to ENST00000389524 R992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:72191291 C>A maps to ENST00000424560 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr15:72190148 G>C maps to ENST00000424560 T1565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr15:72338222 G>A maps to ENST00000424560 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:72208824 T>C maps to ENST00000424560 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:72122610 C>A maps to ENST00000424560 S2364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:72227691 C>A maps to ENST00000424560 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr15:72144596 A>G maps to ENST00000424560 A2188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:72191153 T>A maps to ENST00000424560 S1230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:72252401 T>G maps to ENST00000424560 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:72195370 G>A maps to ENST00000424560 R971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:17213240 G>A maps to NM_004145.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17296810 G>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr19:17264842 C>G maps to NM_004145.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr19:17311620 G>T maps to NM_004145.3 E1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:17309027 G>A maps to NM_004145.3 A1383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr19:17305637 G>T maps to NM_004145.3 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:17264819 G>T maps to NM_004145.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:171605715 G>A maps to NM_000261.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:171605352 C>T maps to NM_000261.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:12666918 C>A maps to NM_001146312.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:12656521 G>T maps to NM_001146312.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:12656506 C>A maps to NM_001146312.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:12626275 G>C maps to NM_001146312.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr17:12666801 C>A maps to NM_001146312.1 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr17:12656347 T>C maps to NM_001146312.1 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:12647600 G>A maps to NM_001146312.1 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:17743007 C>T maps to NM_002478.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:17741496 C>T maps to NM_002478.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:17742856 C>T maps to NM_002478.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:95162102 G>A maps to NM_013451.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:95148893 C>A maps to NM_013451.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:95116583 G>A maps to NM_013451.3 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:95111577 G>C maps to NM_013451.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:95121314 C>G did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr10:95155908 C>A maps to NM_013451.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:95162072 G>C maps to NM_013451.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:203054888 C>T maps to NM_002479.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:203054630 C>T maps to NM_002479.4 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:203054711 G>T maps to NM_002479.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr1:203053043 G>T maps to NM_002479.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr18:3134706 C>A maps to NM_003803.3 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr18:3071837 C>T maps to NM_003803.3 E1586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:3089173 T>A maps to NM_003803.3 K1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr18:3067286 G>T maps to NM_003803.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr18:3089174 G>T maps to NM_003803.3 C1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr18:3188807 C>A maps to NM_003803.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:2092877 C>A maps to NM_003970.2 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:2017596 G>T maps to NM_003970.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:2054353 G>T maps to NM_003970.2 G989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:2057200 C>A maps to NM_003970.2 S1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:2037847 C>A maps to NM_003970.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:2021569 G>C maps to NM_003970.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:2088652 A>T maps to NM_003970.2 K1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:2056575 G>T did not map to a codon.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr8:2046715 C>T maps to NM_003970.2 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr8:2044147 C>A maps to NM_003970.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:2027641 C>T maps to NM_003970.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:2017480 G>T maps to NM_003970.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:2041799 C>T maps to NM_003970.2 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:2063831 C>A maps to NM_003970.2 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:2048735 G>T maps to NM_003970.2 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr8:2021431 A>G maps to NM_003970.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:24388532 G>A maps to ENST00000330966 H1282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:24406538 G>A maps to ENST00000330966 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:24401864 T>C maps to ENST00000330966 K935K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:24419596 C>T maps to ENST00000330966 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:24426234 G>A maps to ENST00000330966 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:24401951 G>A maps to ENST00000330966 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:24435041 C>A maps to ENST00000330966 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:24383946 G>C maps to ENST00000330966 V1410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:24433711 G>A maps to ENST00000330966 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:137211544 T>C maps to NM_006790.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:75391695 C>A maps to NM_021245.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr4:120085429 C>T maps to NM_016599.3 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:150051462 G>A maps to NM_133371.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:150056313 C>A maps to NM_133371.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr10:69881363 C>T maps to NM_032578.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr10:69948774 G>T maps to NM_032578.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr10:69959229 C>T maps to NM_032578.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:69954181 A>T maps to NM_032578.2 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr10:69961616 G>T maps to NM_032578.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:69966658 C>A maps to NM_032578.2 Y1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:69925567 C>T maps to NM_032578.2 H531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:69948774 G>T maps to NM_032578.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr10:69902780 G>A maps to NM_032578.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:69948765 G>A maps to NM_032578.2 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:69881590 C>A maps to NM_032578.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr10:69881413 C>T maps to NM_032578.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr10:69961613 C>T maps to NM_032578.2 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:40192631 C>A maps to NM_015460.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:39942312 G>C maps to NM_015460.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr3:40251559 G>A maps to NM_015460.2 Q627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr3:40231368 T>C maps to NM_015460.2 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:40231855 C>A maps to NM_015460.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:59148139 C>T maps to NM_001085487.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr16:31138574 C>T maps to NM_182958.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr16:31142153 C>A maps to NM_182958.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:47875696 T>G maps to NM_007067.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:41790451 G>A maps to NM_006766.3 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr8:41791381 C>A maps to NM_006766.3 A1452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr8:41791407 G>A maps to NM_006766.3 Q1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:41836296 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:41792281 C>T maps to NM_006766.3 W1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:41834583 C>T maps to NM_006766.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:41790298 G>A maps to NM_006766.3 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr8:41791419 C>A maps to NM_006766.3 E1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:41791425 C>A maps to NM_006766.3 E1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:41836244 G>A maps to NM_006766.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:76788499 G>A maps to NM_012330.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:76736088 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:76789342 G>T maps to NM_012330.2 T1587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:76735732 G>T maps to NM_012330.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:76780502 G>C maps to NM_012330.2 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr10:76603031 C>A maps to NM_012330.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:62836920 C>A maps to NM_004535.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr20:62854713 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62850369 A>T maps to NM_004535.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:62853401 T>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:62837069 C>A maps to NM_004535.2 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:62839649 G>A maps to NM_004535.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:62848564 C>T maps to NM_004535.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr20:62831275 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr20:62851064 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr20:62854694 C>A maps to NM_004535.2 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr20:62836963 C>T maps to NM_004535.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:62836947 C>A maps to NM_004535.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:1926361 C>T maps to ENST00000399161 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:1893090 G>T maps to ENST00000399161 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:1946753 C>A maps to ENST00000399161 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:1926244 G>T maps to ENST00000399161 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:1843126 C>A maps to ENST00000399161 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:1893072 G>T maps to ENST00000399161 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:1982999 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:1926498 C>A maps to ENST00000399161 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:1926807 G>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:1947096 A>T maps to ENST00000399161 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:1914082 C>A maps to ENST00000399161 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:1890379 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:1906867 G>T maps to ENST00000399161 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:1926807 G>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:1926883 G>A maps to ENST00000399161 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr2:1914043 G>C maps to ENST00000399161 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:1906915 A>G maps to ENST00000399161 Y656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:1926886 C>G maps to ENST00000399161 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:1915811 G>A maps to ENST00000399161 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:1805557 A>G maps to ENST00000399161 D1062D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:1891330 G>A maps to ENST00000399161 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:1926247 C>A maps to ENST00000399161 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:1983534 G>C maps to ENST00000399161 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:1926751 G>A maps to ENST00000399161 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:59080679 G>A maps to NM_198055.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr16:48581955 C>A maps to NM_153029.3 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:48580109 C>A maps to NM_153029.3 G761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:40104130 C>T maps to NM_018177.3 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:40146364 G>C maps to NM_018177.3 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:40122700 A>G maps to NM_018177.3 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr4:40104479 A>T maps to NM_018177.3 K339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:40122931 A>G maps to NM_018177.3 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:40113713 A>T maps to NM_018177.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:40104286 C>T maps to NM_018177.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr4:40115054 C>T maps to NM_018177.3 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:32978378 G>A maps to NM_001079691.1 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr13:33110699 T>C maps to ENST00000505213 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:177546898 G>T maps to NM_015111.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:177548131 G>T maps to NM_015111.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr21:30255347 A>C maps to NM_013240.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr13:21306049 C>T maps to NM_174928.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:153197845 C>T did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr4:80246365 T>C maps to NM_032693.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr4:80246395 A>G maps to NM_032693.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:80246953 G>T maps to NM_032693.2 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:80246770 G>T maps to NM_032693.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr4:140265338 G>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr4:140306133 T>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr4:140265374 A>G maps to NM_057175.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:140299928 A>G maps to NM_057175.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:41941682 A>C maps to NM_024561.4 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:41894956 C>A maps to NM_024561.4 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr12:112516500 C>A maps to NM_024953.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:112528569 T>A maps to NM_024953.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:112506752 G>A maps to NM_024953.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr14:57858148 G>T maps to NM_001011713.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:57863468 G>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:117828411 G>T maps to NM_016200.4 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:89907011 G>T maps to NM_005467.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:89891356 C>T maps to NM_005467.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:89896503 C>A maps to NM_005467.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr11:89885503 C>A maps to NM_005467.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:89868776 C>T maps to NM_005467.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:89916114 C>T maps to NM_005467.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:89883720 C>T maps to NM_005467.3 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:89896520 T>C maps to NM_005467.3 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:89885503 C>A maps to NM_005467.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr11:89868006 G>A maps to NM_005467.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:89892451 C>A maps to NM_005467.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:64825655 C>T maps to ENST00000340252 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:64825655 C>G maps to ENST00000340252 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:175184863 T>G maps to NM_207015.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:174814952 G>A maps to NM_207015.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:175165126 G>T maps to NM_207015.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:175184874 C>G maps to NM_207015.2 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:174974223 G>T maps to NM_207015.2 G282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:174814684 G>A maps to NM_207015.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:57486978 G>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:57485105 C>T maps to NM_005967.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr12:57110314 G>A maps to NM_001113203.1 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:57110842 T>A maps to NM_001113203.1 K1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:57112841 G>C maps to NM_001113203.1 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr12:57112307 A>G maps to NM_001113203.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr12:57108217 C>G maps to NM_001113203.1 A1917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr12:57115187 T>A maps to NM_001113203.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:59668400 G>T maps to NM_199290.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:59668498 C>A maps to NM_199290.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:13247139 T>C maps to NM_052876.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:1685645 T>G maps to ENST00000344463 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:71195411 C>T maps to NM_018161.4 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:71164425 G>A maps to NM_018161.4 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr11:71209480 C>T maps to NM_018161.4 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:66847734 A>T maps to ENST00000359087 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:66850921 G>A maps to ENST00000359087 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr4:164087831 G>A maps to NM_138386.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:164087651 G>A maps to NM_138386.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:164050299 G>A maps to NM_138386.2 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr4:164050297 C>T maps to NM_138386.2 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:42461774 C>T maps to NM_000262.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr22:42462722 G>A maps to NM_000262.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:71303831 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:71299780 G>T maps to NM_017567.4 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:71299831 C>T maps to NM_017567.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:40690376 G>C maps to NM_000263.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr17:40696048 G>A maps to NM_000263.3 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr16:5083365 C>T maps to NM_016256.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:5078017 G>A maps to NM_016256.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:42082135 G>A maps to NM_153006.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:42082045 G>A maps to NM_153006.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:42083114 C>T maps to NM_153006.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:42084748 G>A maps to NM_153006.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr17:42083066 C>T maps to NM_153006.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:130829230 G>A maps to NM_197956.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:130825793 G>A maps to NM_197956.3 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:70308531 C>A maps to NM_004536.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:101717914 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:101763039 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:102030992 G>T maps to NM_052867.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:101890209 C>A maps to NM_052867.2 G444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:102029287 G>A maps to NM_052867.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:101721104 A>T maps to NM_052867.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101710323 G>A maps to NM_052867.2 Q1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:101936319 G>C maps to NM_052867.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr13:101890222 A>T maps to NM_052867.2 C439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:101714424 C>A maps to NM_052867.2 L1550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:101714412 C>A maps to NM_052867.2 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr13:101795541 G>T maps to NM_052867.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr13:101763578 T>C did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr13:101748032 T>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr13:101707769 A>T maps to NM_052867.2 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:101735161 C>A maps to NM_052867.2 E1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:101756711 G>A maps to NM_052867.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr13:101728292 C>G did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr13:101714423 C>A maps to NM_052867.2 E1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr13:102029329 G>T maps to NM_052867.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:101890144 T>C maps to NM_052867.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr13:101712241 C>T maps to NM_052867.2 P1611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr13:101756964 G>T maps to NM_052867.2 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr13:101728231 C>A maps to NM_052867.2 G1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:101707700 G>T maps to NM_052867.2 T1721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr13:101881928 G>T maps to NM_052867.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr13:101755660 A>T maps to NM_052867.2 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr13:102029275 A>G maps to NM_052867.2 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:102051435 T>C maps to NM_052867.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr13:101795487 G>A maps to NM_052867.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr13:101726010 C>A maps to NM_052867.2 S1374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr13:101742055 G>T maps to NM_052867.2 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr13:101717811 G>T maps to NM_052867.2 C1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr13:101735484 G>T maps to NM_052867.2 I1216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:105902109 G>C maps to NM_005746.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:105909740 G>A maps to NM_005746.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:7947054 G>A maps to NM_024865.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120790053 C>A maps to NM_199461.2 Y247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:46417798 C>T maps to NM_001029861.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:13991268 C>T maps to NM_001098622.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:13988557 C>T maps to NM_001098622.1 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:25596689 T>C maps to NM_152667.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr20:25596775 C>A maps to NM_152667.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr9:100845291 C>T maps to NM_018946.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:72434119 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:72433697 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:72433352 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:72433875 T>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:72433138 C>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:72433768 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:72433311 C>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr23:72433188 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:72433572 A>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:72433877 T>C did not map to a codon.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr23:72434051 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:92927734 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:92927893 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:92927565 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:92927796 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:92927485 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:92928085 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:92928087 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:92926977 G>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:92927524 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:92926870 A>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:92927181 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:92927203 T>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:92927111 C>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:92927253 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:92927018 T>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:92926825 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:92927449 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:92927529 T>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:92928285 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:92926928 C>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:92928145 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:92927878 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:92927989 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:92927306 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:92928108 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:2981070 G>A maps to ENST00000399624 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:47996259 C>A maps to NM_003827.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:23361955 T>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:102760346 C>T maps to ENST00000455523 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:102760609 C>A maps to ENST00000455523 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:10548348 A>G maps to NM_003826.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr18:10550088 C>T maps to NM_003826.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:144660048 C>A maps to ENST00000276844 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:50862276 G>A maps to NM_004851.1 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:50862783 C>A maps to NM_004851.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:50865479 G>T maps to NM_004851.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:80436674 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:780983 C>A maps to NM_022493.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:784252 G>C maps to NM_022493.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr16:784288 G>A maps to NM_022493.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:787272 C>A maps to NM_022493.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr15:60760340 C>A maps to NM_024611.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:78277201 T>C maps to NM_024678.4 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:78154804 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr1:46067954 C>T maps to NM_002482.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:18079763 C>T maps to NM_001160176.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr8:18080398 C>A maps to NM_001160176.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr11:34153689 T>C maps to NM_024662.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:34149017 T>C maps to NM_024662.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:34167642 G>A maps to NM_024662.2 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:34129825 A>G maps to NM_024662.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:34144127 G>T maps to NM_024662.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:34144052 G>A maps to NM_024662.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:34139801 C>T maps to NM_024662.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:34149089 C>G maps to NM_024662.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:34133650 C>T maps to NM_024662.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3532548 G>T maps to NM_024845.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:18258139 G>T maps to NM_000015.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:50334354 C>A maps to NM_012191.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:50334258 G>A maps to NM_012191.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr2:73868506 C>A maps to NM_003960.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:72768372 G>A maps to NM_015654.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:72769121 C>A maps to NM_015654.3 E83*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:201777943 C>A maps to ENST00000367296 R1384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:201618284 G>T maps to ENST00000367296 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr1:201778379 C>T maps to ENST00000367296 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:201777623 G>T maps to ENST00000367296 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:201687682 G>T maps to ENST00000367296 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:20070531 C>T maps to ENST00000396087 N1410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:20070730 C>T maps to ENST00000396087 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:20066721 A>T maps to ENST00000396087 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:19735465 G>T maps to ENST00000396087 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:19890505 A>T maps to ENST00000396087 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:20066787 C>A maps to ENST00000396087 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:20067153 G>T maps to ENST00000396087 P1303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:20065811 G>T maps to ENST00000396087 G1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:20070444 G>A maps to ENST00000396087 K1381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:20113750 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:20136342 T>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:19954929 G>T maps to ENST00000396087 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr11:19954914 G>C maps to ENST00000396087 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:20122655 G>T maps to ENST00000396087 E2178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:20139798 C>T maps to ENST00000396087 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:20129312 C>T maps to ENST00000396087 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:78513203 T>A maps to NM_014903.4 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:78513134 C>T maps to NM_014903.4 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:78574790 A>T maps to NM_014903.4 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:78513152 G>A maps to NM_014903.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:78444769 C>A maps to NM_014903.4 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:78362296 A>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:78510662 C>A maps to NM_014903.4 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr12:78516178 G>T maps to NM_014903.4 T1403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:78388648 T>A maps to NM_014903.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:78415550 C>T maps to NM_014903.4 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:78542636 C>A maps to NM_014903.4 R1575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:78444603 C>T maps to NM_014903.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr12:78400785 C>T maps to NM_014903.4 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:78400473 G>T maps to NM_014903.4 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr12:78225483 G>A maps to NM_014903.4 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:78400484 G>A maps to NM_014903.4 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr12:78400685 C>A maps to NM_014903.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr12:78593172 C>A maps to NM_014903.4 R2171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:78225333 T>C maps to NM_014903.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:78571077 C>A maps to NM_014903.4 S1761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr12:78571093 G>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:78593139 G>T maps to NM_014903.4 E2160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:78513015 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:78562539 T>A maps to NM_014903.4 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:78515819 C>A maps to NM_014903.4 R1284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:78569161 C>A maps to NM_014903.4 G1686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:78570979 A>G maps to NM_014903.4 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:78513131 C>A maps to NM_014903.4 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr12:78592423 A>G maps to NM_014903.4 S2140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr12:78604197 C>A maps to NM_014903.4 L2331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:15555686 G>A maps to NM_015909.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:15557782 A>C maps to NM_015909.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:15432848 C>A maps to NM_015909.2 V1613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:15417225 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:15358905 G>A maps to NM_015909.2 P2141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:15514741 C>A maps to NM_015909.2 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr2:15493754 G>C maps to NM_015909.2 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr2:15629147 T>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:15542343 G>A maps to NM_015909.2 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:15358895 C>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:15555759 C>A maps to NM_015909.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:15651344 C>A maps to NM_015909.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:15644337 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:15496519 G>T maps to NM_015909.2 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:15701344 G>C maps to NM_015909.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:15618410 T>C maps to NM_015909.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:35630160 C>T maps to ENST00000400445 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr13:36046594 G>T maps to ENST00000400445 G2169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr13:36046600 C>G maps to ENST00000400445 L2171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:35517200 C>T maps to ENST00000400445 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr13:36141139 A>C maps to ENST00000400445 R2341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr13:35685095 C>T maps to ENST00000400445 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr13:35683513 T>C maps to ENST00000400445 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:36167463 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:35923250 G>C maps to ENST00000400445 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr13:36229810 G>T maps to ENST00000400445 G2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr13:35747692 G>T maps to ENST00000400445 E1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr13:35683456 C>T maps to ENST00000400445 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:204058615 C>G maps to NM_001114132.1 L2311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:204045222 G>T maps to NM_001114132.1 E2166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:47039672 C>T maps to NM_015175.1 F1025F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:47037927 G>T maps to NM_015175.1 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:47044543 G>T maps to NM_015175.1 E1853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:90965537 T>A maps to NM_002485.4 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:90994958 T>A maps to NM_002485.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:90958457 T>C maps to NM_002485.4 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr8:90983436 G>A maps to NM_002485.4 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:16890538 G>A maps to NM_017940.3 Q1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:16918356 G>T maps to NM_017940.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:16895566 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:16893811 C>A maps to NM_017940.3 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:16907942 C>A maps to NM_017940.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:16914248 A>T maps to NM_017940.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:16892176 G>A maps to NM_017940.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:145296387 C>T maps to NM_001039703.4 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:145368635 G>C maps to NM_001039703.4 V3538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:145302755 C>T maps to NM_001039703.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:145368668 C>T maps to NM_001039703.4 V3549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:145299899 C>T maps to NM_001039703.4 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:145368678 C>T maps to NM_001039703.4 Q3553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:148016460 C>A did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr1:148009458 A>G maps to ENST00000310701 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:144828750 G>T maps to NM_001037675.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:41345113 C>T maps to NM_005899.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr8:102705019 G>A maps to NM_032041.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:102731842 G>A maps to NM_032041.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:113133595 C>A maps to ENST00000397960 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr11:113102470 C>T maps to ENST00000316851 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:113078055 G>C maps to ENST00000316851 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:113102991 A>T maps to ENST00000316851 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:113076777 C>A maps to ENST00000316851 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:113102910 C>A maps to ENST00000316851 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:113111526 T>A maps to ENST00000397960 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:113078065 G>T maps to ENST00000316851 E237*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8302-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:113103000 G>T maps to ENST00000316851 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:113102931 G>A maps to ENST00000316851 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:113076266 G>A maps to ENST00000316851 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:113126629 G>A maps to ENST00000316851 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr11:113075206 C>G maps to ENST00000316851 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr11:113078025 C>T maps to ENST00000316851 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:113133592 C>A maps to ENST00000397960 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:113078566 G>A maps to ENST00000316851 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:22370901 C>T maps to NM_004540.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:22881253 C>T maps to NM_004540.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr21:22658658 C>A maps to NM_004540.2 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr21:22710707 G>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr21:22881295 C>T maps to NM_004540.2 C734C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:22881367 T>G maps to NM_004540.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:22839026 C>A maps to NM_004540.2 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr21:22710823 G>T maps to NM_004540.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr21:22881289 G>A maps to NM_004540.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr21:22906868 C>A maps to NM_004540.2 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:19338711 C>T maps to NM_004386.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:19338660 C>A maps to NM_004386.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:19334855 C>A maps to NM_004386.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:19339041 G>T maps to NM_004386.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:19338835 G>T maps to NM_004386.2 G803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr19:19338672 G>A maps to NM_004386.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:19337841 C>T maps to NM_004386.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:19339150 C>T maps to NM_004386.2 Q908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:19349179 G>T maps to NM_004386.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:19337292 A>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:19360590 G>A maps to NM_004386.2 R1279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:19339356 G>A maps to NM_004386.2 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:6631033 C>G maps to NM_014865.3 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:6604359 G>A maps to NM_014865.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:6635321 C>T maps to NM_014865.3 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:6626626 C>T maps to NM_014865.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr12:6635620 C>A maps to NM_014865.3 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr12:6637369 C>T maps to NM_014865.3 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:6635485 C>T maps to NM_014865.3 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:6624086 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:134073738 C>T maps to NM_015261.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:134073618 G>C maps to NM_015261.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:158482645 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:158468338 C>A maps to NM_017760.5 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:158483361 C>T maps to NM_017760.5 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:158455055 G>A maps to NM_017760.5 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:158468324 C>T maps to NM_017760.5 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:158449053 G>A maps to NM_017760.5 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr7:158449020 G>A maps to NM_017760.5 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:97008911 G>A maps to NM_015341.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:97031790 C>T maps to NM_015341.3 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:97024809 A>T maps to NM_015341.3 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39691003 G>C maps to NM_001001414.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:39691254 G>C did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:36026117 C>A maps to NM_001014839.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:36026228 G>A maps to NM_001014839.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:36029490 G>A maps to NM_001014839.1 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:36026261 G>A maps to NM_001014839.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:172351585 A>T maps to NM_001146276.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:172365892 G>T maps to NM_001146276.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:74197866 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:74197922 C>T maps to NM_000265.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr22:37268424 T>C maps to NM_013416.3 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr22:37266470 G>T maps to NM_013416.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:136664878 A>T maps to NM_006153.4 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:106498469 G>T maps to NM_001004720.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:106497817 G>A maps to NM_001004720.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:183821317 A>G maps to NM_205842.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:183832072 G>C maps to NM_205842.1 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr2:183821251 T>C maps to NM_205842.1 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:183791549 T>C maps to NM_205842.1 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:183791551 G>A maps to NM_205842.1 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:183860434 G>T maps to NM_205842.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:183846072 C>A maps to NM_205842.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:54925123 C>T maps to NM_005337.4 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:54925988 C>A maps to NM_005337.4 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:54929926 G>T maps to NM_005337.4 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:54917191 C>T maps to NM_005337.4 H631H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr12:54914979 C>T maps to NM_005337.4 C612C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr12:54910731 C>T maps to NM_005337.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:133721312 C>A maps to NM_207363.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133540443 G>T maps to NM_207363.2 R1314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:133542196 A>G maps to NM_207363.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:133489352 C>T maps to NM_207363.2 G1800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:133543132 G>T maps to NM_207363.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:133721291 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:133541070 A>G maps to NM_207363.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:133540038 C>A maps to NM_207363.2 G1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:133539997 C>A maps to NM_207363.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:133541887 A>G maps to NM_207363.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:133489454 G>T maps to NM_207363.2 A1766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:133489418 G>A maps to NM_207363.2 D1778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr2:133554220 G>A maps to NM_207363.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:133489361 G>T maps to NM_207363.2 T1797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:133542559 G>T maps to NM_207363.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr2:133541209 T>C maps to NM_207363.2 Q1058Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:133483247 C>A maps to NM_207363.2 G1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:133543027 G>T maps to NM_207363.2 C452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:50189230 C>G maps to NM_001037806.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:50190207 G>A maps to NM_001037806.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:50188717 C>A maps to NM_001037806.3 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr12:50186234 G>A maps to NM_001037806.3 T1262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:50190888 C>A maps to NM_001037806.3 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:50196878 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:48719040 T>C maps to NM_016453.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:48719903 G>A maps to NM_016453.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:48717146 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:232324987 C>A maps to NM_005381.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:232323095 T>G maps to NM_005381.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:24933897 G>A maps to NM_003743.4 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:24929491 C>A maps to NM_003743.4 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:24896314 G>T maps to NM_003743.4 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:24929508 C>T maps to NM_003743.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:24985554 G>C did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:24929669 C>G maps to NM_003743.4 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:24929505 G>T maps to NM_003743.4 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:71075712 G>A maps to NM_006540.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:71075700 T>C maps to NM_006540.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:71036163 C>A maps to NM_006540.2 V1416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:46254146 T>C maps to NM_181659.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:46276055 A>T maps to NM_181659.2 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr20:46264275 A>G maps to NM_181659.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr20:46255823 C>T maps to NM_181659.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:51585289 T>C maps to NM_001145260.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr10:51579258 C>T maps to NM_001145260.1 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695707 G>A maps to NM_020967.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:44695758 G>A maps to NM_020967.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr20:44697168 T>A maps to NM_020967.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:33330705 C>T maps to NM_014071.2 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:33345446 C>A maps to NM_014071.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr20:33334659 G>A maps to NM_014071.2 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr20:33345398 T>C maps to NM_014071.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr20:33345359 G>A maps to NM_014071.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr20:33337974 G>A maps to NM_014071.2 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr20:33329480 T>A maps to NM_014071.2 K1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr20:33328572 G>A maps to NM_014071.2 T1829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:33345890 G>A maps to NM_014071.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:16004982 C>A maps to ENST00000395857 T773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16004784 G>A maps to ENST00000395857 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr17:15973545 C>A maps to ENST00000395857 R1498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:15935792 T>G maps to ENST00000395857 S2394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr17:16055312 C>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:124826521 G>A maps to NM_006312.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:124862882 C>A maps to NM_006312.4 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr12:124840076 G>A maps to NM_006312.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:124812057 G>A maps to NM_006312.4 L2367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:124827677 G>A maps to NM_006312.4 H1610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:124856712 C>A maps to NM_006312.4 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:124826369 T>A maps to NM_006312.4 R1736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:124862822 G>A maps to NM_006312.4 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:124957678 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:124821371 C>A maps to NM_006312.4 S2021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr12:124856701 G>C maps to NM_006312.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:124826398 G>A maps to NM_006312.4 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr12:124824556 G>A maps to NM_006312.4 V1901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:124811958 C>A maps to NM_006312.4 S2400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:55420751 C>A maps to NM_004829.5 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:55418136 C>T maps to NM_004829.5 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:55417574 C>T maps to NM_004829.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:55424184 C>A maps to NM_004829.5 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:41309565 C>T maps to NM_004828.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:31556973 G>C maps to NM_001145466.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr9:132988694 G>T maps to NM_014286.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:160313246 C>T maps to NM_015331.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:160325483 T>C maps to NM_015331.2 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr1:160321959 C>T maps to NM_015331.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:2616503 G>A maps to NM_006101.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:15771719 C>T maps to NM_001143979.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:15758647 G>T maps to NM_001143979.1 G5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:23931902 G>A maps to NM_002487.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:23931652 C>A maps to NM_002487.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:23932115 C>A maps to NM_002487.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr15:23932082 G>C maps to NM_002487.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr15:23931706 G>T maps to NM_002487.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:23932359 G>C maps to NM_002487.2 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr15:23931764 C>T maps to NM_002487.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:23931596 G>T maps to NM_002487.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:23932276 C>A maps to NM_002487.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:43809120 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:43817788 C>T did not map to a codon.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr23:43817760 T>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr8:134269067 G>A maps to NM_006096.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21486633 G>T maps to NM_201537.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:21490240 T>A maps to NM_201537.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr20:35284929 C>T maps to ENST00000373803 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr20:35288784 G>A maps to ENST00000373803 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:58541756 C>A maps to NM_001130487.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr16:58537746 C>A maps to NM_001130487.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr16:58528890 G>A maps to NM_001130487.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:149919744 C>G maps to NM_001543.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:75567204 C>T maps to NM_003635.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr10:75565473 T>C maps to NM_003635.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr4:119059261 C>T maps to NM_004784.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119158233 C>A maps to NM_004784.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:119161770 C>G maps to NM_004784.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:119163304 G>T did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr4:119036051 C>A maps to NM_004784.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:115773902 T>A maps to NM_022569.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:115760593 T>C maps to NM_022569.1 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:115997855 C>A maps to NM_022569.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:115767153 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:115997622 T>C maps to NM_022569.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:115998177 C>T maps to NM_022569.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:115997478 T>C maps to NM_022569.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:115773887 T>C maps to NM_022569.1 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:115997568 G>T maps to NM_022569.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:115998012 A>G maps to NM_022569.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:115997820 G>T maps to NM_022569.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:115792031 G>C maps to NM_022569.1 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr4:115760533 C>T maps to NM_022569.1 Q762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:115773938 G>T maps to NM_022569.1 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:115769465 A>T maps to NM_022569.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:115997889 G>T maps to NM_022569.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:115891728 C>A maps to NM_022569.1 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:115998117 G>A maps to NM_022569.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr4:115997286 C>T maps to NM_022569.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:115997577 G>T maps to NM_022569.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:119007298 G>C did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:119007321 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240954194 G>A maps to ENST00000404554 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:240961673 C>A maps to ENST00000404554 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:240960827 G>A maps to ENST00000404554 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:5894809 G>A maps to NM_175614.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:95365231 G>C maps to NM_018838.3 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:19638158 G>T maps to ENST00000436926 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:19637066 C>T maps to ENST00000436926 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr7:10979641 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:124906575 C>A maps to NM_014222.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:4778905 G>T did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr3:49060178 C>T maps to NM_199069.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr16:2011496 G>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr23:47001816 C>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:47001810 C>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:47003894 C>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:47002080 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:47003879 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:47001789 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:47002066 A>T did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr7:140396597 C>T maps to NM_004546.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:201950244 T>C maps to NM_002491.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr3:120315259 C>T maps to NM_004547.5 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:179336200 A>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:179334810 A>G maps to NM_002492.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr9:32558940 A>G maps to NM_002493.3 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:102286803 G>A maps to NM_005004.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr8:125559308 G>A maps to NM_005005.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:207008740 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:207003265 C>A maps to ENST00000455934 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:206994877 G>A maps to ENST00000455934 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr2:206992594 G>A maps to ENST00000455934 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:206994965 C>T maps to ENST00000455934 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:161173235 G>T maps to NM_004550.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:52979050 G>T maps to NM_002495.2 *176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:1816028 A>T maps to NM_004553.4 *125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:67804058 G>A maps to NM_002496.3 *211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr21:44323959 G>T maps to NM_021075.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr21:44317034 A>T did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:152426723 G>T maps to NM_001164507.1 I5767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:152423687 C>T maps to NM_001164507.1 Q6050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:152410461 G>T maps to NM_001164507.1 A6502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:152507312 G>T maps to NM_001164507.1 S2334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:152507101 C>A maps to NM_001164507.1 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152531008 C>G maps to NM_001164507.1 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:152553914 G>A maps to NM_001164507.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:152522014 C>A maps to NM_001164507.1 G1690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:152467371 G>T maps to NM_001164507.1 Y3938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:152553886 T>A maps to NM_001164507.1 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:152553213 G>A maps to NM_001164507.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:152432207 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:152512819 G>A maps to NM_001164507.1 H2114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:152551034 C>G did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:152426636 G>A maps to NM_001164507.1 N5796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:152553971 C>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr2:152527650 G>A maps to NM_001164507.1 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:152472514 C>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:152483650 C>T maps to NM_001164507.1 V3404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:152470788 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:152467041 G>A maps to NM_001164507.1 D4002D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:152406212 A>G maps to NM_001164507.1 Y6662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:152361992 G>T maps to NM_001164507.1 S7914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:152492823 C>A maps to NM_001164507.1 E3007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr2:152476159 A>G maps to NM_001164507.1 R3559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:152534388 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:152423891 C>T maps to NM_001164507.1 Q5982Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:152426642 G>A maps to NM_001164507.1 D5794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:152470888 T>A maps to NM_001164507.1 V3834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:152543992 G>A maps to NM_001164507.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr2:152470915 C>A maps to NM_001164507.1 V3825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr2:152582032 T>C maps to NM_001164507.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:152500535 C>T maps to NM_001164507.1 Q2584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:152425820 G>A maps to NM_001164507.1 S5832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:152490371 C>T maps to NM_001164507.1 Q3070Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:152553947 T>C maps to NM_001164507.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:152410452 G>C maps to NM_001164507.1 S6505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:152466583 G>T maps to NM_001164507.1 A4023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152499150 A>C maps to NM_001164507.1 Y2770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:152554105 C>T maps to NM_001164507.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr2:152499795 C>T maps to NM_001164507.1 E2676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr2:152417529 A>G maps to NM_001164507.1 N6398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:152548388 G>A maps to NM_001164507.1 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:152474830 C>A maps to NM_001164507.1 P3678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:152507231 C>A maps to NM_001164507.1 V2361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:152404839 G>T maps to NM_001164507.1 V6713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:21074852 C>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr10:21120400 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:21134260 C>A maps to ENST00000430741 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:21124439 A>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:21101767 G>A maps to ENST00000430741 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:21074741 G>A maps to ENST00000430741 Y995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:21108394 C>T maps to ENST00000430741 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:21120446 A>C maps to ENST00000430741 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr10:21461325 C>T maps to NM_213569.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:21148755 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:21250669 C>T maps to NM_213569.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:21124530 C>A maps to ENST00000430741 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:91963392 T>C maps to NM_022351.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:91937843 C>T maps to NM_022351.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:84035949 G>A maps to NM_019065.2 *387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:84031856 G>C maps to NM_019065.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:32258533 C>A maps to NM_031232.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr1:16778418 A>T maps to NM_018090.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:97311455 C>T maps to NM_001135175.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:97313903 G>T did not map to a codon.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr12:97303605 A>C maps to NM_001135175.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:56207619 G>A maps to ENST00000508342 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:11185640 T>A maps to NM_006403.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:11190712 G>A maps to NM_006403.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:11191135 G>C maps to NM_006403.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr22:29879484 G>C maps to NM_021076.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr22:29886352 G>A maps to NM_021076.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr22:29886088 G>T maps to NM_021076.3 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:29881764 C>A maps to NM_021076.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr22:29879417 C>A maps to NM_021076.3 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr22:29885524 C>G maps to NM_021076.3 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr22:29885854 A>G maps to NM_021076.3 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr22:29885371 C>A maps to NM_021076.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr8:24811217 G>A maps to ENST00000221169 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:24771755 C>A maps to NM_005382.2 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:24775338 G>T maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr8:24775284 C>A maps to NM_005382.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:24771965 G>T maps to NM_005382.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:24774646 C>T maps to NM_005382.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:72241942 G>T maps to NM_173808.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:72400909 C>A maps to NM_173808.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:72400930 C>A maps to NM_173808.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:11628970 G>A maps to NM_145043.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:178257372 G>C maps to NM_018248.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr4:178231232 C>A maps to NM_018248.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:178274628 G>T maps to NM_018248.2 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr4:178274876 T>A maps to NM_018248.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:170498204 G>A maps to ENST00000507142 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr4:170477146 G>A maps to ENST00000507142 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:170498201 C>G maps to ENST00000507142 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:27387647 G>A maps to ENST00000396636 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:27332781 C>A maps to ENST00000396636 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr3:27346452 C>T maps to ENST00000396636 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:27346302 G>A maps to ENST00000396636 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:130828741 G>C maps to NM_024800.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:130799420 G>T maps to NM_024800.4 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:130884336 C>T maps to NM_024800.4 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:130884363 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:211848790 A>G maps to NM_002497.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr13:52707316 C>T maps to NM_002498.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:52710339 C>T maps to NM_002498.2 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:52802577 C>A maps to NM_003157.4 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:52802406 G>A maps to NM_003157.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:52693476 T>A maps to NM_199289.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr13:52639626 C>A maps to NM_199289.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr13:52673892 G>A maps to NM_199289.1 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:52639650 G>A maps to NM_199289.1 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr13:52639543 C>T maps to NM_199289.1 *709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:127101940 C>A maps to NM_001166171.1 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:127064308 G>A maps to NM_001166171.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:198222168 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr17:27061970 C>T maps to NM_178170.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr17:27067962 G>A maps to NM_178170.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:75573381 C>A maps to NM_033116.4 G451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr9:140349707 G>A maps to NM_001130969.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:21592477 C>A maps to NM_006157.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:20948921 T>C maps to NM_006157.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:21592380 A>G maps to NM_006157.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:20907086 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:21556037 A>T maps to NM_006157.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr11:21250896 C>T maps to NM_006157.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:21594796 G>T maps to NM_006157.3 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:20869299 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr11:21581786 C>A maps to NM_006157.3 C613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:21594951 C>A maps to NM_006157.3 C793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:20805280 G>T maps to NM_006157.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr11:20939729 G>T maps to NM_006157.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:21392414 C>A maps to NM_006157.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:21581801 G>A maps to NM_006157.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr11:21581912 T>C maps to NM_006157.3 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:45001030 G>T maps to NM_001145107.1 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:45173493 G>T maps to NM_001145107.1 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:45169921 A>T maps to NM_001145107.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:45059387 G>T maps to NM_001145107.1 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:45004704 A>T maps to NM_001145107.1 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:45173780 G>C maps to NM_001145107.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:45209863 C>T maps to NM_001145107.1 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr12:44915845 A>G maps to NM_001145107.1 N754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr12:45269062 G>A maps to NM_001145107.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:212617690 A>T maps to NM_013349.4 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:73575341 G>T maps to NM_002499.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:73562349 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:73418809 C>A maps to NM_002499.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:73552669 C>A maps to NM_002499.3 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:73552693 G>A maps to NM_002499.3 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:156642539 C>T maps to NM_006617.1 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:156642185 C>T maps to NM_006617.1 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:156640009 G>A maps to NM_006617.1 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:156641615 C>A maps to NM_006617.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:156646984 G>T maps to NM_006617.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:156643270 G>C maps to NM_006617.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:156640181 C>T maps to NM_006617.1 L1266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:156641771 T>G maps to NM_006617.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:156639928 C>A maps to NM_006617.1 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:156639119 C>T maps to NM_006617.1 E1620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:156646840 C>T maps to NM_006617.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:156640298 C>A maps to NM_006617.1 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:156646678 C>G maps to NM_006617.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:156642985 C>A maps to NM_006617.1 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:156640979 C>T maps to NM_006617.1 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr10:5468684 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:5498650 T>C maps to NM_001047160.1 C495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:70417718 G>C maps to NM_153181.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:70417313 G>A maps to NM_153181.2 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:70423368 G>T maps to NM_153181.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr18:70416304 A>G maps to NM_153181.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr18:70451041 T>A maps to NM_153181.2 K246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:70417787 G>A maps to NM_153181.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr18:70417389 G>T maps to NM_153181.2 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:70461639 C>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr18:70417796 G>T maps to NM_153181.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:47117290 T>C maps to NM_018092.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:31827582 G>T maps to NM_000434.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:233898902 G>T maps to NM_005383.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:233899028 C>A maps to NM_005383.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:233899004 C>T maps to NM_005383.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:233899562 G>A maps to NM_005383.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:233898954 G>T maps to NM_005383.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:233897539 C>G maps to NM_005383.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:233899169 G>T maps to NM_005383.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:74717302 C>T maps to NM_006656.5 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:242757737 C>T maps to NM_001167599.1 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:242757739 G>A maps to NM_001167599.1 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:242755755 C>A maps to NM_001167599.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:242756339 G>C maps to NM_001167599.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:242758328 G>T maps to NM_001167599.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:105330647 C>T maps to NM_004210.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:44518887 C>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:7227487 G>A maps to NM_032442.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:7220797 G>A maps to NM_032442.2 R1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:7230116 C>T maps to NM_032442.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:7226285 C>A maps to NM_032442.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr17:7225207 C>T maps to NM_032442.2 E949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:182543485 G>A maps to NM_002500.2 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr2:182543430 G>A maps to NM_002500.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:182543539 G>T maps to NM_002500.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:182543083 G>A maps to NM_002500.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:182543230 C>A maps to NM_002500.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:182542870 G>A maps to NM_002500.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55420632 G>A maps to NM_021191.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:55421050 C>G maps to NM_021191.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:55421014 C>G maps to NM_021191.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:55420402 G>A maps to NM_021191.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:55420819 C>T maps to NM_021191.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:55420926 C>A maps to NM_021191.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr7:31378432 C>A maps to NM_022728.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:31378609 C>T maps to NM_022728.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:31378045 C>T maps to NM_022728.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr7:31378327 G>A maps to NM_022728.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr5:134870855 A>G maps to NM_006161.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:113436202 G>C maps to NM_024019.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:113436286 C>A maps to NM_024019.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:113436574 C>A maps to NM_024019.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr4:113436339 G>T maps to NM_024019.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr10:71332667 C>T maps to NM_020999.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:71332415 G>T maps to NM_020999.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:78392496 C>A maps to NM_144573.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:29663768 G>C maps to NM_001042492.2 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:29670032 G>T maps to NM_001042492.2 E2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr17:29664476 T>G maps to NM_001042492.2 A2173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:29654663 C>T maps to NM_001042492.2 Q1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr17:29548865 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:29527460 C>T maps to NM_001042492.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr17:29490290 G>T maps to NM_001042492.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:29541556 T>A maps to NM_001042492.2 L494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:29553701 G>T maps to NM_001042492.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:29661881 G>T maps to NM_001042492.2 E1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:29665720 G>C did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr17:29664868 G>A maps to NM_001042492.2 W2225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:29562634 C>T maps to NM_001042492.2 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:29654690 C>T maps to NM_001042492.2 Q1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr17:29652836 G>T did not map to a codon.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr17:29550460 G>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:29528426 A>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:29663413 G>T maps to NM_001042492.2 G2024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr17:29559716 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:29654857 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr17:29553454 T>C maps to NM_001042492.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr17:29663891 C>T maps to NM_001042492.2 I2129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:29550531 A>T maps to NM_001042492.2 K598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:29528173 T>C maps to NM_001042492.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:29557871 A>G maps to NM_001042492.2 V1042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr22:30035168 C>T maps to NM_181832.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr22:30061030 C>G maps to NM_181832.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:204951080 C>T maps to ENST00000367172 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:204953161 G>A maps to ENST00000367172 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:204939792 C>T maps to ENST00000367172 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:204955153 C>T maps to ENST00000367172 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr1:204966442 C>T maps to ENST00000367172 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:204948499 C>T maps to ENST00000367172 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr1:204942474 A>C maps to ENST00000367172 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:204951050 C>A maps to ENST00000367172 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:204978688 C>A maps to ENST00000367172 Y1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:204943865 C>A maps to ENST00000367172 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:204957824 G>T maps to ENST00000367172 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:204971876 G>T did not map to a codon.
Alternatively spliced codon TCGA-86-8073-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:204937425 C>T maps to ENST00000367172 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204943310 G>T maps to ENST00000367172 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:204924074 C>T maps to ENST00000367172 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:69681330 A>G maps to NM_138713.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:69660387 C>T maps to NM_138713.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:69711161 G>A maps to NM_138713.2 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:69724897 G>A maps to NM_138713.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:69718865 C>T maps to NM_138713.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:69725936 A>T maps to NM_138713.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr16:69703976 G>A maps to NM_138713.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:77221366 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr18:77170445 G>T maps to NM_172387.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:77227511 C>T maps to NM_172387.1 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:77246410 G>A maps to NM_172387.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr18:77193605 G>A maps to NM_172387.1 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr18:77170430 C>T maps to NM_172387.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr18:77227580 C>T maps to NM_172387.1 N684N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:77170562 G>C maps to NM_172387.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:50048655 C>A maps to NM_012340.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr20:50090661 A>C maps to NM_012340.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:50140439 C>A maps to NM_012340.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:50048685 C>A maps to NM_012340.3 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:50140533 G>A maps to NM_012340.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:50139924 G>A maps to NM_012340.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:28967296 A>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:28970310 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr16:28970177 C>T maps to NM_032815.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr16:28970369 C>A maps to NM_032815.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:68156553 C>T maps to NM_173165.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr16:68156766 A>T maps to NM_173165.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:68224926 T>A maps to NM_173165.2 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:68224794 G>T maps to NM_173165.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:68200748 T>A maps to NM_173165.2 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr14:24839230 T>C maps to NM_001136022.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:24846004 G>A maps to NM_001136022.1 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:24845993 G>T maps to NM_001136022.1 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr14:24839713 G>A maps to NM_001136022.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:24839563 C>A maps to NM_001136022.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:54686508 G>A maps to NM_001136023.1 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:54686352 G>A maps to NM_001136023.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:46128845 C>T maps to ENST00000362042 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:46128596 C>T maps to ENST00000362042 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr17:46135949 C>G maps to ENST00000362042 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:178098809 C>A maps to NM_006164.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:61554014 A>T maps to NM_001145512.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:61849026 A>G maps to NM_001145512.1 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr9:14150264 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:14146718 A>T maps to ENST00000397581 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:14307438 T>A maps to ENST00000397581 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:14307369 C>T maps to ENST00000397581 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:14146700 G>A maps to ENST00000397581 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:3381996 C>G maps to ENST00000269778 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:3452573 C>T maps to ENST00000269778 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:3381909 G>T maps to ENST00000269778 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:94171717 C>T maps to NM_005384.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:94172452 G>A maps to NM_005384.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:13192575 G>T maps to ENST00000397661 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:103531828 G>A maps to NM_003998.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr4:103517298 C>G maps to NM_003998.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:103528834 C>A maps to NM_003998.3 Y718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:103504054 G>T maps to NM_003998.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:103534718 C>T maps to NM_003998.3 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr4:103534676 G>A maps to NM_003998.3 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104157428 C>T maps to NM_001077494.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:104156243 C>T maps to NM_001077494.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr10:104157407 G>A maps to NM_001077494.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr14:35873697 C>T maps to NM_020529.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:35872428 G>A maps to NM_020529.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr14:35871599 C>T maps to NM_020529.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:35871224 C>G maps to NM_020529.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr19:36387392 C>T maps to ENST00000352614 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:36380880 G>A maps to ENST00000352614 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:44228229 G>C maps to NM_004556.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr8:145659142 C>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:101573502 G>T maps to NM_031419.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:101576170 C>A maps to NM_031419.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:129739493 T>C maps to NM_006165.3 V1167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:129754772 C>A maps to NM_006165.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:129748202 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:129740009 C>A maps to NM_006165.3 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:129748436 G>A maps to NM_006165.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:129754655 C>A maps to NM_006165.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:129753092 C>T maps to NM_006165.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr20:34260737 C>A maps to NM_021100.4 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr20:34263122 C>A maps to NM_021100.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:69633214 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr9:33364013 A>G maps to NM_002504.4 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:33318726 A>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr4:47880673 T>A maps to NM_152995.4 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:41062140 C>T maps to NM_002505.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:41060811 A>G maps to NM_002505.4 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:41215345 C>T maps to ENST00000308733 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:41232319 C>G maps to ENST00000308733 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:41232362 C>T maps to ENST00000308733 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:41213213 C>T maps to ENST00000308733 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:23944435 G>A maps to NM_001042635.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:23944501 G>T maps to NM_001042635.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:233785157 C>A maps to NM_019850.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:233834988 G>T maps to NM_019850.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:233785095 G>A maps to NM_019850.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:233791855 C>A maps to NM_019850.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:233759608 G>C maps to NM_019850.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:233839368 T>A maps to NM_019850.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:233785020 T>C maps to NM_019850.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:233745955 G>T maps to NM_019850.2 C614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:115829119 G>A maps to NM_002506.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr17:47583904 C>T maps to NM_002507.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:47583738 C>A maps to NM_002507.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:102632568 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:102632635 G>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:25781254 C>A maps to NM_018297.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr3:25781183 T>A maps to NM_018297.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr3:25778861 A>T maps to NM_018297.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:25805754 C>A maps to NM_018297.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:90808964 C>T maps to NM_001033088.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr4:103910989 G>A maps to NM_139173.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr4:103822393 G>T maps to NM_139173.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:103964602 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:103950040 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:103947549 C>A maps to NM_178833.4 G531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219942057 G>T maps to NM_024782.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:160340529 C>T maps to NM_005598.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:116380681 C>A maps to NM_005599.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:18122333 C>T maps to NM_198586.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:18122804 C>G maps to NM_198586.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:115664628 A>G maps to NM_198514.3 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:115636547 C>T maps to NM_198514.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:177580532 C>A maps to NM_017838.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:42076368 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:17744754 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:17745106 A>G did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:17745406 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:17705956 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:17744627 T>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:17739710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:17750407 G>C did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:17744496 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:17746075 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:17743881 G>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:17743933 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:17743553 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:17744443 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:17750340 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:17744528 C>G did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr23:17394367 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:17745929 C>T did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr23:17744123 A>C did not map to a codon.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr23:17745912 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:17742548 A>G did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:17742485 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:17746877 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:17739607 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:17743769 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:17750170 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:17750171 A>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:71359878 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:71359503 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:71360425 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:71360052 C>G did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:71360514 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:71358693 T>A did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:71359233 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:71358508 G>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:71359764 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:71360026 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:71360076 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:71360365 C>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:236176843 G>T maps to NM_002508.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:236148781 G>A maps to NM_002508.2 A984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:236192967 G>T maps to NM_002508.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:236205428 C>A maps to NM_002508.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:236144993 C>T maps to NM_002508.2 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:236205318 G>C maps to NM_002508.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:236187490 C>T maps to NM_002508.2 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:236228240 C>A maps to NM_002508.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:236192919 C>A maps to NM_002508.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:236212120 G>A maps to NM_002508.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:236175323 T>G maps to NM_002508.2 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:236154281 G>T maps to NM_002508.2 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:236208833 T>C maps to NM_002508.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:236195947 G>T maps to NM_002508.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:236211987 A>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:52520737 C>A maps to NM_007361.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:52508880 C>A maps to NM_007361.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52509063 T>A maps to NM_007361.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:52494051 T>A maps to NM_007361.3 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr14:52481082 C>T maps to NM_007361.3 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:52520984 G>T maps to NM_007361.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:52485783 G>T maps to NM_007361.3 S1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:52505471 C>A maps to NM_007361.3 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr14:52520642 C>T maps to NM_007361.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr14:52520909 G>A maps to NM_007361.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:201758086 A>T maps to NM_001136039.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:201760029 C>T maps to NM_001136039.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:201768358 T>C maps to NM_001136039.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:51192619 G>A maps to NM_182946.1 N2081N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:51288609 C>T maps to NM_020921.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:51223244 C>G maps to NM_020921.3 T1501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:51223741 G>A maps to NM_020921.3 Q1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr14:51288687 C>A maps to NM_020921.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:51226915 G>C maps to NM_020921.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:51233536 G>A maps to NM_020921.3 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:675314 G>T maps to NM_016533.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:772526 C>T maps to NM_016533.4 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:25481598 C>G maps to NM_025176.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:25485522 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:25481559 G>A maps to NM_025176.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:25470570 C>T maps to NM_025176.4 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr20:25459683 G>A maps to NM_025176.4 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr20:25481502 C>A maps to NM_025176.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr20:25456785 G>A maps to NM_025176.4 T1047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:25450718 A>G maps to NM_025176.4 H1087H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:25507046 G>A maps to NM_025176.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr15:23060867 C>A maps to NM_144599.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:23049044 C>A maps to NM_144599.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr15:23048974 C>A maps to NM_144599.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:24795650 C>G maps to NM_020448.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:24771673 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:24785404 C>T maps to NM_020448.4 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:24786968 A>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:24768624 C>T maps to NM_020448.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:24768625 C>T maps to NM_020448.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:156890270 C>G maps to NM_001099287.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:156890225 T>C maps to NM_001099287.1 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:156898709 G>T maps to NM_001099287.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:37027498 G>A maps to NM_133433.3 E1949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr5:37020710 G>T maps to NM_133433.3 E1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr5:36985802 C>T maps to NM_133433.3 R841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:36976484 A>C maps to NM_133433.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr5:37022344 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:36985081 T>C maps to NM_133433.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:37007477 A>T maps to NM_133433.3 R1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:37014783 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:36985250 A>T maps to NM_133433.3 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:107533127 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:52505827 A>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:52514219 C>T maps to NM_007184.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:52524742 C>A maps to NM_007184.3 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:100058048 G>T maps to NM_020202.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:100058771 C>A maps to NM_020202.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:31655425 G>A maps to NM_024522.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:125139560 T>C maps to NM_001040214.1 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:124979486 C>A maps to NM_001040214.1 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:124676488 C>A maps to NM_001040214.1 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:124676441 G>T maps to NM_001040214.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:63831056 G>T maps to NM_173688.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:63502280 G>T maps to NM_173688.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:63492147 G>T maps to NM_173688.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:61873916 G>T maps to NM_152864.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr20:61881322 G>A maps to NM_152864.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:119077252 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:119070589 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:119064114 G>C did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:119077527 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:119077332 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:119077345 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:119077509 C>G did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:119059198 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr23:119066178 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:119077418 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:119077244 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:28227391 C>T maps to NM_001007531.1 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:28227361 G>A maps to NM_001007531.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:50664758 A>C maps to NM_033119.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr16:50659415 C>A maps to NM_033119.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr16:50666257 G>A maps to NM_033119.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr16:50664740 G>T maps to NM_033119.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1038187 C>A maps to NM_033120.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr5:1038313 G>A maps to NM_033120.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:1036405 C>A maps to NM_033120.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:1034941 C>T maps to NM_033120.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:51875430 G>A maps to NM_005601.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr19:51875206 G>T maps to NM_005601.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:40175883 C>T maps to ENST00000316082 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:118723932 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:118723885 T>C did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:118723607 C>G did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:118723543 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:118724895 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:118724576 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:118723346 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:118723758 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:118724568 G>C did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr3:42679412 T>C maps to NM_005385.3 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr3:42685391 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:21492968 C>T maps to NM_002509.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:21494265 G>A maps to NM_002509.2 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:21494244 G>C maps to NM_002509.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr20:21492977 G>A maps to NM_002509.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:21376830 G>T maps to NM_033176.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:172660065 G>T maps to NM_004387.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:172659697 C>A maps to NM_004387.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:23538979 T>C maps to NM_006167.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr8:23539109 G>T maps to NM_006167.3 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:13543757 G>T maps to NM_001189.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:85416845 C>G maps to NM_006168.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:134598455 G>T maps to NM_177400.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr10:134598650 G>T maps to NM_177400.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:33462470 C>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:33464162 G>T maps to NM_018096.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:33464163 C>T maps to NM_018096.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:33467046 A>C maps to NM_018096.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:173997032 T>C maps to NM_014932.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:173997118 G>A maps to NM_014932.2 W443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:173322579 G>T maps to NM_014932.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:173996666 A>T maps to NM_014932.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:173998674 C>G maps to NM_014932.2 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:173998771 T>G maps to NM_014932.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:173998780 T>C maps to NM_014932.2 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:173997176 C>T maps to NM_014932.2 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr3:173996885 A>C maps to NM_014932.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:7317980 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr17:7315482 C>T maps to NM_020795.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:7312024 G>T maps to NM_020795.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:7319153 C>G maps to NM_020795.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr17:7320632 G>T maps to NM_020795.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:70389914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:70389249 G>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:70389604 A>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:70387433 G>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:70384153 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:70389503 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:70389159 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:70389657 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:70384144 G>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:70389452 G>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:70373330 C>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:70367875 T>A did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:70387439 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:70387539 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:5811256 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:5821842 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:5827224 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:5821356 C>G did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:5821877 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:5821138 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:5821359 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:5827246 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:6069309 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:5811256 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:5811549 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:5827265 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:5821161 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr23:5827178 C>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:5821808 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:5827163 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:5821791 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:5821397 C>A did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:5821248 A>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:6069452 C>A did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:5821682 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:5811274 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:5811508 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:5947445 G>T did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr23:5811409 C>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:6069326 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:5821839 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:5810993 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:6069137 G>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:5821824 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:5821335 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:5821595 C>G did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:6069172 T>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:5821851 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:6069375 C>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:5821877 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:6069321 T>A did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr23:5811618 G>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:5821829 T>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:5810939 T>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:5811461 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:6069432 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:5811562 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:5827151 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:6069149 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:5811607 C>A did not map to a codon.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr23:5811124 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:5821397 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:5810984 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:5821158 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:5811205 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:5811170 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:5821253 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:6069135 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:5821158 G>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:6069363 G>C did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:6069323 A>T did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:5811180 G>A did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:5821825 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:5827216 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:6069173 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:5821328 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:6069296 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr23:5821805 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:6069338 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:6069339 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:5811348 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:5821610 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:5811301 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:5821303 A>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr24:16734014 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr24:16734056 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:65084125 C>G maps to NM_020726.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:65073270 G>A maps to NM_020726.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr5:65105927 G>T maps to NM_020726.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:3606913 C>T maps to ENST00000448023 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr16:3600415 C>T maps to ENST00000448023 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:3613764 A>G maps to ENST00000448023 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:3614681 T>G maps to ENST00000448023 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr16:3614255 G>A maps to ENST00000448023 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr16:3613821 G>A maps to ENST00000448023 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:32476635 G>A maps to NM_021209.4 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:32477680 G>T maps to NM_021209.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:32476122 G>T maps to NM_021209.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:32463285 G>A maps to NM_021209.4 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:57111714 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr16:57059670 A>G maps to NM_032206.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr16:57063702 C>T maps to NM_032206.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:57104527 G>C maps to NM_032206.3 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr16:57085489 C>T maps to NM_032206.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr16:57112964 A>T maps to NM_032206.3 L1695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:57060810 C>T maps to NM_032206.3 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:57113514 G>C maps to NM_032206.3 T1765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr16:57104459 C>T maps to NM_032206.3 Q1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr16:57062238 C>T maps to NM_032206.3 R729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr16:57063720 G>C maps to NM_032206.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr16:57111270 G>T maps to NM_032206.3 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr16:57059865 G>A maps to NM_032206.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5463314 C>T maps to NM_033004.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:5462875 G>C maps to NM_033004.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:5462839 C>A maps to NM_033004.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:5487226 C>T maps to NM_033004.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr17:5405148 G>A maps to NM_001033053.2 D1371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:5456764 A>G maps to NM_033004.3 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:5462578 C>A maps to NM_033004.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:5463331 C>T maps to NM_033004.3 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:5418226 G>T maps to NM_033004.3 P1423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:5485232 C>A maps to NM_033004.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr17:5436227 C>T maps to NM_033004.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:7982525 C>A maps to NM_176821.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:7982783 G>T maps to NM_176821.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:7981510 C>A maps to NM_176821.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:7981814 A>G maps to NM_176821.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:7982252 G>A maps to NM_176821.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:7981772 G>T maps to NM_176821.3 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr11:7981382 A>G maps to NM_176821.3 N592N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr11:7982675 C>T maps to NM_176821.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7981826 G>T maps to NM_176821.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr11:7982582 G>T maps to NM_176821.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:7981478 G>T maps to NM_176821.3 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:7981664 C>G maps to NM_176821.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:7981955 G>T maps to NM_176821.3 C401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr11:7981424 A>T maps to NM_176821.3 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:7982837 G>T maps to NM_176821.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:7981801 G>A maps to NM_176821.3 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56320397 C>T maps to NM_145007.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:56303673 C>A maps to NM_145007.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:56321473 A>G maps to NM_145007.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:56320319 A>G maps to NM_145007.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:56321417 G>A maps to NM_145007.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr19:56307480 G>T maps to NM_145007.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:56313041 C>A maps to NM_145007.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:56329359 C>A maps to NM_145007.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:56307570 G>A maps to NM_145007.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:56313105 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr19:56329268 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:56297071 A>G maps to NM_145007.3 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:54327410 G>C maps to ENST00000391773 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:54313960 G>T maps to ENST00000391773 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:54313063 A>G maps to ENST00000391773 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:54313760 C>A maps to ENST00000391773 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:54304548 C>A maps to ENST00000391773 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:54304527 C>A maps to ENST00000391773 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:54313571 C>A maps to ENST00000391773 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:54301507 G>A maps to ENST00000391773 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54304613 C>A maps to ENST00000391773 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:54312854 C>A maps to ENST00000391773 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:54310816 C>A maps to ENST00000391773 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:54310870 C>A maps to ENST00000391773 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:54314258 C>T maps to ENST00000391773 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:54299228 C>A maps to ENST00000391773 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56410251 G>T maps to NM_176810.2 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:56424607 C>T maps to NM_176810.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:56424252 A>G maps to NM_176810.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:56413552 C>A maps to NM_176810.2 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:56436006 C>A maps to NM_176810.2 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:56423977 G>T maps to NM_176810.2 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr19:56423402 T>A maps to NM_176810.2 K594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:56407338 G>T maps to NM_176810.2 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:56424027 C>A maps to NM_176810.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56424210 C>T maps to NM_176810.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:56416457 G>T maps to NM_176810.2 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:56443533 G>T maps to NM_176810.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:56443457 C>A maps to NM_176810.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:56443371 T>C maps to NM_176810.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:7063622 T>C maps to NM_176822.3 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr11:7071069 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:7059876 G>A maps to NM_176822.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:7091675 A>T maps to NM_176822.3 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:7070901 G>T maps to NM_176822.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:7063772 C>G maps to NM_176822.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:7064693 C>T maps to NM_176822.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:55481502 G>A maps to NM_017852.3 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:55493962 G>T maps to NM_017852.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr19:55494004 G>C maps to NM_017852.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr19:55497539 T>A maps to NM_017852.3 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:55495054 G>A maps to NM_017852.3 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:55502028 G>A maps to NM_017852.3 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:55494829 C>T maps to NM_017852.3 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:55481508 C>T maps to NM_017852.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:247587488 C>G maps to NM_004895.4 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247592922 G>T maps to NM_004895.4 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:247608105 C>A maps to NM_004895.4 C998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:247587725 G>T maps to NM_004895.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247586535 A>C maps to NM_004895.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:247587296 G>A maps to NM_004895.4 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:247588095 C>T maps to NM_004895.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247587737 C>T maps to NM_004895.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247607997 C>A maps to NM_004895.4 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr1:247587617 G>C maps to NM_004895.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:247587689 A>T maps to NM_004895.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:247607376 G>T maps to NM_004895.4 G925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:247582298 G>A maps to NM_004895.4 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:247588043 C>A maps to NM_004895.4 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:247588838 C>A maps to NM_004895.4 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:247587720 G>T maps to NM_004895.4 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:247587422 G>C maps to NM_004895.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:247587422 G>T maps to NM_004895.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:247587719 C>A maps to NM_004895.4 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:247611745 G>T maps to NM_004895.4 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:247608057 C>A maps to NM_004895.4 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:247587866 C>A maps to NM_004895.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247592910 C>A maps to NM_004895.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:247588856 G>C maps to NM_004895.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:247611772 T>C maps to NM_004895.4 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:247586621 C>A maps to NM_004895.4 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:247587965 C>A maps to NM_004895.4 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:247587983 G>T maps to NM_004895.4 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:247599304 T>C maps to NM_004895.4 C844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:247588781 G>C maps to NM_004895.4 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr1:247587470 C>T maps to NM_004895.4 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:247597425 G>C maps to NM_004895.4 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:247582260 C>A maps to NM_004895.4 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247582215 C>A maps to NM_004895.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:247588619 C>A maps to NM_004895.4 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:247597516 G>T maps to NM_004895.4 G814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:247588838 C>A maps to NM_004895.4 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:247588784 C>A maps to NM_004895.4 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:247607988 G>A maps to NM_004895.4 W959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:247597575 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:56369119 C>T maps to NM_134444.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:56369277 G>T maps to NM_134444.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:56382294 G>T maps to NM_134444.4 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:56369427 G>T maps to NM_134444.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:56363726 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:56369521 C>A maps to NM_134444.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:56379073 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:56369253 G>C maps to NM_134444.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:56388360 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:56369781 G>T maps to NM_134444.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56382249 G>A maps to NM_134444.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr19:56369781 G>T maps to NM_134444.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:56390294 C>A maps to NM_134444.4 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:56363454 C>A maps to NM_134444.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:56379119 T>A maps to NM_134444.4 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:56369622 G>C maps to NM_134444.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:56369394 C>T maps to NM_134444.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:56369553 G>A maps to NM_134444.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:56565063 G>A maps to NM_153447.4 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:56538819 C>A maps to NM_153447.4 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr19:56572883 G>A maps to NM_153447.4 W1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:56552449 G>A maps to NM_153447.4 Q983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:56543980 C>A maps to NM_153447.4 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:56549543 C>A maps to NM_153447.4 C923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:56569689 C>T maps to NM_153447.4 N1128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56544054 G>A maps to NM_153447.4 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:56561897 C>T maps to NM_153447.4 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:56539578 G>C maps to NM_153447.4 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:56539560 C>A maps to NM_153447.4 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:56545006 G>T maps to NM_153447.4 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:56544114 G>C maps to NM_153447.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:56538870 C>A maps to NM_153447.4 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:56544052 C>T maps to NM_153447.4 Q785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:56544099 C>A maps to NM_153447.4 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:56539266 C>A maps to NM_153447.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr19:56539032 C>T maps to NM_153447.4 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr19:56539518 C>T maps to NM_153447.4 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:56539572 C>G maps to NM_153447.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:56552344 C>A maps to NM_153447.4 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:282700 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:281092 C>T maps to NM_138329.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:284493 C>T maps to NM_138329.1 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:284283 G>A maps to NM_138329.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:55451463 G>A maps to ENST00000446217 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:55451424 G>T maps to ENST00000446217 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:55452863 C>T maps to ENST00000446217 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:55452323 T>C maps to ENST00000446217 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:55447800 T>C did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr19:55450791 G>A maps to ENST00000446217 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:55450425 C>A maps to ENST00000446217 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:55451462 G>A maps to ENST00000446217 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr19:55450746 G>T maps to ENST00000446217 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:55450277 C>A maps to ENST00000446217 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:55450961 G>T maps to ENST00000446217 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:55451340 G>T maps to ENST00000446217 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr19:55452959 C>T maps to ENST00000446217 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:55451565 C>A maps to ENST00000446217 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:55453061 T>C maps to ENST00000446217 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:55449503 A>G maps to ENST00000446217 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:55450992 G>T maps to ENST00000446217 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:55451568 G>T maps to ENST00000446217 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:55447765 C>T maps to ENST00000446217 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:56490757 A>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:56485016 G>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:56490772 C>T maps to NM_176811.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr19:56466500 G>A maps to NM_176811.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:56466758 G>A maps to NM_176811.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56466488 G>T maps to NM_176811.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:56482062 G>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:56466134 C>A maps to NM_176811.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:56490763 G>T maps to NM_176811.2 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:56466374 C>T maps to NM_176811.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:56487516 G>A maps to NM_176811.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:56243815 G>T maps to NM_176820.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:56243627 T>A maps to NM_176820.2 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:56223290 G>T maps to NM_176820.2 A906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:56226466 G>A maps to NM_176820.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:56244282 G>T maps to NM_176820.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:56244353 T>C maps to NM_176820.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:56226545 G>A maps to NM_176820.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:56223263 C>T maps to NM_176820.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:85198533 G>T maps to NM_205858.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:142409564 G>T maps to NM_002511.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:142396982 G>T maps to NM_002511.2 Y325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr6:142399901 G>T maps to NM_002511.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:160965078 G>A maps to ENST00000472947 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:49245625 G>A maps to ENST00000393198 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:152132105 T>A maps to NM_004688.2 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:10041187 A>G maps to NM_022787.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:183247711 G>A maps to NM_015039.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:183230189 C>A maps to NM_015039.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:183221826 C>T maps to NM_015039.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr1:183221826 C>T maps to NM_015039.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:101093866 T>A maps to NM_001011717.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr2:101089997 T>G maps to NM_001011717.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr17:43175845 G>T maps to NM_021079.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:43183000 A>G maps to NM_021079.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr17:43176874 G>A maps to NM_021079.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:15172175 C>G maps to ENST00000378143 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr10:15151837 T>A maps to ENST00000378143 K478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:232389975 G>T maps to NM_006056.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:232390131 G>A maps to NM_006056.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:232389987 C>G maps to NM_006056.4 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr2:232393701 G>A maps to NM_006056.4 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:232393101 C>A maps to NM_006056.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:232389993 C>T maps to NM_006056.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr2:232389975 G>A maps to NM_006056.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151784224 G>A maps to NM_020167.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:151784305 C>G maps to NM_020167.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:151784152 G>A maps to NM_020167.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:151784185 G>T maps to NM_020167.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:151771874 G>T maps to NM_020167.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:151784149 C>A maps to NM_020167.4 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:151784215 G>A maps to NM_020167.4 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:36149768 C>T maps to NM_005386.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:114182961 A>T maps to NM_006169.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:114167427 C>T maps to NM_006169.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:114183168 G>T maps to NM_006169.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr5:43613235 C>G maps to NM_182977.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:43609434 G>T maps to NM_182977.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr5:43609420 C>T maps to NM_182977.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:43645475 C>T maps to NM_182977.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:43656851 G>T maps to NM_182977.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:43656845 C>T maps to NM_182977.2 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:144097390 G>A maps to ENST00000467773 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:144098308 G>T maps to ENST00000467773 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:144098190 G>T maps to ENST00000467773 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:144098577 G>T maps to ENST00000467773 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:144096866 A>T maps to ENST00000467773 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:144096937 G>T maps to ENST00000467773 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:880904 C>A maps to NM_015658.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:887453 C>G maps to NM_015658.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:881034 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:96122586 C>A maps to NM_022451.9 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:96099535 G>T maps to NM_022451.9 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:96099594 C>T maps to NM_022451.9 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:132636666 C>T maps to NM_024078.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:30490919 G>T maps to NM_006092.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr7:30492654 C>T maps to NM_006092.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr7:30491514 G>A maps to NM_006092.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:30494867 G>C maps to NM_006092.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:30490878 G>A maps to NM_006092.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:30492288 C>A maps to NM_006092.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:30475651 C>T maps to NM_006092.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:50744598 C>A maps to NM_022162.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:50733414 G>T maps to NM_022162.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:50745597 G>T maps to NM_022162.1 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:50733451 G>T maps to NM_022162.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:50750867 G>A maps to NM_022162.1 Q871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:50745495 G>C maps to NM_022162.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:50753904 C>A maps to NM_022162.1 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:50745426 G>T maps to NM_022162.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:50744733 C>A maps to NM_022162.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:50745463 C>T maps to NM_022162.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr16:50744742 G>T maps to NM_022162.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:50744742 G>A maps to NM_022162.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr16:50733865 G>T did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr10:72195116 G>A maps to NM_018055.4 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:72195365 G>T maps to NM_018055.4 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:54671766 G>A maps to NM_005450.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:10729816 G>A maps to NM_024894.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:10712240 C>A maps to NM_024894.2 G675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr17:65722702 A>G maps to NM_015462.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:31432982 G>A maps to NM_003787.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:31537450 A>G maps to NM_003787.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:31709891 C>G maps to NM_003787.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr18:31599331 G>A maps to NM_003787.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr18:31803022 G>T maps to NM_003787.4 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:33467823 C>T maps to NM_022917.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr9:33472114 C>A maps to NM_022917.4 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:33462768 C>A maps to NM_022917.4 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:33465805 C>T maps to NM_022917.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:95076671 C>A maps to NM_017948.5 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr9:95077880 T>C maps to NM_017948.5 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:6610603 G>A maps to NM_024654.4 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:6586754 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:103921998 C>T maps to ENST00000405356 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:103919188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr16:14970222 C>T maps to ENST00000456867 C788C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:14951443 C>G maps to ENST00000456867 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr16:14982981 C>A maps to ENST00000456867 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr16:14988853 G>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr16:14978233 G>A maps to ENST00000456867 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr16:14972645 C>T maps to ENST00000456867 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr23:70517740 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:70510514 G>T did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:70511690 C>T did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr23:70511680 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:70517784 T>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:2964863 C>A maps to NM_003703.1 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:2945797 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:6669387 T>A maps to ENST00000382421 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr12:6675947 T>C maps to ENST00000382421 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:2636372 C>G maps to NM_006392.2 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:117726018 C>A maps to ENST00000338101 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:117657885 C>A maps to ENST00000338101 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr12:117715774 G>A maps to ENST00000338101 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr12:117710191 C>A maps to ENST00000338101 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr12:117723101 C>T maps to ENST00000338101 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:117658025 G>A maps to ENST00000338101 R1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr12:117681122 C>A maps to ENST00000338101 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:117768757 C>A maps to ENST00000338101 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:117701734 G>T maps to ENST00000338101 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:117749383 T>A maps to ENST00000338101 K247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:117662917 C>A maps to ENST00000338101 R1277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:117660522 T>A maps to ENST00000338101 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr12:117718541 C>A maps to ENST00000338101 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr12:117768585 G>A maps to ENST00000338101 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:117701724 G>T maps to ENST00000338101 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr12:117658020 G>T maps to ENST00000338101 A1377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:162313766 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:162337163 C>A maps to NM_014697.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:162313681 C>T maps to NM_014697.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:162257210 G>A maps to NM_014697.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:26116677 G>A maps to NM_000625.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:26114744 T>C maps to NM_000625.4 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:26094791 C>A maps to NM_000625.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:26108163 C>T maps to NM_000625.4 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:26109132 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:26110041 G>A maps to NM_000625.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr17:26086079 G>T maps to NM_000625.4 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr17:26096026 G>A maps to NM_000625.4 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:26125763 G>A maps to NM_000625.4 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:26107872 G>T maps to NM_000625.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:26096595 C>A maps to NM_000625.4 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:150696412 G>A maps to NM_000603.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:150697596 C>A maps to NM_000603.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:150695714 C>A maps to NM_000603.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:150698951 A>T maps to NM_000603.4 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:169707820 G>A maps to NM_001171631.1 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:139411823 C>T maps to NM_017617.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:139395165 T>G maps to NM_017617.3 T1924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr9:139395152 C>A maps to NM_017617.3 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:139409986 G>A maps to NM_017617.3 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:139399873 G>A maps to NM_017617.3 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr9:139393422 G>A maps to NM_017617.3 A2036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:139404255 G>A maps to NM_017617.3 S966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr9:139399811 G>A maps to NM_017617.3 A1512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:120478158 C>T maps to NM_024408.2 Q1197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:120461116 G>A maps to NM_024408.2 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:120466411 C>A maps to NM_024408.2 L1569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:120539848 G>A maps to NM_024408.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120468433 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:120510148 C>A maps to NM_024408.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:120510123 G>C maps to NM_024408.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:120547952 T>A maps to NM_024408.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:120458345 C>A maps to NM_024408.2 A2333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:120461933 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:120471797 C>A maps to NM_024408.2 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:120457929 C>T maps to NM_024408.2 *2472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:120468093 G>A maps to NM_024408.2 Q1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:120480030 C>T maps to NM_024408.2 T1132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:120491109 G>T maps to NM_024408.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:120462956 G>A maps to NM_024408.2 Q1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:145273424 C>T maps to ENST00000454606 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:145273313 G>C maps to ENST00000454606 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:145281549 C>T maps to ENST00000454606 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:15302286 G>C maps to NM_000435.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:15273347 C>A maps to NM_000435.2 A1947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:15299046 C>G maps to NM_000435.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:15273311 G>C maps to NM_000435.2 L1959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:15302574 C>T maps to NM_000435.2 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:15299869 C>A maps to NM_000435.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:32169165 C>A maps to NM_004557.3 G1289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:32169992 C>A maps to NM_004557.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr6:32169087 C>G maps to NM_004557.3 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:32181886 C>A maps to NM_004557.3 G723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr6:32168901 G>A maps to NM_004557.3 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:32168996 G>T maps to NM_004557.3 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:32180909 A>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:32165249 G>T maps to NM_004557.3 P1626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:32187963 C>A maps to NM_004557.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:32180371 G>T maps to NM_004557.3 C853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr6:32182028 G>A maps to NM_004557.3 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:32190533 G>A maps to NM_004557.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:120429207 G>T maps to NM_002514.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:120435206 C>A maps to NM_002514.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:26917499 C>A maps to ENST00000449198 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr14:26917551 C>A maps to ENST00000449198 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr14:26917569 G>A maps to ENST00000449198 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:26917494 A>G maps to ENST00000449198 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:26917985 C>A maps to ENST00000449198 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:46443288 G>A maps to NM_002516.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:100117172 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:100099014 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:100106266 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:100103633 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:100105366 C>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:100104355 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:100103736 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:100103701 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:100117725 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:155749950 G>T maps to NM_015718.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr6:155776233 C>A maps to NM_015718.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:155750178 C>A maps to NM_015718.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:155743923 G>T maps to NM_015718.2 C404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:155743902 G>T maps to NM_015718.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr6:155776016 C>T maps to NM_015718.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:155750055 G>T maps to NM_015718.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:89133460 G>T maps to NM_016931.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:89060018 C>A maps to NM_016931.3 G548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:89088202 G>A maps to NM_016931.3 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:89185033 T>A maps to NM_016931.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:89069011 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:89166013 C>G maps to NM_016931.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:89106597 A>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:89184979 G>A maps to NM_016931.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:89088128 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:89166019 A>G maps to NM_016931.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:89133420 G>A maps to NM_016931.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr11:89133528 C>A maps to NM_016931.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr15:69320610 C>T maps to NM_024505.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:2029346 G>T maps to NM_172168.1 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:2030142 A>T maps to NM_172168.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:101604707 G>T maps to NM_002518.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:101604650 G>T maps to NM_002518.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:101582157 G>T maps to NM_002518.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:101598835 C>G maps to NM_002518.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:34243682 T>C maps to NM_001164749.1 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr14:34269441 C>A maps to NM_001164749.1 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr14:34269657 C>A maps to NM_001164749.1 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:34270251 G>C maps to NM_001164749.1 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:34247778 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr14:34269355 C>A maps to NM_001164749.1 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:34266695 C>T maps to NM_001164749.1 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr14:34269549 C>A maps to NM_001164749.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:34269177 C>A maps to NM_001164749.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:66188688 G>T maps to NM_178864.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:66191383 C>T maps to NM_178864.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:66189681 A>C maps to NM_178864.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:66191659 C>G maps to NM_178864.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:66189699 C>G maps to NM_178864.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:66190262 A>C maps to NM_178864.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:66191383 C>A maps to NM_178864.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:66192325 C>T maps to NM_178864.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:66190226 C>A maps to NM_178864.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:66192355 G>A maps to NM_178864.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:66190199 A>C maps to NM_178864.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:108043481 G>A maps to NM_002519.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:108059913 G>A maps to NM_002519.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:108057297 T>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:108043049 T>A maps to NM_002519.2 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:108059884 C>A maps to NM_002519.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:108057288 G>A maps to NM_002519.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:108060037 A>G maps to NM_002519.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:53852565 G>A maps to NM_005285.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:53853264 C>A maps to NM_005285.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr8:53853135 T>C maps to NM_005285.3 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:53853024 C>A maps to NM_005285.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:62737698 C>A maps to NM_005286.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:62737584 G>A maps to NM_005286.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:62737844 C>A maps to NM_005286.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr20:62738105 G>A maps to NM_005286.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:21140247 G>A maps to NM_000271.4 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:21113481 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:21115555 G>T maps to NM_000271.4 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr18:21136521 C>A maps to NM_000271.4 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:44576028 T>C did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:44571747 C>A maps to NM_013389.2 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:44571765 C>A maps to NM_013389.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:44579149 C>T maps to NM_013389.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr7:44579719 G>A maps to NM_013389.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:44560607 G>A maps to NM_013389.2 N1021N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr7:44555688 T>A maps to NM_013389.2 G1236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57269553 C>A maps to NM_024663.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:57288529 C>T maps to NM_024663.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:45668160 G>T maps to NM_006310.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr17:45689929 G>T maps to NM_006310.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr17:45673789 C>T maps to NM_006310.3 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:72015084 G>T maps to ENST00000277942 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:72020415 C>A maps to ENST00000277942 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:72020427 G>A maps to ENST00000277942 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:72025848 C>A maps to ENST00000277942 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr4:73012877 C>G maps to NM_004885.2 Y306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:73012883 C>A maps to NM_004885.2 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:73013162 C>A maps to NM_004885.2 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:110917823 C>T maps to NM_000272.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:132407564 A>T maps to ENST00000393156 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:132440851 C>T maps to ENST00000393156 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr3:132440851 C>T maps to ENST00000393156 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:132416115 C>T maps to ENST00000393156 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:132415658 T>G did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:5925160 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:6027357 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:5993290 G>A maps to NM_015102.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:5947484 G>A maps to NM_015102.2 H782H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:6008260 C>A maps to NM_015102.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:36339974 G>T maps to NM_004646.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36340176 G>T maps to NM_004646.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:36334378 T>A maps to NM_004646.3 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:36332707 G>A maps to NM_004646.3 N908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:36322196 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:36338986 A>G maps to NM_004646.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:36321793 C>A maps to NM_004646.3 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:36338978 G>A maps to NM_004646.3 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr19:36321858 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:36330256 G>A maps to NM_004646.3 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:36336384 G>T maps to NM_004646.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:36342574 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:179526326 G>A maps to NM_014625.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:179530486 C>A maps to NM_014625.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:179521776 C>G maps to NM_014625.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:179520477 G>A maps to NM_014625.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:15045797 A>G maps to NM_006985.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:15045756 G>T maps to NM_006985.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:182785876 G>T maps to NM_030769.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:182783955 T>A maps to NM_030769.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:79580489 C>A maps to NM_017921.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:170819786 G>T maps to NM_002520.6 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:170814963 G>C maps to NM_002520.6 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:106858223 C>T maps to ENST00000503451 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr4:106858223 C>A maps to ENST00000503451 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:11918460 G>A maps to NM_002521.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:11917728 C>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:153659681 C>T maps to NM_000906.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:153661696 G>T maps to NM_000906.3 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:153655007 C>T maps to NM_000906.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:153661495 G>T maps to NM_000906.3 E829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:35802273 C>G maps to NM_003995.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:35793019 A>G maps to NM_003995.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:35799659 C>T maps to NM_003995.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:35794018 A>T maps to NM_003995.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:35792872 A>G maps to NM_003995.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:32724852 G>T maps to ENST00000265074 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:32739136 G>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:32784902 A>T maps to ENST00000265074 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:32712583 C>A maps to ENST00000265074 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:32739066 T>A maps to ENST00000265074 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:32780870 T>C maps to ENST00000265074 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:32712046 G>T maps to ENST00000265074 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:162774 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:142602 A>G maps to ENST00000399953 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr10:129350834 A>T maps to NM_001030013.1 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:34889212 G>T maps to NM_207172.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:34867157 C>A maps to NM_207172.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr7:34888168 G>T maps to NM_207172.1 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:34698050 C>T maps to NM_207172.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr15:73862611 G>A maps to NM_012428.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:78449350 G>A maps to NM_002522.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:98254453 C>A maps to NM_002523.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:98256542 C>A maps to NM_002523.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr22:39224290 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:25266429 C>T maps to NM_022150.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr7:25266591 A>G maps to NM_022150.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:24324909 C>T maps to NM_000905.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164247105 G>A maps to NM_000909.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:164247684 G>A maps to NM_000909.4 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:164246586 C>A maps to NM_000909.4 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:164247648 C>A maps to NM_000909.4 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr4:164247376 C>T maps to NM_000909.4 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:156135258 C>A maps to NM_000910.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr4:156135900 G>C maps to NM_000910.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:156135528 G>T maps to NM_000910.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:156136062 C>A maps to NM_000910.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:156135228 G>A maps to NM_000910.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr4:156136041 C>T maps to NM_000910.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:156136233 C>A maps to NM_000910.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:156135577 C>T maps to NM_000910.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:156135827 T>A maps to NM_000910.2 L246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr4:156135552 C>T maps to NM_000910.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:164271730 C>A maps to NM_006174.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:164271826 A>T maps to NM_006174.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr4:164271982 A>T maps to NM_006174.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr4:164271629 A>T maps to NM_006174.2 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr4:164272189 C>T maps to NM_006174.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:164272514 C>A maps to NM_006174.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:164271487 C>A maps to NM_006174.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr4:164271556 G>T maps to NM_006174.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:69744935 C>T maps to NM_000903.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr16:69744881 T>C maps to NM_000903.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:30327198 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:30322835 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:30326949 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:30326994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr23:30322722 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:30322721 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:30326405 G>C did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:30327113 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:30322842 G>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:30326433 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:30326397 G>C did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:30322937 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:30326723 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:30327328 C>T did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr23:30327299 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:30327008 C>T did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:27238519 C>T maps to NM_021969.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:27238431 G>A maps to NM_021969.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:27240368 G>T maps to NM_021969.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:50881425 G>T maps to NM_007121.4 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr11:47283258 G>A maps to NM_005693.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:100928737 C>A maps to ENST00000392986 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:100928725 T>C maps to ENST00000392986 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:100926299 G>A maps to ENST00000392986 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:100904814 C>T maps to ENST00000392986 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:100934573 G>A maps to ENST00000392986 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr12:100904814 C>A maps to ENST00000392986 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:119531735 C>T maps to NM_022002.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:119533824 G>T did not map to a codon.
Alternatively spliced codon TCGA-17-Z055-01A-01W-0747-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:161200618 G>A maps to NM_001077482.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:161205670 C>T maps to NM_001077482.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:15057666 G>T maps to NM_003298.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:108501528 G>A maps to ENST00000368983 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:108496053 G>T maps to ENST00000368983 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr6:108502053 C>A maps to ENST00000368983 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:92923848 C>A maps to NM_005654.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:92929472 C>T maps to NM_005654.4 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:92923752 C>T maps to NM_005654.4 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr5:92924055 C>A maps to NM_005654.4 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:92923650 C>A maps to NM_005654.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:96877534 G>T maps to NM_021005.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:17346350 C>T maps to NM_005234.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:142780340 C>A maps to NM_001024094.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:142680273 G>C maps to NM_001024094.1 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:142779798 C>T maps to NM_001024094.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:149357468 T>A maps to ENST00000511528 K182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:149002644 C>T maps to ENST00000511528 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:149356881 A>G maps to ENST00000511528 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:52449824 G>A maps to ENST00000360284 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:157186158 T>C maps to NM_006186.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr9:102595772 C>T maps to NM_173199.1 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:102595601 C>T maps to NM_173200.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:127262439 T>A maps to NM_004959.4 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr9:127255380 C>T maps to NM_004959.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:200017309 C>T maps to NM_205860.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:200080374 T>C maps to NM_205860.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:200143262 C>T maps to NM_205860.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:200017459 C>T maps to NM_205860.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:200014582 C>A maps to NM_205860.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr10:115391687 C>A maps to ENST00000369358 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr10:115356916 A>G maps to ENST00000369358 S1461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:115405667 T>C maps to ENST00000369358 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:115380467 C>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:115384619 G>A maps to ENST00000369358 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:115384638 G>A maps to ENST00000369358 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:115423620 A>G maps to ENST00000369358 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr10:115374046 G>T maps to ENST00000369358 Y1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:115251275 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:115256578 C>T maps to NM_002524.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:64913380 C>T maps to NM_030759.3 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:27659969 G>T maps to ENST00000379863 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:27660165 C>G maps to ENST00000379863 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:27657348 C>T maps to ENST00000379863 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:27657623 C>T maps to ENST00000379863 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr8:144917855 G>C maps to NM_178564.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:107878194 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:107818537 A>T maps to ENST00000379032 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:107871485 C>T maps to ENST00000379032 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:107818552 G>A maps to ENST00000379032 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:107790397 G>T maps to ENST00000379032 S1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:107820808 G>A maps to ENST00000379032 I903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:107836278 G>T maps to ENST00000379032 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:107832197 G>C maps to ENST00000379032 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:107808782 G>A maps to ENST00000379032 I1084I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:107823166 A>T maps to ENST00000379032 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr7:107823196 C>A maps to ENST00000379032 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:107849965 A>T maps to ENST00000379032 L325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:107872865 C>A maps to ENST00000379032 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr7:107790356 A>T maps to ENST00000379032 *1309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:52283747 G>A maps to NM_002525.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:52301821 C>T maps to NM_002525.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:52299741 G>A maps to NM_002525.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:129349024 C>T maps to ENST00000393231 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr7:129357121 G>T maps to ENST00000393231 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:129350355 C>A maps to ENST00000393231 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr7:129367174 G>T maps to ENST00000393231 G440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:129351328 A>T maps to ENST00000393231 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:32620795 C>A maps to NM_001160004.1 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:32621577 G>T maps to NM_013956.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr8:32453385 G>T maps to NM_013956.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:32585596 G>A maps to NM_004495.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:32621714 C>A maps to NM_013956.3 S578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:32621403 C>T maps to NM_013956.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr8:32611923 C>T maps to NM_013956.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr8:32505334 G>T maps to NM_013959.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:32617783 A>T maps to NM_013956.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:32621289 G>T maps to NM_013956.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:139232108 G>T maps to NM_013982.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:139231258 G>T maps to NM_013982.2 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr5:139260462 C>A maps to NM_013982.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:139260444 G>A maps to NM_013982.2 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:84733611 C>A maps to ENST00000404547 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr10:83635620 C>T maps to ENST00000404547 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr10:84744852 G>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:84118493 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:84745240 C>A maps to ENST00000404547 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:83635848 C>A maps to ENST00000404547 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:84118543 A>T maps to ENST00000404547 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr10:83635734 A>T maps to ENST00000404547 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:83635515 C>A maps to ENST00000404547 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:76248309 G>A maps to NM_138573.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:2939957 G>T maps to NM_031474.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:2936793 G>C maps to NM_031474.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:105167241 G>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr23:105190393 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:105075046 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:105167114 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:105179198 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:105168747 G>C did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:105197056 G>T did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:105181438 T>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:105153551 T>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:105150542 A>G did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:105153138 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:105168968 A>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:105152951 A>C did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr23:105153376 C>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:105167149 T>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:105181472 T>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:105153041 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:105150487 A>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:105181508 T>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:105181571 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:105153051 G>T did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:105075044 A>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:105190360 G>C did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:105153580 G>C did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:105167172 G>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:105153511 C>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:105193616 G>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:105181571 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:105179266 A>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:105152723 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:105142674 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:105189872 G>T did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr14:24551822 G>A maps to NM_006177.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr6:6006964 G>A maps to NM_016588.2 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:67919706 C>T maps to NM_198443.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr10:33510715 G>A maps to NM_003873.5 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:33542984 C>A maps to NM_003873.5 G318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr10:33515145 C>T maps to NM_003873.5 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr10:33496557 C>T maps to NM_003873.5 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:206641177 C>T maps to NM_018534.3 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:206590697 T>C maps to NM_201266.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:206610594 G>T maps to NM_201266.1 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:206659562 G>C maps to NM_201266.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:206581060 G>T maps to NM_201266.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:206610585 G>A maps to NM_201266.1 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:206610567 G>A maps to NM_201266.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:206659577 C>A maps to NM_201266.1 P864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:24145855 C>T maps to NM_080723.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:24134590 G>A maps to NM_080723.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr6:24146170 C>T maps to NM_080723.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:24134623 C>G maps to NM_080723.4 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:24134623 C>A maps to NM_080723.4 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:50149312 C>G maps to ENST00000404971 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:50724852 C>A did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr2:50282122 G>A maps to ENST00000404971 R1300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:50765685 C>T maps to ENST00000404971 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:50280582 G>T maps to ENST00000404971 I1358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:51255087 C>G maps to ENST00000404971 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:50847159 C>T maps to ENST00000404971 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:50850507 C>A maps to ENST00000404971 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:50699459 C>A maps to ENST00000404971 G1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr2:50850753 C>A maps to NM_001135659.1 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:50149312 C>A maps to ENST00000404971 T1471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:50149279 G>C maps to ENST00000404971 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:50280528 A>T maps to ENST00000404971 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:50850559 C>A maps to ENST00000404971 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:50280717 G>T maps to ENST00000404971 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:51254823 G>T maps to ENST00000404971 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:50280728 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:50724469 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:50149333 G>A maps to ENST00000404971 I1464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:50318578 A>G maps to ENST00000404971 I1240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:50850542 G>C maps to ENST00000404971 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:51254658 G>T maps to ENST00000404971 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:50463983 G>A maps to ENST00000404971 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:50318467 G>T maps to ENST00000404971 Y1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:50850507 C>A maps to ENST00000404971 G393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:51255105 C>A maps to ENST00000404971 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:50850469 G>T maps to ENST00000404971 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr2:50850487 G>T maps to ENST00000404971 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:50463953 G>T maps to ENST00000404971 G1213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:50149324 G>T maps to ENST00000404971 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:64480927 G>A maps to NM_015080.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:64402832 C>A maps to NM_015080.3 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:64434818 C>A maps to NM_015080.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:64390551 T>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:64415749 C>T maps to NM_015080.3 W1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:64465256 G>A maps to NM_015080.3 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:64428237 C>A maps to NM_015080.3 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:64418776 C>A maps to NM_015080.3 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:64434731 A>G maps to NM_015080.3 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:64418768 G>T maps to NM_015080.3 S959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:64434815 G>A maps to NM_015080.3 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:64436067 G>T maps to NM_015080.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:64393932 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:64434869 C>A maps to NM_015080.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:79270161 C>T maps to NM_004796.4 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:80130239 C>A maps to NM_004796.4 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr14:80164063 C>G maps to NM_004796.4 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:79175700 G>T maps to NM_004796.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr14:79181126 G>A maps to NM_004796.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:79933640 C>A maps to NM_004796.4 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:80328195 C>T maps to NM_004796.4 N1025N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:79175639 C>A maps to NM_004796.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:79434537 G>T maps to NM_004796.4 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr14:79270062 C>A maps to NM_004796.4 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr14:80328222 C>T maps to NM_004796.4 N1034N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:79432644 C>A maps to NM_004796.4 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:79432422 C>A maps to NM_004796.4 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr14:79175972 G>A maps to NM_004796.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr14:79175810 C>A maps to NM_004796.4 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:79181240 C>G maps to NM_004796.4 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr14:79181277 C>T maps to NM_004796.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:176637040 C>T maps to NM_022455.4 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:176562676 C>T maps to NM_022455.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:176673677 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:176722249 G>T maps to NM_022455.4 L2627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:176707798 G>T maps to NM_022455.4 R1952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:176722108 G>A maps to NM_022455.4 A2580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152014960 G>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:152031184 G>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:152018809 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:152027359 C>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:152034483 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:152036207 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:152018930 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:152031266 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:152031162 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:1426309 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:212964937 G>A maps to NM_015471.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:212911977 C>T maps to NM_015471.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:212964925 G>C maps to NM_015471.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr8:59520390 C>A maps to NM_001144772.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:59518563 G>A maps to NM_001144772.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:59502046 G>A maps to NM_001144772.1 N756N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:59500260 C>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr8:126194397 G>A maps to NM_173685.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:6607416 G>A maps to NM_017755.5 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:93802948 A>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:93812982 G>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:93845108 G>A maps to NM_022072.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:93813893 G>T maps to NM_022072.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:46827466 C>G maps to NM_199044.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr7:72718747 G>A maps to NM_148956.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:18885148 T>A maps to NM_182543.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr10:18874950 C>A maps to NM_182543.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:40752994 C>T maps to NM_024677.4 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:40810349 G>C maps to NM_024677.4 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:40131283 G>T maps to NM_032526.1 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:40131790 C>A maps to NM_032526.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:40124891 C>A maps to NM_032526.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:40131833 G>A maps to NM_032526.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:40124834 G>T maps to NM_032526.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:18745190 G>A maps to ENST00000455492 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:18745157 G>C maps to ENST00000455492 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:18757470 A>T maps to ENST00000455492 C513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:18765911 G>T maps to ENST00000455492 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:18766132 G>A maps to ENST00000455492 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:18767603 G>T maps to ENST00000455492 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:104849449 C>T maps to NM_001134373.1 E555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr7:33057179 T>C maps to NM_001002010.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:33055307 G>A maps to NM_001002010.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:33057182 G>A maps to NM_001002010.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:39985170 G>A maps to NM_052935.4 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:116542281 G>T maps to NM_152729.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr3:52562285 C>T maps to NM_001134231.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:52563210 G>A maps to NM_001134231.1 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:104179253 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:104171765 G>A maps to NM_001031701.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:104200707 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr12:104190757 C>A maps to NM_001031701.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:86180988 A>T maps to NM_002526.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr17:17209910 C>T maps to ENST00000379552 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:15141947 G>T maps to NM_173474.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:15141369 G>A maps to NM_173474.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:5603587 C>A maps to NM_001102654.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:5603742 G>A maps to NM_001102654.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:49565008 C>T maps to NM_006179.4 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:132177642 C>A maps to NM_001144058.1 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:132177676 G>T maps to NM_001144058.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:132016328 G>T maps to NM_001144058.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr11:131781443 C>T maps to NM_001144058.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:132016250 G>A maps to NM_001144058.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:132082030 C>A maps to NM_001144058.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:132016187 C>T maps to NM_001144058.1 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:132204976 G>C maps to NM_001144058.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:132177605 G>T maps to NM_001144058.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:132081913 A>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:9083205 G>T maps to NM_004822.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr17:8926265 C>T maps to NM_004822.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr19:49173880 C>A maps to NM_145807.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:49167496 A>G maps to NM_145807.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:107979326 T>A maps to NM_001113226.1 C432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:107979285 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:107867517 G>T maps to NM_001113226.1 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:107691418 G>T maps to NM_001113226.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:107867409 G>A maps to NM_001113226.1 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:107937886 T>A maps to NM_001113226.1 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:107866971 G>T maps to NM_001113226.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:107691461 G>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:107867268 C>T maps to NM_001113226.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:107691316 G>A maps to NM_001113226.1 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:107979308 C>A maps to NM_001113226.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:107867472 G>A maps to NM_001113226.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:107979389 G>T maps to NM_001113226.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:135073436 G>T maps to NM_032536.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr9:135102362 C>A maps to NM_032536.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr9:135073777 C>T maps to NM_032536.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:135073901 C>A maps to NM_032536.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr9:135073528 C>A maps to NM_032536.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:135073441 G>A maps to NM_032536.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr9:135114647 C>T maps to NM_032536.2 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:135073627 C>A maps to NM_032536.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr9:135073411 G>A maps to NM_032536.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr9:135116405 G>A maps to NM_032536.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:156846196 G>A maps to NM_002529.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:156846229 C>T maps to NM_002529.3 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156845458 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:156838012 C>T maps to NM_002529.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:156841428 G>A maps to NM_002529.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:156837894 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:156837895 G>T maps to NM_002529.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:156834151 C>A maps to NM_002529.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:156846280 C>T maps to NM_002529.3 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:156846277 G>T maps to NM_002529.3 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:156849828 G>T maps to NM_002529.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:87339227 T>C maps to NM_006180.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:87635143 C>A maps to NM_006180.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr9:87285782 C>A maps to NM_006180.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr9:87635122 C>A maps to NM_006180.3 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:87570332 C>T maps to NM_006180.3 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr9:87635228 G>T maps to NM_006180.3 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:87317134 G>T maps to NM_006180.3 G92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr9:87338592 G>A maps to NM_006180.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:87342833 G>A maps to NM_006180.3 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr15:88420186 G>T maps to NM_001012338.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:88483883 C>A maps to NM_001012338.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:88576115 C>T maps to NM_001012338.1 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr15:88476241 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:88679798 G>T maps to NM_001012338.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:88680695 G>A maps to NM_001012338.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr15:88669510 C>A maps to NM_001012338.1 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:88690615 C>A maps to NM_001012338.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr15:88678413 G>T maps to NM_001012338.1 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:88420314 G>T maps to NM_001012338.1 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:88476289 G>A maps to NM_001012338.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:88483958 G>A maps to NM_001012338.1 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr15:88472451 G>T maps to NM_001012338.1 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:88690600 C>A maps to NM_001012338.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:86268246 G>T maps to NM_006183.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:61391393 C>A maps to NM_002531.2 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:61340876 C>A maps to NM_002531.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:61386116 C>T maps to NM_002531.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr20:61340903 C>A maps to NM_002531.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr20:61386212 C>A maps to NM_002531.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:61340910 C>T maps to NM_002531.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:11802243 G>C maps to NM_012344.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:11802177 G>T maps to NM_012344.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:106500285 A>T maps to NM_014840.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:106460708 C>A maps to NM_014840.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:205290687 C>A maps to ENST00000441520 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:151042433 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:1836553 C>T maps to NM_012225.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr14:32030657 C>T maps to NM_025152.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:32257002 G>T maps to NM_025152.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:49424448 G>A maps to NM_006184.5 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:49416365 A>G maps to NM_006184.5 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:49404088 G>C maps to NM_006184.5 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:17316911 G>A maps to ENST00000458064 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:205696876 G>A maps to NM_022731.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:110308671 C>A maps to NM_032869.3 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:110255339 T>C maps to NM_032869.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:44524852 G>A maps to NM_015332.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:51075885 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:51239056 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:102891787 G>A maps to NM_031438.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:102895771 C>A maps to NM_031438.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:74879876 C>G maps to NM_015901.4 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:74890528 G>A maps to NM_015901.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:48619793 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:21964954 C>A maps to NM_024815.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:56485054 G>A maps to NM_007006.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:63994327 G>T maps to NM_032344.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:34263447 C>G maps to NM_006703.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr10:12209787 G>A maps to ENST00000378937 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:123814180 G>A maps to NM_007083.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr16:77775522 C>T maps to NM_001105663.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:67396389 C>T maps to ENST00000376693 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:88356225 G>A maps to NM_024047.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:163325228 G>A maps to NM_145697.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:163298634 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:163309230 A>G maps to NM_145697.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:163317665 A>T maps to NM_145697.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:163297276 G>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:163298025 G>C maps to NM_145697.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:163317550 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27613886 C>A maps to NM_020772.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr17:27613316 G>A maps to NM_020772.2 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:71716299 G>T maps to ENST00000393695 T1942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:71726318 G>A maps to ENST00000393695 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:71727041 G>A maps to ENST00000393695 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr11:71717189 A>C maps to ENST00000393695 G1867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr11:71726240 G>A maps to ENST00000393695 R776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:73743881 G>A maps to NM_001005743.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:73743741 G>A maps to NM_001005743.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:69124945 T>C maps to NM_020401.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:69121133 G>T maps to NM_020401.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:69103079 A>T maps to NM_020401.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:69085776 A>T maps to NM_020401.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:229588381 C>A maps to NM_018230.2 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:229636556 G>A maps to NM_018230.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:229625781 G>A maps to NM_018230.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229613446 C>T maps to NM_018230.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:229622275 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:229588298 T>C maps to NM_018230.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:229631692 T>C maps to NM_018230.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr6:17624951 G>A maps to ENST00000430136 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr5:37305172 C>A maps to NM_153485.1 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr5:37292141 T>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:37370995 C>A maps to NM_153485.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr5:37370992 G>A maps to NM_153485.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:37292070 C>T maps to NM_153485.1 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:47829997 G>A maps to NM_015231.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:47843374 T>A did not map to a codon.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr11:47808038 G>A maps to NM_015231.1 Q1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:47808066 T>C maps to NM_015231.1 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:47826138 C>A maps to NM_015231.1 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr9:131745598 G>A maps to NM_015354.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:131760827 A>T maps to NM_015354.1 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:131735482 T>C maps to NM_015354.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:131761474 C>A maps to NM_015354.1 I1180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:131765217 G>A maps to NM_015354.1 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:131750353 C>T maps to NM_015354.1 Q808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr9:131762056 G>T maps to NM_015354.1 R1272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr9:131767757 G>A maps to NM_015354.1 L1562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr9:131752417 C>G maps to NM_015354.1 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:135262699 C>T maps to NM_015135.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:135310103 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:135303236 G>C maps to NM_015135.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:135322680 C>T maps to NM_015135.2 R1713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:135279334 G>A maps to NM_015135.2 W624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:135333219 A>G maps to NM_015135.2 L1985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:135322690 G>T maps to NM_015135.2 G1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:135304259 C>G maps to NM_015135.2 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr7:135277876 C>T maps to NM_015135.2 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:135286202 C>G maps to NM_015135.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:13363717 C>G maps to NM_024923.2 V1630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr3:13370299 G>A maps to NM_024923.2 H1419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:13441296 G>A maps to NM_024923.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:13395160 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:13417889 C>T maps to NM_024923.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:154112394 G>A maps to NM_207308.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:153967591 G>T maps to NM_207308.2 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr1:154098867 G>T maps to NM_207308.2 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:153995617 C>T maps to NM_207308.2 Q1426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:154076560 T>A maps to NM_207308.2 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:153995739 G>A maps to NM_207308.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr1:153973371 C>T maps to NM_207308.2 E1782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014771 A>T maps to ENST00000451030 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:134014780 G>T maps to ENST00000451030 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:134077032 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:134098171 T>C maps to ENST00000451030 S1920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr9:134050988 G>A maps to ENST00000451030 Q1101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr9:134015981 A>T maps to ENST00000451030 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr9:134073548 T>C maps to ENST00000451030 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr9:134019889 C>G maps to ENST00000451030 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:134074070 A>T maps to ENST00000451030 S1731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:184022189 T>G maps to NM_138285.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:102512138 A>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:102512214 C>A maps to NM_024057.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:102512146 C>A maps to NM_024057.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:77057380 C>A maps to ENST00000458189 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:50412419 G>T maps to NM_012346.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:50411624 C>A maps to NM_012346.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:106391024 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:73230880 C>T maps to NM_024844.3 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:73229200 C>T maps to NM_024844.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr17:73206051 G>T maps to NM_024844.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:73206068 C>T maps to NM_024844.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:73228075 T>C did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr17:5317414 G>A maps to NM_002532.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:56871537 G>T maps to NM_014669.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr16:56875615 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:56878487 G>A maps to NM_014669.3 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:3707285 T>C maps to NM_016320.4 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:3707285 T>C maps to NM_016320.4 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:3712667 C>A maps to NM_016320.4 E1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:3721924 G>C maps to NM_016320.4 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:23240331 A>T maps to NM_007342.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr15:41667973 G>A maps to NM_016359.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:224488274 C>A maps to NM_002533.2 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:224475614 T>C maps to NM_002533.2 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16910854 G>A maps to ENST00000438489 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:16860106 T>G maps to ENST00000438489 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:16874685 G>T maps to ENST00000438489 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:16870092 G>T maps to ENST00000438489 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:16910887 C>G maps to ENST00000438489 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr19:16870182 A>G maps to ENST00000438489 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:16860133 C>G maps to ENST00000438489 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62569424 C>A maps to NM_006362.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:62569273 G>A maps to NM_006362.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:62568673 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:101623758 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr23:101581407 G>C did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:101581404 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:101620164 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr23:101623731 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:101576801 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:101615555 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:102334757 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:102337995 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:102337944 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:102335099 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:102337744 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:102338132 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:102334542 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:102339664 G>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:102339803 A>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:102339308 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:102339810 C>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:102334376 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:102334746 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:102337931 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:102333558 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:102334544 C>G did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:102333521 G>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr23:102333542 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:102332600 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:102337205 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:102338593 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:102334689 C>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:102338169 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:101092564 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:101096044 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:101096676 C>T did not map to a codon.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr23:101096473 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:101092627 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:101092589 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:101096644 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:101095987 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:101095867 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:101092806 T>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:101096691 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:101092784 A>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:101092602 G>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:101092606 T>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:101096946 T>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:101092550 T>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:101092545 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:17571645 G>T maps to NM_138454.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:17571669 G>A maps to NM_138454.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:91150522 G>A maps to NM_001161625.1 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:8790639 C>G maps to NM_152745.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:8475397 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:8790940 G>T maps to NM_152745.2 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:139428797 G>T maps to NM_007226.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:139429118 C>A maps to NM_007226.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:139429190 C>A maps to NM_007226.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr17:47656496 C>T maps to ENST00000513748 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:47656115 G>T maps to ENST00000513748 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr17:47656160 G>A maps to ENST00000513748 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr17:47656172 C>T maps to ENST00000513748 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:47656253 C>T maps to ENST00000513748 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:108785909 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:108780243 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:108780216 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:24884149 G>T maps to NM_025081.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:24878082 G>T maps to NM_025081.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:24878208 G>A maps to NM_025081.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:24884815 C>T maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr14:24885565 G>A maps to NM_025081.2 P1537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:24884536 C>A maps to NM_025081.2 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:24878022 G>T maps to NM_025081.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr14:24885568 G>A maps to NM_025081.2 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:41333565 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:41333678 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:41333693 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:120097703 A>G maps to NM_178507.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:120097541 G>A maps to NM_178507.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:113445592 G>T maps to NM_016817.2 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:113433239 A>G maps to NM_016817.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:113442938 G>A maps to NM_016817.2 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:113403718 C>G maps to NM_006187.2 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:113385900 G>C maps to NM_006187.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:113400593 G>T maps to NM_006187.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr12:113398948 C>A maps to NM_006187.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:121461897 T>A maps to NM_003733.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:121465578 G>C maps to NM_003733.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:151742668 C>A maps to ENST00000321531 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105659883 C>T maps to NM_024928.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:138439089 C>T maps to NM_014582.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:228444508 C>T maps to NM_001098623.1 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:228550382 C>T maps to NM_001098623.1 P6256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:228565291 C>A maps to NM_001098623.1 S7794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:228437915 G>C maps to NM_001098623.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:228482093 C>T maps to NM_001098623.1 T3791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228464949 G>C maps to NM_001098623.1 A2230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:228523917 C>A maps to NM_001098623.1 S5495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:228402004 G>T maps to NM_001098623.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:228550328 G>A maps to NM_001098623.1 L6238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:228444427 C>A maps to NM_001098623.1 L1462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:228401926 G>T maps to NM_001098623.1 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:228432120 T>C maps to NM_001098623.1 D1110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228529167 G>T maps to NM_001098623.1 E5963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:228559661 C>T maps to NM_001098623.1 F7061F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:228412280 G>A maps to NM_001098623.1 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:228466414 G>T maps to NM_001098623.1 P2295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:228495873 G>T maps to NM_001098623.1 E4177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:228505240 C>T maps to NM_001098623.1 P4546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:228401920 C>T maps to NM_001098623.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr1:228479862 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:228497225 C>T maps to NM_001098623.1 G4326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:228466468 G>T maps to NM_001098623.1 V2313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:228495020 C>G maps to NM_001098623.1 A4085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:228402013 G>T maps to NM_001098623.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:228468274 G>T maps to NM_001098623.1 E2659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:228412409 G>T maps to NM_001098623.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:228547903 C>G maps to NM_052843.2 A6437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:228466504 C>T maps to NM_001098623.1 G2325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:228553829 G>A maps to NM_001098623.1 T6373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:228560438 C>T maps to NM_001098623.1 F7320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:228559463 C>T maps to NM_001098623.1 I6995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:228468087 G>T maps to NM_001098623.1 A2624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:228469871 G>A maps to NM_001098623.1 R2812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:228503569 G>C maps to NM_001098623.1 G4345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:228557765 C>T maps to NM_001098623.1 F6697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:228403333 C>T maps to NM_001098623.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:228548089 G>T maps to NM_052843.2 V6499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:228464986 C>T maps to NM_001098623.1 Q2243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:228495848 G>T maps to NM_001098623.1 A4168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:228547549 G>C maps to NM_052843.2 S6319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:228464889 G>A maps to NM_001098623.1 T2210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:228432120 T>C maps to NM_001098623.1 D1110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:228475825 G>T maps to NM_001098623.1 T3292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:228522211 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220421266 G>T maps to NM_015311.2 I1415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:220424001 G>T maps to NM_015311.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:220419217 G>A maps to NM_015311.2 C1618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:220424025 A>T maps to NM_015311.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:220423026 C>A maps to NM_015311.2 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:220418343 C>G maps to NM_015311.2 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:220423971 C>A maps to NM_015311.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:133051248 C>T maps to ENST00000262283 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:133053776 A>T maps to ENST00000262283 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:133036910 C>A maps to ENST00000262283 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:133051266 G>T maps to ENST00000262283 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:133053884 G>A maps to ENST00000262283 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:28000605 T>A maps to NM_000275.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:28000611 G>C maps to NM_000275.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28090144 C>A maps to NM_000275.2 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:28096534 G>A maps to NM_000275.2 C777C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:28000590 G>T maps to NM_000275.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:28230274 C>A maps to NM_000275.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:28231771 T>A maps to NM_000275.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:28116362 C>G maps to NM_000275.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr15:28235783 T>A maps to NM_000275.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:28096606 C>A maps to NM_000275.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr15:28116371 G>T maps to NM_000275.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr15:28326921 G>T maps to NM_000275.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr15:28090121 G>A maps to NM_000275.2 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr15:28326978 C>T maps to NM_000275.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr15:28228523 G>A maps to NM_000275.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:28200348 C>T maps to NM_000275.2 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:28096606 C>A maps to NM_000275.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:28211926 C>A maps to NM_000275.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:28260047 G>T maps to NM_000275.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:28263614 C>T maps to NM_000275.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr15:28230312 G>T maps to NM_000275.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr15:28117043 C>A maps to NM_000275.2 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:28273018 C>A maps to NM_000275.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr4:48853936 C>T maps to NM_001168254.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:48899869 C>T maps to NM_001014446.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:97617831 G>A maps to NM_006188.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:97619368 G>T maps to NM_006188.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:97617758 G>A maps to NM_006188.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:97617750 C>A maps to NM_006188.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:128699805 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:128722860 A>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:128692648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:128723861 G>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:128694568 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:128692701 C>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr23:128699792 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:128691358 C>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:128674754 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:128696581 A>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:128695182 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:128692824 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:128722932 T>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:128692883 T>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:128709135 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:71066319 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:71063864 C>T maps to NM_017855.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:71063850 C>T maps to NM_017855.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:10584716 C>T maps to NM_002539.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:10584716 C>T maps to NM_002539.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:103572953 G>T maps to NM_024410.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:103572794 G>T maps to NM_024410.3 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr9:131222920 G>A maps to NM_153435.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:131235917 C>T maps to NM_153435.1 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:86826107 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:86818660 C>A maps to ENST00000370567 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr1:86822222 C>T maps to ENST00000370567 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:197627 C>A maps to NM_053280.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:50969206 C>A maps to NM_001014440.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:463977 C>A maps to NM_182577.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:463924 G>T maps to NM_182577.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:124028143 C>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:123554305 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:123838918 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:123517812 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:123615650 G>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:124097539 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:123514786 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:123539000 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:123680901 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:124097464 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:123515110 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:123785892 G>C did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:123680733 A>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:123870868 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:123518371 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:123680930 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:123556171 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:123870931 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:123554178 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:123517707 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:123805639 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:123519886 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:123785935 G>T did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:123525994 C>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:123514909 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:123516527 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:124097429 T>G did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr23:123780626 C>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:123839005 G>A did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:123870988 C>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:123785873 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:123518484 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:123805640 C>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:123657420 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:123515009 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:123805543 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:123519721 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:123540179 A>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:123637469 C>G did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:123631059 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:123526089 C>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:123654436 A>T did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:123805646 C>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:123587249 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:123654531 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:123587251 T>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:123517901 G>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:124097525 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:124097565 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:123637427 T>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:123654553 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:124028169 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:123519820 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:123838885 G>C did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:123787524 T>G did not map to a codon.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr23:123554469 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:123556155 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:124097384 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123514662 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123540184 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123554635 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123637452 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123657475 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123785917 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:123556171 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:123526197 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:124030090 C>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:123780637 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:123518549 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:123538979 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:123631015 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:123556415 T>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:124028174 C>G did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:124029981 G>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:123517896 C>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:123516627 T>C did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:123587224 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:123838988 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:123839040 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:123519791 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:123554452 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:123785832 G>T did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:123657296 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:123554294 C>A did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:123787579 C>A did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr23:123587297 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:123540245 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:123554362 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:123556351 T>C did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:123779097 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:123779113 C>A did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:123838899 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:123556387 C>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:123587341 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:123514555 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:123631039 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:123556328 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:123637454 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:123657354 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:123519833 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:123615741 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:123615742 T>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:167545348 C>T maps to NM_001122679.1 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:167654945 G>A maps to NM_001122679.1 R1768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:167642068 C>A maps to NM_001122679.1 Y1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:167671429 T>C maps to NM_001122679.1 H1833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:167674517 C>T maps to NM_001122679.1 L2183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr5:167675294 G>T maps to NM_001122679.1 E2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:167420062 G>A maps to NM_001122679.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr5:167551957 C>A maps to NM_001122679.1 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:167625974 C>A maps to NM_001122679.1 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:167673883 C>T maps to NM_001122679.1 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:167643927 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:167671537 C>A maps to NM_001122679.1 R1869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:167689181 C>A maps to NM_001122679.1 T2555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:167674738 C>T maps to NM_001122679.1 D2256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr5:167673931 C>T maps to NM_001122679.1 V1987V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr5:167645192 G>T maps to NM_001122679.1 E1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr5:167645263 C>T maps to NM_001122679.1 C1447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:167674057 C>A maps to NM_001122679.1 V2029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:167379731 C>G maps to NM_001122679.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:167553867 C>T maps to NM_001122679.1 R773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:183713605 C>T maps to NM_001080477.1 D1927D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:183652153 C>A maps to NM_001080477.1 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:183522270 C>T maps to NM_001080477.1 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:183650130 C>T maps to NM_001080477.1 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:183652147 C>A maps to NM_001080477.1 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:183694725 C>G maps to NM_001080477.1 S1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:183651437 G>T maps to NM_001080477.1 E891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:183594350 C>A maps to NM_001080477.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:183675776 T>A maps to NM_001080477.1 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:183696201 A>C maps to NM_001080477.1 R1734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:183713935 G>T maps to NM_001080477.1 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr4:183713424 A>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:183714955 G>A maps to NM_001080477.1 K2377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:183675599 G>T maps to NM_001080477.1 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr4:183696137 G>A maps to NM_001080477.1 L1712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:183603129 G>T maps to NM_001080477.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr4:183522200 G>A maps to NM_001080477.1 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr4:183594344 G>T maps to NM_001080477.1 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:183635316 G>T maps to NM_001080477.1 G767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:183710440 C>T maps to NM_001080477.1 R1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:183635268 G>T maps to NM_001080477.1 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:78412998 G>T maps to NM_001098816.2 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:78381152 G>A maps to NM_001098816.2 A2079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:78399144 T>G maps to NM_001098816.2 I1738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:78369638 G>T maps to NM_001098816.2 R2592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:78387378 G>A maps to NM_001098816.2 L1772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:78412982 G>A maps to NM_001098816.2 R1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr11:78413334 G>T maps to NM_001098816.2 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:78433920 G>A maps to NM_001098816.2 Q1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:78383280 G>A maps to NM_001098816.2 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:78369690 C>T maps to NM_001098816.2 L2574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:78381365 G>T maps to NM_001098816.2 R2008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:78412989 C>T maps to NM_001098816.2 G1556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr11:78381202 G>A maps to NM_001098816.2 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:78440613 G>A maps to NM_001098816.2 Y1071Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:78443411 C>T maps to NM_001098816.2 T1029T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:78369786 G>A maps to NM_001098816.2 L2542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:78380492 G>C maps to NM_001098816.2 R2299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:13785313 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:13775791 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:13778750 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:13762577 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:13769418 G>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:13775792 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:13786286 T>C did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:13785401 G>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr23:13753439 A>G did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:13778480 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:13764934 A>G did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:13778742 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:13771518 T>C did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:13764450 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:13786255 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:13753405 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr23:13781934 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr23:13764991 G>C did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr7:44747320 C>T maps to ENST00000444676 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:44736067 C>T maps to ENST00000444676 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr7:44733542 C>T maps to ENST00000444676 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:50952127 G>T maps to NM_018245.2 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50952076 G>T maps to NM_018245.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr10:50953849 C>A maps to NM_018245.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:50964931 G>T maps to NM_018245.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:50953476 G>C maps to NM_018245.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr10:50953987 G>T maps to NM_018245.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr10:50950995 C>T maps to NM_018245.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr10:50960244 C>T maps to NM_018245.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr10:50953437 G>T maps to NM_018245.2 Y527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:50953542 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:50964944 G>T maps to NM_018245.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:56500800 G>A maps to NM_018233.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:123463484 C>T maps to ENST00000228922 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr20:61444193 G>A maps to NM_007346.2 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr20:61444143 G>T maps to NM_007346.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:72011637 C>A maps to NM_024576.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:9792035 G>A maps to NM_016821.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:9807578 C>T maps to NM_016821.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:95163437 C>T maps to NM_033014.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:95165620 G>T maps to NM_033014.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:95163389 G>T maps to NM_033014.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr9:95163460 C>A maps to NM_033014.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:70774415 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:70775074 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:70767787 C>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:70777048 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:70793527 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:70787502 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:70783032 A>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:70782806 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:70787406 G>C did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:70764468 G>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:70756130 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:70776804 C>T did not map to a codon.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr23:70775056 T>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:70764461 C>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:70779443 T>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:70783196 G>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:70787517 G>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:70783044 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:70782993 C>G did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:70782789 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:70784508 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr23:70782819 C>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:70767809 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr23:70784554 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:70757865 G>A did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:70781667 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:74692242 G>C maps to NM_152635.1 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr10:74666351 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:74660144 C>T maps to NM_152635.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:175006615 G>A maps to ENST00000409546 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:174943776 T>G maps to ENST00000409546 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:15107657 G>T maps to NM_018324.2 G213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:138011774 G>T maps to NM_014279.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:138011927 C>T maps to NM_014279.4 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:138011957 G>A maps to NM_014279.4 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr9:138011948 G>T maps to NM_014279.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr9:137982045 G>T maps to NM_014279.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:9965536 G>A maps to NM_058164.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:9968408 G>C maps to NM_058164.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:9968408 G>A maps to NM_058164.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:102270472 T>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:102269967 G>T maps to ENST00000338858 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:102269916 G>T maps to ENST00000338858 Y438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:102290756 C>A maps to ENST00000338858 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:102269862 C>T maps to ENST00000338858 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:102290642 C>T maps to ENST00000338858 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:53624884 T>A maps to NM_006418.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr13:53616043 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr13:53617316 C>A maps to NM_006418.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:53602979 C>A maps to NM_006418.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr13:53603156 C>T maps to NM_006418.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:53616109 T>A maps to NM_006418.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:7531355 C>A maps to NM_198474.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:7507165 G>T maps to NM_198474.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:7530833 C>A maps to NM_198474.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:7530965 C>A maps to NM_198474.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr9:127572585 C>T maps to NM_182487.2 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:161953962 G>T maps to ENST00000451379 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:161970074 G>T maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:161967726 G>A maps to ENST00000451379 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:161968139 C>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:161970074 G>A maps to ENST00000451379 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:161969906 C>T maps to ENST00000451379 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:161953506 G>A maps to ENST00000451379 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:161953797 G>T maps to ENST00000451379 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:161953953 G>A maps to ENST00000451379 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:161989750 G>A maps to ENST00000451379 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:161967783 C>T maps to ENST00000451379 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:161970017 G>T maps to ENST00000451379 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:114523871 G>A maps to NM_020190.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr21:34399193 G>T maps to NM_005806.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr21:34399436 G>C maps to NM_005806.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:137815157 C>T maps to NM_175747.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:137815060 G>A maps to NM_175747.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:137814806 C>T maps to NM_175747.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:10313440 C>A maps to NM_002543.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:59004831 A>G maps to NM_145243.3 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:59004729 T>A maps to NM_145243.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:95179236 G>A maps to NM_005014.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:29622581 G>T maps to NM_002544.4 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr17:29622473 C>G maps to NM_002544.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:76814355 C>T maps to NM_006189.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:53081700 G>A maps to NM_004498.1 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:55103906 C>A maps to NM_004852.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:55103682 T>C maps to NM_004852.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:55103328 G>A maps to NM_004852.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:55103646 C>T maps to NM_004852.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:74079479 C>T maps to NM_001080507.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:193377301 A>T maps to NM_130837.2 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr3:193372740 A>T maps to NM_130837.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:193364865 A>G maps to NM_130837.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:193360810 G>A maps to NM_130837.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:46056783 C>T maps to NM_025136.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr19:46032613 C>A maps to NM_001017989.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:98105778 C>A maps to NM_033207.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:132306118 A>T maps to NM_002545.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:132307137 C>T maps to NM_002545.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:132812897 G>T maps to NM_002545.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:132290113 G>T maps to NM_002545.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:132399048 G>A maps to NM_002545.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:132812822 G>T maps to NM_002545.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:67417058 A>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:67283935 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:67283821 G>A did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr23:67430107 G>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:67413738 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:67426433 T>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:67433733 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:67421505 T>C did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:67426496 C>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:67518842 C>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:67284001 T>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:67283996 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:67333082 T>G did not map to a codon.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr23:67283860 A>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:67454406 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:67339134 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:145113226 C>G maps to ENST00000360660 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:145111104 C>A maps to ENST00000360660 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr8:145112602 T>A maps to ENST00000360660 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr8:145111990 C>A maps to ENST00000360660 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:145111987 G>A maps to ENST00000360660 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr8:145111641 C>A maps to ENST00000360660 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:153420134 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153421871 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153421946 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:153421992 C>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:153416197 C>T did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:153418557 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153421915 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153416359 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153420199 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153421924 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:153420158 T>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:153420088 G>C did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:153416309 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:153496192 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:153458998 G>A did not map to a codon.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr23:153496074 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:153496122 A>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:128415640 G>T maps to NM_001708.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr7:128414566 C>G maps to NM_001708.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:241767855 G>A maps to NM_014322.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:241757994 T>A did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:241803375 G>A maps to NM_014322.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:88416012 C>T maps to NM_001030015.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr10:88418409 C>A maps to NM_001030015.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr10:88416036 G>A maps to NM_001030015.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:47763199 C>A maps to ENST00000489301 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr6:47775960 T>A maps to ENST00000489301 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:47754281 C>T maps to ENST00000489301 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:47776035 C>A maps to ENST00000489301 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:47749819 T>A maps to ENST00000489301 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:47763236 G>T maps to ENST00000489301 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:29189408 C>T maps to NM_000911.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:54163342 G>T maps to NM_000912.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:54147394 G>A maps to NM_000912.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:54163444 G>C maps to NM_000912.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:54142117 G>T maps to NM_000912.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:54141958 T>C maps to NM_000912.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr8:54141988 G>A maps to NM_000912.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:54163420 C>A maps to NM_000912.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:54142069 G>T maps to NM_000912.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr8:54142270 G>A maps to NM_000912.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:62729792 C>T maps to NM_000913.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr20:62729692 C>A maps to NM_000913.3 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:62729489 C>A maps to NM_000913.3 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr20:62729935 C>T maps to NM_000913.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr20:62729199 G>T maps to NM_000913.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:62724237 G>T maps to NM_000913.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr20:62729779 G>T maps to NM_000913.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr20:62724084 C>G maps to NM_000913.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:154412189 C>T maps to NM_001145279.1 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:203472091 T>C maps to NM_014359.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:203472721 C>A maps to NM_014359.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:203468945 C>A maps to NM_014359.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:203472694 C>A maps to NM_014359.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:203465261 T>C maps to NM_014359.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:203472808 C>G maps to NM_014359.3 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:13175537 G>T maps to NM_021980.4 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr10:13154607 A>G maps to NM_021980.4 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6891128 C>T maps to NM_001004460.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:6891596 C>G maps to NM_001004460.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:6891884 C>T maps to NM_001004460.1 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:6891794 C>A maps to NM_001004460.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr11:6891878 C>T maps to NM_001004460.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:7960722 C>T maps to NM_001003745.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:7961051 G>A maps to NM_001003745.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr11:7960401 C>A maps to NM_001003745.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr11:7960521 G>A maps to NM_001003745.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr11:7960533 G>A maps to NM_001003745.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:7960286 G>A maps to NM_001003745.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:7960584 A>T maps to NM_001003745.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:7960703 G>T maps to NM_001003745.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr11:6898405 C>T maps to NM_207186.2 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:6898489 T>G maps to NM_207186.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:6897967 C>T maps to NM_207186.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:6898666 C>A maps to NM_207186.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:6898519 G>T maps to NM_207186.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:6866922 G>T maps to ENST00000379831 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:6866969 C>A maps to ENST00000379831 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:6867338 G>T maps to ENST00000379831 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6867089 C>A maps to ENST00000379831 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:6867697 G>A maps to ENST00000379831 W266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:6867386 T>A maps to ENST00000379831 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:6867095 C>G maps to ENST00000379831 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:6867159 C>T maps to ENST00000379831 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:7949816 G>A maps to NM_001004461.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:7950013 A>G maps to NM_001004461.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:7949837 A>T maps to NM_001004461.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:7949729 T>C maps to NM_001004461.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr11:7949930 A>G maps to NM_001004461.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:55615131 C>A maps to NM_001005280.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:55615377 G>A maps to NM_001005280.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:55615500 C>A maps to NM_001005280.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:55615704 G>T maps to NM_001005280.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:55615644 T>A maps to NM_001005280.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:48596694 G>A maps to NM_001004134.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr11:55735795 A>G maps to NM_001005491.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:55735246 G>A maps to NM_001005491.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:55735684 C>T maps to NM_001005491.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:55735297 G>A maps to NM_001005491.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:55735792 G>C maps to NM_001005491.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr11:55735852 G>T maps to NM_001005491.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr11:55735561 C>A maps to NM_001005491.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:55735034 C>G maps to NM_001005491.1 *302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:55735738 G>T maps to NM_001005491.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:29408119 G>T maps to NM_013941.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:29408139 C>T maps to NM_013941.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr6:29408310 C>A maps to NM_013941.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:29407911 C>A maps to NM_013941.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29407950 C>T maps to NM_013941.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:29407860 G>A maps to NM_013941.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:29407926 G>A maps to NM_013941.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:22102443 G>A maps to NM_001005466.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr14:22102533 G>T maps to NM_001005466.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr14:22102424 G>A maps to NM_001005466.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:22038044 G>A maps to NM_001005465.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:22037987 C>T maps to NM_001005465.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:22038359 G>T maps to NM_001005465.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123886969 C>G maps to NM_001004462.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:123886883 C>T maps to NM_001004462.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr11:123886667 C>A maps to NM_001004462.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:123886334 C>A maps to ENST00000375021 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123909483 C>A maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr11:123909324 C>T maps to NM_001004463.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr11:123909360 G>A maps to NM_001004463.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:123909489 A>T maps to NM_001004463.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123909453 G>C maps to NM_001004463.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123909147 G>T maps to NM_001004463.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr11:123908790 T>C maps to NM_001004463.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:123909087 C>T maps to NM_001004463.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:123908877 C>G maps to NM_001004463.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:123908952 G>A maps to NM_001004463.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:123909114 G>T maps to NM_001004463.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:123908877 C>A maps to NM_001004463.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:123900934 T>G maps to ENST00000375021 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:123900412 C>T maps to NM_001004464.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:123900427 C>A maps to NM_001004464.1 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:123901144 C>T maps to ENST00000375021 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:123900637 T>C maps to NM_001004464.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:123900695 C>T maps to ENST00000375021 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123900721 C>A maps to ENST00000375021 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:123900547 T>G maps to NM_001004464.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:123900952 C>A maps to ENST00000375021 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:123900898 C>T maps to ENST00000375021 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:123900847 C>A maps to ENST00000375021 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:123901126 T>A maps to ENST00000375021 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:123894264 C>A maps to NM_001001953.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:123893725 A>T maps to NM_001001953.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:123894339 G>T maps to NM_001001953.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:123894261 G>T maps to NM_001001953.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:123894621 G>T maps to NM_001001953.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:123894321 C>T maps to NM_001001953.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:123894339 G>T maps to NM_001001953.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:123894351 C>T maps to NM_001001953.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:123894444 C>A maps to NM_001001953.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:15918232 G>A maps to NM_013940.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:15918727 C>A maps to NM_013940.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:15839101 C>T maps to NM_013939.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15838972 G>T maps to NM_013939.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:15839524 C>T maps to NM_013939.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:15839755 C>G maps to NM_013939.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:15852501 T>C maps to NM_013938.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:16059889 C>T maps to NM_001004465.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:16060155 C>A maps to NM_001004465.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:15904893 C>T maps to NM_001004466.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:15905245 C>T maps to NM_001004466.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:15905664 G>T maps to NM_001004466.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:15904956 G>C maps to NM_001004466.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:159410294 C>T maps to NM_012351.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:159410378 C>A maps to NM_012351.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:159410333 C>A maps to NM_012351.2 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:159409907 C>T maps to NM_012351.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:159410228 T>C maps to NM_012351.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:159410063 A>T maps to NM_012351.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:159283597 A>G maps to NM_001004467.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:159283996 C>A maps to NM_001004467.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:159283978 G>T maps to NM_001004467.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:159284104 C>A maps to NM_001004467.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:159284047 T>G maps to NM_001004467.1 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:159284173 G>A maps to NM_001004467.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:159283531 C>G maps to NM_001004467.1 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:159283786 G>A maps to NM_001004467.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:159505254 G>T maps to NM_001004469.1 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:159505014 C>T maps to NM_001004469.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158435416 G>A maps to NM_001004473.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:158435354 G>T maps to NM_001004473.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr1:158436190 C>A maps to NM_001004473.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158435884 C>T maps to NM_001004473.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:158436016 C>A maps to NM_001004473.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:158436004 C>T maps to NM_001004473.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr1:158436013 C>A maps to NM_001004473.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:158435683 C>T maps to NM_001004473.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr1:158435440 C>T maps to NM_001004473.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:158435461 C>T maps to NM_001004473.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:158435748 C>A maps to NM_001004473.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158389726 G>A maps to NM_001004476.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:158390596 C>A maps to NM_001004476.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:158390611 G>A maps to NM_001004476.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158390620 G>T maps to NM_001004476.1 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:56031202 G>T maps to NM_206899.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr12:56030836 C>T maps to NM_206899.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:56030944 C>T maps to NM_206899.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:57996203 G>T maps to NM_001004471.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:57995885 G>T maps to NM_001004471.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:57996245 G>C maps to NM_001004471.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:57995948 C>A maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:57995558 C>A maps to NM_001004471.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:57996272 A>G maps to NM_001004471.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:57996110 G>T maps to NM_001004471.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:57995948 C>T maps to NM_001004471.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr11:57996155 A>G maps to NM_001004471.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:57995426 C>T maps to NM_001004471.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:158450420 G>T maps to NM_001004472.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:158450320 G>C maps to NM_001004472.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158450005 C>A maps to NM_001004472.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:158450125 C>G maps to NM_001004472.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158450116 G>T maps to NM_001004472.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158450077 G>A maps to NM_001004472.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:158450024 C>T maps to NM_001004472.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:158450524 T>C maps to NM_001004472.1 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:158449828 G>T maps to NM_001004472.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:158450449 C>A maps to NM_001004472.1 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:123847657 G>C maps to NM_001004474.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:123848122 G>T maps to NM_001004474.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:123848356 C>T maps to NM_001004474.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:123847627 G>T maps to NM_001004474.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:123847567 G>A maps to NM_001004474.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:123847564 G>T maps to NM_001004474.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:123847693 G>A maps to NM_001004474.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:123847681 C>T maps to NM_001004474.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:123847663 G>T maps to NM_001004474.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158368993 G>T maps to NM_001004475.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:158368647 G>A maps to NM_001004475.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:158368638 C>A maps to NM_001004475.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:158369009 G>A maps to NM_001004475.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:158368635 T>A maps to NM_001004475.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:158369175 C>A maps to NM_001004475.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:158369193 C>G maps to NM_001004475.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59481231 C>A maps to NM_001005324.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr11:59480649 C>A maps to NM_001005324.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:59480964 G>T maps to NM_001005324.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:59480877 T>A maps to NM_001005324.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:58035219 C>A maps to NM_207374.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:58034628 G>T maps to NM_207374.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:58034595 G>T maps to NM_207374.3 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:58034412 C>A maps to NM_207374.3 *306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:158549248 T>C maps to NM_001004477.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:158549587 A>G maps to NM_001004477.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:158549194 G>T maps to NM_001004477.1 C165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr1:158549494 A>C maps to NM_001004477.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:158548786 G>A maps to NM_001004477.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:158549134 G>A maps to NM_001004477.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:158549266 G>T maps to NM_001004477.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:158576518 T>C maps to NM_001004478.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:158576833 C>T maps to NM_001004478.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:158576545 A>G maps to NM_001004478.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr1:158576752 G>A maps to NM_001004478.1 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:158576527 G>A maps to NM_001004478.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158576327 C>T maps to NM_001004478.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158576251 C>A maps to NM_001004478.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:158576566 C>T maps to NM_001004478.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:158577109 T>C maps to NM_001004478.1 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:158576617 C>T maps to NM_001004478.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:158577001 G>A maps to NM_001004478.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr1:158577046 T>A maps to NM_001004478.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29395094 T>A maps to NM_013937.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29395247 G>T maps to NM_013937.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:29394971 G>T maps to NM_013937.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr6:29394500 G>T maps to NM_013937.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:20666363 C>A maps to NM_001005503.1 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:20665697 C>G maps to NM_001005503.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr14:20666363 C>T maps to NM_001005503.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:20665718 G>T maps to NM_001005503.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr14:20665895 C>A maps to NM_001005503.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr22:16449093 C>T maps to NM_001005239.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr22:16449113 C>A maps to NM_001005239.1 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr22:16449669 G>T maps to NM_001005239.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:19378075 A>C maps to NM_001013354.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:19378078 G>T maps to NM_001013354.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:19378072 C>A maps to NM_001013354.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr14:19378025 T>C maps to NM_001013354.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:20711257 C>G maps to NM_001004479.1 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:20711192 C>A maps to NM_001004479.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:20692095 C>A maps to NM_001004480.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20691978 T>C maps to NM_001004480.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr14:20692791 T>C maps to NM_001004480.1 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20692662 G>C maps to NM_001004480.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:20692356 C>A maps to NM_001004480.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20692479 A>T maps to NM_001004480.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr14:20692140 C>A maps to NM_001004480.1 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:248004694 G>A maps to NM_001001959.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:248004583 G>T maps to NM_001001959.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr1:248004355 G>T maps to NM_001001959.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:248004460 A>C maps to NM_001001959.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:248004379 G>T maps to NM_001001959.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:248004436 G>T maps to NM_001001959.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:248005038 G>A maps to NM_001001959.1 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:248004726 G>A maps to NM_001001959.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:248004547 G>T maps to NM_001001959.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:248004940 C>G maps to NM_001001959.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:29364670 C>A maps to NM_013936.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:29365228 T>C maps to NM_013936.3 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:29365234 T>A maps to NM_013936.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr6:29364790 G>T maps to NM_013936.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr6:29365366 G>A maps to NM_013936.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:29343003 G>A maps to ENST00000396806 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:29343052 G>A maps to ENST00000396806 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:29342227 G>T maps to NM_030959.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:45799762 C>A maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:45798998 A>T maps to NM_001004297.2 L291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr10:45799859 C>T maps to NM_001004297.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:45799069 G>T maps to NM_001004297.2 C267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:45799705 C>A maps to NM_001004297.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:45799501 C>A maps to NM_001004297.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:45799822 G>A maps to NM_001004297.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:107367887 G>A maps to NM_001004481.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:107367419 C>A maps to NM_001004481.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:107367233 G>A maps to NM_001004481.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr9:107367887 G>T maps to NM_001004481.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:107298632 C>A maps to NM_001001961.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr9:107298914 G>T maps to NM_001001961.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:107288830 G>A maps to NM_001001919.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:107289307 G>A maps to NM_001001919.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:107288800 C>T maps to NM_001001919.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:107289316 G>T maps to NM_001001919.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr9:107289058 C>A maps to NM_001001919.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:107361214 T>G maps to NM_001004482.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:107361001 C>A maps to NM_001004482.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:107331852 C>T maps to NM_001004483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr9:107332203 T>C maps to NM_001004483.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:107331795 C>A maps to NM_001004483.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332059 G>C maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:107332125 G>A maps to NM_001004483.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:107332059 G>T maps to NM_001004483.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:107331900 T>G maps to NM_001004483.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr9:107331759 T>A maps to NM_001004483.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:107331999 C>A maps to NM_001004483.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107380044 C>G maps to NM_001001956.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:107379867 G>A maps to NM_001001956.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:107379807 G>C maps to NM_001001956.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr9:107379837 G>T maps to NM_001001956.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:107380296 C>A maps to NM_001001956.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:107457136 C>A maps to NM_001004484.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr9:107457304 T>A maps to NM_001004484.1 C201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr9:107457178 C>A maps to NM_001004484.1 C159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:107267268 A>G maps to NM_001004485.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:107266854 C>T maps to NM_001004485.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:107267231 C>A maps to NM_001004485.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:107266860 C>T maps to NM_001004485.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr9:107267409 C>A maps to NM_001004485.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:247836100 G>T maps to NM_001005487.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:247836344 C>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr1:247836181 C>A maps to NM_001005487.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr1:247835491 C>G maps to NM_001005487.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:247835437 A>G maps to NM_001005487.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:247835509 C>A maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:247835785 A>G maps to NM_001005487.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr1:247836208 G>A maps to NM_001005487.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:247836181 C>A maps to NM_001005487.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:247835485 C>A maps to NM_001005487.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:247835950 A>G maps to NM_001005487.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:130678153 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:130678718 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:130678560 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:130678917 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:130678903 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:130678093 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:130678890 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:130678285 A>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:130678553 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:130678917 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:130678458 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:35869684 G>A maps to NM_001004487.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:35869735 G>A maps to NM_001004487.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:35869786 G>T maps to NM_001004487.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:35869665 G>A maps to NM_001004487.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:35869978 G>A maps to NM_001004487.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:247978920 C>T maps to NM_001001966.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247978137 C>T maps to NM_001001966.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247978623 C>T maps to NM_001001966.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:247978146 C>T maps to NM_001001966.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:247978212 C>A maps to NM_001001966.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:247978692 G>A maps to NM_001001966.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:247978983 A>G maps to NM_001001966.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:247978599 A>T maps to NM_001001966.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:248512354 G>C maps to NM_001001918.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248512807 G>T maps to NM_001001918.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248512219 C>T maps to NM_001001918.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:248512711 C>A maps to NM_001001918.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248512966 G>T maps to NM_001001918.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248512747 C>A maps to NM_001001918.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:248513001 C>A maps to NM_001001918.1 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:248512311 C>G maps to NM_001001918.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:248512633 T>G maps to NM_001001918.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr1:248512609 C>T maps to NM_001001918.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:248512624 G>A maps to NM_001001918.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:248512672 C>A maps to NM_001001918.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:248845196 C>A maps to NM_001004734.1 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:248844993 C>T maps to NM_001004734.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248845176 T>A maps to NM_001004734.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr1:248845464 G>T maps to NM_001004734.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:248845182 C>T maps to NM_001004734.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:248844882 G>A maps to NM_001004734.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:248845497 C>T maps to NM_001004734.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:248845368 G>T maps to NM_001004734.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:248844747 G>T maps to NM_001004734.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:248845569 C>G maps to NM_001004734.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:248845026 T>C maps to NM_001004734.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr6:29274771 C>T maps to NM_030946.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:3119639 C>A maps to NM_014565.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:3119387 C>A maps to NM_014565.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:3119336 T>A maps to NM_014565.2 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr17:3119741 C>A maps to NM_014565.2 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:3101420 C>T maps to NM_012352.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr17:3101508 C>T maps to NM_012352.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:3100943 C>T maps to NM_012352.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:3100857 G>T maps to NM_012352.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr9:125391040 G>A maps to NM_001004450.1 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:125391436 C>A maps to NM_001004450.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:247921321 G>A maps to NM_012353.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247921240 G>T maps to NM_012353.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:247920883 G>T maps to NM_012353.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:247921474 G>T maps to NM_012353.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:247921159 A>G maps to NM_012353.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:247921053 C>A maps to NM_012353.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:247921357 C>T maps to NM_012353.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:247921081 C>A maps to NM_012353.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:247920988 G>T maps to NM_012353.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:247921009 G>T maps to NM_012353.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:247921333 C>A maps to NM_012353.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:2995603 G>C maps to NM_002548.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr17:2996215 C>A maps to NM_002548.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:3301515 G>T maps to NM_003553.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:3301587 G>T maps to NM_003553.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:3301407 G>A maps to NM_003553.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:3336373 G>C maps to NM_003554.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3336583 G>T maps to NM_003554.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:3337039 C>T maps to NM_003554.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:3255073 G>T maps to NM_012360.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:3254992 C>A maps to NM_012360.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:3030713 G>T maps to ENST00000381953 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:15198124 G>A maps to NM_001004713.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:125239269 A>G maps to NM_001004451.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:125240058 G>A maps to NM_001004451.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:125273574 G>A maps to ENST00000444856 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:125273565 C>A maps to ENST00000444856 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:125273175 G>T maps to ENST00000444856 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:125273130 C>A maps to ENST00000444856 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:125273661 C>G maps to NM_054107.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:125282273 G>C maps to NM_001004452.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr9:125282003 T>C maps to NM_001004452.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr9:125281712 A>G maps to ENST00000444856 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr9:125562400 C>A did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr9:125562913 T>G maps to NM_080859.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr9:125563279 C>T maps to NM_080859.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr9:125562994 G>A maps to NM_080859.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr9:125424279 G>T maps to ENST00000373686 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:125424134 G>A maps to ENST00000373686 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr9:125424272 T>C maps to ENST00000373686 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:125437680 C>T maps to NM_001005234.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:125486741 G>A maps to NM_001005235.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:125486954 C>A maps to NM_001005235.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:125486684 A>G maps to NM_001005235.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:125486717 C>A maps to NM_001005235.1 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr9:125486610 C>T maps to NM_001005235.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:125486858 G>A maps to NM_001005235.1 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:125512599 G>A maps to ENST00000373684 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:125512434 C>A maps to ENST00000373684 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:125330687 C>T maps to NM_001004454.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:125330210 G>T maps to NM_001004454.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:9204054 C>T maps to ENST00000305465 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr19:9204690 C>T maps to ENST00000305465 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:9204066 C>T maps to ENST00000305465 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:9204165 G>T maps to ENST00000305465 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:9204720 C>A maps to ENST00000305465 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:125289308 G>A maps to ENST00000359439 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:125289494 G>A maps to ENST00000359439 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr9:125288810 G>A maps to ENST00000359439 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:125288840 G>A maps to ENST00000359439 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr9:125288753 A>T maps to ENST00000359439 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:125289071 A>G maps to ENST00000359439 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:125316158 C>A maps to NM_001004457.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr9:125315564 G>A maps to NM_001004457.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr9:125316137 G>A maps to NM_001004457.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr9:125315717 C>T maps to NM_001004457.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:57982974 T>C maps to NM_001004458.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:57983115 C>G maps to NM_001004458.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:57982308 C>T maps to NM_001004458.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr11:57982240 C>T maps to NM_001004458.1 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:57970963 G>T maps to NM_001004459.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:57971443 G>A maps to NM_001004459.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:57971020 C>G maps to NM_001004459.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:57970917 C>A maps to NM_001004459.1 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:57970918 C>T maps to NM_001004459.1 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:57970939 G>A maps to NM_001004459.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:57970676 C>G maps to NM_001004459.1 *326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:57970804 A>T maps to NM_001004459.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:57970864 C>A maps to NM_001004459.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:144015468 C>A maps to NM_001005287.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143792895 C>A maps to NM_001004135.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:143792733 T>C maps to NM_001004135.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:143792514 G>A maps to NM_001004135.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:143793021 C>A maps to NM_001004135.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr7:143792934 C>A maps to NM_001004135.1 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:143792487 C>T maps to NM_001004135.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:143792832 C>T maps to NM_001004135.1 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr7:143826246 G>A maps to NM_001001659.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:143826999 T>C maps to NM_001001659.1 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:143826987 C>A maps to NM_001001659.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr7:143826870 C>A maps to NM_001001659.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:143807166 G>A maps to NM_001005480.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:143807142 G>T maps to NM_001005480.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:143771993 C>T maps to NM_001004488.1 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:143771764 A>T maps to NM_001004488.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr7:143771563 C>A maps to NM_001004488.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:143771506 G>A maps to NM_001004488.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:143771332 C>A maps to NM_001004488.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:143771563 C>G maps to NM_001004488.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:143747931 C>T maps to NM_012365.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr7:143748000 T>A maps to NM_012365.1 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:143748126 C>G maps to NM_012365.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:6806426 C>A maps to NM_001004489.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:6806427 C>A maps to NM_001004489.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:6806978 C>A maps to NM_001004489.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:6806723 A>G maps to NM_001004489.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr11:6806453 G>T maps to NM_001004489.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr11:6807053 C>A maps to NM_001004489.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:6807218 G>T maps to NM_001004489.2 *317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:6806405 C>A maps to NM_001004489.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6789843 C>A maps to NM_001004490.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr11:6789735 C>A maps to NM_001004490.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:6789237 C>G maps to NM_001004490.1 *317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:6789861 G>A maps to NM_001004490.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:6790028 G>T maps to NM_001004490.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129412 G>A maps to NM_001004491.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248129469 C>T maps to NM_001004491.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248128875 C>A maps to NM_001004491.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248128866 C>A maps to NM_001004491.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248128911 G>T maps to NM_001004491.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248129451 C>A maps to NM_001004491.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr1:248129008 G>T maps to NM_001004491.1 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:248128776 C>A maps to NM_001004491.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:248129043 C>T maps to NM_001004491.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:248129013 C>A maps to NM_001004491.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:248128812 G>T maps to NM_001004491.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:248128905 C>A maps to NM_001004491.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:248128812 G>T maps to NM_001004491.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:248129592 G>A maps to NM_001004491.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:248128656 C>A maps to NM_001004491.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:248129574 G>A maps to NM_001004491.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:247614729 C>A maps to NM_001004492.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:247614654 G>A maps to NM_001004492.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:247615008 G>T maps to NM_001004492.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:247614600 T>A maps to NM_001004492.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:247614513 T>A maps to NM_001004492.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:27879545 C>T maps to NM_033057.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:27879653 G>T maps to NM_033057.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:29054920 G>A maps to NM_001005226.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29054161 G>A maps to NM_001005226.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:29054812 G>T maps to NM_001005226.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:29054161 G>A maps to NM_001005226.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:29054629 A>G maps to NM_001005226.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:27925332 G>T maps to NM_012367.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:27925440 C>A maps to NM_012367.1 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:27925656 C>A maps to NM_012367.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:27925275 C>A maps to NM_012367.1 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:3406338 C>T maps to NM_012368.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr16:3406350 C>T maps to NM_012368.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:247695441 G>A maps to NM_198074.4 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247695435 G>T maps to NM_198074.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247694973 G>A maps to NM_198074.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:247695585 C>G maps to NM_198074.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:247695357 C>T maps to NM_198074.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:247695143 G>T maps to NM_198074.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:247695120 T>A maps to NM_198074.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:247695564 C>A maps to NM_198074.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:247695306 C>A maps to NM_198074.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:247695609 G>A maps to NM_198074.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:247695459 G>C maps to NM_198074.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:247695645 G>T maps to NM_198074.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:247695552 C>T maps to NM_198074.4 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:247694868 G>T maps to NM_198074.4 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:247695801 T>A maps to NM_198074.4 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:247695732 G>T maps to NM_198074.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:247694973 G>T maps to NM_198074.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6913518 G>A maps to NM_003700.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:6913671 C>A maps to NM_003700.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:6913155 G>T maps to NM_003700.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:6912996 G>A maps to NM_003700.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr11:6942267 G>A maps to NM_001004684.1 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:6942648 T>C maps to NM_001004684.1 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6942636 C>A maps to NM_001004684.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr11:6942343 C>T maps to NM_001004684.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:6943060 C>T maps to NM_001004684.1 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr11:6942528 T>C maps to NM_001004684.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:6942603 G>T maps to NM_001004684.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:6942411 C>A maps to NM_001004684.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr11:6942930 T>G maps to NM_001004684.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:143657782 G>T maps to NM_012369.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:143657536 G>C maps to NM_012369.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:143657161 C>A maps to NM_012369.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:143657206 G>T maps to NM_012369.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:143657797 C>A maps to NM_012369.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:143657689 A>T maps to NM_012369.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:143633080 C>T maps to NM_001004685.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:143632386 G>A maps to NM_001004685.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:143632996 C>A maps to NM_001004685.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:143633044 G>C maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:143632715 C>T maps to NM_001004685.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr7:143632558 C>A maps to NM_001004685.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:247751879 C>A maps to NM_001001915.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:247752014 G>T maps to NM_001001915.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247752137 C>A maps to NM_001001915.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:247752434 C>A maps to NM_001001915.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247751823 G>T maps to NM_001001915.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:247752426 G>T maps to NM_001001915.1 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:247752073 T>A maps to NM_001001915.1 L138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:247752413 C>T maps to NM_001001915.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247751822 G>T maps to NM_001001915.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247752092 C>A maps to NM_001001915.1 C144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:247752011 C>A maps to NM_001001915.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:247752173 C>T maps to NM_001001915.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:247751891 C>A maps to NM_001001915.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:247752242 C>T maps to NM_001001915.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:247768886 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:247769735 C>A maps to NM_001001914.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:247769129 C>T maps to NM_001001914.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:247769355 C>T maps to NM_001001914.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:247769699 G>A maps to NM_001001914.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:247769669 A>G maps to NM_001001914.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:247769066 C>G maps to NM_001001914.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:247768910 C>A maps to NM_001001914.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr1:247769714 C>A maps to NM_001001914.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:247768922 C>T maps to NM_001001914.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:247768979 C>G maps to NM_001001914.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:247768913 A>C maps to NM_001001914.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:247769093 G>T maps to NM_001001914.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:247769537 C>A maps to NM_001001914.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248685896 A>G maps to NM_001013355.1 *317W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:248684958 C>A maps to NM_001013355.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248685078 C>A maps to NM_001013355.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248685462 C>T maps to NM_001013355.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248685279 G>A maps to NM_001013355.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248685219 C>A maps to NM_001013355.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:248685328 C>A maps to NM_001013355.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:248685321 T>G maps to NM_001013355.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:248684953 G>T maps to NM_001013355.1 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:248685663 G>A maps to NM_001013355.1 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:248685672 G>T maps to NM_001013355.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:248685484 G>T maps to NM_001013355.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:248685146 C>A maps to NM_001013355.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248685603 C>T maps to NM_001013355.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248685705 G>T maps to NM_001013355.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:248685228 C>A maps to NM_001013355.1 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr6:29429911 G>T maps to NM_030883.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr6:29429827 A>C maps to NM_030883.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:29430206 C>T maps to NM_030883.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29555741 A>G maps to NM_007160.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:29555765 C>T maps to NM_007160.3 F15F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-6712-01A-11D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:29556083 C>T maps to NM_007160.3 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr6:29556027 C>T maps to NM_007160.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:29141762 G>C maps to NM_030905.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:29142164 C>G maps to NM_030905.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:29141789 T>C maps to NM_030905.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:29142068 T>G maps to NM_030905.2 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr6:29141531 G>A maps to NM_030905.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr6:29141462 A>G maps to NM_030905.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:29079940 G>T maps to NM_001005216.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:29080182 T>A maps to NM_001005216.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29080005 A>T maps to NM_001005216.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:29080107 G>T maps to NM_001005216.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr9:114090197 G>A maps to ENST00000374428 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:114090555 G>C maps to ENST00000374428 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:114090286 G>T maps to ENST00000374428 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:248263534 C>A maps to NM_175911.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248263030 C>A maps to NM_175911.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:248262961 A>T maps to NM_175911.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:248263129 G>T maps to NM_175911.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:248263048 C>A maps to NM_175911.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248262730 C>A maps to NM_175911.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248263099 G>T maps to NM_175911.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:248263255 C>G maps to NM_175911.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:248262793 G>C maps to NM_175911.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:248262904 C>A maps to NM_175911.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:248263054 C>A maps to NM_175911.2 C126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:248262884 C>T maps to NM_175911.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr1:248263324 C>A maps to NM_175911.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:248262756 T>A maps to NM_175911.2 L27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:248262964 T>C maps to NM_175911.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:248263417 G>A maps to NM_175911.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:248263108 T>A maps to NM_175911.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:248263132 C>A maps to NM_175911.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:248262904 C>A maps to NM_175911.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:248263153 A>T maps to NM_175911.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:248263327 T>C maps to NM_175911.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:248263162 C>A maps to NM_175911.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:248201628 A>T maps to NM_001004686.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248202222 C>A maps to NM_001004686.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:248201901 G>T maps to NM_001004686.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:248201697 C>A maps to NM_001004686.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:248202303 T>G maps to NM_001004686.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:248202246 C>G maps to NM_001004686.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:248201637 C>A maps to NM_001004686.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:248224138 C>T maps to NM_001004687.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248224540 G>C maps to NM_001004687.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr1:248224699 C>A maps to NM_001004687.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:248224408 G>A maps to NM_001004687.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:248224543 C>A maps to NM_001004687.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248112716 G>C maps to NM_001001963.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:248113082 C>T maps to NM_001001963.1 C308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248112896 A>T maps to NM_001001963.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:248112647 C>T maps to NM_001001963.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:248113085 T>G maps to NM_001001963.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:248112404 T>A maps to NM_001001963.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:248112557 C>A maps to NM_001001963.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:248112524 C>T maps to NM_001001963.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:248112719 C>A maps to NM_001001963.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:248112302 C>A maps to NM_001001963.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:248343316 C>A maps to NM_001004688.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:248343685 C>A maps to NM_001004688.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248344003 G>T maps to NM_001004688.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:248343379 C>A maps to NM_001004688.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:248343824 G>T maps to NM_001004688.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:248343772 C>A maps to NM_001004688.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:248343685 C>A maps to NM_001004688.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:248343418 C>A maps to NM_001004688.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:248344003 G>C maps to NM_001004688.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:248344043 G>T maps to NM_001004688.1 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248343445 C>G maps to NM_001004688.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:248344072 C>T maps to NM_001004688.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:248343811 C>A maps to NM_001004688.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:248343361 G>T maps to NM_001004688.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:248343514 C>T maps to NM_001004688.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:248344223 G>T maps to NM_001004688.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:248343691 C>T maps to NM_001004688.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:248344102 G>A maps to NM_001004688.1 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:248367103 C>A maps to NM_001004689.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248366413 G>T maps to NM_001004689.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:248366863 C>T maps to NM_001004689.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:248366685 C>A maps to NM_001004689.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:248367062 G>T maps to NM_001004689.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248366413 G>T maps to NM_001004689.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:248367166 C>A maps to NM_001004689.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:248366542 C>A maps to NM_001004689.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:248367019 C>A maps to NM_001004689.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:248366833 T>C maps to NM_001004689.1 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:248366944 A>T maps to NM_001004689.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:248366749 C>T maps to NM_001004689.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248366566 G>C maps to NM_001004689.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:248402274 G>T maps to NM_017504.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:248402275 G>T maps to NM_017504.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:248402508 T>C maps to NM_017504.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:248402652 T>C maps to NM_017504.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248402586 T>A maps to NM_017504.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:248402298 C>A maps to NM_017504.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248402422 C>T maps to NM_017504.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:248402385 G>A maps to NM_017504.1 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:248402783 T>A maps to NM_017504.1 L185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:248402643 G>T maps to NM_017504.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:248309177 T>C maps to NM_001004690.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:248308448 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:248308877 T>A maps to NM_001004690.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:248308454 A>G maps to NM_001004690.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr1:248308637 C>A maps to NM_001004690.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr1:248308721 C>G maps to NM_001004690.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:248309246 C>A maps to NM_001004690.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:248308607 C>G maps to NM_001004690.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:248308962 C>A maps to NM_001004690.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:248308514 C>A maps to NM_001004690.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr1:248308973 C>A maps to NM_001004690.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:248308490 C>G maps to NM_001004690.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:248308685 C>A maps to NM_001004690.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:248309285 C>A maps to NM_001004690.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:248487666 G>C maps to NM_001004691.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248487860 C>A maps to NM_001004691.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248487006 G>A maps to NM_001004691.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248487613 A>T maps to NM_001004691.1 L86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:248486946 G>T maps to NM_001004691.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248487471 G>T maps to NM_001004691.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:248487648 G>A maps to NM_001004691.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:248487597 G>T maps to NM_001004691.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:248487432 G>T maps to NM_001004691.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:248487780 C>A maps to NM_001004691.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:248487522 A>G maps to NM_001004691.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:248487824 C>A maps to NM_001004691.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:248487825 C>A maps to NM_001004691.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:35957690 C>A maps to NM_019897.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248569765 T>A maps to NM_030904.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:248569630 C>G maps to NM_030904.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:248569299 G>A maps to NM_030904.1 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:248570314 C>A maps to NM_030904.1 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr1:248570293 C>A maps to NM_030904.1 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:248569819 C>A maps to NM_030904.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:248569429 C>A maps to NM_030904.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:248569678 G>C maps to NM_030904.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248569918 C>A maps to NM_030904.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:248569558 A>G maps to NM_030904.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248569420 A>G maps to NM_030904.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248756857 A>T maps to NM_001004693.1 L71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248756475 G>A maps to NM_001004693.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:248756712 G>T maps to NM_001004693.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:248756460 A>G maps to NM_001004693.1 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr1:248756337 G>A maps to NM_001004693.1 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248790327 C>A maps to NM_001001964.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:248789556 G>A maps to NM_001001964.1 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:248790267 G>T maps to NM_001001964.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248789924 G>T maps to NM_001001964.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr1:248790050 G>A maps to NM_001001964.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:248789952 G>T maps to NM_001001964.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:248790324 G>T maps to NM_001001964.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248789790 A>T maps to NM_001001964.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr1:248790194 G>A maps to NM_001001964.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:248790324 G>T maps to NM_001001964.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:248790366 G>T maps to NM_001001964.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:248458256 G>T maps to NM_001004692.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248458256 G>T maps to NM_001004692.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458340 G>A maps to NM_001004692.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:248458343 G>C maps to NM_001004692.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:248458397 G>T maps to NM_001004692.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:248457965 C>A maps to NM_001004692.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr1:248458124 A>G maps to NM_001004692.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:248458100 G>T maps to NM_001004692.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:248458340 G>T maps to NM_001004692.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:248458292 G>A maps to NM_001004692.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:248458790 C>A maps to NM_001004692.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:248458160 A>G maps to NM_001004692.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:248458304 G>C maps to NM_001004692.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:248616139 C>A maps to NM_001004136.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:248616383 C>T maps to NM_001004136.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248616316 C>A maps to NM_001004136.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:248616355 C>G maps to NM_001004136.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:248616757 G>A maps to NM_001004136.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:248616247 C>A maps to NM_001004136.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:248616202 C>A maps to NM_001004136.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:248616139 C>A maps to NM_001004136.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:248617030 C>A maps to NM_001004136.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:248616418 C>A maps to NM_001004136.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:248616712 G>T maps to NM_001004136.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:248616425 G>T maps to NM_001004136.1 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:248616418 C>A maps to NM_001004136.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:248617042 C>T maps to NM_001004136.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:248813330 G>C maps to NM_001001824.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:248813366 A>G maps to NM_001001824.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248813465 G>T maps to NM_001001824.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:248813770 T>A maps to NM_001001824.1 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr1:248814181 C>A maps to NM_001001824.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:248813378 C>T maps to NM_001001824.1 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:248813816 G>T maps to NM_001001824.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:248814053 G>C maps to NM_001001824.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248813507 A>T maps to NM_001001824.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:248637391 C>A maps to NM_001005495.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:248637271 C>A maps to NM_001005495.1 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:248637469 T>A maps to NM_001005495.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:248637256 G>T maps to NM_001005495.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr1:248637203 G>T maps to NM_001005495.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr1:248637421 C>T maps to NM_001005495.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:248637457 C>T maps to NM_001005495.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:248637244 C>A maps to NM_001005495.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:248637535 C>A maps to NM_001005495.1 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:248637571 G>A maps to NM_001005495.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:248636962 C>T maps to NM_001005495.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:248637271 C>A maps to NM_001005495.1 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:248436682 G>T maps to NM_001004695.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:248436633 G>T maps to NM_001004695.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:248436330 G>T maps to NM_001004695.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:248436672 G>A maps to NM_001004695.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:248436682 G>T maps to NM_001004695.1 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248436750 C>A maps to NM_001004695.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:248436888 C>G maps to NM_001004695.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:248436657 G>A maps to NM_001004695.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:248436498 C>A maps to NM_001004695.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:248436765 G>T maps to NM_001004695.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:248436791 C>A maps to NM_001004695.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:248436336 G>T maps to NM_001004695.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:248437020 G>T maps to NM_001004695.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:248437044 G>T maps to NM_001004695.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:248737449 G>A maps to NM_001001821.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:248738046 C>A maps to NM_001001821.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:248737410 G>A maps to NM_001001821.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:248737461 G>A maps to NM_001001821.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:248738034 A>T maps to NM_001001821.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:248737761 C>T maps to NM_001001821.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:248737470 G>A maps to NM_001001821.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:248737692 G>T maps to NM_001001821.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:248737431 G>A maps to NM_001001821.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:248525428 C>T maps to NM_001004696.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:248525346 C>A maps to NM_001004696.1 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:248525016 C>A maps to NM_001004696.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:248525193 G>A maps to NM_001004696.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:248525592 C>A maps to NM_001004696.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:248525529 A>G maps to NM_001004696.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:248525577 C>G maps to NM_001004696.1 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:248524935 G>A maps to NM_001004696.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:248651963 C>A maps to NM_001004697.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:248651987 G>T maps to NM_001004697.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:248550950 C>T maps to NM_001005471.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:248551472 C>A maps to NM_001005471.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:248551127 C>A maps to NM_001005471.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:248551196 C>A maps to NM_001005471.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248551229 T>C maps to NM_001005471.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:248551235 G>T maps to NM_001005471.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:248551250 G>C maps to NM_001005471.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:248084348 C>T maps to NM_001005522.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:248084531 G>T maps to NM_001005522.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:248085098 C>A maps to NM_001005522.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:248084414 C>T maps to NM_001005522.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:180582494 T>C maps to NM_206880.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr5:180582664 C>T maps to NM_206880.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:180582115 C>T maps to NM_206880.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:180581965 C>A maps to NM_206880.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:180582568 C>G maps to NM_206880.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:29012466 G>A maps to NM_030903.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:29012091 C>A maps to NM_030903.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:29012676 G>A maps to NM_030903.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:248059190 C>T maps to NM_001001957.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059202 G>T maps to NM_001001957.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:248059496 G>T maps to NM_001001957.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:248059046 C>A maps to NM_001001957.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:248058992 C>A maps to NM_001001957.2 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:248059388 C>A maps to NM_001001957.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:248059118 C>A maps to NM_001001957.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:248059283 C>A maps to NM_001001957.2 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:248059634 C>A maps to NM_001001957.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:248059652 C>A maps to NM_001001957.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:248059550 T>A maps to NM_001001957.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:248059298 C>T maps to NM_001001957.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:248059439 G>A maps to NM_001001957.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:248059610 C>A maps to NM_001001957.2 C241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:248059674 G>T maps to NM_001001957.2 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:248059634 C>A maps to NM_001001957.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:248059202 G>T maps to NM_001001957.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:248059292 C>A maps to NM_001001957.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:248059127 G>A maps to NM_001001957.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:248059022 C>A maps to NM_001001957.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:248059311 C>A maps to NM_001001957.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:248059388 C>A maps to NM_001001957.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr1:248059388 C>G maps to NM_001001957.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:248059169 C>A maps to NM_001001957.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:247654701 C>G maps to NM_001004698.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:247655349 G>C maps to NM_001004698.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:247654602 C>A maps to NM_001004698.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:247655346 G>T maps to NM_001004698.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:247654578 C>A maps to NM_001004698.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:247654726 C>T maps to NM_001004698.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:247655049 T>A maps to NM_001004698.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:247655149 C>T maps to NM_001004698.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:180166173 G>A maps to NM_001001657.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:180166827 G>T maps to NM_001001657.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:180166745 G>A maps to NM_001001657.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:8841573 C>T maps to NM_001004699.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:8842091 A>G maps to NM_001004699.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:8841554 C>A maps to NM_001004699.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:3195612 G>T maps to ENST00000397187 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:3195447 G>T maps to ENST00000397187 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:3195486 G>T maps to ENST00000397187 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:3195678 C>T maps to ENST00000397187 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr17:3181523 G>A maps to NM_002551.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:3324736 C>A maps to NM_012373.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:55136381 G>A maps to NM_001005275.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr11:55135667 T>C maps to NM_001005275.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136264 T>A maps to NM_001005275.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55136270 T>G maps to NM_001005275.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:55136142 C>T maps to NM_001005275.1 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:55136240 C>A maps to NM_001005275.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:55136183 C>A maps to NM_001005275.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr11:55136240 C>A maps to NM_001005275.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:55135424 G>A maps to NM_001005275.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:55135817 C>G maps to NM_001005275.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr11:55135508 G>A maps to NM_001005275.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:55135631 G>T maps to NM_001005275.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:55135642 C>G maps to NM_001005275.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr11:55136057 G>C maps to NM_001005275.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:55135589 C>T maps to NM_001005275.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr11:55135909 C>A maps to NM_001005275.1 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:55110930 T>C maps to NM_001005274.1 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55110711 C>A maps to NM_001005274.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:55111428 C>A maps to NM_001005274.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:55111359 G>A maps to NM_001005274.1 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:55110861 C>A maps to NM_001005274.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:55111533 G>T maps to NM_001005274.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:55110822 C>A maps to NM_001005274.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:55111467 C>T maps to NM_001005274.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:55111086 G>C maps to NM_001005274.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:48511135 C>T maps to NM_001005512.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:48510640 C>A maps to NM_001005512.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:48510901 C>T maps to NM_001005512.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:48511135 C>A maps to NM_001005512.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:51411645 G>T maps to NM_001005272.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:51411696 G>T maps to NM_001005272.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:51411669 G>C maps to NM_001005272.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr11:51412272 C>A maps to NM_001005272.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:51412201 G>T maps to NM_001005272.3 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr11:51411694 A>T maps to NM_001005272.3 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:48238837 C>T maps to NM_001005470.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr11:48238705 G>T maps to NM_001005470.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:48238444 G>T maps to NM_001005470.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:48238556 T>C maps to NM_001005470.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:48238927 C>T maps to NM_001005470.1 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:55371294 A>T maps to NM_001004700.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55370921 C>A maps to NM_001004700.1 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:55371654 G>A maps to NM_001004700.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:55371141 G>A maps to NM_001004700.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:55371304 A>T maps to NM_001004700.1 L182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:55371129 A>T maps to NM_001004700.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:55371072 G>T maps to NM_001004700.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:50003261 G>T maps to NM_001005270.2 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:50003623 C>T maps to NM_001005270.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:49974693 C>A maps to NM_001001955.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:49974684 C>G maps to NM_001001955.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:49974018 T>C maps to NM_001001955.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:49974147 C>G maps to NM_001001955.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr11:49974387 T>A maps to NM_001001955.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:49974513 C>A maps to NM_001001955.2 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:49974726 C>A maps to NM_001001955.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr11:49974550 C>T maps to NM_001001955.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:49974450 C>T maps to NM_001001955.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55322042 C>A maps to NM_001001920.1 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:55322558 C>A maps to NM_001001920.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:55322372 G>A maps to NM_001001920.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:55322399 C>T maps to NM_001001920.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:55322195 C>T maps to NM_001001920.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:55322291 C>T maps to NM_001001920.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:55322039 C>A maps to NM_001001920.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:55322198 C>G maps to NM_001001920.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:55321936 T>A maps to NM_001001920.1 L52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr11:55322010 G>T maps to NM_001001920.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr11:55322150 T>C maps to NM_001001920.1 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:55322786 C>G maps to NM_001001920.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr11:55321820 A>T maps to NM_001001920.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr11:55322396 C>G maps to NM_001001920.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr11:55321895 C>T maps to NM_001001920.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr11:55339899 C>A maps to NM_001004701.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:55339950 G>T maps to NM_001004701.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:55339950 G>C maps to NM_001004701.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:55339944 C>T maps to NM_001004701.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:55340040 C>A maps to NM_001004701.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr11:55339920 C>A maps to NM_001004701.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:48347427 T>A maps to NM_001004702.1 Y312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:48347480 A>T maps to NM_001004702.1 *330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:48346725 C>T maps to NM_001004702.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr11:48347184 C>A maps to NM_001004702.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:51515646 G>T maps to NM_001004703.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:51515364 G>T maps to NM_001004703.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:51515605 G>T maps to NM_001004703.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:51515307 G>A maps to NM_001004703.1 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:51515703 G>C maps to NM_001004703.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:51515952 G>A maps to NM_001004703.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:51515577 C>T maps to NM_001004703.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:51515319 G>A maps to NM_001004703.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:51516183 T>C maps to NM_001004703.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:51515838 C>A maps to NM_001004703.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:51515997 C>A maps to NM_001004703.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:55433433 C>T maps to NM_001004704.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:55432992 C>T maps to NM_001004704.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:55433271 T>C maps to NM_001004704.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:55433367 C>A maps to NM_001004704.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:55433223 C>A maps to NM_001004704.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:55433082 G>A maps to NM_001004704.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:55433502 G>A maps to NM_001004704.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr11:55433391 C>T maps to NM_001004704.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:55433304 C>A maps to NM_001004704.1 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:55432656 C>T maps to NM_001004704.1 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:55433076 G>T maps to NM_001004704.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:55433189 T>A maps to NM_001004704.1 L183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:56233443 G>A maps to NM_012374.1 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:56232888 C>T maps to NM_012374.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:56232726 C>G maps to NM_012374.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr11:59245744 G>T maps to NM_001004705.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:59245090 C>A maps to NM_001004705.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:59245788 C>G maps to NM_001004705.1 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:59271425 C>T maps to NM_001004706.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:59271344 A>G maps to NM_001004706.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:59271632 T>A maps to NM_001004706.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59271728 T>C maps to NM_001004706.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:59271158 G>T maps to NM_001004706.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:59271548 T>A maps to NM_001004706.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:56247354 C>T maps to NM_001004707.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:56247585 T>A maps to NM_001004707.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:56247936 T>A maps to NM_001004707.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:56247174 C>A maps to NM_001004707.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:123810905 T>C maps to NM_001001965.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr11:123810709 C>A maps to NM_001001965.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:123810869 C>T maps to NM_001001965.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:123810835 T>C maps to NM_001001965.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:123811219 G>A maps to NM_001001965.1 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr11:123810601 C>T maps to NM_001001965.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123811223 C>T maps to NM_001001965.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:123811054 T>A maps to NM_001001965.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:59224645 C>T maps to NM_001004708.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:59224870 G>A maps to NM_001004708.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:59225047 G>T maps to NM_001004708.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr11:59224534 G>A maps to NM_001004708.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:59224567 T>A maps to NM_001004708.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:59225152 C>A maps to NM_001004708.1 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:59224553 G>T maps to NM_001004708.1 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr11:59225215 C>T maps to NM_001004708.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:59225092 C>T maps to NM_001004708.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:59224660 C>A maps to NM_001004708.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:59283041 G>T maps to NM_001004711.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:59282630 G>A maps to NM_001004711.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:59283059 G>A maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:59282963 C>T maps to NM_001004711.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:59283101 C>A maps to NM_001004711.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:22133667 G>T maps to NM_001001912.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr14:22133769 G>T maps to NM_001001912.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr14:22133529 G>T maps to NM_001001912.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:22133934 C>G maps to NM_001001912.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr14:22133542 G>T maps to NM_001001912.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:102358679 T>A maps to NM_001001674.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:102358574 C>A maps to NM_001001674.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:102358499 G>A maps to NM_001001674.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:110701 G>T maps to NM_001005240.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:69515 G>A maps to NM_001005484.1 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr15:102346710 C>T maps to NM_001005326.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:20404274 G>A maps to NM_001004063.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20403986 T>C maps to NM_001004063.2 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:20404493 C>A maps to NM_001004063.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20404199 C>T maps to NM_001004063.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:20404562 G>T maps to NM_001004063.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:20403983 C>A maps to NM_001004063.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:20404280 C>T maps to NM_001004063.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:20404499 C>A maps to NM_001004063.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr14:20502512 G>T maps to NM_001004714.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20502862 T>A maps to NM_001004714.1 K19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:20502450 G>T maps to NM_001004714.1 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:20502223 G>T maps to NM_001004714.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:20502143 G>T maps to NM_001004714.1 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr14:20502818 C>A maps to NM_001004714.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:20502644 G>T maps to NM_001004714.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:20483241 G>A maps to NM_001004712.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:20483178 G>C maps to NM_001004712.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20482704 C>G maps to NM_001004712.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr14:20482821 G>A maps to NM_001004712.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr14:20482587 G>T maps to NM_001004712.1 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:20482659 G>T maps to NM_001004712.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:20444600 T>C maps to NM_001005486.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:20443736 C>A maps to NM_001005486.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr14:20443946 G>C maps to NM_001005486.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:20443787 G>T maps to NM_001005486.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20444177 G>C maps to NM_001005486.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20444456 C>A maps to NM_001005486.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr14:20444045 C>A maps to NM_001005486.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr14:20444045 C>A maps to NM_001005486.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20585585 C>T maps to NM_001004715.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:20586107 C>A maps to NM_001004715.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:20586167 T>G maps to NM_001004715.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:20586176 G>T maps to NM_001004715.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr14:20586230 C>T maps to NM_001004715.1 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:20586104 G>A maps to NM_001004715.1 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:20586260 C>T maps to NM_001004715.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:20586029 G>T maps to NM_001004715.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:20586311 C>G maps to NM_001004715.1 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:20344995 G>C maps to NM_001005501.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr14:20344566 C>A maps to NM_001005501.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:20344869 C>A maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:20344476 C>A maps to NM_001005501.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr14:20345085 T>A maps to NM_001005501.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:20345370 G>T maps to NM_001005501.1 *315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:20344722 C>A maps to NM_001005501.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:20345097 T>C maps to NM_001005501.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr14:20389718 G>T maps to NM_001005483.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20389217 G>C maps to NM_001005483.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr14:20389553 C>T maps to NM_001005483.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:20389361 T>C maps to NM_001005483.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:20389622 T>C maps to NM_001005483.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:20389616 C>T maps to NM_001005483.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:20389632 A>C maps to NM_001005483.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr14:20388776 C>A maps to NM_001005483.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr14:20389037 C>G maps to NM_001005483.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr14:20388992 T>C maps to NM_001005483.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20528424 C>T maps to NM_001004717.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:20528382 C>A maps to NM_001004717.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr14:20528430 C>A maps to NM_001004717.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:20528617 A>T maps to NM_001004717.1 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:20528260 C>A maps to NM_001004717.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr14:20528289 G>T maps to NM_001004717.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:20248993 C>A maps to NM_001005500.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:20248528 C>A maps to NM_001005500.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:20248810 G>C maps to NM_001005500.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr14:20248933 G>T maps to NM_001005500.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:20248534 C>A maps to NM_001005500.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr14:20248945 T>C maps to NM_001005500.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:20249158 G>A maps to NM_001005500.1 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr14:20249146 G>T maps to NM_001005500.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr14:20249414 G>T maps to NM_001005500.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr14:20248684 C>A maps to NM_001005500.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:20248501 C>A maps to NM_001005500.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:20248711 A>T maps to NM_001005500.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:22369033 C>T maps to NM_001004719.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:22369132 G>T maps to NM_001004719.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:22368784 T>C maps to NM_001004719.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr15:22368727 A>G maps to NM_001004719.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr15:22368718 C>G maps to NM_001004719.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:22369228 T>C maps to NM_001004719.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr15:22368925 G>A maps to NM_001004719.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr15:22368700 T>C maps to NM_001004719.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:22369216 G>T maps to NM_001004719.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:20296218 C>T maps to NM_001004723.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20295924 C>T maps to NM_001004723.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:20295864 C>A maps to NM_001004723.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:20295897 C>A maps to NM_001004723.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20296191 G>A maps to NM_001004723.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:20295855 G>T maps to NM_001004723.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr14:20296383 G>A maps to NM_001004723.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr14:20295676 C>T maps to NM_001004723.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr14:20295900 C>A maps to NM_001004723.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:20296297 G>T maps to NM_001004723.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:20295687 C>A maps to NM_001004723.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:20296254 C>A maps to NM_001004723.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:22383395 T>A maps to NM_001005241.1 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr15:22382660 G>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr15:22382660 G>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr15:22382658 C>T maps to NM_001005241.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr15:22382495 A>T maps to NM_001005241.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:22383071 C>T maps to NM_001005241.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:22382627 C>T maps to NM_001005241.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:22383041 C>A maps to NM_001005241.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr15:22382891 C>T maps to NM_001005241.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:22383203 C>T maps to NM_001005241.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr15:22382498 G>T maps to NM_001005241.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr15:22383053 G>A maps to NM_001005241.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:20612580 C>A maps to NM_001004724.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:20612553 C>T maps to NM_001004724.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20611947 C>A maps to NM_001004724.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:20612592 G>A maps to NM_001004724.1 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:20612415 C>A maps to NM_001004724.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:20612058 C>T maps to NM_001004724.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr14:20612770 G>T maps to NM_001004724.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:20612328 G>C maps to NM_001004724.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr14:20612196 C>A maps to NM_001004724.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:55406717 C>A maps to NM_001004124.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:55406057 G>A maps to NM_001004124.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:55406105 C>A maps to NM_001004124.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:55405856 T>A maps to NM_001004124.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:55405982 C>T maps to NM_001004124.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55405904 C>T maps to NM_001004124.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:55406750 G>A maps to NM_001004124.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:55406631 A>T maps to NM_001004124.1 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:55406171 C>T maps to NM_001004124.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:55406027 A>G maps to NM_001004124.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:55406033 C>G maps to NM_001004124.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20216395 G>A maps to NM_172194.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:20216281 G>A maps to NM_172194.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20216350 C>T maps to NM_172194.1 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr14:20215963 C>A maps to NM_172194.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:20216296 C>A maps to NM_172194.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:20216461 T>C maps to NM_172194.1 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr14:20215939 C>A maps to NM_172194.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr14:20215981 C>A maps to NM_172194.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr14:20216020 G>A maps to NM_172194.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:48328562 G>T maps to NM_001004725.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:48328541 C>A maps to NM_001004725.1 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:48328182 C>A maps to NM_001004725.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:48328453 C>A maps to NM_001004725.1 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:48328157 G>T maps to NM_001004725.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr11:55419044 C>A maps to NM_001004059.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr11:55418436 G>T maps to NM_001004059.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:55419008 T>A maps to NM_001004059.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:55418651 C>G maps to NM_001004059.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:55418426 T>C maps to NM_001004059.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr11:55418703 G>T maps to NM_001004059.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:55418852 G>T maps to NM_001004059.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:55418792 A>T maps to NM_001004059.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:55419047 G>A maps to NM_001004059.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:55418546 C>G maps to NM_001004059.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:55419058 C>A maps to NM_001004059.2 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:55418542 C>A maps to NM_001004059.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr11:55419083 C>A maps to NM_001004059.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:55418855 T>A maps to NM_001004059.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:48286047 G>A maps to NM_001004726.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:48285576 C>T maps to NM_001004726.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr11:48285957 G>T maps to NM_001004726.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:4976325 G>A maps to NM_001004748.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:4976400 A>T maps to NM_001004748.1 C181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:4976703 C>A maps to NM_001004748.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:4976805 G>T maps to NM_001004748.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4967799 G>A maps to NM_001005329.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:4967816 T>A maps to NM_001005329.1 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:4968294 G>T maps to NM_001005329.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:4967751 G>A maps to NM_001005329.1 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:4967712 G>C maps to NM_001005329.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:4968003 G>A maps to NM_001005329.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:4967517 G>T maps to NM_001005329.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:4929495 G>A maps to NM_001004749.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr11:4929366 C>A maps to NM_001004749.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr11:4929321 C>T maps to NM_001004749.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5345398 G>T maps to NM_033180.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:5344660 G>T maps to NM_033180.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:5344954 A>T maps to NM_033180.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:5344969 A>G maps to NM_033180.4 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:5345005 A>T maps to NM_033180.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:5345278 T>C maps to NM_033180.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:5345062 C>A maps to NM_033180.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:5322777 A>T maps to NM_033179.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:5323125 G>T maps to NM_033179.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:5363818 G>A maps to NM_001005567.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:5363848 A>G maps to NM_001005567.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:5364616 G>A maps to NM_001005567.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr11:5364343 A>G maps to NM_001005567.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:5364118 G>A maps to NM_001005567.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:5364532 G>T maps to NM_001005567.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5373150 G>A maps to NM_001004750.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:5372874 C>A maps to NM_001004750.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:4661751 G>T maps to NM_001004751.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:4661547 C>G maps to NM_001004751.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:4661247 G>C maps to NM_001004751.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:4661634 C>G maps to NM_001004751.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4661967 C>A maps to NM_001004751.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:4661475 T>C maps to NM_001004751.2 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4673878 T>A maps to NM_152430.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:4674575 C>T maps to NM_152430.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:4674112 G>T maps to NM_152430.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:4673770 C>A maps to NM_152430.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:4674604 G>T maps to NM_152430.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:4673875 T>A maps to NM_152430.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:4674622 C>G maps to NM_152430.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:4703242 C>A maps to NM_030774.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:4703889 C>A maps to NM_030774.3 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:4703107 G>T maps to NM_030774.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:4703621 G>T maps to NM_030774.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4790454 G>A maps to ENST00000380383 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:4790229 G>A maps to ENST00000380383 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:4790810 C>A maps to ENST00000380383 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr11:4790207 T>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:4843367 C>A maps to NM_001004753.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4843568 C>T maps to NM_001004753.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4843074 C>T maps to NM_001004753.1 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:4843472 C>A maps to NM_001004753.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4842746 T>A maps to NM_001004753.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4843385 C>A maps to NM_001004753.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:4843361 G>C maps to NM_001004753.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:4843323 C>T maps to NM_001004753.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:4842710 A>T maps to NM_001004753.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr11:4843481 C>A maps to NM_001004753.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:4944804 G>T maps to NM_001005237.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4944708 G>T maps to NM_001005237.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:4944909 G>T maps to NM_001005237.1 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:4944942 C>A maps to NM_001005237.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:4944843 G>T maps to NM_001005237.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:4945494 G>T maps to NM_001005237.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:4944909 G>T maps to NM_001005237.1 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:4945464 G>A maps to NM_001005237.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:4944804 G>T maps to NM_001005237.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:4945413 A>G maps to NM_001005237.1 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:4936137 A>G maps to NM_001005238.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:4936311 A>T maps to NM_001005238.1 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5462057 G>T maps to NM_001005288.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:5461846 C>A maps to NM_001005288.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:5462624 G>T maps to NM_001005288.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:5462024 G>C maps to NM_001005288.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:5461916 G>T maps to NM_001005288.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:5462540 G>T maps to NM_001005288.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:5462723 G>A maps to NM_001005288.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:5474876 C>A maps to NM_001004754.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:5474972 C>T maps to NM_001004754.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:5475623 C>A maps to NM_001004754.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:5021019 C>T maps to NM_001004755.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5020469 G>T maps to NM_001004755.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:5020849 C>G maps to NM_001004755.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5021144 A>G maps to NM_001004755.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:5020421 G>T maps to NM_001004755.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr11:5020307 C>G maps to NM_001004755.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:5411261 C>T maps to NM_001004756.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5410855 C>A maps to NM_001004756.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:5411020 C>A maps to NM_001004756.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:5411542 C>T maps to NM_001004756.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:5443759 C>T maps to NM_001004757.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:5444218 T>A maps to NM_001004757.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:5444011 C>A maps to NM_001004757.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:5444305 C>A maps to NM_001004757.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:5444176 T>A maps to NM_001004757.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr11:5443900 G>A maps to NM_001004757.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:5444287 C>T maps to NM_001004757.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:5443825 C>G maps to NM_001004757.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:4869646 G>T maps to NM_001004758.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr11:4869598 A>G maps to NM_001004758.1 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:4870357 G>T maps to NM_001004758.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr11:4870012 C>A maps to NM_001004758.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:4870050 G>T maps to NM_001004758.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr11:4870117 T>A maps to NM_001004758.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:4903659 C>T maps to NM_001004759.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:4904110 T>A maps to NM_001004759.1 *355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:4903926 C>A maps to NM_001004759.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:4903674 C>A maps to NM_001004759.1 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:4903377 G>T maps to NM_001004759.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:4903239 C>T maps to NM_001004759.1 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:4904022 C>G maps to NM_001004759.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:4903651 G>T maps to NM_001004759.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5220985 G>C maps to NM_001004760.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:5221507 A>G maps to NM_001004760.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5221657 C>A maps to NM_001004760.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:5221384 G>A maps to NM_001004760.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:5221759 C>A maps to NM_001004760.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:5221534 G>A maps to NM_001004760.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:5221795 G>T maps to NM_001004760.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:5173455 C>T maps to NM_012375.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5173071 G>T maps to NM_012375.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr11:5172978 G>A maps to NM_012375.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:5172786 G>T maps to NM_012375.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5142799 C>A maps to NM_001005222.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5153244 G>A maps to NM_001005160.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5153245 G>T maps to NM_001005160.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:5153347 T>A maps to NM_001005160.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:5153416 G>C maps to NM_001005160.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr11:5153683 A>T maps to NM_001005160.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:5153014 G>T maps to NM_001005160.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr11:6191529 G>A maps to NM_001004052.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:6191451 G>A maps to NM_001004052.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:6190689 C>A maps to NM_001004052.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:4389381 G>T maps to NM_001005161.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:4389408 G>A maps to NM_001005161.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:4388805 G>C maps to NM_001005161.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:4389060 A>G maps to NM_001005161.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr11:4389489 T>A maps to NM_001005161.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:5510136 C>A maps to NM_001005163.2 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr11:5510859 A>G maps to NM_001005163.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:5079999 T>A maps to NM_001005164.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:5080734 G>A maps to NM_001005164.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:5079888 C>A maps to NM_001005164.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr11:5080460 G>A maps to NM_001005164.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:5080089 G>T maps to NM_001005164.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5905567 C>T maps to NM_001005165.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5906065 G>T maps to NM_001005165.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:5906109 C>A maps to NM_001005165.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:5906319 C>G maps to NM_001005165.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:5905707 C>T maps to NM_001005165.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:5862710 G>C maps to ENST00000379946 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5862467 G>T maps to ENST00000379946 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:5862539 G>T maps to ENST00000379946 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr11:5862668 C>T maps to ENST00000379946 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:5862245 C>A maps to ENST00000379946 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:5862764 G>T maps to ENST00000379946 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:5862773 C>G maps to ENST00000379946 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:5862503 C>T maps to ENST00000379946 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr11:5862729 C>T maps to ENST00000379946 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:5862659 G>C maps to ENST00000379946 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:5862663 A>T maps to ENST00000379946 L159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr11:5878152 T>A maps to NM_001005168.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:5878911 C>A maps to NM_001005168.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr11:5878253 G>A maps to NM_001005168.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr11:5565817 T>A maps to NM_001005289.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:5566147 G>A maps to NM_001005289.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:5566402 G>T maps to NM_001005289.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:5566630 G>A maps to NM_001005289.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:4615654 C>T maps to ENST00000450052 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:4616128 C>A maps to ENST00000450052 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:4615648 T>C maps to ENST00000450052 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:4608962 A>T maps to NM_001005170.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:4608443 C>A maps to NM_001005170.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:5068432 C>A maps to NM_001001916.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:5068621 C>T maps to NM_001001916.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:5068582 T>A maps to NM_001001916.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:5068234 C>G maps to NM_001001916.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr11:4510219 C>A maps to NM_001005171.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4471180 G>T maps to NM_001005172.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4470649 C>A maps to NM_001005172.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:4470601 A>T maps to NM_001005172.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:4470976 G>A maps to NM_001005172.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:4471273 C>G maps to NM_001005172.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:4470691 G>T maps to NM_001005172.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr11:4471033 G>T maps to NM_001005172.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr11:4470611 T>C maps to NM_001005172.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:4470637 A>G maps to NM_001005172.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:4470979 C>A maps to NM_001005172.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:4471054 C>T maps to NM_001005172.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:6007542 G>T maps to NM_001005173.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:6007893 C>A maps to NM_001005173.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:6007392 A>G maps to NM_001005173.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:6007674 G>A maps to NM_001005173.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6008098 G>C maps to NM_001005173.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr11:6008151 C>T maps to NM_001005173.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr11:6007326 G>A maps to NM_001005173.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:4566860 G>A maps to NM_001004137.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:4566821 T>C maps to NM_001004137.1 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr11:4566848 G>T maps to NM_001004137.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:5809158 C>A maps to NM_001001913.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:5809515 G>T maps to NM_001001913.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:5842332 T>A maps to NM_001005174.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:5841930 G>T maps to NM_001005174.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:5841573 G>T maps to NM_001005174.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:5841901 G>T maps to NM_001005174.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:5776425 G>C maps to NM_001005175.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5776386 C>A maps to NM_001005175.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:5776692 T>C maps to NM_001005175.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:5776461 C>T maps to NM_001005175.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:5776242 C>G maps to NM_001005175.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:5776764 C>T maps to NM_001005175.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:5776644 G>T maps to NM_001005175.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:5776036 G>T maps to NM_001005175.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:5776476 C>T maps to NM_001005175.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:5799838 C>T maps to NM_001001922.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5799255 G>T maps to NM_001001922.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:5799747 G>A maps to NM_001001922.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr11:5799681 C>T maps to NM_001001922.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:4825052 A>T maps to ENST00000380382 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:4824734 G>A maps to ENST00000380382 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:4824944 C>A maps to ENST00000380382 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:4825511 C>A maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr11:4824685 C>A maps to ENST00000380382 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:4825133 C>A maps to ENST00000380382 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:4824716 T>C maps to ENST00000380382 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:6220887 T>C maps to NM_001005178.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:6048373 G>T maps to NM_001001917.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:6047983 C>A maps to NM_001001917.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:6048541 C>T maps to NM_001001917.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:6048349 G>A maps to NM_001001917.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:6048640 C>A maps to NM_001001917.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr11:5968809 C>A maps to NM_001003443.2 C78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:5968749 T>A maps to NM_001003443.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:5969235 C>G maps to NM_001003443.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:5969346 C>A maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:5969355 G>A maps to NM_001003443.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr11:5969310 T>A maps to NM_001003443.2 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:5969346 C>A maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:5969253 G>T maps to NM_001003443.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:5968695 C>A maps to NM_001003443.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:5968956 T>C maps to NM_001003443.2 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:5969286 C>A maps to NM_001003443.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:6024333 G>A maps to NM_001005179.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:6024012 G>C maps to NM_001005179.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:6024195 A>G maps to NM_001005179.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:6023781 G>A maps to NM_001005179.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5758675 C>A maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:5758483 C>G maps to NM_001005180.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:5757856 T>A maps to NM_001005180.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:6129205 C>A maps to NM_001005181.1 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:59211009 C>T maps to NM_001004728.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59211573 G>A maps to NM_001004728.1 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:59211048 C>A maps to NM_001004728.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:59211377 C>A maps to NM_001004728.1 S246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr11:59211012 C>T maps to NM_001004728.1 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:59210994 G>T maps to NM_001004728.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:59211267 C>T maps to NM_001004728.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:59211168 C>A maps to NM_001004728.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr11:59211157 G>T maps to NM_001004728.1 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:59189871 G>T maps to NM_001001954.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:97806151 G>T maps to NM_054106.1 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:97806571 C>T maps to NM_054106.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:97806732 C>G maps to NM_054106.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:97806522 T>G maps to NM_054106.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:97806510 A>T maps to NM_054106.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:59132050 G>T maps to NM_001004729.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:59132125 T>C maps to NM_001004729.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:59132371 G>C maps to NM_001004729.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:59131996 C>A maps to NM_001004729.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:56409809 A>G maps to NM_001002925.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:56409510 G>T maps to NM_001002925.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr11:56409828 T>A maps to NM_001002925.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:56409177 G>A maps to NM_001002925.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:56409483 C>A maps to NM_001002925.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56431718 C>A maps to NM_001004730.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:56431457 C>A maps to NM_001004730.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:56431667 T>A maps to NM_001004730.1 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55798328 T>C maps to NM_001001921.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:55798169 C>A maps to NM_001001921.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:55798577 C>A maps to NM_001001921.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:55798490 C>G maps to NM_001001921.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:55798391 G>T maps to NM_001001921.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:55798658 C>A maps to NM_001001921.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:55798634 A>G maps to NM_001001921.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:55798642 T>A maps to NM_001001921.1 L250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:55798067 C>T maps to NM_001001921.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:21623953 C>T maps to NM_001004731.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:21623230 G>A maps to NM_001004731.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:58207549 G>C maps to NM_001004733.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:58207462 G>A maps to NM_001004733.2 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:58126400 G>A maps to NM_001005489.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:58125639 C>T maps to NM_001005489.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:58125858 T>A maps to NM_001005489.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:58190686 G>T maps to NM_001005566.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:58190536 C>A maps to NM_001005566.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:58189954 G>T maps to NM_001005566.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:58190023 G>C maps to NM_001005566.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:58190266 G>A maps to NM_001005566.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:58275239 C>A maps to NM_001005218.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:58275101 T>A maps to NM_001005218.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:58170852 G>A maps to NM_001005469.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:58170489 G>T maps to NM_001005469.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:58170033 C>A maps to NM_001005469.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:58170846 A>T maps to NM_001005469.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:58170426 C>A maps to NM_001005469.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:58170447 G>T maps to NM_001005469.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:58170111 G>C maps to NM_001005469.1 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:125551303 C>T maps to NM_001001923.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr9:125552134 C>A maps to NM_001001923.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:125552141 C>T maps to NM_001001923.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:125552026 G>A maps to NM_001001923.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:55541278 T>C maps to NM_001001967.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr11:55541603 C>T maps to NM_001001967.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:55541527 C>A maps to NM_001001967.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:55541386 C>T maps to NM_001001967.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:55541092 C>A maps to NM_001001967.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55563947 T>G maps to NM_001004735.1 L306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:55563606 T>A maps to NM_001004735.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:55563648 C>T maps to NM_001004735.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:55563765 C>A maps to NM_001004735.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:55563351 C>A maps to NM_001004735.1 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:55563381 G>C maps to NM_001004735.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:55563357 T>A maps to NM_001004735.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:55563195 C>T maps to NM_001004735.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:55563153 G>C maps to NM_001004735.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:55607015 A>G maps to NM_001005496.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:55606871 C>A maps to NM_001005496.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:55606406 C>A maps to NM_001005496.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:55606604 G>A maps to NM_001005496.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr11:55606364 G>T maps to NM_001005496.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:55606406 C>G maps to NM_001005496.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr11:55606982 C>A maps to NM_001005496.1 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:55606760 T>C maps to NM_001005496.1 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr11:55606802 T>C maps to NM_001005496.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:55607039 C>T maps to NM_001005496.1 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:55606478 G>T maps to NM_001005496.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:55607147 C>A maps to NM_001005496.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55587575 C>T maps to ENST00000395203 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55587851 C>T maps to ENST00000395203 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55587545 G>T maps to ENST00000395203 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:55587563 A>T maps to ENST00000395203 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:55587308 C>G maps to ENST00000395203 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587140 G>T maps to ENST00000395203 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:55587800 C>T maps to ENST00000395203 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55587431 G>A maps to ENST00000395203 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:55587647 G>A maps to ENST00000395203 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:55587974 C>T maps to ENST00000395203 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr11:55587404 A>T maps to ENST00000395203 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:55587398 C>A maps to ENST00000395203 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:55587534 C>T maps to ENST00000395203 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:55587956 C>T maps to ENST00000395203 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:55587800 C>A maps to ENST00000395203 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:55587188 C>A maps to ENST00000395203 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:55761252 G>C maps to NM_003697.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:55761407 C>A maps to NM_003697.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:55761408 C>A maps to NM_003697.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55761412 G>T maps to NM_003697.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr11:55761522 G>T maps to NM_003697.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr11:55761684 G>T maps to NM_003697.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:55761237 C>A maps to NM_003697.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:55761960 G>T maps to NM_003697.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr3:97852217 T>A maps to NM_001005338.1 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:97852074 C>A maps to NM_001005338.1 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:97852028 T>A maps to NM_001005338.1 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr3:97852149 A>T maps to NM_001005338.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:97868306 C>A maps to NM_001005514.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:97868307 C>T maps to NM_001005514.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr3:97868993 C>T maps to NM_001005514.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:97868666 C>A maps to NM_001005514.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:97887788 G>A maps to NM_001005515.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr3:97887573 G>T maps to NM_001005515.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:97887749 G>A maps to NM_001005515.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:97887953 C>A maps to NM_001005515.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:97887590 A>C maps to NM_001005515.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:97887620 C>A maps to NM_001005515.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:97887971 G>T maps to NM_001005515.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:98002177 G>T maps to NM_001005482.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:98001859 T>C maps to NM_001005482.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:97983472 A>T maps to NM_001005479.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:97983439 G>A maps to NM_001005479.1 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:97983202 G>T maps to NM_001005479.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:97983940 C>T maps to NM_001005479.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr3:97984018 A>T maps to NM_001005479.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:97983943 C>A maps to NM_001005479.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:97984036 C>T maps to NM_001005479.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:55703540 T>A maps to NM_006637.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr11:55703624 C>G maps to NM_006637.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr11:55703582 C>A maps to NM_006637.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55703123 C>A maps to NM_006637.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr11:55703674 G>A maps to NM_006637.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:55703699 G>A maps to NM_006637.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:55944329 C>A maps to NM_001005492.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:55944911 G>T maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:55944179 G>T maps to NM_001005492.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:55944521 G>A maps to NM_001005492.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:55944481 T>A maps to NM_001005492.1 L130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr11:55944911 G>A maps to NM_001005492.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:55944439 C>A maps to NM_001005492.1 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:55944497 C>A maps to NM_001005492.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98188737 T>A maps to NM_001004736.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:98188902 G>T maps to NM_001004736.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:98188533 C>G maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr3:98188518 C>A maps to NM_001004736.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr3:98188969 T>C maps to NM_001004736.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:98189142 T>A maps to NM_001004736.2 C241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:98217147 C>A maps to NM_001004737.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:98110225 T>A maps to NM_001005516.1 C239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:98072804 G>T maps to NM_001005517.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:98073304 C>A maps to NM_001005517.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:98073317 A>G maps to NM_001005517.1 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55579238 G>A maps to NM_001004738.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:55579085 G>C maps to NM_001004738.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55579853 G>C maps to NM_001004738.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:55579094 C>A maps to NM_001004738.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:55579751 T>A maps to NM_001004738.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:55579361 G>T maps to NM_001004738.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:55579670 C>T maps to NM_001004738.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:55579823 T>C maps to NM_001004738.1 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr11:55579616 C>A maps to NM_001004738.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55595458 C>A maps to NM_001004739.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:55594894 C>G maps to NM_001004739.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:55594858 C>A maps to NM_001004739.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:55595446 C>T maps to NM_001004739.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:55594984 C>A maps to NM_001004739.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr11:55594984 C>T maps to NM_001004739.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:55595458 C>A maps to NM_001004739.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr11:55595368 C>A maps to NM_001004739.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:55595299 G>A maps to NM_001004739.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:55594867 C>T maps to NM_001004739.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:55594990 G>A maps to NM_001004739.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:55595152 G>A maps to NM_001004739.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56380834 C>A maps to NM_001004740.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:56380753 G>A maps to NM_001004740.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56380108 A>G maps to NM_001004740.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:56380708 C>T maps to NM_001004740.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:56380330 C>A maps to NM_001004740.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56380870 T>A maps to NM_001004740.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:56380558 G>A maps to NM_001004740.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:56344618 A>T maps to NM_001004741.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56344906 G>T maps to NM_001004741.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:56344786 G>C maps to NM_001004741.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:56344765 C>A maps to NM_001004741.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:56345056 C>A maps to NM_001004741.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:56344660 G>A maps to NM_001004741.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:56344314 T>A maps to NM_001004741.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:56310499 G>T maps to NM_001005245.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:56310157 A>T maps to NM_001005245.1 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:56310715 G>T maps to NM_001005245.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:56310559 G>T maps to NM_001005245.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:56310154 G>C maps to NM_001005245.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:56310562 C>A maps to NM_001005245.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56237709 T>C maps to NM_001004742.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56237376 T>A maps to NM_001004742.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:56237246 G>A maps to NM_001004742.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:56237442 A>G maps to NM_001004742.1 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:56237871 G>T maps to NM_001004742.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56258336 G>T maps to NM_001005282.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr11:56258675 G>T maps to NM_001005282.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56258246 A>T maps to NM_001005282.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr11:56258450 G>T maps to NM_001005282.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:56258723 G>A maps to NM_001005282.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56258012 G>T maps to NM_001005282.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:56258732 C>A maps to NM_001005282.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:56230487 A>G maps to NM_001004743.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:56230565 G>T maps to NM_001004743.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56230508 G>T maps to NM_001004743.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56230559 G>A maps to NM_001004743.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56230094 G>T maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:56230094 G>T maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:56230202 G>A maps to NM_001004743.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:56230456 G>T maps to NM_001004743.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:56230127 A>T maps to NM_001004743.1 Y250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:56230115 G>A maps to NM_001004743.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:7818087 T>A maps to NM_153444.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr11:7818471 G>A maps to NM_153444.1 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:7847495 A>T maps to NM_153445.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:7847204 C>T maps to NM_153445.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:7847495 A>G maps to NM_153445.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:7847234 A>G maps to NM_153445.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:7847132 G>A maps to NM_153445.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr11:56185333 G>T maps to NM_001004744.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:56185519 G>A maps to NM_001004744.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:56185684 A>T maps to NM_001004744.1 Y8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:56185387 G>A maps to NM_001004744.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:56185159 G>A maps to NM_001004744.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:56185377 C>A maps to NM_001004744.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:56043986 C>A maps to NM_001004745.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:56043713 T>A maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:56043776 C>G maps to NM_001004745.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:56044013 C>T maps to NM_001004745.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:56043302 G>T maps to NM_001004745.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:56043650 C>A maps to NM_001004745.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:56043563 C>A maps to NM_001004745.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr11:56043302 G>C maps to NM_001004745.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:56044092 T>C maps to NM_001004745.1 *327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55999893 G>C maps to NM_001004746.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr11:56000091 A>T maps to NM_001004746.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:55999926 G>T maps to NM_001004746.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:55999872 G>T maps to NM_001004746.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:56000133 T>A maps to NM_001004746.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr11:55999866 C>T maps to NM_001004746.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr11:55999947 G>T maps to NM_001004746.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:56020313 T>A maps to NM_001004747.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:56019821 T>C maps to NM_001004747.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:56020157 G>A maps to NM_001004747.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:56020163 A>G maps to NM_001004747.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr11:56020493 T>A maps to NM_001004747.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:56019915 G>T maps to NM_001004747.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:56020601 A>G maps to NM_001004747.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:29323885 G>T maps to NM_030876.5 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:29323942 A>G maps to NM_030876.5 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:29323759 G>T maps to NM_030876.5 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:55681455 G>A maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:55681464 C>T maps to NM_001001960.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:55681779 G>T maps to NM_001001960.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:55681185 G>A maps to NM_001001960.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:6816648 G>T maps to NM_003696.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:143701965 C>A maps to NM_001005281.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr7:143701547 T>C maps to NM_001005281.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:143701574 C>T maps to NM_001005281.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:143701655 C>A maps to NM_001005281.1 C189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr7:143701217 G>A maps to NM_001005281.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr7:143701253 G>T maps to NM_001005281.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:143701160 G>T maps to NM_001005281.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr7:143701706 C>A maps to NM_001005281.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:143701142 T>A maps to NM_001005281.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:143701236 C>T maps to NM_001005281.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:240969525 C>G maps to NM_001005853.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:240969768 C>A maps to NM_001005853.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240969744 G>T maps to NM_001005853.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:240969756 G>C maps to NM_001005853.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:240969108 G>T maps to NM_001005853.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:240969651 G>T maps to NM_001005853.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr2:240969237 G>T maps to NM_001005853.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:240984556 G>T maps to NM_173351.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:240984703 G>T maps to NM_173351.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:55715171 A>G maps to NM_001005182.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55715312 A>C maps to NM_001005182.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:55715042 C>A maps to NM_001005182.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr12:55715319 T>A maps to NM_001005182.1 *313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:55714962 G>T maps to NM_001005182.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr12:55714895 T>A maps to NM_001005182.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:55846626 T>G maps to NM_054105.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:55726035 A>G maps to NM_054104.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55725637 C>T maps to NM_054104.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:55725522 C>A maps to NM_054104.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:55726116 G>A maps to NM_054104.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:55725825 C>A maps to NM_054104.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr12:55725573 C>T maps to NM_054104.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr12:55945510 T>C maps to NM_001005494.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr12:55945334 G>T maps to NM_001005494.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:55688350 G>T maps to NM_001005493.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:55688557 G>A maps to NM_001005493.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:55794779 C>A maps to NM_001005518.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:55886197 C>T maps to NM_001005519.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr12:55863742 G>A maps to NM_001005499.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:55641136 G>A maps to NM_001005490.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:55641625 C>T maps to NM_001005490.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:55759802 C>A maps to NM_001005497.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55820396 T>C maps to NM_001005183.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:55820132 G>T maps to NM_001005183.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:55820792 C>A maps to NM_001005183.1 C252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:247875435 G>A maps to NM_001005286.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:247875403 A>G maps to NM_001005286.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:247875385 G>T maps to NM_001005286.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:247875475 T>G maps to NM_001005286.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr1:247875471 C>A maps to NM_001005286.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:247875709 T>A maps to NM_001005286.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr1:247875712 C>A maps to NM_001005286.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:247876018 G>T maps to NM_001005286.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:247875406 G>T maps to NM_001005286.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr1:247875280 G>A maps to NM_001005286.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:247875463 C>A maps to NM_001005286.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:158669884 C>G maps to NM_001005279.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:158670321 C>A maps to NM_001005279.1 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:158669977 G>T maps to NM_001005279.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:158670175 C>T maps to NM_001005279.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:158670187 C>A maps to NM_001005279.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:158669932 C>A maps to NM_001005279.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:158669515 A>T maps to NM_001005279.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:158670334 A>T maps to NM_001005279.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:158669544 C>A maps to NM_001005279.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:158670346 G>C maps to NM_001005279.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:158687356 A>G maps to ENST00000368146 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:158687392 G>T maps to ENST00000368146 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:158687536 G>A maps to ENST00000368146 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:158687440 G>A maps to ENST00000368146 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:158687239 A>T maps to ENST00000368146 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:158687659 G>C maps to ENST00000368146 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr1:158687500 G>A maps to ENST00000368146 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:158687242 G>T maps to ENST00000368146 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:158687488 C>A maps to ENST00000368146 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:158725559 C>T maps to NM_001005184.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:158724748 G>A maps to NM_001005184.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:158724742 G>T maps to NM_001005184.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr1:158725612 G>A maps to NM_001005184.1 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123676202 A>G maps to NM_001005325.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:123676223 C>A maps to NM_001005325.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:123676814 G>T maps to NM_001005325.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:123676118 A>C maps to NM_001005325.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:123676361 C>T maps to NM_001005325.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr11:123676163 C>T maps to NM_001005325.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:158735769 T>G maps to NM_001005185.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:158735629 G>T maps to NM_001005185.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158736112 G>C maps to NM_001005185.1 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:158736043 C>T maps to NM_001005185.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:158735614 G>A maps to NM_001005185.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:158736070 G>T maps to NM_001005185.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:158735989 G>C maps to NM_001005185.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:158735725 G>A maps to NM_001005185.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:158735857 G>T maps to NM_001005185.1 C205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158746534 G>A maps to NM_001005278.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr1:158747011 G>A maps to NM_001005278.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:158746644 G>T maps to NM_001005278.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158747405 G>T maps to NM_001005278.1 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158747163 C>A maps to NM_001005278.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:158746834 C>A maps to NM_001005278.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:158746798 G>T maps to NM_001005278.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:158746765 C>T maps to NM_001005278.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:57799342 C>T maps to NM_001005186.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:57799281 G>T maps to NM_001005186.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr11:57798589 C>T maps to NM_001005186.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:57799083 G>T maps to NM_001005186.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:57799173 T>A maps to NM_001005186.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr11:57799059 G>A maps to NM_001005186.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:57798732 C>T maps to NM_001005186.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:21109499 C>T maps to NM_001001968.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21109584 G>C maps to NM_001001968.1 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr14:21109484 C>T maps to NM_001001968.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:21109394 C>A maps to NM_001001968.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:21108971 A>G maps to NM_001001968.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:21109019 C>A maps to NM_001001968.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:21109703 C>A maps to NM_001001968.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:123813849 A>T maps to NM_001005187.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:123814446 C>A maps to NM_001005187.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:123813615 G>T maps to NM_001005187.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:123813816 C>A maps to NM_001005187.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:123814425 T>A maps to NM_001005187.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:123813639 T>C maps to NM_001005187.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:123813848 C>A maps to NM_001005187.1 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:123813681 G>A maps to NM_001005187.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:123814218 G>T maps to NM_001005187.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:123814233 G>T maps to NM_001005187.1 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:142749622 C>A maps to NM_001001667.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr7:142749649 A>T maps to NM_001001667.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:142750144 C>T maps to NM_001001667.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:142749586 C>T maps to NM_001001667.1 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:142750054 C>T maps to NM_001001667.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:142750303 C>A maps to NM_001001667.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:123624623 G>A maps to NM_001005188.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:123624623 G>T maps to NM_001005188.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:123624809 G>T maps to NM_001005188.1 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr11:123624881 G>A maps to NM_001005188.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr11:123624359 A>T maps to NM_001005188.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:158517592 G>T maps to NM_001005189.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158517481 T>C maps to NM_001005189.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:158517160 G>T maps to NM_001005189.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:158517679 G>T maps to NM_001005189.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:158517802 G>T maps to NM_001005189.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:14952562 G>A maps to NM_001005190.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:14952212 T>C maps to NM_001005190.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:14952191 C>A maps to NM_001005190.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:14952491 C>A maps to NM_001005190.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:14952632 C>T maps to NM_001005190.1 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:14991762 G>T maps to NM_030901.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr19:14992092 G>T maps to NM_030901.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:14991321 G>T maps to NM_030901.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr19:14991870 G>C maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:14991762 G>A maps to NM_030901.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:14991975 G>T maps to NM_030901.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:14992035 G>T maps to NM_030901.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:14991684 T>C maps to NM_030901.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14938678 G>A maps to NM_017506.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:14938363 T>C maps to NM_017506.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr19:14938324 A>C maps to NM_017506.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:14910186 C>A maps to NM_198944.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:14910177 C>A maps to NM_198944.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:14910759 G>T maps to NM_198944.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr19:15053211 C>A maps to NM_012377.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr19:9296960 C>T maps to NM_175883.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:9296520 G>T maps to NM_175883.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9324916 C>T maps to NM_001005191.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:9325114 C>A maps to NM_001005191.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:9325149 G>T maps to NM_001005191.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:9361886 G>A maps to NM_001079935.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr19:9361928 C>T maps to NM_001079935.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:9361943 C>A maps to NM_001079935.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:9361817 G>T maps to NM_001079935.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:9361880 G>A maps to NM_001079935.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:9362621 C>A maps to NM_001079935.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:9361871 C>A maps to NM_001079935.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:9362501 T>C maps to NM_001079935.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:9361931 C>T maps to NM_001079935.1 S71S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z030-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:9225998 G>T maps to ENST00000293614 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:9226301 G>C maps to ENST00000293614 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr19:9226408 C>A maps to ENST00000293614 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:9226190 C>T maps to ENST00000293614 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:9225956 C>T maps to ENST00000293614 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:9225958 G>A maps to ENST00000293614 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:9225932 G>T maps to ENST00000293614 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr19:9213199 G>T maps to NM_001005193.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:9213382 A>T maps to NM_001005193.1 C200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:9213805 G>T maps to NM_001005193.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:9213241 C>T maps to NM_001005193.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:9213343 G>T maps to NM_001005193.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:9213202 G>T maps to NM_001005193.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:9237032 C>A maps to NM_001001958.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:9237506 C>A maps to NM_001001958.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:9237083 T>C maps to NM_001001958.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:9236945 T>C maps to NM_001001958.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:9236777 G>T maps to NM_001001958.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr19:9237521 G>T maps to NM_001001958.1 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:9236786 C>A maps to NM_001001958.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:124440002 C>G maps to NM_001005194.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:124440911 C>A maps to NM_001005194.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:124440818 C>A maps to NM_001005194.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:124440746 T>A maps to NM_001005194.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:124413355 G>C maps to NM_001005195.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124413478 G>T maps to NM_001005195.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:124413489 C>A maps to NM_001005195.1 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:124413322 G>T maps to NM_001005195.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:124412647 C>T maps to NM_001005195.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr11:124412752 G>T maps to NM_001005195.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:124412911 G>T maps to NM_001005195.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:124413268 T>A maps to NM_001005195.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr11:124413307 C>T maps to NM_001005195.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:124252846 C>G maps to NM_001005468.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:124252801 A>G maps to NM_001005468.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:124252357 C>T maps to NM_001005468.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr11:124266587 G>A maps to NM_001005467.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr11:124294722 C>A maps to NM_001005196.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:124294272 C>A maps to NM_001005196.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:124294647 C>A maps to NM_001005196.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:124294048 C>T maps to NM_001005196.1 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:124294221 G>T maps to NM_001005196.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr11:124310357 A>C maps to NM_012378.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:124310873 C>T maps to NM_012378.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:124180113 G>T maps to NM_001002917.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:124179837 A>G maps to NM_001002917.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:124180512 T>A maps to NM_001002917.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr11:124180044 G>A maps to NM_001002917.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:124179962 G>T maps to NM_001002917.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:124189357 A>G maps to NM_001002918.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr11:124189501 G>A maps to NM_001002918.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:124189265 C>T maps to NM_001002918.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:124189724 A>G maps to NM_001002918.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:123777581 C>A maps to NM_001005197.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:123777146 A>T maps to NM_001005197.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:123777146 A>T maps to NM_001005197.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:123777158 C>T maps to NM_001005197.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:123777257 G>T maps to NM_001005197.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:123777258 G>T maps to NM_001005197.1 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:123777515 C>A maps to NM_001005197.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:123777893 T>A maps to NM_001005197.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr11:56058355 A>G maps to NM_001005199.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:56057902 T>G maps to NM_001005199.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:56057629 G>T maps to NM_001005199.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:56057941 G>A maps to NM_001005199.1 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:56058409 C>A maps to NM_001005199.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:55872680 C>T maps to NM_001005200.1 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr11:55872949 C>A maps to NM_001005200.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:55873051 C>T maps to NM_001005200.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:55872763 C>A maps to NM_001005200.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:55873256 G>T maps to NM_001005200.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:55873240 C>A maps to NM_001005200.1 C241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:55873186 T>C maps to NM_001005200.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr11:55872751 C>T maps to NM_001005200.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:55872769 G>A maps to NM_001005200.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:55872769 G>A maps to NM_001005200.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr11:55873212 C>A maps to NM_001005200.1 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:55873322 G>T maps to NM_001005200.1 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:55890174 T>C maps to NM_001005201.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:55890586 G>T maps to NM_001005201.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:55890480 T>G maps to NM_001005201.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:55890408 G>T maps to NM_001005201.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:55889871 A>T maps to NM_001005201.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:55890462 C>A maps to NM_001005201.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:55860900 T>C maps to NM_001003750.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55861579 C>A maps to NM_001003750.1 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55861151 C>A maps to NM_001003750.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:55861055 C>A maps to NM_001003750.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:55861457 G>T maps to NM_001003750.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr11:55861180 C>A maps to NM_001003750.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:55861154 A>T maps to NM_001003750.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr11:55861484 G>A maps to NM_001003750.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:55860791 C>A maps to NM_001003750.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr11:55861040 A>G maps to NM_001003750.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:56128117 C>T maps to NM_001005205.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:56127955 C>A maps to NM_001005205.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:56128651 C>A maps to NM_001005205.1 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:56128507 C>A maps to NM_001005205.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:56128531 T>A maps to NM_001005205.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:56128646 C>T maps to NM_001005205.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:56128025 G>T maps to NM_001005205.1 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:56128129 G>T maps to NM_001005205.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:56128117 C>G maps to NM_001005205.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:56128012 T>A maps to NM_001005205.1 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:56127835 C>G maps to NM_001005205.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:56128573 T>A maps to NM_001005205.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:56128024 G>T maps to NM_001005205.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:56127850 G>T maps to NM_001005205.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904483 G>T maps to NM_001004064.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:55904891 C>A maps to NM_001004064.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:55904779 G>T maps to NM_001004064.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr11:55904813 A>G maps to NM_001004064.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:55905005 C>T maps to NM_001004064.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr11:55904969 A>T maps to NM_001004064.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:55904447 C>A maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:55904333 G>T maps to NM_001004064.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr11:55904330 C>T maps to NM_001004064.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:55905080 G>T maps to NM_001004064.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:56113543 G>C maps to NM_001002907.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:56113903 A>T maps to NM_001002907.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:56113825 C>A maps to NM_001002907.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:56113888 C>A maps to NM_001002907.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:56113750 C>A maps to NM_001002907.1 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:56113927 C>T maps to NM_001002907.1 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:56113900 C>A maps to NM_001002907.1 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56086191 C>A maps to NM_001005202.1 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56085805 G>T maps to NM_001005202.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:56085827 G>T maps to NM_001005202.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:56086306 T>C maps to NM_001005202.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:56085898 G>A maps to NM_001005202.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr11:56085805 G>T maps to NM_001005202.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:56086249 T>C maps to NM_001005202.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:55927528 G>T maps to NM_001004058.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr11:55927729 C>A maps to NM_001004058.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:55927547 C>T maps to NM_001004058.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:48920046 C>T maps to NM_001005203.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr12:48919740 G>T maps to NM_001005203.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:48919524 G>T maps to NM_001005203.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:48921693 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:48921774 C>A maps to NM_001005203.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:142723538 G>A maps to NM_001001658.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:142723472 G>T maps to NM_001001658.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:142723378 G>A maps to NM_001001658.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:142723319 C>T maps to NM_001001658.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:142724021 A>T maps to NM_001001658.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:141618908 C>T maps to NM_001001656.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:141619430 C>A maps to NM_001001656.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr7:141619586 G>C maps to NM_001001656.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:141619190 T>C maps to NM_001001656.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr7:141619370 T>G maps to NM_001001656.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:141618890 C>T maps to NM_001001656.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56468741 T>C maps to NM_001013358.1 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:56468504 G>T maps to NM_001013358.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:56468594 G>T maps to NM_001013358.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:56468588 C>A maps to NM_001013358.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:56468309 T>C maps to NM_001013358.1 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:56468516 C>T maps to NM_001013358.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:56468282 T>C maps to NM_001013358.1 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:56468471 C>T maps to NM_001013358.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:56468603 C>G maps to NM_001013358.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:56468495 G>A maps to NM_001013358.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:56468059 C>A maps to NM_001013358.1 S66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:56468177 G>T maps to NM_001013358.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:56468108 G>A maps to NM_001013358.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:56468177 G>C maps to NM_001013358.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:56510822 G>C maps to NM_001005284.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:56511218 G>T maps to NM_001005284.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:56510306 T>C maps to NM_001005284.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:56511221 G>T maps to NM_001005284.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr11:56510969 G>C maps to NM_001005284.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr11:56510846 A>G maps to NM_001005284.1 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:56510405 G>T maps to NM_001005284.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr11:57886055 A>T maps to NM_001005211.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:57886528 G>A maps to NM_001005211.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr11:57886583 C>T maps to NM_001005211.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:55524458 C>T maps to NM_001005243.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:55524037 C>A maps to NM_001005243.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr12:55524127 T>G maps to NM_001005243.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:55523707 C>A maps to NM_001005243.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:55523902 C>A maps to NM_001005243.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:55523944 C>T maps to NM_001005243.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:57946993 T>C maps to NM_001005212.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:57947581 C>A maps to NM_001005212.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr11:57947392 G>T maps to NM_001005212.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:57947779 C>A maps to NM_001005212.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:57958654 T>C maps to NM_001005283.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:57958804 G>A maps to NM_001005283.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:57958024 C>G maps to NM_001005283.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:57958039 T>C maps to NM_001005283.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:122064793 G>T maps to NM_032790.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr7:102087126 G>A maps to NM_032831.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:69488078 C>A maps to ENST00000376587 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr1:52867115 G>A maps to NM_004153.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr1:52867034 A>G maps to NM_004153.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:52854938 G>A maps to NM_004153.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:52859451 G>A maps to NM_004153.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:52847400 T>A maps to NM_004153.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:201785051 A>C maps to NM_006190.4 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:201800585 C>A maps to NM_006190.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr2:201822818 T>A maps to NM_006190.4 K10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:88375548 C>T maps to NM_181837.2 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:88344666 A>T maps to NM_181837.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:148715892 C>A maps to NM_181742.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:148733485 T>A maps to NM_181742.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:148730379 C>A maps to NM_181742.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:148705694 T>A maps to NM_181742.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103838231 C>A maps to NM_002553.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103808890 C>A maps to NM_181747.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:103808966 C>T maps to NM_002553.3 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:58114581 G>T maps to NM_006812.3 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:58109616 T>A maps to NM_006812.3 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr11:59376079 T>A maps to NM_002556.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:59382831 G>A maps to NM_002556.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:59367986 G>C maps to NM_002556.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr11:59377943 G>A maps to NM_002556.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr22:31091087 G>T maps to NM_030758.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr22:31266431 C>T maps to NM_030758.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:31286743 C>T maps to NM_030758.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:125298817 C>T maps to NM_022776.4 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:125279255 C>T maps to NM_022776.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:125286263 G>C maps to NM_022776.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:125271279 C>A maps to NM_022776.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr3:125271433 G>T maps to NM_022776.4 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr18:21750344 G>A maps to NM_080597.2 D788D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr18:21897288 A>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:21891946 C>A did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr18:21747355 T>C maps to NM_080597.2 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60864346 C>T maps to NM_144498.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:24901332 G>T maps to NM_015550.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:24874131 C>A maps to NM_015550.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:24881966 G>A maps to NM_015550.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:3114884 G>A maps to NM_020896.3 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:3114833 C>T maps to NM_020896.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:3111786 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:3114893 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:3121424 C>T maps to NM_020896.3 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr11:3125496 G>T maps to NM_020896.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179214116 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:179226407 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:179255853 G>T maps to ENST00000392505 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:179248839 A>T maps to ENST00000392505 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179209050 G>A maps to ENST00000392505 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:179248904 T>C did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:179247976 G>A maps to ENST00000392505 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:179197660 C>T maps to ENST00000392505 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:45896420 C>A maps to NM_145798.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr17:45886293 C>A maps to NM_145798.2 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:45893992 G>A maps to NM_145798.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:45891147 C>T maps to NM_145798.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr17:45886268 G>T maps to NM_145798.2 S753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:76750466 C>A maps to NM_020841.4 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:76752582 G>A maps to NM_020841.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:76786452 C>T maps to NM_020841.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:76779953 A>G maps to NM_020841.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:76788491 C>T maps to NM_020841.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:76778052 C>A maps to NM_020841.4 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:54604074 C>A maps to NM_130771.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr19:54600428 A>T maps to NM_130771.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:54598551 G>T maps to NM_130771.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr19:54598590 G>A maps to NM_130771.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:54598536 G>T maps to NM_130771.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:54603065 G>A maps to NM_130771.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20917121 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr14:20922833 C>T maps to NM_017807.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr14:20917173 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190619988 A>T maps to NM_022353.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:190620066 A>G maps to NM_022353.2 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:83992863 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr16:83999017 G>T maps to NM_013370.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr16:83999434 G>T maps to NM_013370.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr22:30660258 C>T maps to NM_020530.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr22:30660135 G>T maps to NM_020530.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:38919156 C>T maps to NM_003999.2 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr5:38925342 G>T maps to NM_003999.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:38925399 C>T maps to NM_003999.2 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:38885505 G>A maps to NM_003999.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:38933464 G>A maps to NM_003999.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:19553251 T>G maps to NM_145260.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:99962907 C>T maps to ENST00000457907 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:99961383 C>A maps to ENST00000457907 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr8:99961617 C>T maps to ENST00000457907 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:99961557 G>T maps to ENST00000457907 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr8:99961587 G>C maps to ENST00000457907 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr15:65345483 A>G maps to NM_178859.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:109571950 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr4:109571865 C>T maps to ENST00000512478 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:77732460 A>T maps to NM_012383.4 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:77745522 C>T maps to NM_012383.4 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr3:190967906 C>A maps to NM_198184.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:190936624 T>A maps to NM_198184.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:195953989 G>A maps to NM_152672.5 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:195960060 C>G maps to NM_152672.5 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:38271169 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:38226590 T>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:38229079 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:38262931 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:38226662 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:38271133 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:38262993 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:38268136 C>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:38262961 T>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:38262951 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:38260567 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:21726421 C>A maps to ENST00000286149 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:21737979 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:21739596 C>T maps to ENST00000286149 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr16:21693115 G>T maps to ENST00000286149 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr16:21734263 A>G maps to ENST00000286149 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr16:21712279 G>T maps to ENST00000286149 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr2:26695490 G>A maps to NM_194248.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:26696879 C>A maps to NM_194248.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:26689580 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:26683599 C>A maps to NM_194248.2 E1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr2:26684612 G>C maps to NM_194248.2 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:26717863 G>A maps to NM_194248.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:26706329 C>T maps to NM_194248.2 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:26705388 G>A maps to NM_194248.2 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:26750698 C>A did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr2:26702188 C>G maps to NM_194248.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:26690337 C>T maps to NM_194248.2 K1374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr2:26691278 C>A maps to NM_194248.2 E1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr2:26739455 G>T maps to NM_194248.2 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:161221369 C>T maps to NM_001080440.1 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr3:161221657 C>A maps to NM_001080440.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:161220138 G>T maps to NM_001080440.1 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr4:4199744 G>T maps to NM_177998.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr4:4214687 G>T maps to NM_177998.1 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr4:4190544 G>C maps to NM_177998.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:4190607 G>T maps to NM_177998.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr4:4199063 G>T maps to NM_177998.1 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:72921750 G>T maps to NM_178160.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:72920957 C>A maps to NM_178160.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:72926572 T>A maps to NM_178160.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr17:72943236 C>T maps to NM_178233.1 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:72942966 C>T maps to NM_178233.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr20:16729510 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:241078630 G>A maps to NM_148961.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:241078673 G>T maps to NM_148961.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:241078727 G>T maps to NM_148961.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:20216955 G>T maps to NM_015207.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:48780528 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:48781241 G>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:48783165 C>A did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr23:48791831 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:48781241 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:69282976 C>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:69283032 T>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:69283008 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:69283038 T>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:69283182 A>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:69283108 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:69282925 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:69282871 T>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:69283018 A>G did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:69283068 C>A did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr23:69282642 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:69282899 A>G did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:69283122 T>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:69283211 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:69282385 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:69282947 C>A did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:69282482 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:92090699 T>C maps to NM_016023.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:92083504 T>C maps to NM_016023.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:31819479 C>A maps to ENST00000382902 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:31776660 C>A maps to ENST00000382902 V546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:31862302 A>G maps to ENST00000382902 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:31776741 G>C maps to ENST00000382902 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:149943153 G>A maps to NM_020205.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr1:149936221 T>C maps to NM_020205.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:149943015 G>C maps to NM_020205.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:149915756 C>A maps to NM_020205.2 *844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:149916619 C>G maps to NM_020205.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:149919236 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:63280139 C>T maps to NM_014562.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:63280222 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:63282685 G>T maps to NM_014562.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr14:57268909 G>T maps to NM_021728.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:57268854 G>A maps to NM_021728.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:57268455 C>T maps to NM_021728.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:29648296 A>T maps to NM_183378.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:29604464 G>A maps to NM_183378.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:29614864 A>G maps to NM_183378.2 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:29604478 C>A maps to NM_183378.2 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:29592259 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:29627992 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:29642558 G>C maps to NM_183378.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr12:29614909 A>T maps to NM_183378.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:29630271 A>T did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr12:29624865 G>T maps to NM_183378.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:29614828 G>T maps to NM_183378.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:29640680 G>T maps to NM_183378.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:29614941 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:29639281 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr12:29617626 C>T maps to NM_183378.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:29648338 C>T maps to NM_183378.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:29642558 G>C maps to NM_183378.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr12:29639252 T>C maps to NM_183378.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:29630154 A>T maps to NM_183378.2 C419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:29642558 G>T maps to NM_183378.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:29631787 G>T maps to NM_183378.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:7722002 C>A maps to NM_198185.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:7712602 G>T maps to NM_198185.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr14:23239012 C>G maps to NM_005015.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:23237369 C>T maps to NM_005015.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:41762286 C>A maps to NM_000436.3 G422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:41870397 C>T maps to NM_000436.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:41739503 C>G maps to NM_000436.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr5:41862831 G>A maps to NM_000436.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:41870433 G>A maps to NM_000436.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:41853622 C>A maps to NM_000436.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:41842841 T>A maps to NM_000436.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:40236168 A>G maps to NM_022120.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:42991091 C>A maps to NM_148962.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:42991238 G>C maps to NM_148962.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr13:97639077 A>G maps to NM_080818.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr13:97639788 C>A maps to NM_080818.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr13:97639371 C>T maps to NM_080818.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:107763108 T>C maps to NM_001198533.1 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:107752608 A>G maps to NM_001198533.1 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:107691472 G>T maps to NM_001198533.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:107751702 C>T maps to NM_001198533.1 D685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:107754475 A>G maps to NM_001198533.1 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:107726140 A>T maps to NM_001198533.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:107691490 C>T maps to NM_001198533.1 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr8:107719107 T>C maps to NM_001198533.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:25833305 A>G maps to NM_017897.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:25833257 C>G maps to NM_017897.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:38266059 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:38287588 G>T maps to NM_005109.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr3:8809555 G>A maps to NM_000916.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr3:8809378 C>T maps to NM_000916.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:3802968 C>G maps to NM_002558.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:3807292 G>T maps to NM_002558.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:3802962 G>T maps to NM_002558.2 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr17:3802230 G>A maps to NM_002558.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr17:3808612 G>A maps to NM_002558.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:133196906 C>A maps to NM_170683.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:133196473 C>A maps to NM_170683.2 C142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:133197925 G>T maps to NM_170683.2 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:133198152 C>T maps to NM_170683.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:57114658 G>T maps to NM_002559.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:57114032 C>T maps to NM_002559.2 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:57114086 G>A maps to NM_002559.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:121670267 C>T maps to NM_002560.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:121660768 C>T maps to NM_002560.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3593444 C>A did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:3591920 T>A maps to ENST00000435558 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr22:21377448 C>A maps to NM_005446.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr22:21377427 C>A maps to NM_005446.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:121603860 G>C maps to NM_002562.5 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:121613189 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:152553900 C>G maps to NM_002563.2 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:152553813 G>A maps to NM_002563.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:152554644 C>T maps to NM_002563.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:78216451 G>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:78216968 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:78216602 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:78216045 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:78216670 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:78217003 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:78216959 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:78216791 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:78216857 C>G did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:78216858 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:78216920 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:78216921 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:78216846 G>C did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:78216468 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:78216607 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:78216337 G>C did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:78216864 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:78216153 T>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:78216191 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:78216350 C>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:78216424 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:78216120 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:78216520 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:78217035 A>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:78216072 G>C did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr23:78217035 A>G did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:78216381 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:78216208 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:78216849 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:78216670 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:151055928 G>A maps to NM_022788.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr3:150931543 T>A maps to NM_014879.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:150931951 G>T maps to NM_014879.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:72945674 G>T maps to NM_176071.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:69479164 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:69478985 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:69478528 G>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:69478946 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:69478591 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:69478546 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:73008426 G>A maps to NM_004154.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:73007895 C>T maps to NM_004154.3 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:73008273 G>T maps to NM_004154.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:1584525 C>G did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:1584584 G>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:1584614 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:1585307 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:1585308 A>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:1584789 A>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:1584779 C>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:1585187 G>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:1585175 C>A did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:1584435 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:1584596 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:1584743 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:1584493 T>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:1585326 A>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:1585172 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:1584428 A>T did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr10:74813241 G>A maps to NM_000917.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr10:74813306 C>A maps to NM_000917.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:131544998 C>G maps to NM_001142599.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:131534589 C>T maps to NM_001142599.1 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:131539794 G>T maps to NM_001142599.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr5:131546064 T>A maps to NM_001142599.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:73988086 C>A maps to NM_182904.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:73979201 C>A maps to NM_182904.3 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:73988125 G>A maps to NM_182904.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:79813035 C>A maps to NM_000918.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:79817263 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:79804358 C>T maps to NM_000918.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:79813068 G>A maps to NM_000918.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr17:79805208 C>G maps to NM_000918.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:49042347 G>T maps to NM_177938.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:56500855 C>T maps to NM_006191.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:73620585 G>T maps to NM_025155.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:73625494 C>G maps to NM_025155.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:101718959 G>A maps to NM_002568.3 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:101721761 T>A maps to NM_002568.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:43552897 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr20:43538804 C>T maps to NM_001124756.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:43552821 G>A maps to NM_001124756.1 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:43559303 G>A maps to NM_001124756.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr13:25671838 C>T maps to NM_030979.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr13:25670398 C>T maps to NM_030979.2 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr1:40035544 G>A maps to NM_001135653.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:40030415 A>T maps to NM_001135653.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:40028025 T>A maps to NM_001135653.1 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:90691247 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:90691097 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:90691482 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:90690870 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:90690937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:90690786 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:90691662 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:90690838 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:90690947 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:90690915 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:90690794 G>C did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:90690775 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:90690940 T>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:90691001 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:90691473 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:90691643 A>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:90691702 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:90691150 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:90691714 G>C did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:90690800 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:90691231 T>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:90691081 G>T did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:90691564 G>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:90690696 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:90690955 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:90690969 A>G did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:90691683 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:90691595 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:90691532 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:23792259 C>T maps to NM_004643.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr14:23792632 C>G maps to NM_004643.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr14:23793489 C>T maps to NM_004643.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:163235180 G>A maps to NM_152410.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr4:20709440 C>A maps to ENST00000503585 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr4:20714529 G>T maps to ENST00000503585 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:66001696 G>A maps to NM_018026.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:65998371 C>T maps to NM_018026.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr11:65983734 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:65988099 A>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:105818725 A>G maps to ENST00000458164 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:105814895 G>T maps to ENST00000458164 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr14:105833557 A>G maps to ENST00000458164 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr14:105849202 G>A maps to ENST00000458164 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:34499493 C>T maps to NM_020804.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:34498310 G>T maps to NM_020804.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr22:43272320 C>T maps to NM_001184970.1 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:43284729 G>A maps to NM_001184970.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:47204065 G>A maps to NM_016223.4 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:17555219 G>T maps to NM_013358.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:17559429 C>T maps to NM_013358.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:17570584 G>A maps to NM_013358.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:17418972 G>T maps to NM_007365.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:17413135 C>A maps to NM_007365.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr1:17413183 G>A maps to NM_007365.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:17593245 C>A maps to NM_016233.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:17599914 G>A maps to NM_016233.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:17575700 G>A maps to NM_016233.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:17593260 G>T maps to NM_016233.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:17597415 C>A maps to NM_016233.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:17594365 G>A maps to NM_016233.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:17668496 C>T maps to NM_012387.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:17674518 G>A maps to NM_012387.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:17664567 C>T maps to NM_012387.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:17634767 C>A maps to NM_012387.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:17666216 G>A maps to NM_012387.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:17690069 C>A maps to NM_012387.2 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:17682573 G>T maps to NM_012387.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:17725321 G>A maps to NM_207421.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:17708468 G>A maps to NM_207421.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:2583588 G>T maps to NM_000430.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:42804210 C>A maps to NM_001145940.1 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr8:81899638 G>A maps to NM_018440.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:49455911 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:49458769 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:49454071 C>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:49458730 C>G did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:55117811 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:55117841 A>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:55116964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:55103863 G>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:55103103 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:49597216 C>G did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:49597219 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:55249083 T>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:55248205 C>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:55248300 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:55248249 T>C did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:55249154 G>C did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:55247074 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:55247846 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:55247880 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:103249049 C>G maps to NM_000277.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:103240675 G>T maps to NM_000277.1 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:103246728 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:43535035 G>C maps to NM_006451.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:77070047 C>A maps to NM_001128620.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:77064627 C>A maps to NM_001128620.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:77070062 C>G did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:77090367 T>C maps to NM_001128620.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr11:77054933 C>A maps to NM_001128620.1 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:10702847 C>A maps to NM_017906.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:10707697 C>G maps to NM_017906.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:196509690 A>T maps to NM_002577.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:196509564 G>A maps to NM_002577.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:110406154 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:110459766 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:110439736 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:110439095 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:110459750 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:110435807 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:110439860 C>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:110439767 G>A did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:110385360 T>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:110366400 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:110390964 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:110366340 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:110463589 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:110395674 G>C did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:110439077 A>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:110459766 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:110463670 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39665644 C>G maps to NM_005884.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:39660360 C>T maps to NM_005884.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr15:40566419 G>A maps to NM_020168.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr15:40568141 G>T maps to NM_020168.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:40558062 G>A maps to NM_020168.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:40564711 A>T maps to NM_020168.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:9525047 C>A maps to NM_177990.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:9546641 G>T maps to NM_177990.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:9546830 C>A maps to NM_177990.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:9520258 A>C maps to NM_177990.2 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:9624771 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:9546656 G>T maps to NM_177990.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:9543539 G>A maps to NM_177990.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr20:9546590 C>T maps to NM_177990.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr20:9546719 C>T maps to NM_177990.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:9560827 G>T maps to NM_177990.2 Y318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:9561328 G>T maps to NM_177990.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr20:9520195 G>T maps to NM_177990.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:9561031 C>T maps to NM_177990.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:9525047 C>A maps to NM_177990.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:9561250 G>A maps to NM_177990.2 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:9546845 C>A maps to NM_177990.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr16:23614845 C>T maps to NM_024675.3 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:23646429 C>T maps to NM_024675.3 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:169632954 C>T maps to NM_001166108.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:169611776 G>A maps to NM_001166108.1 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:169611825 C>T maps to NM_001166108.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:169842779 G>T maps to NM_001166108.1 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:169602531 A>G maps to NM_001166108.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr4:169602546 A>G maps to NM_001166108.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:169632828 C>A maps to NM_001166108.1 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:169606710 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:100155279 T>A maps to NM_017734.4 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:100152285 G>A maps to NM_017734.4 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:102361024 A>C maps to NM_000919.3 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:102285238 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr5:102260735 G>A maps to NM_000919.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:35454104 G>T maps to NM_015430.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:35454044 C>A maps to NM_015430.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:35463194 C>A maps to NM_015430.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:35453912 A>G maps to NM_015430.2 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:35463053 T>A maps to NM_015430.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:35456352 C>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr11:35453993 C>T maps to NM_015430.2 W708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:56713244 C>G maps to NM_001127460.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:56712093 G>A maps to NM_001127460.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:56712161 G>A maps to NM_001127460.2 Q1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:56720555 G>A maps to NM_001127460.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:56726625 C>A maps to NM_001127460.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr13:28855516 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:28835535 A>G did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr13:28855450 G>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:91404708 C>T maps to NM_148977.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:91359244 C>G maps to NM_148977.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:91404900 G>T maps to NM_148977.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:3869921 C>T maps to NM_153638.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr20:3891394 C>T maps to NM_153638.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:167995914 T>C maps to NM_024594.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:2452748 T>A maps to ENST00000425477 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:2452730 C>A maps to ENST00000425477 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:2441344 C>A maps to ENST00000425477 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:2451330 C>T maps to ENST00000425477 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:93912878 G>C maps to NM_015368.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:93886732 G>A maps to NM_015368.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:93913423 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:124489662 C>T maps to NM_052959.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr11:124489323 C>T maps to NM_052959.2 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:135193659 G>T maps to NM_152911.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:135204975 C>G maps to NM_207128.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:78915545 G>C maps to NM_173797.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr5:78915519 C>T maps to NM_173797.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr16:50250030 C>G maps to NM_001040284.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:6750511 G>T maps to NM_006999.4 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:6749705 G>A maps to NM_006999.4 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:39591612 C>A maps to NM_001004318.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:39591586 A>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr14:73733265 C>G maps to ENST00000427855 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:73720460 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr14:73721604 G>T maps to ENST00000427855 S502S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8507-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:73719442 C>A maps to ENST00000427855 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:97009143 G>T maps to NM_032632.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:97022201 A>T maps to NM_032632.3 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:4900090 C>A maps to NM_020144.4 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:61010338 A>G maps to NM_022894.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:60998765 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:61009051 C>T maps to NM_022894.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:118989775 T>A maps to NM_002581.3 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr9:118982342 G>T maps to NM_002581.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:118974077 G>A maps to NM_002581.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr9:118949433 G>A maps to NM_002581.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr9:118950087 G>A maps to NM_002581.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:118949474 G>A maps to NM_002581.3 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:118989707 A>G did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr9:119124911 C>T maps to NM_002581.3 T1463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:118950339 C>A maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:118969866 C>A maps to NM_002581.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr9:119115903 G>A maps to NM_002581.3 R1393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr9:119097263 G>C maps to NM_002581.3 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr9:119097320 G>A maps to NM_002581.3 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:176709119 C>T maps to NM_020318.2 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:176679221 C>A maps to NM_020318.2 Y1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:176661379 T>C maps to NM_020318.2 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:176762726 C>G maps to NM_020318.2 P1684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:176526297 T>A maps to NM_020318.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:176734816 C>A maps to NM_020318.2 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:176526165 G>A maps to NM_020318.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:176564365 G>T maps to NM_020318.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:176525706 C>A maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:176526270 G>T maps to NM_020318.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:176526315 G>T maps to NM_020318.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:176525865 G>A maps to NM_020318.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:176564455 C>A maps to NM_020318.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:176525706 C>T maps to NM_020318.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:176762717 T>C maps to NM_020318.2 C1681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:176563987 G>T maps to NM_020318.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:176740127 T>A maps to NM_020318.2 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:176668419 C>G maps to NM_020318.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:176526088 G>T maps to NM_020318.2 G211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:176564300 G>T maps to NM_020318.2 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:176762729 C>G maps to NM_020318.2 P1685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:176564659 C>T maps to NM_020318.2 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:176759077 C>T maps to NM_020318.2 Q1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:176738882 C>T maps to NM_020318.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:176564446 C>A maps to NM_020318.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:176563797 T>A maps to NM_020318.2 L353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:176738759 A>G maps to NM_020318.2 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:176661344 G>T maps to NM_020318.2 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:176734957 C>A maps to NM_020318.2 Y1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:176664878 C>A maps to NM_020318.2 S877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:176564227 C>A maps to NM_020318.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:176564104 C>A maps to NM_020318.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:176661388 C>T maps to NM_020318.2 I853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:176738825 G>A maps to NM_020318.2 P1469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:176708896 G>T maps to NM_020318.2 G1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:176526315 G>T maps to NM_020318.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:176564386 G>T maps to NM_020318.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:176668545 G>C maps to NM_020318.2 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:176738909 C>T maps to NM_020318.2 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:176668356 C>A maps to NM_020318.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:176760503 G>T maps to NM_020318.2 E1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:108576015 C>A maps to NM_005443.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:108566002 C>A maps to NM_005443.4 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:89475486 A>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:89475535 C>G maps to NM_001015880.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:79856273 C>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr15:69692414 C>T maps to NM_017705.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr15:69696022 C>A maps to NM_017705.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:156214603 G>C maps to NM_024897.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr1:26189835 G>A maps to NM_178422.5 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr6:52269009 C>T maps to ENST00000361841 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:142681359 G>T maps to NM_198504.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142681452 C>A maps to NM_198504.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:142681338 G>C maps to NM_198504.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:142681275 C>A maps to NM_198504.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:34690797 T>C maps to NM_019619.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:34400443 G>A maps to NM_019619.3 Q1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr10:34573100 T>G maps to NM_019619.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:34688330 T>A maps to NM_019619.3 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:34806021 C>A maps to NM_019619.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:206166422 G>A maps to ENST00000406610 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:206265803 C>T maps to ENST00000406610 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:206023444 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:206480372 A>T maps to ENST00000406610 K1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:205986560 G>A maps to ENST00000406610 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:206364737 G>T maps to ENST00000406610 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:205986567 C>T maps to ENST00000406610 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr2:206364755 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:206418046 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:206036932 A>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr20:49366454 A>G maps to NM_032521.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:162475169 G>T maps to NM_004562.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr6:161781118 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:161969911 C>A maps to NM_004562.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:162683596 G>A maps to NM_004562.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:161970004 C>A maps to NM_004562.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:162683713 G>T maps to NM_004562.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:161969903 G>T maps to NM_004562.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:162206909 G>A maps to NM_004562.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:162683677 C>A maps to NM_004562.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:183547409 G>A maps to NM_018622.5 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:14540931 T>A maps to NM_002582.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:14687235 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:14576589 C>T maps to NM_002582.2 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr16:14645890 C>T maps to NM_002582.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226576434 C>T maps to NM_001618.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:226574073 C>A maps to NM_001618.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:226553693 A>G maps to NM_001618.3 H822H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:145057391 G>A maps to NM_032789.3 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:145058996 A>T maps to NM_032789.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:145058990 C>A maps to NM_032789.3 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:145059359 A>G maps to NM_032789.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145060241 G>C maps to NM_032789.3 L54L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:3921378 G>A maps to NM_020367.4 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:139724635 G>A maps to NM_022750.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:139741442 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:139756776 C>T maps to NM_022750.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:122446792 C>T maps to NM_017554.2 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:122432420 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr3:122437575 C>A maps to NM_017554.2 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:122422782 G>T maps to NM_017554.2 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:122353865 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:65559013 G>A maps to NM_017851.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr15:65553240 G>C maps to NM_017851.4 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr15:65553263 T>A maps to NM_017851.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr15:65559052 C>T maps to NM_017851.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20824168 C>T maps to NM_005484.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:20811811 G>T maps to NM_005484.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:51978184 C>A maps to NM_001003931.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:51978524 G>A maps to NM_001003931.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:25000736 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:25029153 C>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr13:25021219 G>A maps to NM_006437.3 A1073A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr13:25023876 G>A maps to NM_006437.3 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr13:25060418 C>T maps to NM_006437.3 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr13:25075912 G>T maps to NM_006437.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:25017844 T>A maps to NM_006437.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr13:25009357 T>A maps to NM_006437.3 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:72549733 C>G maps to NM_020214.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr15:72552002 C>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr15:72554008 C>G maps to NM_020214.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:50111264 G>T did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr5:50111357 G>A maps to ENST00000505697 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr5:50091198 C>G maps to ENST00000505697 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:50073901 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:50055519 A>G maps to ENST00000505697 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:55223832 C>A maps to NM_152268.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr22:44527412 C>T maps to NM_001003828.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr22:44532398 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:44527487 G>T maps to NM_001003828.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr22:44585088 C>A maps to NM_001137606.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:150817160 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:150841004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:150789452 G>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:150840928 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:150832784 T>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:150832591 C>G did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:150832661 G>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:150780188 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:150780225 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:150832646 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:150842573 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:150842425 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:150842426 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:150844492 G>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:150839610 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:150832708 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:150828194 A>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:150839638 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:150828285 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:150840993 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:150840241 C>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:150773188 A>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:150840244 C>G did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:150840163 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:150828214 T>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:150773155 T>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:150840151 C>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:150828208 G>T did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:150840875 G>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:150773198 C>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:150789476 C>G did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr23:150842554 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:150840122 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:150773179 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:242066562 C>A maps to ENST00000358649 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:242065749 T>C maps to ENST00000358649 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:242066663 C>A maps to ENST00000358649 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:242065725 G>A maps to ENST00000358649 N868N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:242077445 C>A maps to ENST00000358649 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:242075337 C>A maps to ENST00000358649 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:242066202 C>A maps to ENST00000358649 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:242066604 C>A maps to ENST00000358649 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:242054765 T>C maps to ENST00000358649 K1045K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:125616205 A>T maps to NM_138294.2 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr11:59417005 T>C maps to NM_152716.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:59406552 C>G maps to NM_152716.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:31740991 G>A maps to NM_014323.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:79986433 G>A maps to NM_002583.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:80014935 C>A maps to NM_002583.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:21689879 C>G maps to NM_006192.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:21687544 C>A maps to NM_006192.3 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:21687187 C>A maps to NM_006192.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr20:21687574 C>G maps to NM_006192.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr20:21687580 C>G maps to NM_006192.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr20:21687130 C>A maps to NM_006192.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:21695212 C>A maps to NM_006192.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr10:102586787 G>T maps to NM_003987.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:102509611 C>A maps to NM_003987.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:102509554 C>T maps to NM_003987.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:102566265 C>G maps to NM_003987.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:223084954 G>T maps to NM_181459.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:223160316 G>T maps to NM_181459.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:223158476 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:223158468 G>C maps to NM_013942.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:127251681 G>A maps to NM_006193.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:127255535 G>T maps to NM_006193.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:127251135 T>A maps to NM_006193.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:127255514 C>T maps to NM_006193.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr7:127253551 G>T maps to NM_006193.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:127255044 A>T maps to NM_006193.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr7:127251159 G>A maps to NM_006193.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36882088 C>A maps to NM_016734.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:36882058 G>A maps to NM_016734.1 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:36846920 C>A maps to NM_016734.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:36966698 C>T maps to NM_016734.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr9:36846873 G>A maps to NM_016734.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:36966712 C>A maps to NM_016734.1 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr9:36882073 G>A maps to NM_016734.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:31812321 G>T maps to NM_001604.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:31811520 A>G maps to NM_001604.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr11:31815102 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:31823442 T>C maps to NM_001604.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:31812339 C>A maps to NM_001604.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:31811562 G>T maps to NM_001604.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:31815227 G>T maps to NM_001604.4 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:31815012 G>A maps to NM_001604.4 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:19062358 C>A maps to NM_002584.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19062124 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:19018402 G>T maps to NM_002584.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:19018323 G>C maps to NM_002584.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:19027163 C>T maps to NM_002584.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:19062343 C>A maps to NM_002584.2 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:114002023 G>C maps to NM_003466.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:114002064 G>T maps to NM_003466.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:154775015 C>A maps to NM_007349.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:154755398 G>A maps to NM_007349.3 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr7:154738231 G>C maps to NM_007349.3 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:70048378 C>A maps to NM_022129.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:70045147 G>C maps to NM_022129.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:70056646 T>A maps to NM_022129.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr3:52584761 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:52623228 G>C maps to ENST00000296302 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr3:52623228 G>C maps to ENST00000296302 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:52713718 G>T maps to ENST00000296302 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:164761872 T>C maps to NM_002585.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:164761969 G>T maps to NM_002585.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:32155933 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:32154221 G>A maps to NM_002586.4 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:128697855 G>C maps to ENST00000373487 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:128722998 A>T maps to ENST00000373487 K315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr9:128724492 G>A maps to ENST00000373487 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:19681571 C>G maps to NM_025245.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:154919081 C>T maps to NM_020524.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:154918694 C>T maps to NM_020524.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:154919934 G>A maps to NM_020524.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154918706 C>T maps to NM_020524.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:154920024 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:66617696 G>C maps to NM_022172.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:66620060 C>T maps to NM_022172.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:66636435 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr11:66631268 C>A maps to NM_022172.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr11:66620018 G>A maps to NM_022172.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:66619931 G>C maps to NM_022172.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:66638804 C>A maps to NM_022172.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:53849271 G>T maps to NM_005016.5 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr21:47359948 A>T maps to NM_020528.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr21:47337539 G>A maps to NM_020528.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr13:100953793 C>T maps to NM_000282.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr3:135975416 C>T maps to NM_001178014.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:141248393 C>A maps to NM_032420.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr5:141244681 G>C maps to NM_032420.2 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:141244260 C>A maps to NM_032420.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:141243093 C>T maps to NM_032420.2 Q934Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr5:141248805 G>A maps to NM_032420.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:141244740 G>A maps to NM_032420.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:141244218 G>A maps to NM_032420.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:141243882 C>G maps to NM_032420.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:134073016 C>A maps to NM_032961.1 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072017 G>T maps to NM_032961.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134072782 C>A maps to NM_032961.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:134073067 C>A maps to NM_032961.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:134084250 C>T maps to NM_032961.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:134075508 C>T maps to NM_032961.1 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:134072044 C>T maps to NM_032961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:134071516 C>T maps to NM_032961.1 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr4:134073430 A>G maps to NM_032961.1 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr4:134072275 C>G maps to NM_032961.1 Y327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:134071900 C>A maps to NM_032961.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:134084243 C>A maps to NM_032961.1 R970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:134072089 A>C maps to NM_032961.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:134073226 C>A maps to NM_032961.1 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:134084153 C>T maps to NM_032961.1 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:134073203 G>T maps to NM_032961.1 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:134073850 C>A maps to NM_032961.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:134071513 G>T maps to NM_032961.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:134073550 G>A maps to NM_032961.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:134072737 C>A maps to NM_032961.1 Y481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr4:134073643 C>T maps to NM_032961.1 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:91134262 C>G did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:91873722 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:91134267 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:91134001 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:91873566 T>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:91873595 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:91873454 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:91131874 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:91090849 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:91132635 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:91642766 G>T did not map to a codon.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr23:91134022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:91134183 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:91090514 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:91133597 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:91133014 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:91873561 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:91873577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:91090668 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:91132419 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:91873876 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:91132884 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:91090764 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:91133249 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:91133252 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:91873625 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:91873298 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:91642838 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:91134238 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:91134029 G>T did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:91133832 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:91090840 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:91873485 C>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:91133546 C>G did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:91132807 T>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:91131883 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:91090513 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:91090670 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:91131908 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:91132777 C>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:91134115 G>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:91132546 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:91873601 C>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:91134200 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:91131799 C>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:91134010 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:91518113 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:91133848 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:91134053 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:91134267 G>T did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:91133291 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:91133113 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:91090680 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:91133454 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:91873752 T>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:91131800 G>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:91133871 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:91456417 T>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:91131896 A>C did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:91642829 A>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:91132040 G>A did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr23:91134201 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:91642791 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:91456414 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:91134241 C>T did not map to a codon.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr23:91873618 G>C did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:91131902 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:91133633 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:91090517 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:91134191 A>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:91090975 A>T did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:91133467 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:91873764 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:91873710 C>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:91132538 A>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:91131865 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:91873372 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:91873441 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:91133827 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:91090998 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:91133003 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:91873756 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:91873777 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:91132648 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:91137921 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:91133669 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:91134127 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:91134128 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:91134081 T>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:91873895 C>A did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr23:91131958 T>C did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:91873900 A>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:91133400 G>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:91873895 C>G did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:91133301 C>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:91133909 A>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:91873329 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:91134202 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:91873372 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:91873744 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:91873527 A>G did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:91090815 C>G did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:91873811 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:91873835 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:91133694 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:91133961 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:91873432 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:91133800 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:91873429 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:91873703 G>C did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:91132555 A>G did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:91134011 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:91132950 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:91133689 T>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:91133757 C>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:91133758 A>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:91873604 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:91132950 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:91134172 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:91134047 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:91132932 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:91132559 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr24:5605584 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr24:4968733 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr24:4968082 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr24:5605401 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr24:4925347 G>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr24:4967790 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr24:4968235 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr24:4925272 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr24:4968619 G>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr24:4967014 A>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr24:5605529 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr24:4968667 A>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr24:5369218 A>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr24:5369234 C>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr24:5605964 G>T did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr24:4924870 A>T did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr24:4967036 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr24:4966381 G>C did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr24:4968038 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr24:5605438 A>T did not map to a codon.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr24:4968283 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr24:4967198 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:141335022 C>T maps to NM_016580.2 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr5:141325367 G>A maps to NM_016580.2 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:141336066 G>T maps to NM_016580.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:141336579 C>T maps to NM_016580.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:141334599 A>T maps to NM_016580.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:55839090 C>A maps to NM_001142763.1 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr10:55755477 C>A maps to NM_001142763.1 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:56077051 G>A maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:55582502 T>G maps to NM_001142763.1 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr10:56423944 G>T maps to NM_001142763.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:55581629 A>C maps to NM_001142763.1 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:55582805 A>G maps to NM_001142763.1 S1567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:55913024 G>T maps to NM_001142763.1 S545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr10:56287632 G>A maps to NM_001142763.1 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:55570365 C>A maps to NM_001142769.1 E1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr10:55912863 G>T maps to NM_001142763.1 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:55912885 C>G maps to NM_001142763.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:55617002 C>T maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55566680 G>T maps to ENST00000373965 S1571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:55943218 C>T maps to NM_001142763.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:55782675 A>T maps to NM_001142763.1 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr10:55626443 A>T maps to NM_001142763.1 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr10:55721651 C>A maps to NM_001142763.1 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:55626401 G>T maps to NM_001142763.1 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:55626422 C>A maps to NM_001142763.1 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr10:55849793 T>A maps to NM_001142763.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:55582709 T>A maps to NM_001142763.1 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:55582431 G>T maps to NM_001142763.1 S1692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:55912972 G>T maps to NM_001142763.1 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:55587223 C>T maps to NM_001142763.1 V1437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:56077038 T>A maps to NM_001142763.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:55569180 G>T maps to NM_001142769.1 A1548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:55583014 C>A maps to NM_001142763.1 E1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:55912942 G>A maps to NM_001142763.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:55943254 G>T maps to NM_001142763.1 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr10:55566839 G>T maps to ENST00000373965 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:55568823 T>G maps to NM_001142769.1 A1667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:56138691 C>G maps to NM_001142763.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr10:55912897 C>A maps to NM_001142763.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:55912945 G>T maps to NM_001142763.1 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr10:55663077 T>C maps to NM_001142763.1 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:55826618 C>T maps to NM_001142763.1 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55582280 G>T maps to NM_001142763.1 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:55944962 A>T maps to NM_001142763.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:55566680 G>A maps to ENST00000373965 S1571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr10:55955643 T>C maps to NM_001142763.1 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr10:55892757 G>A maps to NM_001142763.1 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:55569224 T>A maps to NM_001142769.1 K1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:55587193 C>A maps to NM_001142763.1 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr10:55600185 G>T maps to NM_001142763.1 R1298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:58207804 G>T maps to NM_001040429.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr13:58207105 G>T maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr13:58207612 T>C maps to NM_001040429.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:58299397 G>C maps to NM_001040429.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr13:58299214 C>A maps to NM_001040429.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:58208383 G>C maps to NM_001040429.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:58209102 C>A maps to NM_001040429.2 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:58207732 C>A maps to NM_001040429.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr13:58299397 G>T maps to NM_001040429.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr13:58208572 C>T maps to NM_001040429.2 N631N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr13:58207409 G>T maps to NM_001040429.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:58209169 G>C maps to NM_001040429.2 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:58208636 G>T maps to NM_001040429.2 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr13:58207783 C>A maps to NM_001040429.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr13:58207963 C>T maps to NM_001040429.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr13:58208152 G>C maps to NM_001040429.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr13:58207234 C>T maps to NM_001040429.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:58208941 G>T maps to NM_001040429.2 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr13:58207159 C>T maps to NM_001040429.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr13:58208728 G>A maps to NM_001040429.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr13:58208911 C>A maps to NM_001040429.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr13:58299166 C>T maps to NM_001040429.2 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:138449938 C>A maps to NM_019035.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:138453098 T>A maps to NM_019035.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:138453001 C>A maps to NM_019035.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:138453116 T>G maps to NM_019035.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:138451382 T>A maps to NM_019035.3 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:138451145 G>T maps to NM_019035.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:138452819 G>A maps to NM_019035.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:138442737 C>A maps to NM_019035.3 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:138451877 G>A maps to NM_019035.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:99657616 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:99662937 C>A did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:99661646 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:99551725 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:99551692 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:99663167 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:99662047 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:99663319 C>G did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:99661990 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:99662980 G>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:99597070 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:99663475 G>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:99551622 C>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:99662621 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:99551397 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:99551398 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:99657784 C>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:99551650 T>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:99663106 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:99596915 G>A did not map to a codon.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr23:99662888 G>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:99662342 T>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:99661861 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:99551539 G>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:99662702 A>C did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:99596975 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:99551344 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:99663434 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:61985942 C>A maps to NM_022843.3 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:61985376 C>G maps to NM_022843.3 *952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr13:61987354 C>A maps to NM_022843.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr13:61986962 G>A maps to NM_022843.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:61987634 G>A maps to NM_022843.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:61987481 C>A maps to NM_022843.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:31144128 G>T maps to NM_001173523.1 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:31144175 G>A maps to NM_001173523.1 W1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:30724315 C>A maps to NM_001173523.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:30725905 G>C maps to NM_001173523.1 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:30724786 C>A maps to NM_001173523.1 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:30724795 C>A maps to NM_001173523.1 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:30724069 G>A maps to NM_001173523.1 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:30921947 C>A maps to NM_001173523.1 T1116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:30726007 C>A maps to NM_001173523.1 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:31144137 T>A maps to NM_001173523.1 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr4:30723214 C>T maps to NM_001173523.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr4:30725929 G>A maps to NM_001173523.1 Q962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr13:53418774 G>A maps to NM_002590.2 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr13:53422136 G>A maps to NM_002590.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr13:53421704 G>T maps to NM_002590.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:53420644 C>A maps to NM_002590.2 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr13:53420690 G>T maps to NM_002590.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:53420389 C>A maps to NM_002590.2 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:53420801 G>T maps to NM_002590.2 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:53419557 A>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr13:53419725 G>A maps to NM_002590.2 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:53418745 G>T maps to NM_002590.2 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:67800922 A>C maps to NM_203487.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:67800784 C>A maps to NM_203487.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr13:67205363 A>G maps to NM_203487.2 D1106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr13:67802317 A>T maps to NM_203487.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr13:67800211 C>T maps to NM_203487.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr13:67801312 C>T maps to NM_203487.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr13:67801795 C>G maps to NM_203487.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:67205544 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:67802359 C>A maps to NM_203487.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:67801401 T>A maps to NM_203487.2 K391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr13:67802281 G>C maps to NM_203487.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140168128 C>T maps to NM_018900.2 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140166919 G>T maps to NM_018900.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140167893 C>T maps to NM_018900.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr5:140167782 C>G maps to NM_018900.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:140166960 C>T maps to NM_018900.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140167047 C>A maps to NM_018900.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:140167314 G>A maps to NM_018900.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:140167629 G>T maps to NM_018900.2 V585V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-69-7980-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:140166502 T>C maps to NM_018900.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140166213 G>A maps to NM_018900.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:140167440 C>A maps to NM_018900.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr5:140389281 C>A maps to NM_018909.2 Y871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:140167227 C>T maps to NM_018900.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:140165958 C>T maps to NM_018900.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:140166918 A>G maps to NM_018900.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:140167311 G>A maps to NM_018900.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:140167621 C>A maps to NM_018900.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:140168034 G>C maps to NM_018900.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:140167410 G>C maps to NM_018900.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr5:140167227 C>T maps to NM_018900.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr5:140235731 A>C maps to NM_018901.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:140236733 C>G maps to NM_018901.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:140236160 T>C maps to NM_018901.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140236392 C>T maps to NM_018901.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140237057 G>T maps to NM_018901.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:140235842 C>T maps to NM_018901.2 H70H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140237759 G>C maps to NM_018901.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr5:140237381 G>A maps to NM_018901.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:140237240 G>A maps to NM_018901.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:140235971 G>C maps to NM_018901.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140249659 G>A maps to NM_018902.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr5:140249779 C>T maps to NM_018902.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140249938 G>A maps to NM_018902.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:140249875 G>A maps to NM_018902.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr5:140249914 C>T maps to NM_018902.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140250526 G>T maps to NM_018902.3 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr5:140250403 G>A maps to NM_018902.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:140250091 A>C maps to NM_018902.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:140250220 G>T maps to NM_018902.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140256795 T>A maps to NM_018903.2 L580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr5:140255725 A>G maps to NM_018903.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140255191 G>T maps to NM_018903.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140255899 C>T maps to NM_018903.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:140256412 G>T maps to NM_018903.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:140256556 C>A maps to NM_018903.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr5:140256739 C>T maps to NM_018903.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr5:140255494 G>A maps to NM_018903.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140263697 G>T maps to NM_018904.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140263034 C>T maps to NM_018904.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140264057 C>A maps to NM_018904.2 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr5:140262053 G>A maps to NM_018904.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140263226 C>A maps to NM_018904.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:140263145 C>A maps to NM_018904.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:140264144 G>T maps to NM_018904.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:140175811 T>C maps to NM_018905.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:140177023 G>T maps to NM_031495.1 *825Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr5:140174708 C>T maps to NM_018905.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140176160 C>A maps to NM_018905.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr5:140176283 G>T maps to NM_018905.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:140174650 C>G maps to NM_018905.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:140176687 C>T maps to NM_018905.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140175014 G>T maps to NM_018905.2 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:140176177 G>A maps to NM_018905.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:140176253 A>C maps to NM_018905.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140176296 G>A maps to NM_018905.2 W583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140181570 C>A maps to NM_018906.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:140182307 C>A maps to NM_018906.2 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140181957 C>T maps to NM_018906.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140181996 C>T maps to NM_018906.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140182644 G>A maps to NM_018906.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:140180925 C>T maps to NM_018906.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:140181954 C>A maps to NM_018906.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:140182635 G>A maps to NM_018906.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:140182887 C>T maps to NM_018906.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr5:140182665 G>T maps to NM_018906.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:140182383 G>A maps to NM_018906.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:140181069 C>A maps to NM_018906.2 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:140181945 G>T maps to NM_018906.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:140182332 G>T maps to NM_018906.2 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:140182209 G>T maps to NM_018906.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr5:140182995 G>T maps to NM_018906.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:140182980 G>T maps to NM_018906.2 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140181220 C>T maps to NM_018906.2 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr5:140182407 G>A maps to NM_018906.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140188757 G>T maps to NM_018907.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:140188796 G>A maps to NM_018907.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140187311 G>T maps to NM_018907.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:140188673 G>C maps to NM_018907.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140186909 C>A maps to NM_018907.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:140188373 G>A maps to NM_018907.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:140186807 G>T maps to NM_018907.2 R12R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8302-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140189024 G>T maps to NM_018907.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:140187569 C>A maps to NM_018907.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:140187571 C>A maps to NM_018907.2 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140189051 T>C maps to NM_018907.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:140187275 C>T maps to NM_018907.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr5:140188066 C>A maps to NM_018907.2 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:140188280 G>A maps to NM_018907.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:140188049 C>G maps to NM_018907.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:140188625 G>T maps to NM_018907.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140203111 G>A maps to NM_018908.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140203276 C>A maps to NM_018908.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr5:140201933 G>T maps to NM_018908.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr5:140203339 C>T maps to NM_018908.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr5:140203729 A>G maps to NM_031501.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr5:140203498 G>A maps to NM_018908.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:140201761 A>G maps to NM_018908.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:140203435 G>T maps to NM_018908.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr5:140202976 G>C maps to NM_018908.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140207846 G>T maps to NM_018909.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:140209439 C>A maps to NM_018909.2 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:140208839 G>T maps to NM_018909.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:140209793 G>A maps to NM_018909.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:140208044 G>A maps to NM_018909.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr5:140209754 G>A maps to NM_018909.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140207687 C>A maps to NM_018909.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140209901 C>A maps to NM_018909.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:140208978 C>T maps to NM_018909.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:140208227 A>T maps to NM_018909.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140209367 G>T maps to NM_018909.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140209368 C>T maps to NM_018909.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:140207852 G>C maps to NM_018909.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:140209640 T>C maps to NM_018909.2 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr5:140209730 C>T maps to NM_018909.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:140215143 C>T maps to NM_018910.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140215965 G>A maps to NM_018910.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140215842 G>T maps to NM_018910.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140215323 C>A maps to NM_018910.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:140216115 G>T maps to NM_018910.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140215056 C>A maps to NM_018910.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:140216097 G>T maps to NM_018910.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:140215131 C>A maps to NM_018910.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140216112 G>T maps to NM_018910.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr5:140215971 G>A maps to NM_018910.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr5:140215836 C>A maps to NM_018910.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:140222066 C>A maps to NM_018911.2 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140220965 C>A maps to NM_018911.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140222982 C>T maps to NM_018911.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:140222270 C>T maps to NM_018911.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr5:140222138 C>T maps to NM_018911.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140222228 G>A maps to NM_018911.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:140222792 C>A maps to NM_018911.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr5:140222534 G>T maps to NM_018911.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:140222375 G>C maps to NM_018911.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:140222195 G>T maps to NM_018911.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:140222981 G>T maps to NM_018911.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140228508 G>A maps to NM_031857.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:140230314 G>T maps to NM_031857.1 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140230311 G>C maps to NM_031857.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr5:140230155 G>T maps to NM_031857.1 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140229633 C>A maps to NM_031857.1 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:140230535 T>G maps to NM_014005.3 L819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr5:140230331 C>A maps to NM_031857.1 S751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:140229519 G>A maps to NM_031857.1 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:140230278 G>A maps to NM_031857.1 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr5:140228142 C>T maps to NM_031857.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140306845 C>T maps to NM_018898.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140306689 C>A maps to NM_018898.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140307478 C>T maps to NM_018898.3 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:140347670 A>T maps to NM_018899.5 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:140432665 G>T maps to NM_013340.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:140433172 C>T maps to NM_013340.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140432183 C>A maps to NM_013340.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140433274 G>A maps to NM_013340.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140433352 T>C maps to NM_013340.2 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:140432998 C>T maps to NM_013340.2 H648H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:140432647 G>T maps to NM_013340.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140572892 C>A maps to NM_018930.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140573618 G>T maps to NM_018930.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:140573672 C>G maps to NM_018930.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140572514 G>T maps to NM_018930.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140573762 G>T maps to NM_018930.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr5:140573612 G>T maps to NM_018930.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:140572280 G>T maps to NM_018930.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:140574155 C>A maps to NM_018930.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:140574290 C>T maps to NM_018930.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140574377 C>A maps to NM_018930.3 Y751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:140572577 A>T maps to NM_018930.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:140581714 C>T maps to NM_018931.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr5:140580678 C>A maps to NM_018931.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:140581683 T>C maps to NM_018931.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140580417 A>T maps to NM_018931.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr5:140580729 C>T maps to NM_018931.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:140581560 C>T maps to NM_018931.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr5:140581503 G>T maps to NM_018931.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:140581419 G>T maps to NM_018931.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:140579943 G>T maps to NM_018931.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:140581599 C>A maps to NM_018931.2 Y751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:140581425 G>A maps to NM_018931.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr5:140580846 C>T maps to NM_018931.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:140579689 C>T maps to NM_018931.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:140589828 C>T maps to NM_018932.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:140590653 C>T maps to NM_018932.3 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:140588871 C>A maps to NM_018932.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140590239 C>A maps to NM_018932.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:140589096 G>T maps to NM_018932.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:140589507 C>T maps to NM_018932.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr5:140590308 G>A maps to NM_018932.3 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr5:140590188 G>A maps to NM_018932.3 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140590431 G>T maps to NM_018932.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140590566 A>G maps to NM_018932.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr5:140590251 G>T maps to NM_018932.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:140589645 C>T maps to NM_018932.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr5:140589930 C>A maps to NM_018932.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:140590251 G>T maps to NM_018932.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:140589141 C>A maps to NM_018932.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140594393 C>A maps to NM_018933.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140595758 C>A maps to NM_018933.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:140594669 T>A maps to NM_018933.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140595122 A>G maps to NM_018933.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:140596013 C>T maps to NM_018933.2 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr5:140595062 C>A maps to NM_018933.2 Y456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr5:140595674 G>T maps to NM_018933.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr5:140594639 C>A maps to NM_018933.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:140595851 G>T maps to NM_018933.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140605335 G>T maps to NM_018934.2 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140605056 G>T maps to NM_018934.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:140605188 G>T maps to NM_018934.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140605065 G>T maps to NM_018934.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:140605230 G>A maps to NM_018934.2 R718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:140604624 C>A maps to NM_018934.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr5:140604342 C>A maps to NM_018934.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr5:140603407 G>T maps to NM_018934.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr5:140603144 T>A maps to NM_018934.2 L23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:140605020 C>T maps to NM_018934.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:140605137 C>T maps to NM_018934.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr5:140605062 G>C maps to NM_018934.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:140604501 C>A maps to NM_018934.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:140605041 C>T maps to NM_018934.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr5:140603169 A>G maps to NM_018934.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140603151 G>A maps to NM_018934.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:140627194 C>A maps to NM_018935.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr5:140625592 G>C maps to NM_018935.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140626792 G>C maps to NM_018935.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:140627302 G>C maps to NM_018935.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:140627359 C>T maps to NM_018935.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr5:140627194 C>T maps to NM_018935.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140625382 G>T maps to NM_018935.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:140626564 C>G maps to NM_018935.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr5:140625607 G>T maps to NM_018935.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:140627113 C>A maps to NM_018935.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr5:140627173 G>T maps to NM_018935.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:140564341 G>T maps to NM_020957.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140563360 C>A maps to NM_020957.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140563600 G>T maps to NM_020957.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr5:140564275 C>T maps to NM_020957.1 C714C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:140562313 C>A maps to NM_020957.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140562562 G>T maps to NM_020957.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563489 C>T maps to NM_020957.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:140563648 C>A maps to NM_020957.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:140562592 T>C maps to NM_020957.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr5:140562298 G>A maps to NM_020957.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:140564263 G>T maps to NM_020957.1 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140564194 T>C maps to NM_020957.1 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr5:140563504 C>A maps to NM_020957.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr5:140563072 G>A maps to NM_020957.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr5:140563816 G>T maps to NM_020957.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:140563599 C>A maps to NM_020957.1 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr5:140476014 G>T maps to NM_018936.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:140475996 G>A maps to NM_018936.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:140476464 C>A maps to NM_018936.2 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr5:140475630 C>A maps to NM_018936.2 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr5:140475912 C>A maps to NM_018936.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:140475165 C>A maps to NM_018936.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr5:140476386 C>A maps to NM_018936.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr5:140476413 G>A maps to NM_018936.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140474442 G>T maps to NM_018936.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140481801 C>A maps to NM_018937.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:140480403 G>A maps to NM_018937.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140482344 G>T maps to NM_018937.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140480847 G>A maps to NM_018937.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:140481423 A>G maps to NM_018937.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:140480362 T>C maps to NM_018937.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140481672 A>T maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140480949 A>T maps to NM_018937.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:140481828 C>T maps to NM_018937.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:140482365 G>T maps to NM_018937.2 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr5:140480871 C>A maps to NM_018937.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr5:140480898 G>T maps to NM_018937.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:140480989 G>T maps to NM_018937.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140502029 A>G maps to NM_018938.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr5:140503214 G>A maps to NM_018938.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140503613 C>A maps to NM_018938.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr5:140502488 A>G maps to NM_018938.2 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr5:140502746 G>A maps to NM_018938.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:140503751 C>T maps to NM_018938.2 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:140502449 T>A maps to NM_018938.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140503841 G>A maps to NM_018938.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:140502212 C>T maps to NM_018938.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140502590 G>T maps to NM_018938.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140503754 G>T maps to NM_018938.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140516258 G>T maps to NM_015669.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140517151 G>A maps to NM_015669.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140515334 C>T maps to NM_015669.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140515357 G>C maps to NM_015669.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr5:140516239 G>C maps to NM_015669.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140516197 C>A maps to NM_015669.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:140515628 C>A maps to NM_015669.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:140516437 C>A maps to NM_015669.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr5:140516311 C>T maps to NM_015669.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140531910 G>C maps to NM_018939.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:140531775 C>A maps to NM_018939.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140530411 G>T maps to NM_018939.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140530554 C>A maps to NM_018939.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:140531097 G>A maps to NM_018939.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr5:140531307 G>A maps to NM_018939.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:140530737 G>T maps to NM_018939.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr5:140529990 G>A maps to NM_018939.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:140531994 G>C maps to NM_018939.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:140530674 C>A maps to NM_018939.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140531364 C>T maps to NM_018939.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140552727 G>C maps to NM_018940.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140553012 G>T maps to NM_018940.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr5:140554533 C>T maps to NM_018940.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr5:140553606 C>A maps to NM_018940.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140552679 G>A maps to NM_018940.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:140553150 G>A maps to NM_018940.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:140553817 C>T maps to NM_018940.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:140553498 C>G maps to NM_018940.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:140554008 G>A maps to NM_018940.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:140552826 G>A maps to NM_018940.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140553847 A>T maps to NM_018940.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140554053 G>T maps to NM_018940.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:140554488 G>T maps to NM_018940.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140554542 G>T maps to NM_018940.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140553204 C>T maps to NM_018940.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:140553102 C>T maps to NM_018940.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr5:140553780 C>T maps to NM_018940.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:140553858 C>A maps to NM_018940.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:140554443 G>T maps to NM_018940.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr5:140553264 C>T maps to NM_018940.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr5:140552499 C>A maps to NM_018940.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140554759 G>T maps to NM_018940.2 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140554463 C>A maps to NM_018940.2 S683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:140554147 C>A maps to NM_018940.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140559783 G>T maps to NM_019120.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140559228 C>A maps to NM_019120.2 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140559207 G>A maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:140558991 G>T maps to NM_019120.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140559504 G>A maps to NM_019120.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:140558440 G>T maps to NM_019120.2 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:140559693 G>T maps to NM_019120.2 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:140559893 C>G maps to NM_019120.2 S760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:140558697 G>T maps to NM_019120.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:140559960 A>T maps to NM_019120.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140558769 C>A maps to NM_019120.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:140559585 C>A maps to NM_019120.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140558592 A>T maps to NM_019120.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:140558230 G>T maps to NM_019120.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr5:140559723 C>T maps to NM_019120.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:140559207 G>T maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr5:140558943 G>C maps to NM_019120.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr5:140559036 C>A maps to NM_019120.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:140710331 G>T maps to NM_018912.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140712338 G>T maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:140712365 G>T maps to NM_018912.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140711648 C>T maps to NM_018912.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:140711132 A>G maps to NM_018912.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:140884971 C>T maps to NM_018915.2 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:140710790 G>T maps to NM_018912.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140890661 A>G maps to NM_018915.2 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:140711484 A>T maps to NM_018912.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr5:140711075 G>T maps to NM_018912.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:140712359 C>G maps to NM_018912.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr5:140712440 C>T maps to NM_018912.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:140710925 C>A maps to NM_018912.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140711006 C>A maps to NM_018912.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr5:140711918 C>T maps to NM_018912.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:140794434 G>T maps to NM_018913.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140794976 G>T maps to NM_018913.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:140794526 G>T maps to NM_018913.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:140792798 G>T maps to NM_018913.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:140793564 G>T maps to NM_018913.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:140794244 G>A maps to NM_018913.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:140794396 T>A maps to NM_018913.2 L552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140801456 C>T maps to NM_018914.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr5:140802011 A>T maps to NM_018914.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:140800976 G>A maps to NM_018914.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:140802743 C>T maps to NM_018914.2 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:140800955 G>C maps to NM_018914.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr5:140802866 G>A maps to NM_018914.2 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:140801027 G>A maps to NM_018914.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:140811612 C>T maps to NM_003735.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:140810505 G>T maps to NM_003735.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140812311 G>T maps to NM_003735.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140812209 G>T maps to NM_003735.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:140812476 G>T maps to NM_003735.2 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr5:140810955 G>T maps to NM_003735.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr5:140810964 G>T maps to NM_003735.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140811193 C>T maps to NM_003735.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:140812530 G>A maps to NM_003735.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:140812203 G>T maps to NM_003735.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:140812536 G>T maps to NM_003735.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:140719050 A>T maps to NM_018915.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140720007 T>A maps to NM_018915.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:140720931 C>A maps to NM_018915.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:140719743 C>A maps to NM_018915.2 Y402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140720760 G>T maps to NM_018915.2 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:140720218 G>T maps to NM_018915.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:140720430 C>A maps to NM_018915.2 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr5:140719314 C>A maps to NM_018915.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr5:140720583 C>A maps to NM_018915.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:140719830 C>A maps to NM_018915.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr5:140720583 C>A maps to NM_018915.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:140719962 G>C maps to NM_018915.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr5:140718765 T>C maps to NM_018915.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140720280 C>A maps to NM_018915.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:140725093 G>T maps to NM_018916.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:140725411 G>T maps to NM_018916.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:140725510 G>T maps to NM_018916.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:140725936 C>T maps to NM_018916.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:140725309 C>T maps to NM_018916.3 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:140723873 C>A maps to NM_018916.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:140725982 C>T maps to NM_018916.3 Q795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:140723758 G>A maps to NM_018916.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:140723887 C>A maps to NM_018916.3 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:140725396 C>A maps to NM_018916.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:140724490 G>C maps to NM_018916.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140723666 C>T maps to NM_018916.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:140725834 G>T maps to NM_018916.3 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr5:140725147 G>T maps to NM_018916.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:140736242 C>A maps to NM_018917.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140735630 A>T maps to NM_018917.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140736947 T>A maps to NM_018917.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:140736530 G>T maps to NM_018917.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:140736275 C>G maps to NM_018917.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:140736509 C>A maps to NM_018917.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr5:140736222 C>T maps to NM_018917.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr5:140736603 G>T maps to NM_018917.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:140736860 C>T maps to NM_018917.2 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr5:140735711 T>A maps to NM_018917.2 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:140735120 G>A maps to NM_018917.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:140736237 C>T maps to NM_018917.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:140737049 G>C maps to NM_018917.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:140745189 C>A maps to NM_018918.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:140746230 G>T maps to NM_018918.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:140745822 C>G maps to NM_018918.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:140744068 G>T maps to NM_018918.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:140743926 C>T maps to NM_018918.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr5:140743980 C>T maps to NM_018918.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:140745864 C>T maps to NM_018918.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:140746035 G>T maps to NM_018918.2 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr5:140744898 G>T maps to NM_018918.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140744960 C>A maps to NM_018918.2 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:140755905 C>A maps to NM_018919.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:140753847 C>A maps to NM_018919.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:140754055 G>T maps to NM_018919.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr5:140753952 G>A maps to NM_018919.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:140755329 C>T maps to NM_018919.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:140755563 C>A maps to NM_018919.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:140755329 C>A maps to NM_018919.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:140755506 G>A maps to NM_018919.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:140755008 C>G maps to NM_018919.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:140754885 G>T maps to NM_018919.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr5:140755486 G>T maps to NM_018919.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:140755486 G>T maps to NM_018919.2 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr5:140755005 C>T maps to NM_018919.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:140753829 G>A maps to NM_018919.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140763011 G>A maps to NM_018920.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr5:140764229 G>C maps to NM_018920.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:140764133 T>C maps to NM_018920.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr5:140764586 C>T maps to NM_018920.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:140762681 G>T maps to NM_018920.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140773661 G>T maps to NM_032088.1 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:140773999 G>A maps to NM_032088.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140774233 G>C maps to NM_032088.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:140774464 G>T maps to NM_032088.1 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:140774113 G>T maps to NM_032088.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:140774086 A>G maps to NM_032088.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:140773984 C>T maps to NM_032088.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:140774158 G>T maps to NM_032088.1 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr5:140772413 G>T maps to NM_032088.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:140774609 G>T maps to NM_032088.1 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr5:140772466 A>G maps to NM_032088.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:140774263 G>T maps to NM_032088.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:140784117 G>A maps to NM_018921.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:140782983 A>G maps to NM_018921.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:140783352 A>T maps to NM_018921.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:140782869 C>T maps to NM_018921.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr5:140784591 C>G maps to NM_018921.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:140784027 C>T maps to NM_018921.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:140784469 C>T maps to NM_018921.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:140782698 G>T maps to NM_018921.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:140784597 C>G maps to NM_018921.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:140729928 G>A maps to NM_018922.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140731095 G>A maps to NM_018922.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:140731740 G>T maps to NM_018922.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:140731824 G>A maps to NM_018922.2 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:140731392 C>A maps to NM_018922.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:140730453 G>A maps to NM_018922.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:140731920 C>G maps to NM_018922.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:140732047 G>T maps to NM_018922.2 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:140740130 C>G maps to NM_018923.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:140740421 A>C maps to NM_018923.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:140740472 G>T maps to NM_018923.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr5:140741282 C>T maps to NM_018923.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr5:140740859 G>T maps to NM_018923.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr5:140740397 C>T maps to NM_018923.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:140741213 C>A maps to NM_018923.2 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr5:140740130 C>T maps to NM_018923.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:140741774 C>A maps to NM_018923.2 Y691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:140741738 G>T maps to NM_018923.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:140739881 C>T maps to NM_018923.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:140739819 G>T maps to NM_018923.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:140741831 A>T maps to NM_018923.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:140750197 C>A maps to NM_018924.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:140750983 T>C maps to NM_018924.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:140752015 G>A maps to NM_018924.2 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:140751041 G>T maps to NM_018924.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:140750263 G>T maps to NM_018924.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr5:140751679 G>A maps to NM_018924.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr5:140769091 C>T maps to NM_003736.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:140768713 G>A maps to NM_003736.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr5:140769310 C>A maps to NM_003736.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:140769607 C>T maps to NM_003736.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140769610 C>T maps to NM_003736.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr5:140769382 G>T maps to NM_003736.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:140768314 C>G maps to NM_003736.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:140768899 C>A maps to NM_003736.2 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:140789007 G>A maps to NM_018926.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr5:140788612 C>A maps to NM_018926.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:140788221 A>T maps to NM_018926.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:140799010 G>T maps to NM_018927.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:140799835 A>T maps to NM_018927.2 K804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:140799828 G>A maps to NM_018927.2 K801K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:140798054 T>A maps to NM_018927.2 L210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr5:140798769 C>T maps to NM_018927.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:140799282 G>T maps to NM_018927.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:140798841 G>T maps to NM_018927.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:140856927 G>T maps to NM_002588.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:140866245 A>G maps to NM_018928.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:140864841 G>T maps to NM_018928.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:140867175 G>A maps to NM_018928.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:140869286 G>A maps to NM_018929.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr5:140870003 T>A maps to NM_018929.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:120387531 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:120388168 G>A maps to NM_001029996.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr2:120388401 C>A maps to NM_001029996.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr2:120383253 G>T maps to NM_001029996.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:82877480 G>T maps to NM_015885.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:82893517 T>C maps to NM_015885.3 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr11:82868591 C>T maps to NM_015885.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:82876986 G>T maps to NM_015885.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:82879652 C>A maps to NM_015885.3 S759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:82868654 C>T maps to NM_015885.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:74733991 C>T maps to NM_032673.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:36896595 G>C maps to NM_007144.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr17:36894635 G>A maps to NM_007144.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:113852579 T>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:44576186 C>G maps to NM_022104.3 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:56138619 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:56139285 G>A maps to NM_002591.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr20:56140517 C>A maps to NM_002591.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:56139592 C>T maps to NM_002591.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr20:56140749 A>T maps to NM_002591.3 K587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr20:56137914 C>T maps to NM_002591.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr20:56139536 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:56140120 C>G maps to NM_002591.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:56137240 C>A maps to NM_002591.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:56140138 C>A maps to NM_002591.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr20:56138655 G>A maps to NM_002591.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr20:56138195 C>A maps to NM_002591.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr20:56138114 G>A maps to NM_002591.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr14:24566320 C>T maps to NM_004563.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr14:24569243 G>T maps to NM_004563.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr14:24567861 C>T maps to NM_004563.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:82764744 C>T maps to NM_033026.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:82579982 C>A maps to NM_033026.5 L3307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:82582432 A>G maps to NM_033026.5 D2612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:82387974 G>T maps to NM_033026.5 A5115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:82595230 T>A maps to NM_033026.5 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr7:82784288 T>C maps to NM_033026.5 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:82532039 C>G maps to NM_033026.5 G4485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr7:82583173 C>T maps to NM_033026.5 E2365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:82584924 C>A maps to NM_033026.5 E1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:82595464 T>G maps to NM_033026.5 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:82583785 C>A maps to NM_033026.5 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:82582363 T>C maps to NM_033026.5 S2635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:82474676 T>A maps to NM_033026.5 S4652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr7:82580111 C>T maps to NM_033026.5 K3264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82387922 T>A maps to NM_033026.5 K5133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr7:82784915 C>A maps to NM_033026.5 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583766 C>A maps to NM_033026.5 E2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82583851 T>C maps to NM_033026.5 E2139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:82784422 G>A maps to NM_033026.5 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr7:82785428 A>G maps to NM_033026.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:82579279 G>T maps to NM_033026.5 R3542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:82584973 A>G maps to NM_033026.5 P1765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:82585287 C>A maps to NM_033026.5 G1661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:82546110 C>A maps to NM_033026.5 E3731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:82581838 T>G maps to NM_033026.5 T2810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:82583160 C>A maps to NM_033026.5 E2370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:82545901 G>T maps to NM_033026.5 Y3800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr7:82430832 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:82474676 T>A maps to NM_033026.5 S4652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:82580711 G>T maps to NM_033026.5 S3064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:82595356 G>A maps to NM_033026.5 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:82581517 T>A maps to NM_033026.5 S2917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:82585972 T>A maps to NM_033026.5 S1432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:82764882 C>T maps to NM_033026.5 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:82595665 C>T maps to NM_033026.5 Q1146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr7:82584421 C>T maps to NM_033026.5 G1949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:82474736 T>A maps to NM_033026.5 S4632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:82584906 C>A maps to NM_033026.5 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:82580372 C>A maps to NM_033026.5 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:82389980 G>A maps to NM_033026.5 L5088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:82476455 G>A maps to NM_033026.5 L4588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:82585369 G>A maps to NM_033026.5 D1633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr7:82764795 T>C maps to NM_033026.5 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:82390735 T>A maps to NM_033026.5 I5027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:82585777 A>G maps to NM_033026.5 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:82784735 T>C maps to NM_033026.5 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:82595458 A>G maps to NM_033026.5 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:17827248 G>A maps to NM_006197.3 E1192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:17849060 G>A maps to NM_006197.3 V1514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:17804747 A>G maps to NM_006197.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:17796487 G>C maps to NM_006197.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr8:17820798 A>T maps to NM_006197.3 K885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:17823621 C>G maps to NM_006197.3 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:17796322 G>A maps to NM_006197.3 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:150114743 A>C maps to NM_005389.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:52732946 A>G maps to NM_052937.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:52758275 C>A maps to NM_052937.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr8:52746116 T>G maps to NM_052937.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr8:52733189 G>T maps to NM_052937.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:52733038 C>A maps to NM_052937.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:52732934 G>T maps to NM_052937.2 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:62904847 G>T maps to NM_018257.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr20:62891578 G>A maps to NM_018257.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:62891623 A>T maps to NM_018257.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:101311479 A>G maps to NM_020357.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:47754561 A>T maps to NM_006031.5 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:47851462 G>A maps to NM_006031.5 E2695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr21:47773117 G>A maps to NM_006031.5 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr21:47805790 C>T maps to NM_006031.5 C1119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr21:47783459 G>A maps to NM_006031.5 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:47783763 G>T maps to NM_006031.5 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:47801664 G>T maps to NM_006031.5 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr21:47850465 G>A maps to NM_006031.5 Q2653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr21:47831534 G>T maps to NM_006031.5 E1850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr21:47836155 C>T maps to NM_006031.5 S2108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr21:47836668 C>T maps to NM_006031.5 S2279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr21:47808655 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr21:47836584 G>A maps to NM_006031.5 L2251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr21:47754603 C>T maps to NM_006031.5 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr21:47851495 G>C maps to NM_006031.5 V2706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:71542903 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:71518645 T>C maps to NM_014982.2 S1498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:71485879 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:71575642 C>A maps to NM_014982.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:71575561 C>T maps to NM_014982.2 S2181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr14:71445030 A>T maps to NM_014982.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:71540487 G>T maps to NM_014982.2 R1693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:233296137 C>A maps to NM_014801.3 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:233190058 C>A maps to NM_014801.3 G1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:233394782 C>A maps to NM_014801.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:233122107 C>T maps to NM_014801.3 S1990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:233394395 G>A maps to NM_014801.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:233136137 G>A maps to NM_014801.3 L1747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:233393861 C>G maps to NM_014801.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr1:233394356 C>A maps to NM_014801.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:233388214 G>T maps to NM_014801.3 I671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr1:233134125 C>A maps to NM_014801.3 G1888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr11:65403698 A>G maps to NM_032223.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385567 C>T maps to NM_032223.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:65385574 G>T maps to NM_032223.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:65386108 G>T maps to NM_032223.2 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:65390964 G>C maps to NM_032223.2 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:65391685 G>C maps to NM_032223.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:65392483 C>T maps to NM_032223.2 I972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:65393400 A>G maps to NM_032223.2 A1085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr11:65392664 C>A maps to NM_032223.2 V981V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr11:65392879 C>T maps to NM_032223.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr11:65393130 C>G maps to NM_032223.2 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:100202834 C>T maps to NM_002593.3 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:142548566 G>A maps to NM_013363.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:142537260 G>T maps to NM_013363.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:142567170 A>T maps to NM_013363.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr3:142542443 G>A maps to NM_013363.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:142567308 G>T maps to NM_013363.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:142537296 G>T maps to NM_013363.3 Y376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:142561834 G>T maps to NM_013363.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:95761537 G>A maps to NM_000439.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:95748051 G>T maps to NM_000439.4 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:95728881 G>T maps to NM_000439.4 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:95761522 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr20:17437054 C>G maps to NM_002594.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr20:17462465 C>A maps to NM_002594.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:17417357 C>A maps to NM_002594.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr20:17208120 C>T maps to NM_002594.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr19:1487980 C>T maps to NM_017573.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:1487193 C>A maps to NM_017573.3 T267T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-69-7979-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr9:78772036 C>A maps to NM_001190482.1 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:78749030 T>C maps to NM_001190482.1 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:78710912 C>T maps to NM_001190482.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:78547385 C>A maps to NM_001190482.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:78771961 G>T maps to NM_001190482.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:101845510 C>T maps to NM_002570.3 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:117100203 A>T maps to NM_004716.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr11:117100518 G>A maps to NM_004716.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:117094010 C>T maps to NM_004716.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr1:55524238 C>T maps to NM_174936.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:53852151 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:148742284 C>A maps to NM_024028.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:195997345 G>C maps to NM_005017.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:195997348 C>G maps to NM_005017.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:195965672 G>T maps to NM_005017.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:195984695 G>A maps to NM_005017.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:24665110 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:24597529 T>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:24580212 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:24608166 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:24690740 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:24608230 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr17:79867408 G>A maps to NM_001184917.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr7:99002493 C>T maps to NM_014891.6 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:186415571 G>T maps to ENST00000340129 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:186415578 T>A maps to ENST00000340129 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:186413119 A>G maps to ENST00000340129 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr10:105166429 A>G maps to NM_014976.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr10:105173784 T>C maps to NM_014976.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:105197798 C>T maps to NM_014976.1 N1291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr10:105173724 C>G maps to NM_014976.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr10:105194594 A>T maps to NM_014976.1 R1236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:105177626 G>T maps to NM_014976.1 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:105201668 G>T maps to NM_014976.1 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr9:5534763 C>A maps to NM_025239.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:5557752 G>A did not map to a codon.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr9:5522563 A>C maps to NM_025239.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr9:5549473 C>A maps to NM_025239.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:170892656 G>T maps to NM_002598.3 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:311474 G>A maps to NM_013232.3 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:33863495 A>G maps to NM_001162429.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:33870349 G>T maps to NM_001162429.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr3:33870388 C>T maps to NM_001162429.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr15:65411715 G>A maps to NM_005707.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:125582561 C>T maps to NM_005388.4 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr4:56448362 A>G maps to NM_152401.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:101192813 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:165801828 G>T maps to NM_001130690.1 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:165863739 G>T maps to NM_001130690.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:165809840 G>A maps to NM_001130690.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:165843833 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr6:165957052 A>T maps to NM_001130690.1 L24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:165808688 G>T maps to NM_001130690.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:165746584 G>A maps to NM_001130690.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr6:165832219 G>A maps to NM_001130690.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr6:165863739 G>A maps to NM_001130690.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:165752814 A>T maps to NM_001130690.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178494167 G>T maps to NM_016953.3 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:178681582 G>A maps to NM_016953.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:178936852 A>G maps to NM_016953.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:178762820 G>A maps to NM_016953.3 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr2:178969105 G>A maps to NM_001077197.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:178969142 G>A maps to NM_001077197.1 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:178936366 C>G maps to NM_016953.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:183051237 C>A maps to NM_005019.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:183011819 C>A maps to NM_005019.3 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:183387061 G>T maps to NM_005019.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:183066164 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:183129073 C>A maps to NM_005019.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:183129065 C>T maps to NM_005019.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:183070792 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:54963069 G>T maps to NM_000924.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr12:54963036 C>T maps to NM_000924.3 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr12:54963088 G>T maps to NM_000924.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:31864496 C>A maps to NM_001191057.1 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:31867987 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:31862792 G>T maps to NM_001191057.1 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:31890286 G>A maps to NM_001191057.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:31855673 G>T maps to NM_001191057.1 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:31918699 G>T maps to NM_001191057.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:31918622 C>A maps to NM_001191057.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:31913021 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:31876811 C>T maps to NM_001191057.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:31877566 T>A maps to NM_001191057.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:31887621 C>A maps to NM_001191057.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:31862810 A>T maps to NM_001191057.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:31862699 G>T maps to NM_001191057.1 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr7:31917642 A>G maps to NM_001191057.1 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr7:31862711 C>T maps to NM_001191057.1 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:31917650 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:31920384 C>A maps to NM_001191057.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:72290424 G>A maps to NM_002599.3 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:72295736 G>A maps to NM_002599.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:72297214 C>A maps to NM_002599.3 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr11:72299886 G>A maps to NM_002599.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:72289311 G>T maps to NM_002599.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:72292013 G>A maps to NM_002599.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:72297128 G>C maps to NM_002599.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:72295352 G>A maps to NM_002599.3 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr11:72292495 G>T maps to NM_002599.3 Y650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:72290583 G>A maps to NM_002599.3 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:20766630 A>T maps to NM_000921.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr12:20769251 T>A maps to NM_000921.3 L453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:20522823 A>T maps to NM_000921.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr12:20833069 A>T maps to NM_000921.3 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr12:20766429 C>A maps to NM_000921.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:20766474 G>T maps to NM_000921.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:20803376 A>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:20803377 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr12:20769268 C>A maps to NM_000921.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:20774298 T>G maps to NM_000921.3 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:20801731 G>T maps to NM_000921.3 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:20801732 G>T maps to NM_000921.3 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:20803533 G>A maps to NM_000921.3 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:20783001 C>A maps to NM_000921.3 Y567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:20522728 G>T maps to NM_000921.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:20807032 G>A maps to NM_000921.3 W1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:14880789 A>T maps to NM_000922.3 K908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:14882865 T>A maps to NM_000922.3 L947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:14665636 C>T maps to NM_000922.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:14889143 C>A maps to NM_000922.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:14666478 G>T maps to NM_000922.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:10578179 C>G maps to NM_001111307.1 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:10572349 C>T maps to NM_001111307.1 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:66713196 C>A maps to NM_001037341.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:66458792 G>T maps to NM_001037340.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:66384347 C>T maps to NM_001037341.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:66384437 G>A maps to NM_001037341.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:18329182 G>T maps to NM_000923.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr19:18329146 G>A maps to NM_000923.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:18331045 C>A maps to NM_000923.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:58273026 G>T maps to NM_001104631.1 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:58271611 G>A maps to NM_001104631.1 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:59284439 G>A maps to ENST00000502484 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144868161 A>T maps to NM_014644.4 T1759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:144879315 C>A maps to NM_014644.4 R1378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:144930943 T>C maps to NM_001002811.1 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:144882508 C>G maps to NM_014644.4 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:144879554 C>A maps to NM_014644.4 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:144946726 C>T maps to NM_014644.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:144866592 C>T maps to NM_014644.4 R1883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:144892527 C>T maps to NM_014644.4 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr1:144874681 T>C maps to NM_014644.4 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:144855816 C>A maps to NM_014644.4 E2246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:144865912 G>A maps to NM_014644.4 F1889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:144877095 G>T maps to NM_014644.4 R1531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:145021124 C>T maps to NM_001198832.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:144877270 C>A maps to NM_014644.4 G1472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:144882514 C>G maps to NM_014644.4 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:144886254 C>T maps to NM_014644.4 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:145015898 G>A maps to NM_001198832.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:144868092 G>A maps to NM_014644.4 N1782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:144912138 C>T maps to NM_014644.4 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:120419773 G>T maps to NM_001083.3 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:120527899 C>A maps to NM_001083.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:120528140 A>T maps to NM_001083.3 L155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:149264108 G>A maps to NM_000440.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149324062 G>A maps to NM_000440.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:149286940 C>A maps to NM_000440.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:149286941 C>G did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:149276333 G>T maps to NM_000440.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:149274853 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:619513 C>A maps to NM_000283.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:647648 G>A maps to NM_000283.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr4:663833 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:619636 C>T maps to NM_000283.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:619759 G>A maps to NM_000283.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:657926 C>T maps to NM_000283.3 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:628497 C>A maps to NM_000283.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr4:628464 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:647708 C>A maps to NM_000283.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:651144 G>A maps to NM_000283.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:95394517 G>T maps to NM_006204.3 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:95425129 A>T maps to NM_006204.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:95380393 C>T maps to NM_006204.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:95394660 C>A maps to NM_006204.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:95389037 T>C maps to NM_006204.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr10:95400214 C>G maps to NM_006204.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr10:95418720 C>A maps to NM_006204.3 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:136472316 G>A maps to NM_018945.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr15:85669586 G>T maps to NM_002605.2 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:76721721 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:76708953 C>A maps to NM_003719.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:76607859 G>C maps to NM_003719.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:76709007 C>T maps to NM_003719.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:76649203 G>T maps to NM_003719.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:44108029 C>T maps to NM_002606.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr21:44108032 G>C maps to NM_002606.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:44151934 G>A maps to NM_002606.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr21:44192568 C>T maps to NM_002606.2 S569S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr7:550630 C>A maps to NM_002607.5 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr11:103814369 G>A maps to NM_025208.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:103814198 G>A maps to NM_025208.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:103818453 T>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:55139721 C>G maps to NM_006206.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:55140698 C>T maps to NM_006206.4 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr4:55156541 T>A maps to ENST00000507166 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:55144559 C>T maps to ENST00000507166 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr4:55156544 G>C maps to ENST00000507166 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:55152084 G>T maps to ENST00000507166 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:55161375 C>T maps to ENST00000507166 D829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:55154984 C>T maps to ENST00000507166 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:55133806 G>T maps to NM_006206.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr4:55152084 G>T maps to ENST00000507166 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr4:55151610 C>A maps to ENST00000507166 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr4:55155206 G>T maps to ENST00000507166 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:55141104 C>A maps to ENST00000507166 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:55133887 G>A maps to NM_006206.4 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:55139895 C>A maps to NM_006206.4 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr4:55133530 G>T maps to NM_006206.4 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:55151574 A>T maps to ENST00000507166 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:149515438 C>A maps to NM_002609.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:149500811 G>A maps to NM_002609.3 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:149515316 C>A maps to NM_002609.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr5:149515373 T>A maps to NM_002609.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr5:149501446 G>T maps to NM_002609.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr5:149513571 C>A did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr5:149498363 G>T maps to NM_002609.3 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:149514547 G>C maps to NM_002609.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:17500264 T>C maps to NM_006207.2 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:19375767 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:19372639 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:19377729 C>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:19369443 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:19377733 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:96762020 C>G maps to NM_005390.4 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:96761627 G>C maps to NM_005390.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:96761472 G>T maps to NM_005390.4 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:96761504 T>A maps to NM_005390.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr4:96761673 C>A maps to NM_005390.4 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:96761789 C>T maps to NM_005390.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:96762440 A>T maps to NM_005390.4 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr4:96762281 C>A maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:96762425 T>G maps to NM_005390.4 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:96762101 A>G maps to NM_005390.4 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:34969154 T>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:335704 T>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr16:335127 C>G maps to NM_006849.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:335386 C>A maps to NM_006849.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr15:44061819 C>G maps to NM_005313.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr15:44038799 C>T maps to NM_005313.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:148702341 C>A maps to NM_004911.4 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr3:122849398 C>T maps to NM_006810.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr3:122865025 G>A maps to NM_006810.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:122873845 G>T maps to NM_006810.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:10933283 G>A maps to ENST00000381611 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:26441053 C>T maps to NM_152835.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:20380966 A>T maps to NM_174924.1 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:20410502 C>A maps to NM_174924.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr16:20410589 C>T maps to NM_174924.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:20376863 T>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr16:20370658 T>C maps to NM_174924.1 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:173451115 G>A maps to ENST00000392571 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr2:173429788 G>T maps to ENST00000392571 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:24512947 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:24537107 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:24546234 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:24523381 G>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:24552144 A>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:24549851 G>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:95216780 T>C maps to NM_002612.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22439035 C>T maps to NM_021630.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:186423462 C>G maps to NM_014476.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:186423471 C>A maps to NM_014476.4 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:186427699 G>A maps to NM_014476.4 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:131606651 T>C maps to NM_003687.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr5:131607088 C>A maps to NM_003687.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:176923489 C>T maps to NM_005451.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:176918101 C>T maps to NM_005451.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:94935645 G>T maps to NM_001161778.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:94935756 C>T maps to NM_001161778.1 N549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:94935757 G>T maps to NM_001161778.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:94934844 G>T maps to NM_001161778.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:94934694 A>G maps to NM_001161778.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:66918315 C>T maps to NM_020786.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:66919296 C>G maps to NM_020786.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr16:2607891 G>A maps to NM_002613.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:70166108 G>T maps to NM_017990.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:70187391 G>A maps to NM_017990.3 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:33320129 A>T maps to ENST00000400481 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:33247429 G>A maps to ENST00000400481 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr13:33334732 A>T maps to ENST00000400481 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:33344485 G>T maps to ENST00000400481 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr13:33344512 A>T maps to ENST00000400481 P1293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr10:27031430 A>T maps to NM_014317.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:107533453 C>G maps to NM_020381.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:28498624 A>T maps to NM_000209.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:28498511 C>A maps to NM_000209.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:28498414 G>T maps to NM_000209.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:15111245 G>T maps to NM_015027.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr16:15102637 C>T maps to NM_015027.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:15095656 C>G maps to NM_015027.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr21:45173596 C>G maps to NM_003681.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:38061658 G>A maps to ENST00000442465 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:1961358 G>A maps to NM_024411.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:1961229 G>T maps to NM_024411.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:1961378 C>A maps to NM_024411.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:32089568 C>A maps to NM_178140.2 V2005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr5:32048789 G>A maps to NM_178140.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:31799690 T>A maps to NM_178140.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:32037440 C>G maps to NM_178140.2 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:32089085 C>T maps to NM_178140.2 G1844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:32077587 C>G maps to NM_178140.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:31799378 C>A maps to NM_178140.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:32048714 C>T maps to NM_178140.2 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:32088395 T>C maps to NM_178140.2 P1614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:31799354 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr5:32087672 C>T maps to NM_178140.2 S1373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr5:32074453 C>G maps to NM_178140.2 S1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr5:32090216 G>A maps to NM_178140.2 R2221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:32072265 G>A did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:119060199 A>G maps to ENST00000392817 *572W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr11:119059375 G>T maps to ENST00000392817 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:153069677 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:153069156 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:153069794 G>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:153068960 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:153070178 G>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:153073879 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:153069119 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:153072735 C>G did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:153070072 G>T did not map to a codon.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr23:153069728 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:153069053 G>C did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:153073936 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:153068879 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:153070160 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:153070010 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr10:102783310 C>A maps to NM_001195263.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr10:102782063 G>A maps to NM_001195263.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr10:102783326 C>G maps to NM_001195263.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:102789826 C>T maps to NM_001195263.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr10:102778630 G>A maps to NM_001195263.1 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:119043129 G>A maps to NM_173791.3 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119044377 C>A maps to NM_173791.3 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:119043972 C>A maps to NM_173791.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:119043174 C>A maps to NM_173791.3 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr10:119043639 C>T maps to NM_173791.3 Q868Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:119044269 G>A maps to NM_173791.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:119044980 A>T maps to NM_173791.3 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:145752462 C>T maps to NM_002614.3 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:145761320 C>A maps to NM_002614.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:145747190 C>T maps to NM_002614.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:73440204 C>T maps to NM_015009.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:73673724 G>T maps to NM_015009.1 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:73433799 C>T maps to NM_015009.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:73651528 C>A maps to NM_015009.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:73432827 C>T maps to NM_015009.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr3:73433091 C>G maps to NM_015009.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:73432878 G>T maps to NM_015009.1 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:73433739 G>T maps to NM_015009.1 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:73453384 G>A maps to NM_015009.1 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:73432530 C>A maps to NM_015009.1 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:73657781 C>A maps to NM_015009.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:73437169 G>C maps to NM_015009.1 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr3:73433913 C>T maps to NM_015009.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:73433148 G>T maps to NM_015009.1 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:73657746 A>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:73433778 G>A maps to NM_015009.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr3:73432743 C>A maps to NM_015009.1 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:41966200 C>T maps to NM_001164595.1 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr12:41966756 G>T maps to NM_001164595.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr12:41966914 C>T maps to NM_001164595.1 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:41966542 C>A maps to NM_001164595.1 C654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:41582587 C>A maps to NM_001164595.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:41966350 G>A maps to NM_001164595.1 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:41967631 G>T maps to NM_001164595.1 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:156874557 G>A maps to NM_001080471.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156880521 C>T maps to NM_001080471.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:156877440 C>T maps to NM_001080471.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:156878709 C>G maps to NM_001080471.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:156883034 C>T maps to NM_001080471.1 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:156873741 C>A maps to NM_001080471.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:156877970 G>T maps to NM_001080471.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:156882352 C>T maps to NM_001080471.1 C716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:156883535 C>A maps to NM_001080471.1 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:156880455 C>A maps to NM_001080471.1 C624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:156876501 C>A maps to NM_001080471.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:156873753 T>A maps to NM_001080471.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:156876136 G>A maps to NM_001080471.1 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:22571032 G>A maps to NM_144962.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:4125572 T>A maps to NM_206836.2 K236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:216914081 G>A maps to NM_018441.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:216930033 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:57328675 A>G maps to NM_006210.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:57333090 C>A maps to NM_006210.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:57327946 A>G maps to NM_006210.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57325591 C>A maps to NM_006210.2 V1406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:57334136 G>T maps to NM_006210.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr19:57325603 G>A maps to NM_006210.2 A1402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:57325231 A>C maps to NM_006210.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:57326710 A>T maps to NM_006210.2 C1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:57327814 G>T maps to NM_006210.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:57325335 C>A maps to NM_006210.2 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:57328075 C>T maps to NM_006210.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr19:57328600 C>A maps to NM_006210.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr19:57335024 G>T maps to NM_006210.2 T139T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8506-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:57335045 G>A maps to ENST00000391708 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:57325485 C>A maps to NM_006210.2 E1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:57327009 T>A maps to NM_006210.2 K934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:57326224 C>T maps to NM_006210.2 G1195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:57328906 C>A maps to NM_006210.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:57328381 T>C maps to NM_006210.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:57326878 G>T maps to NM_006210.2 C977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:57328465 C>A maps to NM_006210.2 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr19:57327217 A>T maps to NM_006210.2 Y864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:57327913 A>G maps to NM_006210.2 C632C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:57327424 C>A maps to NM_006210.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:57325714 T>A maps to NM_006210.2 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:57325966 G>T maps to NM_006210.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:57327814 G>A maps to NM_006210.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:57327304 G>A maps to NM_006210.2 I835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:57325606 A>C maps to NM_006210.2 A1401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:64323336 T>C maps to NM_020651.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:56763320 G>T maps to NM_021255.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:56763457 C>T maps to NM_021255.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr14:56763463 G>A maps to NM_021255.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:56755249 C>T maps to NM_021255.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:66235597 G>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:4575045 T>G maps to ENST00000301396 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:17494896 G>T maps to NM_148172.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:57358430 G>A maps to NM_001135690.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:57354088 C>G maps to NM_001135690.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr8:57354127 A>G maps to NM_001135690.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:57353893 G>T maps to NM_001135690.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr8:57354181 G>A maps to NM_001135690.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:57354421 C>A maps to NM_001135690.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:8051527 G>T maps to NM_002616.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:8047129 T>G maps to NM_002616.2 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr17:8053355 C>A maps to NM_002616.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:8050242 G>A maps to NM_002616.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:8053802 G>A maps to NM_002616.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:239170884 G>A maps to NM_022817.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:239180142 C>T maps to NM_022817.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:239161570 C>T maps to NM_022817.2 Q1031Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:7846895 A>T maps to ENST00000377532 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:7890001 C>T maps to ENST00000377532 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:7858729 G>T maps to ENST00000377532 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr1:7879478 A>T maps to ENST00000377532 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:30974930 G>A maps to NM_014303.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr4:152622521 G>A maps to NM_004564.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:152679921 A>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:92136427 G>A maps to NM_000466.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:92147357 T>A did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr7:92131236 G>A maps to NM_000466.2 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:2339977 G>A maps to NM_153818.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:90226655 T>A maps to NM_003847.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:145522531 C>G maps to NM_003846.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:7543246 C>A maps to NM_080662.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:10690004 G>A maps to NM_004565.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:10659361 C>T maps to NM_004565.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:10689759 G>T maps to NM_004565.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:160249885 C>A maps to NM_002857.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr8:77896273 C>A maps to NM_001172087.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:77895672 C>A maps to NM_001172087.1 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:77895553 T>G maps to NM_001172087.1 V287V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr22:18562678 C>A maps to NM_017929.5 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:143792567 C>T maps to NM_003630.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr12:7361762 C>T maps to NM_001131023.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:7361711 G>A maps to NM_001131023.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:7343063 C>A maps to NM_001131023.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:7362388 G>T maps to NM_001131023.1 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:179615933 G>T maps to NM_016559.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:179597741 G>T maps to NM_016559.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:179605470 G>T maps to NM_016559.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:179576888 G>A maps to NM_016559.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:179754381 G>A maps to NM_016559.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:179592152 C>A maps to NM_016559.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr3:179533762 G>A maps to NM_016559.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:179615998 G>T maps to NM_016559.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:179526077 G>T maps to NM_016559.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:42934364 C>T maps to NM_000287.3 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:42934569 G>C maps to NM_000287.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:74719545 C>T maps to NM_002620.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:8169550 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:161087768 C>A maps to NM_012394.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:54987334 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:54989705 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:54982666 C>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:54987317 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:54982649 C>A did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:54989697 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:54982640 T>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:54978517 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:54978499 C>G did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:207235397 C>T maps to NM_006212.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:207245605 C>T maps to NM_006212.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:45730917 G>A maps to NM_002626.4 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr21:45736373 G>C maps to NM_002626.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr21:45738471 G>A maps to NM_002626.4 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr21:45741640 G>T maps to NM_002626.4 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr21:45741646 C>G maps to NM_002626.4 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:48533132 G>A did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr12:48535580 C>T maps to NM_001166686.1 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr12:48533650 G>T maps to NM_001166686.1 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:3141544 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:4851650 C>A maps to NM_005022.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:24345375 G>A maps to NM_199346.1 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:61017437 C>T maps to ENST00000422676 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:61017422 C>T maps to ENST00000422676 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:61017164 C>T maps to ENST00000422676 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:61015905 C>A maps to ENST00000422676 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:44105092 G>C maps to NM_000290.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:77224973 G>C did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:77224417 A>G did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:77225036 C>T did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr23:77224606 C>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:77225099 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:77224682 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:77225091 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:197784850 C>A maps to NM_024989.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:197711725 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:197705996 G>A maps to NM_024989.3 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:3845192 C>T maps to NM_014489.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:28269748 A>T maps to NM_032507.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:28254866 C>T maps to NM_032507.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr6:28251739 C>T maps to NM_032507.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:28268891 G>T maps to NM_032507.3 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264603 G>A maps to NM_032507.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:28264609 G>A maps to NM_032507.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr6:28253484 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:28269904 G>A maps to NM_032507.3 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr6:28269794 C>T maps to NM_032507.3 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:249211871 G>A maps to NM_170725.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:249211208 G>T maps to NM_170725.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:249211643 G>A maps to NM_170725.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:249211250 C>T maps to NM_170725.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:249212111 G>C maps to NM_170725.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:249211988 C>A maps to NM_170725.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:249211544 C>A maps to NM_170725.2 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:249210882 G>T maps to NM_170725.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr10:50723380 A>G maps to ENST00000515869 *1062Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:34396294 A>G maps to NM_152595.4 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr15:34395532 G>A maps to NM_152595.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:230472852 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:230486820 C>G maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr1:230486706 G>T maps to ENST00000321327 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:230492929 C>A maps to ENST00000321327 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:230492795 G>A maps to ENST00000321327 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:230472902 C>A maps to ENST00000321327 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:41704679 G>T maps to NM_002630.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:41712180 G>A maps to NM_002630.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:41711122 A>G maps to NM_002630.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:98155360 G>A maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr8:97892088 G>T maps to ENST00000325141 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr8:97797325 G>A maps to ENST00000325141 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:97847375 C>A maps to ENST00000325141 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr8:97978224 C>T maps to ENST00000325141 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:98041643 G>A maps to ENST00000325141 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:97978203 G>A maps to ENST00000325141 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:10473252 A>T maps to NM_002631.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:10460607 G>T maps to NM_002631.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:75416137 G>A maps to ENST00000405431 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:77378446 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:77373667 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:77381314 C>T did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:77373664 C>A did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr23:77372870 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:77380448 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:77365414 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:49754363 C>T maps to NM_138733.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:49754614 G>A maps to NM_138733.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:49754639 G>A maps to NM_138733.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:49754588 C>A maps to NM_138733.4 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49754273 C>A maps to NM_138733.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr6:49754624 A>G maps to NM_138733.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:17627040 G>A maps to NM_012088.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:15579521 G>T maps to NM_052890.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:15586643 C>A maps to NM_052890.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:15587313 G>T maps to NM_052890.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:15582834 C>A maps to NM_052890.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:15586643 C>T maps to NM_052890.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:15586768 G>A maps to NM_052890.3 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:153279555 G>T maps to NM_052891.1 C81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:153270488 C>T maps to NM_052891.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:153312855 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:153303329 C>A maps to NM_020393.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:153309768 C>A maps to NM_020393.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:153303332 C>A maps to NM_020393.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:64089163 A>T maps to NM_001172818.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:64059308 G>A maps to NM_002633.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:37848687 A>T maps to NM_018290.3 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:37841686 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:37848863 A>G maps to NM_018290.3 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:37836325 C>T maps to NM_018290.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:37848596 G>T maps to NM_018290.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:74056625 C>T maps to NM_173582.3 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr11:74054018 C>T maps to NM_173582.3 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71002377 G>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:71006564 G>C maps to NM_021965.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:71080083 A>T maps to NM_021965.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:71114207 G>A maps to NM_021965.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:71114171 A>T maps to NM_021965.3 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr9:71006586 G>T maps to NM_021965.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:2263991 T>A maps to NM_001042371.2 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:99512841 C>A maps to NM_001102612.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr15:99512853 G>C maps to NM_001102612.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:100933198 T>A maps to NM_000926.4 K731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:100912824 C>A maps to NM_000926.4 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:100933246 G>A maps to NM_000926.4 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:100922258 A>T maps to NM_000926.4 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:118370573 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:118377131 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:76399769 G>A maps to NM_024419.3 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:76392436 C>T maps to NM_024419.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:13228215 C>T maps to NM_030948.1 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:13283718 C>T maps to NM_030948.1 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:13283760 T>C maps to NM_030948.1 D539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:13230267 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr6:13182881 G>T maps to NM_030948.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr6:144086515 A>G maps to NM_001100164.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:58318160 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:58416514 C>T maps to NM_080672.3 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:58349460 G>T maps to NM_080672.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:58348439 G>T maps to NM_080672.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:58381108 G>C maps to NM_080672.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr20:58349301 C>T maps to NM_080672.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr20:58349429 A>C maps to NM_080672.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:28815702 A>G maps to NM_023923.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:28800618 G>T maps to NM_023923.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:125939788 G>A maps to NM_032177.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:47486767 G>A maps to NM_002634.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr12:7079658 G>A maps to NM_001144831.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:7077177 G>A maps to NM_001144831.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:9087775 G>A maps to ENST00000433083 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:33794654 A>G maps to ENST00000419414 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:33790504 C>T maps to ENST00000419414 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr1:33832750 A>T maps to ENST00000419414 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:22237201 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:22065242 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:22245655 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:22196456 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:22117196 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:22051129 G>C did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:22129676 G>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:22244558 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:22056628 G>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:22108603 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:22196463 C>G did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:22065262 C>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:22132588 C>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:22112123 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:22112187 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:22065310 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:22132684 A>G did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:22095664 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr23:22095661 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:22266063 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:22244621 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr23:22095702 G>A did not map to a codon.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:33382863 C>T maps to NM_024165.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:27251017 C>T maps to NM_001033561.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:27240043 T>A maps to NM_001033561.1 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr17:27240037 T>C maps to NM_001033561.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:11022705 A>T maps to ENST00000303905 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11022087 G>T maps to ENST00000303905 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:11068426 A>T maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11068307 G>T maps to ENST00000303905 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:11022738 G>T maps to ENST00000303905 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr5:133873704 A>C maps to ENST00000448712 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr5:133895664 G>T maps to ENST00000448712 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:133871558 G>A maps to ENST00000448712 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:46845160 A>G did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:46898442 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:46913592 G>T did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:46913644 G>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:46913775 G>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:46898397 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:46917716 C>G did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:46913914 A>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:46918163 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:46918320 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:46917890 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:129770170 G>A maps to NM_199320.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:129767549 C>T maps to NM_199320.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr4:129776951 G>A maps to NM_199320.2 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr4:129783280 C>T maps to NM_199320.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr9:123626343 C>T maps to NM_015651.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:96427979 C>G maps to NM_005392.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:96436115 G>T maps to NM_005392.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr9:96421879 G>T maps to NM_005392.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:96438931 C>T maps to NM_005392.3 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr9:96439906 G>A maps to NM_005392.3 Q1080Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:96408012 G>T maps to NM_005392.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:96428302 G>C maps to NM_005392.3 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:96392312 G>T maps to NM_005392.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:34519295 C>T maps to NM_016436.4 Q744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr20:34451131 G>T maps to NM_016436.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:34526624 G>T maps to NM_016436.4 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:34526625 G>T maps to NM_016436.4 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:34487414 T>A maps to NM_016436.4 L469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr20:34451290 A>G maps to NM_016436.4 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:34526966 G>T maps to NM_016436.4 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr20:34435327 G>T maps to NM_016436.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:133826880 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:133807004 G>C maps to ENST00000395386 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:133806688 G>A maps to ENST00000395386 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:133848836 G>A maps to ENST00000395386 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr8:133855072 A>T maps to ENST00000395386 K902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:133807004 G>A maps to ENST00000395386 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:133816218 T>A maps to ENST00000395386 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:46105752 T>A maps to ENST00000257821 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:45975092 C>A maps to ENST00000257821 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:45992771 G>A maps to ENST00000257821 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr11:45970443 C>T maps to ENST00000257821 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:45992813 G>A maps to ENST00000257821 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:45309811 G>A maps to NM_138415.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr22:45312222 G>A maps to NM_138415.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr22:45312285 C>A maps to NM_138415.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr22:45279171 A>G maps to NM_138415.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr22:45309827 C>T maps to NM_138415.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr22:45312348 C>T maps to NM_138415.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr22:45309876 G>T maps to NM_138415.3 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr22:45283867 C>T maps to NM_138415.3 W391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:64356527 C>T maps to NM_015153.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr6:64422790 C>T maps to NM_015153.2 N1769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:64394398 C>G maps to NM_015153.2 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:64394071 C>G maps to NM_015153.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:64394488 C>G maps to NM_015153.2 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:133559233 A>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:133527956 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:133549066 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:133547964 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:133547666 G>T did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr3:52448546 G>T maps to ENST00000454052 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:54020194 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:54029092 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:54029106 G>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:54011444 C>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:54011567 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:54069222 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:54040928 C>G did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:54020142 C>A did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr23:54040884 G>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:53970626 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:54044163 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:54028635 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:54012258 C>A did not map to a codon.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:120263890 T>A maps to NM_006623.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:120266065 T>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:120279816 T>A maps to NM_006623.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:79697924 C>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:79726318 G>A maps to NM_017934.5 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:79650951 T>A maps to NM_017934.5 K1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:71840576 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:71838618 C>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:71932664 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:71855066 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:71840644 G>C did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:71838659 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:71813029 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:71864267 A>G did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:71887314 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:71895992 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:71895993 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:71856208 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:71856209 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:71800925 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:71864284 C>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:71840618 T>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:71840619 C>G did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:71864286 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:71802253 T>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:18956833 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:18915322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:18912362 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:18943784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:18926945 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:18972503 G>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr23:18926042 C>T did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:18924679 C>G did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr23:18927023 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:18944618 T>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:18944627 T>G did not map to a codon.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr23:18959757 T>A did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:18923880 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:18924665 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr16:47533763 A>G maps to NM_000293.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:47622832 G>T maps to NM_000293.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr16:47698807 C>T maps to NM_000293.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:47581456 G>T maps to NM_000293.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr16:47684468 C>T maps to NM_000293.2 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:56149702 G>T maps to NM_006213.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:56148956 G>A maps to NM_006213.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:30768219 T>C maps to NM_000294.2 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr16:30768315 C>A maps to NM_000294.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr12:76424316 C>G maps to NM_007350.3 *402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:76425197 G>A maps to NM_007350.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr1:201437844 G>A maps to NM_012396.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118509944 G>A maps to NM_015157.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:118498237 G>T maps to NM_015157.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr11:118516194 G>T maps to NM_015157.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:118498105 G>T maps to NM_015157.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr11:118495659 G>A maps to NM_015157.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:111686523 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:111603475 C>T maps to NM_001134438.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr3:111685541 G>T maps to NM_001134438.1 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr3:111603770 C>T maps to NM_001134438.1 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr3:111603682 C>T maps to NM_001134438.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:111632359 G>A maps to NM_001134438.1 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:111603502 C>T maps to NM_001134438.1 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:44008245 C>A maps to NM_198850.3 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:44001308 G>C maps to NM_198850.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:44008063 G>A maps to NM_198850.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:43982284 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:44001362 C>T maps to NM_198850.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:60506076 C>T maps to NM_194449.2 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr18:60506064 G>T maps to NM_194449.2 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr18:60646291 C>T maps to NM_194449.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:71697943 C>A maps to NM_015020.2 G615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:71713314 T>G maps to NM_015020.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:71701198 C>A maps to NM_015020.2 G556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr16:71683002 G>A maps to NM_015020.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr17:47301766 C>G maps to NM_001143804.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:170557702 C>T maps to NM_001008489.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:71952178 C>A maps to NM_005169.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:41750471 C>A maps to NM_003924.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:608851 C>G maps to ENST00000264555 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:609457 C>T maps to ENST00000264555 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:114255906 G>A maps to NM_006608.2 C259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr7:77549682 C>T maps to ENST00000427986 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:13325782 C>A maps to NM_006214.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:22079150 G>T maps to NM_014759.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:22079138 C>A maps to NM_014759.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:60994098 G>T maps to NM_032439.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:61005251 C>G maps to NM_032439.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:75756214 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:75757615 G>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr8:75756295 G>A maps to NM_015886.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:36922667 G>T maps to NM_153370.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr4:25262191 T>A maps to NM_018323.3 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:21157609 T>A did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr22:21083677 C>G maps to NM_058004.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr22:21119495 C>A maps to NM_058004.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:21174156 C>G maps to NM_058004.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr22:21153503 C>T maps to NM_058004.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr22:21073003 G>T maps to NM_058004.2 I1683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:21064218 G>A maps to NM_058004.2 R1992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:21159448 G>A maps to NM_058004.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr22:21161737 G>A maps to NM_058004.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:151276018 G>A maps to NM_002651.2 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:151274761 C>T maps to NM_002651.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:44435526 C>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:145580300 T>C maps to NM_006099.3 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:145580548 A>G maps to NM_006099.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:145580563 A>G maps to NM_006099.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr19:4013225 C>T maps to NM_015897.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:73482667 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr11:85692254 G>A maps to ENST00000393343 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr11:85722152 G>A maps to ENST00000393343 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:85725987 T>C maps to ENST00000393343 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:38468616 G>A maps to NM_012407.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:229890755 G>A maps to NM_017933.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:229890499 C>A maps to NM_017933.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:229890731 C>T maps to NM_017933.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:230020566 C>G maps to NM_017933.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:229890722 T>A maps to NM_017933.4 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr15:65108868 G>A maps to ENST00000333425 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr15:65111420 A>T maps to ENST00000333425 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr15:65114716 G>T maps to ENST00000333425 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr15:65108961 G>T maps to ENST00000333425 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:15349878 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:15339750 C>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:15342891 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:15349465 G>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:15349861 C>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:15339765 G>C did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:15339735 A>G did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:15349799 T>C did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:55611454 A>C maps to ENST00000164305 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr15:55613536 A>T maps to ENST00000164305 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:172411084 C>A maps to NM_153747.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:527725 G>T maps to NM_001127178.1 L897L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-8120-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:533124 G>T maps to NM_001127178.1 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:494290 G>A maps to NM_001127178.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:501315 G>A maps to NM_001127178.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:77676162 T>C maps to NM_005482.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:160001424 A>G maps to NM_145167.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:59739949 G>A maps to NM_176787.4 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr18:59777143 C>G maps to NM_176787.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr18:59828460 T>A maps to NM_176787.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr18:59757810 C>T maps to NM_176787.4 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr9:35091858 C>A maps to NM_032634.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr9:35095172 G>A maps to NM_032634.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr9:35092124 G>A maps to NM_032634.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr9:35095490 G>A maps to NM_032634.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr9:35092167 G>T maps to NM_032634.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:35093137 T>C maps to NM_032634.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr21:38437992 T>C maps to NM_153681.2 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr21:38444732 C>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:633138 G>A maps to NM_148920.1 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:633390 C>T maps to NM_148920.1 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:207111096 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:207107959 G>A maps to NM_002644.3 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:207109004 C>A maps to NM_002644.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:207112587 C>A maps to NM_002644.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:207103737 C>T maps to NM_002644.3 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:207105831 C>A maps to NM_002644.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:207110896 C>T maps to NM_002644.3 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:26890890 G>T maps to NM_033198.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr17:26888617 C>T maps to NM_033198.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr17:26887087 G>C maps to NM_033198.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:26881312 C>T maps to NM_033198.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:26898183 G>A maps to NM_033198.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:26883215 C>T maps to NM_033198.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:44048031 C>T maps to NM_015937.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:44047575 A>T maps to NM_015937.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr20:44054309 C>T maps to NM_015937.4 N527N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:44049301 C>T maps to NM_015937.4 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr20:44052917 C>T maps to NM_015937.4 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr20:44053147 C>T maps to NM_015937.4 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr20:44048214 C>T maps to NM_015937.4 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr20:44050086 G>T maps to NM_015937.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:44049005 C>T maps to NM_015937.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:27117368 G>T maps to NM_017837.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr17:34894228 C>T maps to NM_178517.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr17:34894131 T>A maps to NM_178517.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:89442931 C>A maps to NM_001042616.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:196678779 G>C maps to NM_025163.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:98363771 G>A maps to NM_152309.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98388153 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:98469378 G>A maps to NM_152309.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:98469657 C>A maps to NM_152309.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:98411382 C>T maps to NM_152309.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:98411026 C>T maps to NM_152309.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:98408475 G>A maps to NM_152309.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:98369517 C>G maps to NM_152309.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:98405367 C>A maps to NM_152309.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:98376422 C>A maps to NM_152309.2 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:98416665 G>A maps to NM_152309.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:98386626 G>A maps to NM_152309.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:17124379 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:17191090 C>T maps to NM_002645.2 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr11:17132109 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:204426903 G>A maps to NM_002646.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:204433732 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:204403028 G>A maps to NM_002646.3 N1245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:204413538 C>A maps to NM_002646.3 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:204394101 C>A maps to NM_002646.3 E1595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:204408125 G>A maps to NM_002646.3 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:204412696 G>A maps to NM_002646.3 Q966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:18435366 C>T maps to NM_004570.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:18573926 T>C maps to NM_004570.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:18524164 T>A maps to NM_004570.4 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr12:18715655 G>T maps to NM_004570.4 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:39575852 G>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr18:39617690 G>T maps to ENST00000398870 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:39537582 G>T maps to ENST00000398870 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:178919300 A>T maps to NM_006218.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:178947860 A>T maps to NM_006218.2 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:138383954 C>T maps to NM_006219.1 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr3:138375035 A>T maps to NM_006219.1 L1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:9780179 C>T maps to ENST00000361110 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:9780185 G>T maps to ENST00000361110 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:106508038 G>C maps to NM_002649.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:106545618 C>A maps to NM_002649.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:106509635 C>A maps to NM_002649.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:106509745 C>A maps to NM_002649.2 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:106509706 C>T maps to NM_002649.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:106509208 C>G maps to NM_002649.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:106508179 G>T maps to NM_002649.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:106523544 G>A maps to NM_002649.2 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:106508506 C>T maps to NM_002649.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:106524640 C>T maps to NM_002649.2 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:106513258 G>T maps to NM_002649.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:106508459 C>A maps to NM_002649.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:106508260 G>C maps to NM_002649.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:106523598 T>A maps to NM_002649.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:106508032 C>A maps to NM_002649.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:106513228 G>A maps to NM_002649.2 Q711Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:31688259 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:67589620 G>T maps to ENST00000396611 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr5:67575529 C>T maps to ENST00000396611 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:67588927 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr5:67590997 T>C maps to ENST00000396611 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:67593401 C>T maps to ENST00000396611 Y724Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:67576451 T>G maps to ENST00000396611 L244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:18273926 G>C maps to NM_005027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:18279607 C>T maps to NM_005027.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr19:18278015 C>T maps to NM_005027.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:18272853 G>T maps to NM_005027.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:130437286 G>C maps to NM_014602.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:130435260 A>C maps to NM_014602.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr3:130403128 G>C maps to NM_014602.2 S1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr3:130398310 T>A maps to NM_014602.2 K1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:130399504 T>A maps to NM_014602.2 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:130409377 A>G maps to NM_014602.2 A1073A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:8809051 G>T maps to NM_001142633.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:8784283 G>A maps to NM_001142633.1 N811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr17:8809033 G>A maps to NM_001142633.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:8812395 G>T maps to NM_001142633.1 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:8784262 G>A maps to NM_001142633.1 C818C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:8731975 C>A maps to NM_001010855.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:8725197 C>G maps to NM_001010855.2 *615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr17:8738628 C>A maps to NM_001010855.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr17:8736344 G>T maps to NM_001010855.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:8732149 C>G maps to NM_001010855.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:209188939 A>T maps to NM_015040.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:209218815 C>T maps to NM_015040.3 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:209204747 G>T maps to NM_015040.3 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:209142259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:209191038 C>T maps to NM_015040.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:209190982 A>T maps to NM_015040.3 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr2:209138434 C>T maps to NM_015040.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:209169636 C>T maps to NM_015040.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr2:209190009 G>T maps to NM_015040.3 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:209203254 A>T maps to NM_015040.3 P1545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:209142379 C>T maps to NM_015040.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:209190837 G>A maps to NM_015040.3 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:209185038 A>C maps to NM_015040.3 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:209212619 G>T maps to NM_015040.3 G1749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:99997502 G>A maps to NM_013439.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:99972003 A>T maps to NM_013439.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:99956682 C>T maps to ENST00000413850 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:99956585 C>G maps to ENST00000413850 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:99957040 C>G maps to ENST00000413850 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:37139013 G>C maps to ENST00000373507 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr23:48772394 T>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:48771549 C>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:48772329 G>C did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:48772359 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:48775899 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:48771796 G>C did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:48776078 C>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:48775875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:76984658 G>C maps to NM_017439.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr7:76950084 C>T maps to NM_017439.3 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:76978694 T>C maps to NM_017439.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:77026304 G>A maps to NM_017439.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr7:77006708 T>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:142836647 G>T maps to NM_002652.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:142836632 C>G maps to NM_002652.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:142832324 C>A maps to NM_002652.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:142832325 A>G maps to NM_002652.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:22880658 C>A maps to NM_005028.4 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22880695 C>T maps to NM_005028.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:22828899 G>A maps to NM_005028.4 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr10:22830772 G>A maps to NM_005028.4 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:36935737 C>T maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr17:36936703 C>G did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr12:57992981 G>A maps to NM_024779.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:57994799 G>T maps to NM_024779.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr12:57995328 T>C maps to NM_024779.4 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr12:57989696 C>T maps to NM_024779.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr12:57987806 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:151205137 G>T maps to NM_001135638.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:71532567 T>A maps to NM_003558.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr17:27383321 G>C maps to NM_016518.2 *391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:15425672 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:15444093 G>A did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:15474023 T>A did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:10728816 C>T maps to NM_001101387.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr22:32016568 G>A maps to ENST00000422296 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr22:32015684 C>A maps to ENST00000422296 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr22:28310310 A>G maps to NM_012399.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:65688808 C>A maps to NM_012417.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr11:67263769 C>G maps to NM_004910.2 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:67262385 C>T maps to NM_004910.2 E891E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:67269492 C>A maps to NM_004910.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:67261792 C>T maps to NM_004910.2 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:67269420 C>A maps to NM_004910.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:123485672 T>A maps to NM_020845.2 K361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:123489892 C>T maps to NM_020845.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:6367062 C>A maps to NM_031220.3 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:6367110 G>A maps to NM_031220.3 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:6386988 C>T maps to NM_031220.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr17:6381405 G>A maps to NM_031220.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr17:6380392 G>A maps to NM_031220.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:6386997 C>A maps to NM_031220.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:6374562 T>C maps to NM_031220.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:6367539 C>T maps to NM_031220.3 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:3202410 T>G maps to ENST00000380989 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:3206020 G>A maps to ENST00000380989 H229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr5:134364900 G>T maps to NM_002653.4 Y171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr4:111553592 G>T maps to NM_153426.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:130845801 C>A maps to NM_004764.4 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:130831589 T>A maps to NM_004764.4 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:130845874 C>T maps to NM_004764.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr12:130847581 G>C maps to NM_004764.4 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:130841561 C>T maps to NM_004764.4 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:130845801 C>A maps to NM_004764.4 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr12:130827555 C>T maps to NM_004764.4 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:130841620 C>A maps to NM_004764.4 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:22210597 C>T maps to NM_001135721.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:22210611 G>T maps to NM_001135721.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:22136964 A>T maps to NM_001135721.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr22:25151776 T>C maps to NM_001008496.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:25151806 T>C maps to NM_001008496.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:94301942 C>T maps to NM_152431.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:94330993 A>G maps to NM_152431.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:94310468 G>T maps to NM_152431.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:94316681 G>A maps to NM_152431.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr23:68382048 T>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:68381542 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:68381583 C>T did not map to a codon.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:68381556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:68381181 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:68381828 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:68382066 G>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:68381954 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:68382734 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:68381606 T>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:68382631 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:68381936 C>G did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr23:68381892 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:68382688 A>T did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:68382832 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:68381717 G>T did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:108704448 T>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:108704377 T>C maps to NM_014819.4 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:108714368 A>G maps to NM_014819.4 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:108713992 C>A maps to NM_014819.4 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:2168791 T>A maps to NM_001009944.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:2160772 G>A maps to NM_001009944.2 P1465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr16:2153732 C>G maps to NM_001009944.2 T2775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:2158456 C>A maps to NM_001009944.2 G2237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:2159682 G>A maps to NM_001009944.2 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:2164412 C>A maps to NM_001009944.2 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:2147970 C>A maps to NM_001009944.2 P3355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:2153582 G>T maps to NM_001009944.2 L2825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr16:2161138 C>A maps to NM_001009944.2 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr16:2147376 C>A maps to NM_001009944.2 E3450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2155466 C>A maps to NM_001009944.2 R2624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:2156624 G>A maps to NM_001009944.2 T2421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr16:2164248 C>A maps to NM_001009944.2 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:2162817 C>T maps to NM_001009944.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:47867067 T>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:47979819 C>T maps to NM_138295.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:47852795 C>T maps to NM_138295.3 E2423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:47937646 T>A maps to NM_138295.3 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:47944778 T>A maps to NM_138295.3 K556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:47866970 C>T maps to NM_138295.3 E2277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:47942011 T>G maps to NM_138295.3 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:47870861 C>T maps to NM_138295.3 G2142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr7:47897301 C>A maps to NM_138295.3 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:47854994 C>A maps to NM_138295.3 L2342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:47882628 C>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:47882625 C>T maps to NM_138295.3 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:47882628 C>T maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:47814741 C>T maps to NM_138295.3 *2850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:81187864 G>T maps to NM_052892.3 R1402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:81232342 G>C maps to NM_052892.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81228607 C>A maps to NM_052892.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:81253858 G>A maps to NM_052892.3 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:81208464 C>A maps to NM_052892.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:81208494 C>A maps to NM_052892.3 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:81236247 G>A maps to NM_052892.3 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr16:81181897 G>A maps to NM_052892.3 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr16:81151064 G>T maps to NM_052892.3 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:81214827 G>C maps to NM_052892.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr16:81253873 G>T maps to NM_052892.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:81194294 C>T maps to NM_052892.3 V1231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr16:81134841 G>C maps to NM_052892.3 L2421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:81155283 G>A maps to NM_052892.3 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:81145907 G>A maps to NM_052892.3 L2281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:81145908 G>T maps to NM_052892.3 L2280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr16:81181792 G>T maps to NM_052892.3 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr16:81157273 G>A maps to NM_052892.3 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:81187853 G>T maps to NM_052892.3 A1405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr16:81187675 C>T maps to NM_052892.3 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:88940613 C>T maps to NM_000297.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:88959543 G>T maps to NM_000297.2 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:88967892 G>T maps to NM_000297.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:102053072 T>A maps to NM_016112.2 K575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr10:102059379 G>A maps to NM_016112.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:102057199 G>A maps to NM_016112.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr10:102054718 A>G maps to NM_016112.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:102049823 G>C maps to NM_016112.2 S733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr10:102056835 G>A maps to NM_016112.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:137226200 G>A maps to ENST00000230643 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:137257390 C>A maps to ENST00000230643 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:42284448 G>T maps to NM_138370.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:42282122 A>G maps to NM_138370.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:46656285 C>T maps to NM_006071.1 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr22:46657467 A>G maps to NM_006071.1 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr22:46655393 G>T maps to NM_006071.1 R1276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr22:46654626 C>T maps to NM_006071.1 P1531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr22:46658151 C>G maps to NM_006071.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr22:46657299 A>G maps to NM_006071.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr22:46655313 G>A maps to NM_006071.1 N1302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr22:46654188 G>A maps to NM_006071.1 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr22:46653828 C>T maps to NM_006071.1 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr22:46655130 A>G maps to NM_006071.1 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:51923294 C>A maps to NM_138694.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:51484223 G>T maps to NM_138694.3 V3960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:51512865 T>A maps to NM_138694.3 S3787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:51656118 C>G maps to NM_138694.3 V2785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:51889987 T>A maps to NM_138694.3 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:51612662 C>A maps to NM_138694.3 E3251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr6:51920528 T>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:51907899 C>A maps to NM_138694.3 G952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:51524525 C>T maps to NM_138694.3 R3466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:51938334 T>C maps to NM_138694.3 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr6:51503754 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr6:51908483 G>C maps to NM_138694.3 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:51875133 T>A maps to NM_138694.3 I1908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:51923372 G>T maps to NM_138694.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr6:51913417 C>A did not map to a codon.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr6:51751971 C>T maps to NM_138694.3 P2356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:51824797 C>A maps to NM_138694.3 R1926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr6:51824737 G>A maps to NM_138694.3 V1946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr6:51897942 C>A maps to NM_138694.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:51613440 C>T maps to NM_138694.3 V2991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:51900448 C>A maps to NM_138694.3 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:51777291 C>A maps to NM_138694.3 V2068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:51656067 T>C maps to NM_138694.3 A2802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:51799085 G>A maps to NM_138694.3 I1981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:51524231 G>T maps to NM_138694.3 A3564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:51524558 T>A maps to NM_138694.3 S3455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:51890205 G>A maps to NM_138694.3 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:51917991 G>A maps to NM_138694.3 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:51701241 G>A maps to NM_138694.3 V2711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr6:51503746 G>T maps to NM_138694.3 T3802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr6:51732800 C>A maps to NM_138694.3 L2531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr6:51947263 C>A maps to NM_138694.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:110464484 C>A maps to ENST00000426474 I2161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr8:110516569 G>T maps to ENST00000426474 G3616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr8:110455938 G>T maps to ENST00000426474 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:110455956 A>G maps to ENST00000426474 T1539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:110455957 G>T maps to ENST00000426474 E1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:110477364 G>A maps to ENST00000426474 G2768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:110394799 C>T maps to ENST00000426474 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr8:110476710 C>T maps to ENST00000426474 T2550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:110457306 G>T maps to ENST00000426474 G1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:110535120 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:110509296 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110408304 G>T maps to ENST00000426474 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110432915 G>T maps to ENST00000426474 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:110453507 C>A maps to ENST00000426474 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:110467031 C>T maps to ENST00000426474 V2275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:110539097 T>C maps to ENST00000426474 S4191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:110497337 C>T maps to ENST00000426474 I3214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:110447519 G>T maps to ENST00000426474 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr8:110451321 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:110452936 A>G did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:110457347 C>T maps to ENST00000426474 Y1750Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr8:110457683 A>C maps to ENST00000426474 T1862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:110456948 T>A maps to ENST00000426474 C1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr8:110466980 C>T maps to ENST00000426474 H2258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:110397853 T>A maps to ENST00000426474 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:110509244 T>G maps to ENST00000426474 L3475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:110523009 A>T maps to ENST00000426474 P3801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:110397763 A>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr8:110530507 T>A maps to ENST00000426474 T3935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:110432867 T>C maps to ENST00000426474 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:79513981 G>T maps to NM_181839.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:155264361 G>A maps to ENST00000423816 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr1:155264484 G>A maps to ENST00000423816 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:155265003 G>A maps to ENST00000423816 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:155260452 G>A maps to ENST00000423816 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr15:72499544 C>A maps to ENST00000419739 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr15:72495445 G>A maps to ENST00000419739 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr15:72502176 C>A maps to ENST00000419739 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:72500959 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:3024316 G>A maps to NM_004203.4 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:3025597 A>G maps to NM_004203.4 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:14574748 G>T maps to NM_213560.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:14569147 G>C maps to NM_213560.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:14569148 C>T maps to NM_213560.1 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:89279416 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:89273111 A>G maps to NM_006256.2 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:131469302 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr21:44445024 G>A maps to NM_004571.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr21:44427663 G>T maps to NM_004571.3 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr21:44438241 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr21:44441415 C>T maps to NM_004571.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:125255500 C>A maps to NM_022062.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr11:125255524 C>T maps to NM_022062.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:125301228 G>T maps to NM_022062.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:125280102 G>A maps to NM_022062.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:125280750 C>A maps to NM_022062.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:125221209 A>G maps to NM_022062.2 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:125255569 A>G maps to NM_022062.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:125280186 C>T maps to NM_022062.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:201263115 C>A maps to NM_000299.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:32974457 G>C maps to NM_004572.3 Y659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr12:32974304 C>A maps to NM_004572.3 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr12:32955457 C>T maps to NM_004572.3 Q726Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:33049566 G>T maps to NM_004572.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:33031445 C>T maps to NM_004572.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr12:32975398 A>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:32977014 G>A maps to NM_004572.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:32974409 C>T maps to NM_004572.3 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:33031967 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr12:33003783 C>A maps to NM_004572.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:397118 C>G maps to NM_007183.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:396830 C>A maps to NM_007183.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:159488325 G>T maps to NM_003628.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:159490613 C>T maps to NM_003628.3 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr2:159530505 C>T maps to NM_003628.3 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr2:159499084 C>T maps to NM_003628.3 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:159519884 A>T maps to NM_003628.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:119325777 G>T maps to NM_015900.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:119325792 G>T maps to NM_015900.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:119344080 T>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:119348296 G>A maps to NM_015900.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr3:119347559 A>G maps to NM_015900.2 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:119325678 T>C maps to NM_015900.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:14766511 G>C maps to NM_003561.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6203-01A-11D-1753-08 chr16:14766484 C>T maps to NM_003561.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:74714287 A>G maps to NM_032562.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:68289810 G>A maps to NM_012320.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:63342428 T>C maps to NM_001128203.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:20302259 C>A maps to NM_001161728.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:20442054 G>A maps to ENST00000442610 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:20249183 G>T maps to NM_014589.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:20249234 G>T maps to NM_014589.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:20474887 T>A maps to NM_022819.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186862164 G>T maps to NM_024420.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:186934604 G>T maps to NM_024420.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:186934718 G>T maps to NM_024420.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:186915791 G>T maps to NM_024420.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:186957589 G>T maps to NM_024420.2 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:48558261 G>C maps to NM_003706.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:48609817 C>T maps to NM_001159322.1 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:48565365 G>A maps to NM_003706.2 H382H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:48578087 G>A maps to NM_003706.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr15:42276026 A>G maps to NM_001080490.1 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:42434277 G>A maps to ENST00000397272 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:42436756 C>G maps to ENST00000397272 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr15:42434259 C>T maps to ENST00000397272 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:20416368 G>A maps to NM_000929.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:20416374 C>A maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:20412691 C>A maps to NM_000929.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:20417115 C>T maps to NM_000929.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:38512181 C>T maps to NM_003560.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:38522388 G>A maps to NM_003560.2 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:38524305 G>A maps to NM_003560.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:46672317 T>C maps to NM_001168357.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:160862201 C>A maps to NM_007366.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:160813100 C>T maps to NM_007366.4 W981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:160832629 G>A maps to NM_007366.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160807913 G>C maps to NM_007366.4 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6980-01A-11D-1945-08 chr2:160862238 C>T maps to NM_007366.4 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:160798459 C>T maps to NM_007366.4 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:160813072 G>A maps to NM_007366.4 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:160901444 A>G maps to NM_007366.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr9:26905784 T>C maps to NM_001031689.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:133700519 G>T did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:133700441 T>G did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr11:59812142 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:59811014 A>T maps to NM_173801.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:59814443 T>A maps to NM_173801.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:84015945 T>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:145465022 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:57078966 C>T maps to NM_002655.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:57079653 A>G maps to NM_002655.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr20:30785286 G>A maps to NM_002657.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30789750 C>T maps to NM_002657.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:30785259 C>A maps to NM_002657.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:30785202 C>T maps to NM_002657.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42044932 C>T maps to NM_000930.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:42048919 G>T maps to NM_000930.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:42036483 G>T maps to NM_000930.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:42046461 C>A maps to NM_000930.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:42036486 G>C maps to NM_000930.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:42033558 G>A maps to NM_000930.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:42046465 G>C maps to NM_000930.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:42040259 G>A maps to NM_000930.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr8:42036447 G>T maps to NM_000930.3 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:42037473 C>A maps to NM_000930.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:75673800 G>T maps to NM_002658.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr10:75673357 G>A maps to NM_002658.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44171829 C>A maps to NM_002659.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:28812873 G>C maps to NM_153021.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:28828815 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:28739720 G>A maps to NM_153021.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:28828766 A>G maps to NM_153021.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:28855887 C>T maps to NM_153021.4 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr2:28815537 G>C maps to NM_153021.4 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:28755040 C>T maps to NM_153021.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:28748150 G>A maps to NM_153021.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:28855875 C>T maps to NM_153021.4 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:28752592 A>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:28825741 C>T maps to NM_153021.4 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr2:28854919 C>T maps to NM_153021.4 F1305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:28761238 G>T maps to NM_153021.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:28739672 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr2:28853531 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr12:14706302 T>C maps to NM_024829.5 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:113822700 G>T maps to NM_173542.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:113822706 G>T maps to NM_173542.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113812723 C>T maps to NM_173542.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:113822052 G>A maps to NM_173542.3 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr12:113826319 G>T maps to NM_173542.3 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:113822724 G>T maps to NM_173542.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:8630053 A>T maps to NM_015192.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:8637932 T>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr20:8769322 G>T maps to NM_015192.2 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr20:8626753 G>A maps to NM_015192.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:8769148 G>A maps to NM_015192.2 K1055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:8770892 G>T maps to NM_015192.2 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:8862494 G>C maps to NM_015192.2 *1217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:8717676 T>A maps to NM_015192.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:8770174 G>T maps to NM_015192.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr20:8639340 C>T maps to NM_015192.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:8628600 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr20:8707990 G>T maps to NM_015192.2 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr20:8709753 C>A maps to NM_015192.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:8782713 C>G maps to NM_182734.1 S1145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr20:8782773 C>T maps to NM_182734.1 P1165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr20:8737709 A>G maps to NM_015192.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:8696982 G>T maps to NM_015192.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:8639184 T>C maps to NM_015192.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr20:8705370 C>A maps to NM_015192.2 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr15:40581050 C>T maps to NM_004573.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:40590489 C>A maps to NM_004573.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:40590835 C>A maps to NM_004573.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr15:40590522 G>A maps to NM_004573.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr15:40587215 G>T maps to NM_004573.2 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:64029060 A>T maps to NM_000932.2 K613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:64023284 G>A maps to NM_000932.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:64031508 G>T maps to NM_000932.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:64032517 C>T maps to NM_000932.2 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:64026362 G>A maps to NM_000932.2 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9352969 A>T maps to NM_001172646.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:9368108 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:9404402 G>T maps to NM_001172646.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:9416205 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:9438111 G>C maps to NM_001172646.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr20:9288538 C>G maps to NM_001172646.1 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr20:9459602 C>A maps to NM_001172646.1 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:9402084 G>T maps to NM_001172646.1 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:9368187 A>C maps to NM_001172646.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr20:9319650 C>A maps to NM_001172646.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:9457386 G>T maps to NM_000933.3 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr20:9440443 C>T maps to NM_001172646.1 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr20:9400462 C>G maps to NM_001172646.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr20:9371237 G>A maps to NM_001172646.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:9440373 C>T maps to NM_001172646.1 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:9417689 C>T maps to NM_001172646.1 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:9402014 C>A maps to NM_001172646.1 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr20:9346110 G>A maps to NM_001172646.1 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:9360750 C>T maps to NM_001172646.1 A265A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-2657-01A-01D-1105-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:43192578 C>T maps to NM_133373.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:43194109 G>A maps to NM_133373.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr17:43194010 C>T maps to NM_133373.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:219492944 A>T maps to ENST00000432688 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219495488 G>A maps to ENST00000432688 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:219500598 C>A maps to ENST00000432688 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:95791384 C>T maps to ENST00000371380 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:95791987 G>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:96005701 G>T did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr10:95931188 C>A maps to ENST00000371380 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:95931001 A>T maps to ENST00000371380 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:95791157 C>T maps to ENST00000371380 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:96058403 G>T maps to ENST00000371380 V1812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:96064272 G>A maps to ENST00000371380 E1831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr10:95849042 G>A maps to NM_001165979.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:95994066 G>T maps to ENST00000371380 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr10:95931198 C>T maps to ENST00000371380 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:96068456 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:96028741 G>T maps to ENST00000371380 G1446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:96030304 G>A maps to ENST00000371380 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:39793982 C>G maps to NM_002660.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:39795148 T>C maps to NM_002660.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr16:81934351 G>T maps to NM_002661.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:81953094 G>A maps to NM_002661.2 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr16:81965178 G>T maps to NM_002661.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr16:81902817 G>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr16:81892726 G>A maps to NM_002661.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:81925084 G>A maps to NM_002661.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:81965210 T>C maps to NM_002661.2 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:81942092 G>T maps to NM_002661.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr16:81944139 C>G maps to NM_002661.2 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:155241684 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:155212151 G>A maps to ENST00000340059 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:155203285 G>A maps to ENST00000340059 Q953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:2419130 C>T maps to NM_014638.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr1:2435766 C>T maps to NM_014638.2 S1122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:2428048 G>T maps to NM_014638.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:2436042 C>A maps to NM_014638.2 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:2428139 G>T maps to NM_014638.2 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:2418356 G>T maps to NM_014638.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:2429995 C>A maps to NM_014638.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:198950910 G>T maps to NM_006226.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198949518 T>G maps to NM_006226.3 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:198950364 C>T maps to NM_006226.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:198950307 G>T maps to NM_006226.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:198950308 G>T maps to NM_006226.3 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:198950286 G>T maps to NM_006226.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:199011650 G>T maps to NM_006226.3 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:198966031 C>A maps to NM_006226.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:198950286 G>T maps to NM_006226.3 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:198950856 T>C maps to NM_006226.3 Y872Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:198950262 G>A maps to NM_006226.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:198948519 C>A maps to NM_006226.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:17051998 A>G maps to NM_001144382.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:17056291 G>T maps to NM_001144382.1 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:17053069 A>T maps to NM_001144382.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:215874 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:208263 C>T did not map to a codon.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr23:215941 C>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:215959 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:111394115 G>A maps to ENST00000312791 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:111426974 G>T maps to ENST00000312791 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:41382017 G>T maps to NM_001005473.2 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:41510524 C>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr5:41382253 C>A maps to NM_001005473.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:41313772 G>T maps to NM_001005473.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:41382475 T>C maps to NM_001005473.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr5:41382112 C>G maps to NM_001005473.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr12:18848011 C>A maps to ENST00000266505 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr12:18858219 T>C maps to ENST00000266505 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr12:18858158 C>A maps to ENST00000266505 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:171330157 C>G maps to NM_002662.3 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:171377052 C>A maps to NM_002662.3 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:171451266 T>C maps to NM_002662.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:171394594 C>A maps to NM_002662.3 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:171395479 G>A maps to NM_002662.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:171395354 C>T did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr3:171410233 T>G did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr19:40884019 T>G maps to NM_012268.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:40877596 G>A maps to NM_012268.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:105398444 C>A maps to NM_138790.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:105395256 G>A maps to NM_138790.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:105396325 C>A maps to NM_138790.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:242511433 T>A maps to NM_152666.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:242287870 T>G maps to NM_152666.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:242264083 T>A maps to NM_152666.2 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:242428690 T>A maps to NM_152666.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:242383373 G>C maps to NM_152666.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:242271041 G>A maps to NM_152666.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr17:17106251 C>A maps to NM_178836.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr8:145008877 C>T maps to NM_201380.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr8:144991967 G>A maps to NM_201380.2 A4144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:144995162 C>A maps to NM_201380.2 L3079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:145010068 G>A maps to NM_201380.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr8:144994079 C>A maps to NM_201380.2 L3440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:144992756 C>A maps to NM_201380.2 V3881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr8:145003897 C>A maps to NM_201380.2 G1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr8:144993917 G>A maps to NM_201380.2 L3494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:145049531 C>A maps to NM_000445.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:145008176 G>A maps to NM_201380.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:144998618 C>A maps to NM_201380.2 R1963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:145006188 C>A maps to NM_201380.2 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr8:145011191 G>A maps to NM_201380.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:144998612 C>A maps to NM_201380.2 R1965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:144994217 G>A maps to NM_201380.2 I3394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144991016 G>A maps to NM_201380.2 P4461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:144992483 G>A maps to NM_201380.2 D3972D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr8:144992836 C>A maps to NM_201380.2 E3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:144998492 C>A maps to NM_201380.2 R2005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:145003676 G>A maps to NM_201380.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr8:144993152 C>A maps to NM_201380.2 R3749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr8:144990734 G>A maps to NM_201380.2 D4555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:144997238 C>T maps to NM_201380.2 A2423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:67859504 C>T maps to NM_016445.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:179350366 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:49351252 C>A maps to NM_020904.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:49362832 C>T maps to NM_020904.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:49362230 G>A maps to NM_020904.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:49357335 C>G maps to NM_020904.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:19501349 C>G maps to ENST00000429027 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr12:19506878 G>T maps to ENST00000429027 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:19418717 G>C maps to ENST00000429027 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:204228701 C>A maps to ENST00000367191 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:204234147 C>A maps to ENST00000367191 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:204214838 G>T maps to ENST00000367191 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:204242840 T>A maps to ENST00000367191 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:204197887 C>T maps to ENST00000367191 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:204214785 C>T maps to ENST00000367191 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:204228630 G>A maps to ENST00000367191 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:16838532 C>A maps to ENST00000448080 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:16863109 G>A maps to ENST00000448080 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:16847833 C>T maps to ENST00000448080 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:16877391 C>A maps to ENST00000448080 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr11:16823300 G>A maps to ENST00000448080 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:30092444 C>T maps to ENST00000440706 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:30088837 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:45567058 C>A maps to ENST00000256692 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:45567500 T>C maps to ENST00000256692 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:45568136 T>C maps to ENST00000256692 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:131883345 A>T maps to ENST00000409158 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:131904220 C>T maps to ENST00000409158 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:131904285 G>T maps to ENST00000409158 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr2:131890479 T>C maps to ENST00000409158 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr19:30164790 C>T maps to ENST00000436066 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr19:30164946 C>A maps to ENST00000436066 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:151055095 G>T maps to NM_001029884.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:151130290 C>T maps to NM_001029884.1 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr6:151161686 A>G maps to NM_001029884.1 K1271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:39909403 C>A maps to NM_022835.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:39914268 C>T maps to NM_022835.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39914253 C>T maps to NM_022835.2 Q854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:39907023 C>T maps to NM_022835.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:39911745 A>T maps to NM_022835.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:39911930 G>T maps to NM_022835.2 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:65209850 G>T maps to ENST00000394691 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr14:65208997 C>A maps to ENST00000394691 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr14:65208724 G>A maps to ENST00000394691 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr14:65199519 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:67319225 G>T maps to NM_001129729.1 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:67314354 G>A maps to NM_001129729.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:67321888 C>T maps to NM_001129729.1 R1064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:67322283 G>T maps to NM_001129729.1 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:67318225 G>T maps to NM_001129729.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:67316231 G>T maps to NM_001129729.1 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:67318775 C>G maps to NM_001129729.1 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:143240 G>T maps to NM_052909.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:162014 G>T maps to NM_052909.3 G513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:169707 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:169676 C>G maps to NM_052909.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:163255 G>T maps to NM_052909.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:143351 C>G maps to NM_052909.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr5:169685 G>T maps to NM_052909.3 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:155006 C>G maps to NM_052909.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:163504 C>T maps to NM_052909.3 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:6528570 G>A maps to NM_198681.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:6528640 G>C maps to NM_198681.2 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:6534645 C>A maps to NM_198681.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:6527623 C>G maps to NM_198681.2 *1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:6435619 G>A maps to NM_001144856.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:93163940 C>T maps to NM_001004330.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr14:68042640 G>A maps to NM_020715.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr14:68029322 C>T maps to NM_020715.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr14:68046577 G>A maps to NM_020715.2 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr14:68050717 G>T maps to NM_020715.2 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:43969889 G>T maps to NM_172069.3 G1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:43984325 G>A maps to NM_172069.3 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:43919660 T>A maps to NM_172069.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:43934571 G>T maps to NM_172069.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:43958689 G>C maps to NM_172069.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:43986101 T>A maps to NM_172069.3 C1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:40825721 C>T maps to NM_024927.4 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:40820146 A>T maps to NM_024927.4 *794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr17:43522870 C>A maps to NM_014798.2 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:43545798 G>A maps to NM_014798.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:43516970 G>C maps to NM_014798.2 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:208795743 G>A maps to NM_001080475.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:208866198 T>A maps to NM_001080475.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:208725973 T>A maps to NM_001080475.2 K655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:208795815 C>A maps to NM_001080475.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:208865985 C>T maps to NM_001080475.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:909736 T>A maps to ENST00000379409 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:150131624 G>C maps to ENST00000443480 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:150131408 G>A maps to ENST00000443480 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:150131393 G>A maps to ENST00000443480 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr15:65157576 G>A maps to NM_025201.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr15:65157234 C>T maps to NM_025201.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:161135877 C>A maps to NM_000301.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:161160113 C>G maps to NM_000301.3 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr6:161127551 G>T maps to NM_000301.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:161127548 G>T maps to NM_000301.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr6:161139344 T>A maps to NM_000301.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:161173270 C>T maps to NM_000301.3 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:19119763 C>A maps to NM_001122.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:4847845 G>A maps to NM_005817.4 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr19:4852118 C>T maps to NM_005817.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:4861346 T>A maps to NM_005817.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:4513512 G>T maps to NM_001080400.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:4513701 C>A maps to NM_001080400.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:4512993 A>G maps to NM_001080400.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:4517572 C>T maps to NM_001080400.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:4511322 G>T maps to NM_001080400.1 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:4511535 C>A maps to NM_001080400.1 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:4529858 G>A maps to NM_001013706.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:4529232 G>A maps to NM_001013706.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr16:23691506 C>T maps to NM_005030.3 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr16:23691418 G>T maps to NM_005030.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:23693478 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr20:21142699 C>T maps to NM_018474.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr20:21195336 A>G maps to NM_018474.4 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:57755549 C>T maps to NM_006622.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr5:57750849 T>C did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr5:57751604 G>A maps to NM_006622.2 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr1:45270160 C>A maps to NM_004073.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:45268773 C>G maps to NM_004073.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr4:128815035 T>A maps to NM_014264.4 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:128804506 T>C maps to NM_014264.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:128812263 A>T maps to NM_014264.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:128819694 G>T maps to NM_014264.4 *971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:128807297 C>A maps to NM_014264.4 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:57318395 G>C maps to NM_015993.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12008051 G>C maps to ENST00000376369 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:12012719 C>T maps to ENST00000376369 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:12009870 G>T maps to ENST00000376369 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:145796986 G>C maps to NM_182943.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:145795654 G>A maps to NM_182943.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr3:145788610 G>A maps to NM_182943.2 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:145828165 C>A maps to NM_182943.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:100853845 C>A maps to NM_001084.4 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100855547 G>A maps to NM_001084.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:100850972 C>A maps to NM_001084.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:100859821 C>G maps to NM_001084.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:100849606 C>T maps to NM_001084.4 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr7:100856411 C>A maps to NM_001084.4 V251V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MN-A4N4-01A-12D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:100860065 C>T maps to NM_001084.4 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:103041585 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:103041620 A>G did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:103041592 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:103040646 T>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:103041544 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:103041616 T>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:103042761 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:103045516 C>T did not map to a codon.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr23:49029494 T>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:49030724 A>G did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:49029518 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:49030729 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:155458506 C>T maps to NM_002669.2 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:114856610 G>C did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:114879349 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:114863588 T>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:114874742 T>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:114882229 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:145918865 T>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:145918825 C>A maps to NM_020353.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:145914457 T>C maps to NM_020353.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:145924491 C>A maps to NM_020353.2 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr3:146311745 C>T maps to NM_001085420.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:146318152 T>A maps to NM_001085420.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:44540079 G>A maps to NM_006227.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr20:44536379 G>C maps to NM_006227.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:31825641 T>A maps to NM_130852.2 L42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:31825663 A>G maps to NM_130852.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr20:31829250 C>G maps to NM_130852.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:17476411 G>T maps to NM_031310.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:17487842 G>A maps to NM_031310.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:17476328 C>A maps to NM_031310.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:17476917 C>T maps to NM_031310.1 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:17487895 C>A maps to NM_031310.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr19:17476310 C>T maps to NM_031310.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:17476208 C>A maps to NM_031310.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:37234202 G>C maps to NM_020405.4 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:37265551 C>G maps to NM_020405.4 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:20465997 G>T maps to NM_032812.7 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:20335826 T>A maps to NM_032812.7 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:20466254 A>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:20465965 G>T maps to NM_032812.7 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:20506452 T>C maps to NM_032812.7 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:126708357 G>T maps to NM_032242.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr3:126747836 G>A maps to NM_032242.3 E1557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr3:126741073 G>T maps to NM_032242.3 T1395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr3:126751304 G>T maps to NM_032242.3 T1769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:208270153 C>A maps to NM_025179.3 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:208390135 C>A maps to NM_025179.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:208212979 C>A maps to NM_025179.3 E1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:208315744 C>A maps to NM_025179.3 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:208390424 C>A maps to NM_025179.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr1:208252775 T>A maps to NM_025179.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:208216423 G>A maps to NM_025179.3 P1333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:208206756 C>A maps to NM_025179.3 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:208218556 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:208201401 C>G maps to NM_025179.3 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:153688867 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:153694058 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:153688885 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:153697725 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:153688604 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:153694525 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:153689938 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:153696765 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:153694837 C>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr23:153698804 G>C did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:153693805 G>T did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:153696201 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:153697068 G>A did not map to a codon.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr23:153698357 C>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:153699891 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153692503 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153694566 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153695404 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153697501 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:153692504 C>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:153689813 G>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:153695418 G>C did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:153699968 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:153698331 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:153688973 A>G did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:153694732 C>G did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr23:153694502 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:153695658 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:153690499 G>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:131888168 C>A maps to NM_020911.1 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:131866286 G>T maps to NM_020911.1 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:131913152 C>A maps to NM_020911.1 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:131864551 C>A maps to NM_020911.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:131865425 C>A maps to NM_020911.1 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:132174173 G>T maps to NM_020911.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:131848972 G>T maps to NM_020911.1 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:131866250 G>A maps to NM_020911.1 S1127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:131872243 G>T maps to NM_020911.1 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:131825443 C>A maps to NM_020911.1 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:132169703 C>A maps to NM_181775.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:131982936 C>T maps to NM_020911.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:131925859 G>T maps to NM_020911.1 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr7:131866220 G>T maps to NM_020911.1 T1137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr7:131849959 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:131913209 C>A maps to NM_020911.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr7:131887527 G>A maps to NM_020911.1 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:131825416 C>T maps to NM_020911.1 S1793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:131888124 C>A maps to NM_020911.1 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:131831289 C>A maps to NM_020911.1 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr7:132192498 C>A maps to NM_020911.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:131878898 A>G maps to NM_020911.1 H926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:132192495 C>A maps to NM_020911.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr7:132193284 C>A maps to NM_020911.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:131844346 G>T maps to NM_020911.1 V1515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:132193098 G>A maps to NM_020911.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr7:132169766 G>A maps to NM_181775.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:131829930 A>T maps to NM_020911.1 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:131831331 C>T maps to NM_020911.1 K1664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:131925832 C>T maps to NM_020911.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr7:132069982 A>T maps to NM_001105543.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:132193404 G>T maps to NM_020911.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr7:131864524 G>A maps to NM_020911.1 R1265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:132193254 C>A maps to NM_020911.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr7:131817924 G>A maps to NM_020911.1 I1824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:132192822 C>A maps to NM_020911.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:131910975 G>A maps to NM_020911.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:131888127 G>T maps to NM_020911.1 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:132169772 C>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:48459665 C>A maps to NM_001130082.1 V1052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:48454013 C>A maps to NM_001130082.1 E1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:48462136 G>C maps to NM_001130082.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:48465930 G>A maps to NM_001130082.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:48465345 C>A maps to NM_001130082.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr3:48454579 T>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:50719225 G>A maps to NM_012401.2 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr22:50724600 C>T did not map to a codon.
Sequencing variant TCGA-55-6980-01A-11D-1945-08 chr22:50721831 C>T maps to NM_012401.2 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:50728107 C>A maps to NM_012401.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr22:50716157 G>A maps to NM_012401.2 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:50724455 G>T maps to NM_012401.2 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr22:50716682 C>A maps to NM_012401.2 E1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr22:50718192 C>A maps to NM_012401.2 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr22:50722092 C>T maps to NM_012401.2 Q836Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr22:50728233 C>T maps to NM_012401.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr22:50720742 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr22:50728916 C>A maps to NM_012401.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr22:50719901 C>A maps to NM_012401.2 V1183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr22:50728155 C>T maps to NM_012401.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:153039512 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:153039542 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:153039403 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:153041514 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:153035263 G>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:153036422 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:153033129 G>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:153040721 G>C did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153033744 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:153036514 C>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:153042822 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153032459 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:153039399 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:153036334 C>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:153036814 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153035336 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153041831 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:153043454 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:153035270 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:153039882 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:153033038 G>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:94620959 A>T maps to NM_005761.1 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:94634437 C>A maps to NM_005761.1 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:94580195 G>T maps to NM_005761.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:94618091 G>C did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:94631522 C>T maps to NM_005761.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:94542932 C>T maps to NM_005761.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr12:94694763 C>T maps to NM_005761.1 D1439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:129285419 G>A maps to NM_015103.2 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:129279566 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:129275993 T>A maps to NM_015103.2 K1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:129291745 G>C maps to NM_015103.2 S959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:129284182 C>A maps to NM_015103.2 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:129284752 C>T maps to NM_015103.2 Q1433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:129275271 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:205809436 G>A maps to NM_152491.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:156203519 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:72158692 T>C maps to NM_031293.2 K854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:72156887 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:72184551 G>A maps to NM_031293.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr16:72166805 C>A maps to NM_031293.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr16:72164249 C>T maps to NM_031293.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:72198791 C>A maps to NM_031293.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr16:72163075 T>A maps to NM_031293.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:72166650 C>A maps to NM_031293.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:74315474 G>T maps to NM_033238.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr15:74315630 G>T maps to NM_033238.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr15:74325577 G>T maps to NM_033238.2 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr15:74326882 A>G maps to NM_033240.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:41974849 C>T maps to NM_002676.2 L170L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8089-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr22:41980547 G>A maps to NM_002676.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr16:8898642 T>C maps to NM_000303.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr8:82357105 G>A maps to NM_002677.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:82359622 G>A did not map to a codon.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr17:15142887 G>A maps to NM_000304.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr9:139306550 A>T maps to NM_015160.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr7:102939049 A>C maps to NM_004279.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:102939142 C>G maps to NM_004279.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:102939073 G>T maps to NM_004279.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:190660674 G>T maps to NM_000534.4 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:190719713 G>A maps to NM_000534.4 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:6027150 C>A maps to NM_000535.5 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:6029587 T>C did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr7:6026997 G>A maps to NM_000535.5 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr7:6026805 C>T maps to NM_000535.5 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:6026957 C>A maps to NM_000535.5 G480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:6018320 C>T maps to NM_000535.5 Q727Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:154901622 C>A maps to NM_006556.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:152937076 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:152937445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr23:152936414 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:152938116 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:152938063 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:152937656 T>C did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:152937027 C>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:152938117 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:152937357 C>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr2:219137400 C>T maps to NM_001077399.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:50364719 G>C maps to NM_007254.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:50370364 G>A maps to NM_007254.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr6:160241521 G>A maps to NM_173516.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr6:160229829 G>T maps to NM_173516.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:160234688 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:160237617 C>T maps to NM_173516.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:118313237 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:118314688 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:118314955 G>T maps to NM_000936.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr10:118314996 G>C maps to NM_000936.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:118314904 G>T maps to NM_000936.2 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:118307991 A>T maps to NM_000936.2 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:118360713 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr10:118355763 T>A maps to NM_006229.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:118350658 A>T maps to NM_006229.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr10:118354339 G>T maps to NM_006229.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:118368609 C>T maps to NM_006229.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr10:118360597 G>A maps to NM_006229.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr10:118357601 C>G maps to NM_006229.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:118364983 G>A maps to NM_006229.2 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:118354375 G>A maps to NM_006229.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:118354354 C>A maps to NM_006229.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118386412 G>C maps to NM_005396.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr10:118404543 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:118389573 G>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:118386479 G>T maps to NM_005396.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:118385454 A>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr10:118228809 G>T maps to NM_001011709.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:118236244 C>T maps to NM_001011709.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:118231352 C>A maps to NM_001011709.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr10:118231352 C>A maps to NM_001011709.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr10:118203904 G>A maps to NM_001011709.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:118202625 C>A maps to NM_001011709.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:118196235 C>T maps to NM_001011709.2 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:118220523 C>A maps to NM_001011709.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:118203901 A>G maps to NM_001011709.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:118215293 C>T maps to NM_001011709.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:118220583 C>A maps to NM_001011709.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr10:118228713 T>C maps to NM_001011709.2 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr10:118236600 G>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr10:118236284 T>C maps to NM_001011709.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:118215250 C>A maps to NM_001011709.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:152226179 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:152226784 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:152225753 G>C did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:152225561 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:152226623 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:152226523 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:152226293 G>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:152225684 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:152226043 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:152159023 A>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:152160069 C>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:152159337 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:152159338 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:152159230 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:152159694 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:152159339 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:152159631 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:152159317 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:152158989 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:152159628 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr19:46973122 C>T maps to NM_018215.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:46974055 C>G maps to NM_018215.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr19:46973056 C>T maps to NM_018215.3 E412E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-8091-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:37824838 C>A maps to NM_002686.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr14:39650413 C>T maps to NM_002687.3 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr14:39645281 G>A maps to NM_002687.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:68388899 T>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:20940628 A>T maps to NM_000270.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:36275459 G>T maps to ENST00000457797 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:36260887 G>A maps to ENST00000457797 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr6:36269662 C>T maps to ENST00000457797 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr22:44332967 C>T maps to NM_025225.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr22:44322983 C>T maps to NM_025225.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:44333102 G>T maps to NM_025225.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:7894004 C>A did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:7870100 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:7889854 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:7870029 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:7870119 G>A did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:7870078 T>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:7889849 C>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr22:44285220 G>T maps to ENST00000216177 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:7620625 C>T maps to NM_001166111.1 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:7622060 G>T maps to NM_001166111.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:7618869 G>C maps to NM_001166111.1 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:140400119 C>A maps to NM_001098537.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr9:140400125 C>T maps to NM_001098537.1 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:140356629 C>A did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr9:140414420 G>A maps to NM_001098537.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:140395240 C>A maps to NM_001098537.1 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:140392678 C>A maps to NM_001098537.1 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:140414420 G>T maps to NM_001098537.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:140442060 C>A maps to NM_001098537.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:108113020 C>A maps to NM_015723.2 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr7:108119757 T>C maps to NM_015723.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr7:108119700 C>G maps to NM_015723.2 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:108155041 T>A maps to NM_015723.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:46023994 G>T maps to NM_018129.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:55894184 C>A maps to NM_033109.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:55874525 C>A maps to NM_033109.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:55908016 C>A maps to NM_033109.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:55873548 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:89790744 G>A maps to NM_006813.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:52183872 G>A maps to NM_015426.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:52172223 C>G maps to NM_015426.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:89860636 G>C maps to NM_172240.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr12:89918895 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:89853464 G>A maps to NM_172240.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:74981227 G>C maps to NM_001099271.1 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:74981258 C>A maps to NM_001099271.1 G394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:74988262 T>A maps to NM_001099271.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:53544150 C>T maps to NM_153703.4 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:53544621 G>C maps to NM_153703.4 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:53544069 C>T maps to NM_153703.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:53544240 G>T maps to NM_153703.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:53535628 C>A maps to NM_153703.4 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:53544495 G>T maps to NM_153703.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:53543412 C>A maps to NM_153703.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:14043739 G>A maps to NM_024825.3 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:84563164 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:84563197 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:84586016 C>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:84560879 T>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:84600894 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:84559396 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:84585974 A>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:84586048 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:84558431 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:84562266 T>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:84559420 G>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:84560849 C>G did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:84600908 C>G did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:84562231 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:84569448 A>T did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr23:84634282 C>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:84562227 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:84560870 C>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:84634368 G>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:84560805 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:84600994 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:84569446 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:84585957 C>A did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:84634366 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:84559353 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:84601000 G>T did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr20:30804816 G>A maps to NM_172236.1 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:30804816 G>A maps to NM_172236.1 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:30804434 C>T maps to NM_015352.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr21:46703296 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:151400442 C>A maps to NM_015100.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:151377694 G>C maps to NM_015100.3 V1272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:151380973 T>A maps to NM_015100.3 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:24844571 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:24844713 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:24859837 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:24722558 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:24830822 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:24751886 A>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:24732762 T>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:24757590 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:24742502 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:24745974 G>T did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:24761347 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:24948613 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:24750509 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:24759581 A>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:24761395 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:24767090 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:24735404 A>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:24753518 G>T did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr23:24741378 G>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:24766436 C>G did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:24830860 G>T did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:24746019 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:65048470 C>T maps to NM_002689.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr11:65055232 A>T maps to NM_002689.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:50905994 A>T maps to ENST00000391817 K323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:44156577 G>A maps to NM_006230.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:44156478 G>C maps to NM_006230.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:44154404 T>A maps to NM_006230.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:44157302 T>A maps to NM_006230.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:67120163 G>A maps to NM_021173.3 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr22:42988084 A>C maps to ENST00000415122 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr22:42988051 T>A maps to ENST00000415122 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr22:42991590 C>T maps to ENST00000415122 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:133250241 C>T maps to ENST00000455752 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:133225972 C>A maps to ENST00000455752 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:133234015 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:133225999 C>T maps to ENST00000455752 E1302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:133214628 G>A maps to ENST00000455752 A1886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:133209343 C>A maps to ENST00000455752 G2017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr12:133248869 C>T maps to ENST00000455752 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr12:133249224 G>A maps to ENST00000455752 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:133218934 G>A maps to ENST00000455752 F1670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:75186536 C>T maps to NM_019896.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:89868838 C>A maps to NM_002693.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:89870506 C>A maps to NM_002693.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:89867403 C>G maps to NM_002693.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:89873443 C>A maps to NM_002693.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr15:89870429 G>A maps to NM_002693.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62481961 C>A maps to NM_007215.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:62493020 C>T maps to NM_007215.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr17:62492600 C>T maps to NM_007215.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:62492600 C>T maps to NM_007215.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:62492936 G>A maps to NM_007215.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr18:51820114 G>T maps to NM_007195.2 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr18:51818290 C>A maps to NM_007195.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr10:103345713 C>T maps to NM_013274.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:103339272 A>G maps to NM_013274.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr10:103342588 G>T maps to NM_013274.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:2230952 T>C maps to NM_181808.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr4:2172479 G>A maps to NM_181808.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:2130951 C>A maps to NM_181808.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:2083369 G>A maps to NM_181808.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:121212467 C>A maps to ENST00000393672 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:121207930 C>A maps to ENST00000393672 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:121209248 C>A maps to ENST00000393672 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:121230732 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:121230865 G>A maps to ENST00000393672 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr3:121258346 G>A maps to ENST00000393672 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:121251866 C>G maps to ENST00000393672 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:121206887 T>A maps to ENST00000393672 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:121151257 G>A maps to ENST00000393672 Q2693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:121264694 C>T maps to ENST00000393672 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:121158874 T>A maps to ENST00000393672 P2587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:121229084 T>A maps to ENST00000393672 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr3:121207964 T>A maps to ENST00000393672 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:86266539 G>C maps to NM_015425.3 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:86271324 C>T maps to NM_015425.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:86272748 G>A maps to NM_015425.3 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:86327195 A>G maps to NM_015425.3 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr2:86310234 C>A maps to NM_015425.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:86258473 G>A maps to NM_015425.3 T1519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:113309470 T>C maps to NM_019014.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:113309350 G>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:113300232 C>T maps to NM_019014.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:43488712 C>T maps to NM_203290.1 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:7405882 G>A maps to NM_000937.4 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:7402374 T>C maps to NM_000937.4 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7405852 G>T maps to NM_000937.4 R863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:7411604 G>T maps to NM_000937.4 A1092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr17:7417450 C>A maps to NM_000937.4 L1956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr17:7404338 C>T maps to NM_000937.4 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr4:57889907 T>C maps to NM_000938.1 Y949Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:57857036 G>A maps to NM_000938.1 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:57504901 G>T maps to NM_032940.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:57505024 A>T maps to NM_032940.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr16:57503177 C>T maps to NM_032940.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:57503204 G>A maps to NM_032940.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:128610523 T>A maps to NM_004805.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:1095299 C>T maps to NM_002695.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:62529352 G>A maps to NM_002696.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr3:184081292 C>T maps to NM_006232.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:184081330 G>A maps to NM_006232.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:79782082 A>T maps to NM_007055.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr10:79745854 G>A maps to NM_007055.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:79785863 G>A maps to NM_007055.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:79784816 C>A maps to NM_007055.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr10:79767531 G>A maps to NM_007055.3 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:79737342 C>A maps to NM_007055.3 G1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:106895115 A>G maps to NM_018082.5 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr12:106853101 A>T maps to NM_018082.5 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr12:106857253 A>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:145594088 G>T maps to NM_006468.6 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr1:145608467 G>A maps to NM_006468.6 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:145601801 G>A maps to NM_006468.6 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:22106629 A>T maps to NM_001722.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr16:22330234 G>T maps to NM_018119.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:22325044 G>T maps to NM_018119.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:22326466 G>T maps to NM_018119.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:22328516 G>A maps to NM_018119.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:22330211 C>T maps to NM_018119.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr5:89781467 T>C maps to NM_006467.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:145459706 T>C maps to NM_032305.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr22:41936718 G>A maps to NM_138338.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr22:41926705 A>C maps to NM_138338.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:619716 G>A maps to NM_005035.3 Q979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:619606 C>T maps to NM_005035.3 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:624805 C>G maps to NM_005035.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr19:622753 T>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:72413642 G>A maps to ENST00000434423 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr7:72413366 C>A maps to ENST00000434423 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:75052310 G>A maps to ENST00000257665 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr7:75070314 C>A maps to ENST00000257665 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:75070271 C>A maps to ENST00000257665 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:53103525 C>G maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:53103753 A>T maps to NM_182595.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:53104227 C>T maps to NM_182595.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:53104134 C>A maps to NM_182595.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:53103576 G>T maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:53104215 C>A maps to NM_182595.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:53103525 C>A maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr7:53103432 G>T maps to NM_182595.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:53103858 C>T maps to NM_182595.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:53104089 C>A maps to NM_182595.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:53103417 G>T maps to NM_182595.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:53103645 C>T maps to NM_182595.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:53103525 C>A maps to NM_182595.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr7:53104089 C>A maps to NM_182595.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:53103484 C>T maps to NM_182595.3 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:53103579 G>T maps to NM_182595.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr7:53103858 C>A maps to NM_182595.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:53103546 C>T maps to NM_182595.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:53103576 G>T maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr7:53103447 C>A maps to NM_182595.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr7:53104098 C>T maps to NM_182595.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:53103732 G>T maps to NM_182595.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:53103573 C>G maps to NM_182595.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr7:53103861 C>A maps to NM_182595.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:53103528 G>T maps to NM_182595.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:53103615 G>A maps to NM_182595.3 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:53103417 G>T maps to NM_182595.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr2:25384267 G>A maps to NM_001035256.1 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:25384027 G>T maps to NM_001035256.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:25387560 C>T maps to NM_001035256.1 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:25383954 C>A maps to NM_001035256.1 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:46658030 C>T maps to ENST00000371986 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:46662401 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:46655022 C>A maps to ENST00000371986 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:134394318 C>T maps to NM_007171.3 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr9:134379691 C>T maps to NM_007171.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr9:134385139 C>T maps to NM_007171.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:134394270 C>A maps to NM_007171.3 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr14:77765850 G>A maps to NM_013382.5 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr14:77767498 G>T maps to NM_013382.5 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:76247598 G>A maps to NM_012230.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr7:76254921 C>T maps to NM_012230.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr7:94928338 G>A maps to NM_000446.5 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:94996708 T>A maps to NM_000940.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr8:99169979 C>T maps to NM_015029.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:99135610 C>T maps to NM_015029.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr8:99168472 A>G maps to NM_015029.2 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:99148735 G>A maps to NM_015029.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr8:99142320 G>A maps to NM_015029.2 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:99158832 G>T maps to NM_015029.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:99168551 C>T maps to NM_015029.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:99148942 T>C maps to NM_015029.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:119367416 G>A maps to NM_022135.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:119373368 C>A maps to NM_022135.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr6:105607675 A>G maps to NM_022361.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr6:105609349 G>T maps to NM_022361.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr6:105609468 G>A maps to NM_022361.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:48374533 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:48372654 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:48372655 T>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:48369725 G>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:48372649 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:48368222 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:48374125 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:48372701 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:38172803 G>A maps to NM_006475.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr13:38153364 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr13:38143959 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:38162063 A>G maps to NM_006475.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr13:38154714 T>C maps to NM_006475.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:38153996 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr13:38166302 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr13:38156501 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:124532323 T>A maps to NM_015450.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:124464129 T>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:124475444 T>A maps to NM_015450.2 K465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:124503511 C>A maps to NM_015450.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr7:124464072 T>A maps to NM_015450.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:43197381 C>A maps to NM_001005365.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:43159859 T>C maps to NM_001005365.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:43197328 G>C did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr8:43171052 A>T maps to NM_001005365.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:43152602 G>A did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr8:43197328 G>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:43172495 G>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr18:14542896 A>G maps to ENST00000444806 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:14542947 G>A maps to ENST00000444806 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:14542965 C>T maps to ENST00000444806 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr18:14542791 G>T maps to ENST00000444806 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:14537832 G>C maps to ENST00000444806 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr18:14542914 C>A maps to ENST00000444806 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:14542998 G>A maps to ENST00000444806 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr18:14542926 C>T maps to ENST00000444806 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:131984434 A>T maps to NM_001083538.1 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:131976448 C>A maps to NM_001083538.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:132021820 C>A maps to NM_001083538.1 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:131976379 C>T maps to NM_001083538.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:131976394 G>A maps to NM_001083538.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:132021445 C>T maps to NM_001083538.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:131976232 C>T maps to NM_001083538.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:132010573 C>T maps to NM_001083538.1 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:132021676 G>T maps to NM_001083538.1 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:132021677 G>T maps to NM_001083538.1 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:132021505 C>A maps to NM_001083538.1 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:132021874 C>A maps to NM_001083538.1 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:131976073 C>G maps to NM_001083538.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:132021520 C>G maps to NM_001083538.1 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:131976004 T>G maps to NM_001083538.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr2:132021445 C>A maps to NM_001083538.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:132021601 G>T maps to NM_001083538.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:130832239 G>T maps to NM_001099771.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:130832620 G>T maps to NM_001099771.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:130832524 C>T maps to NM_001099771.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:130832308 G>T maps to NM_001099771.2 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:130832809 C>A maps to NM_001099771.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:130877929 A>T maps to NM_001099771.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:130877668 C>T maps to NM_001099771.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:130832746 G>T maps to NM_001099771.2 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:130877629 G>T maps to NM_001099771.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:130877800 G>A maps to NM_001099771.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr2:130877989 G>A maps to NM_001099771.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:130877830 G>A maps to NM_001099771.2 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:130831863 C>A maps to NM_001099771.2 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:130877617 G>C maps to NM_001099771.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr2:130831863 C>A maps to NM_001099771.2 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:130832404 C>A maps to NM_001099771.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:130831816 C>A maps to NM_001099771.2 *1076Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:19566062 T>C maps to NM_001005356.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:19573143 G>A maps to NM_001005356.2 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr14:19566041 A>G maps to NM_001005356.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:19553586 C>A maps to NM_001005356.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:19553824 C>T maps to NM_001005356.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:19563485 C>T maps to NM_001005356.2 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:19558992 C>A maps to NM_001005356.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr14:19563542 T>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr14:19553787 C>T maps to NM_001005356.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr14:19553754 C>T maps to NM_001005356.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:16287714 G>T maps to NM_001136213.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:16287852 G>T maps to NM_001136213.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:16267026 G>C maps to NM_001136213.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr22:16279253 T>C maps to NM_001136213.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr22:16279208 C>G maps to NM_001136213.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:16287777 C>T maps to NM_001136213.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:16267070 C>A maps to NM_001136213.1 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr22:16287564 G>C maps to NM_001136213.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr22:16287603 G>T maps to NM_001136213.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr22:16267077 C>T maps to NM_001136213.1 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:16287666 C>T maps to NM_001136213.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr22:16287747 A>T maps to NM_001136213.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr22:16287774 C>A maps to NM_001136213.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:20020049 G>T maps to ENST00000439503 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:20019992 G>C maps to ENST00000439503 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:87313651 G>T maps to NM_001122757.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:111229632 C>G maps to NM_006235.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:111229610 G>T maps to NM_006235.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:111225222 C>T maps to NM_006235.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:111225078 G>A maps to NM_006235.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:167370761 C>T maps to NM_002697.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:167358826 A>T maps to NM_002697.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr19:42599695 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:42600286 C>A maps to ENST00000342301 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:42621518 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:42626699 G>A maps to ENST00000342301 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr11:120175881 G>A maps to NM_014352.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:38511275 C>T maps to NM_002699.3 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:105472186 C>G maps to NM_006236.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:105473056 C>T maps to NM_006236.1 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:105473123 G>T maps to NM_006236.1 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:82764134 G>C did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:82764009 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:82763694 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:82763624 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:82763625 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:82763896 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:82763574 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:82763988 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:82763471 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:82763607 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:82764299 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:82763550 C>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:82763777 G>C did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:82763713 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:82763389 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:82763369 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:82763627 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:82763434 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:82764249 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:82764250 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:82763661 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:82763566 C>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:82763848 G>A did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:82763369 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:82764095 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr23:82763435 A>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:79177359 C>A maps to NM_006237.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr13:79177362 C>A maps to NM_006237.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:147561326 G>A maps to NM_004575.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:147560363 C>A maps to NM_004575.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:147561659 T>C maps to NM_004575.2 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:147560396 C>A maps to NM_004575.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:147561257 T>C maps to NM_004575.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:147561805 C>A maps to NM_004575.2 S359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:147560580 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr4:147560543 G>A maps to NM_004575.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:145719676 C>T maps to NM_002700.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:145720005 G>A maps to NM_002700.2 *339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:145719334 C>T maps to NM_002700.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:145719247 G>A maps to NM_002700.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr5:93076687 C>T maps to NM_153216.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:51584374 C>A maps to NM_002702.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:51584290 C>T maps to NM_002702.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:51585529 G>A maps to NM_002702.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51589812 G>A maps to NM_002702.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:39500315 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:39503861 G>A maps to NM_007252.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr7:39379532 G>A maps to NM_007252.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:39472854 G>T maps to NM_007252.3 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:39500185 G>C maps to NM_007252.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr7:39472855 C>T maps to NM_007252.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:39247214 A>G maps to NM_007252.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:39246998 G>A maps to NM_007252.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:39247169 A>T maps to NM_007252.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:54763764 G>T maps to NM_176895.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:288085 G>A maps to NM_177543.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:122334781 C>T maps to NM_001030059.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:122263422 T>A maps to NM_001030059.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:122348908 C>A maps to NM_001030059.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr10:122334667 G>A maps to NM_001030059.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:134165626 C>A maps to NM_032728.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr9:134165560 A>G maps to NM_032728.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr22:46611142 C>T maps to NM_001001928.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr22:46615709 G>A maps to NM_001001928.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr6:35392296 C>G maps to NM_006238.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:12458630 T>A maps to NM_015869.4 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr3:12475577 C>A maps to NM_015869.4 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:12458264 C>T maps to NM_015869.4 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:12458303 C>A maps to NM_015869.4 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:12458241 G>T maps to NM_015869.4 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:23803431 C>T maps to NM_013261.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:23815428 A>G maps to NM_013261.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:23886434 G>A maps to NM_013261.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:23815781 T>A maps to NM_013261.3 K442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:23815725 G>A maps to NM_013261.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr4:23815374 C>T maps to NM_013261.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:23830146 G>C maps to NM_013261.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23816058 C>A maps to NM_013261.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:23833287 G>A maps to NM_013261.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:23803856 G>T maps to NM_013261.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr4:23833203 G>A maps to NM_013261.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:23826099 G>A maps to NM_013261.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:23830042 G>T maps to NM_013261.3 S246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:149210433 G>T maps to NM_133263.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr5:149221869 C>T maps to NM_133263.3 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:149212400 G>T maps to NM_133263.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr5:149212295 C>T maps to NM_133263.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr5:149216201 T>C maps to NM_133263.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:57301532 G>C maps to NM_002703.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:74852990 A>T maps to NM_002704.3 *129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr4:74852991 A>G maps to NM_002704.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr4:74853241 G>T maps to NM_002704.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr4:74853310 G>A maps to NM_002704.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:42923008 G>A maps to NM_024664.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:18802078 A>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:18842156 T>C did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:18822085 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:18836202 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:18822023 G>T did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:18775845 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:18845480 A>T did not map to a codon.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr23:18802164 A>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr4:76793209 G>A maps to NM_006239.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:76797516 C>A maps to NM_006239.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:76782041 G>C maps to NM_006239.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:76781939 G>A maps to NM_006239.2 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:76794372 C>A maps to NM_006239.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:76809403 C>A maps to NM_006239.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:76797786 C>A maps to NM_006239.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:70118298 G>T maps to NM_003626.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:70194392 C>G maps to NM_003626.2 S677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:70171604 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:70176313 C>T maps to NM_003626.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:70201822 A>G maps to NM_003626.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:81851618 T>C maps to NM_003625.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:81751859 C>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:82147850 C>A maps to NM_003625.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:81741467 G>T maps to NM_003625.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr12:81688715 T>C maps to NM_003625.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:81719563 T>C maps to NM_003625.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:81688774 G>T maps to NM_003625.2 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:81839475 G>A maps to NM_003625.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:203029442 G>T maps to ENST00000367238 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:203024682 C>A maps to ENST00000367238 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:203024568 G>A maps to ENST00000367238 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:203036892 C>A maps to ENST00000367238 R1020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:203032954 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:27786364 G>T maps to NM_003622.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:27787876 T>C maps to NM_003622.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr12:27832956 C>T maps to NM_003622.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:27820246 C>T maps to NM_003622.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr12:27845588 G>T maps to NM_003622.3 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:27841316 G>T maps to NM_003622.3 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr12:27832554 C>T maps to NM_003622.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:7654165 G>C did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:42781255 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:42787469 G>A maps to NM_016488.6 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:44838862 C>T maps to NM_021130.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr15:64455119 G>C maps to NM_000942.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:64452332 C>A maps to NM_000942.4 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:159631958 G>A maps to NM_005038.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:159644356 T>A maps to NM_005038.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:81112121 C>T maps to NM_005729.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:170487311 A>G maps to NM_004792.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:170493264 A>G maps to NM_004792.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:43131648 A>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr22:22041184 C>T maps to NM_148175.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr22:22036745 C>T maps to NM_148175.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr2:201741736 A>C maps to ENST00000422134 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:149847909 C>A maps to NM_139126.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:149847908 C>A maps to NM_139126.2 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:43827591 G>A maps to NM_001130858.2 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:43851101 G>A maps to NM_001130858.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:102494992 T>A maps to ENST00000451606 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr5:102465307 C>T maps to ENST00000451606 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr5:102537298 G>A maps to ENST00000451606 T1267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr5:102508921 A>C maps to ENST00000451606 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr5:102522021 G>A maps to ENST00000451606 G1072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:102494219 C>G maps to ENST00000451606 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:102490376 T>C maps to ENST00000451606 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:102522036 C>G maps to ENST00000451606 G1077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4934044 C>T maps to NM_002705.4 V1537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr16:4941885 C>A maps to NM_002705.4 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr16:4934620 C>T maps to NM_002705.4 R1345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr16:4935801 G>A maps to NM_002705.4 Q952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:4934323 C>T maps to NM_002705.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:4934910 G>A maps to NM_002705.4 Q1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:4949121 C>G did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:4935595 C>A maps to NM_002705.4 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr14:60758172 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:60712663 G>A maps to NM_177952.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr14:60749936 A>G maps to NM_177952.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:44428592 T>C maps to NM_002706.4 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:58678245 G>T maps to NM_003620.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:57043136 C>A maps to NM_014906.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:57046943 G>T maps to NM_014906.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:27607728 T>A maps to NM_177983.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:63083556 G>A maps to NM_020700.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr12:63042376 C>A maps to NM_020700.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:63225977 G>T maps to NM_020700.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr12:63225926 G>A maps to NM_020700.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:63042367 C>A maps to NM_020700.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:113253647 G>C maps to NM_005167.5 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr3:160786689 C>T maps to NM_139245.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:160474242 G>C maps to NM_139245.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr3:160786692 G>T maps to NM_139245.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:52283051 C>T maps to NM_144641.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:52282166 A>G did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr11:73914835 T>C maps to NM_016147.1 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:161138873 G>A maps to NM_001122764.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr1:161140728 G>A maps to NM_001122764.1 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:30570322 T>A maps to NM_002714.2 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:80199487 C>T maps to NM_001143885.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202391819 A>G maps to ENST00000367270 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:202391828 C>T maps to ENST00000367270 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:202406947 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:202464797 C>T maps to ENST00000367270 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:202538289 G>T maps to ENST00000367270 E943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:202462445 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:55614841 C>A maps to NM_017607.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:55603622 C>A maps to NM_017607.2 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:104220582 T>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr14:104206829 A>T maps to NM_015316.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr19:45899437 C>T maps to NM_001142502.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:45885836 C>T maps to NM_001142502.1 W799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:45885898 G>A maps to NM_001142502.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:45895536 T>A maps to NM_001142502.1 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:45899995 C>T maps to NM_001142502.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr6:150569943 G>A maps to NM_030949.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:49376607 G>T maps to NM_014330.3 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:49378082 G>T maps to NM_014330.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:49378903 C>T maps to NM_014330.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:204379824 G>A maps to NM_032833.3 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:145725976 C>A maps to NM_032902.5 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:145724388 C>T maps to NM_032902.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:37518308 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:37535620 G>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:37547005 G>A maps to NM_015568.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr20:37547131 G>T maps to NM_015568.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:37546927 C>T maps to NM_015568.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr20:37546819 C>G maps to NM_015568.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:54976576 G>A maps to NM_006741.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr17:37786259 G>A maps to ENST00000394271 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:113519997 G>C maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:113518145 C>A maps to NM_002711.3 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:113558625 G>T maps to NM_002711.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:113518830 C>A maps to NM_002711.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:113518935 T>A maps to NM_002711.3 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:113519424 G>T maps to NM_002711.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:113518029 G>T maps to NM_002711.3 Y1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:113518599 T>C maps to NM_002711.3 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:113519959 G>C maps to NM_002711.3 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:113558724 C>G maps to NM_002711.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:113519091 C>A maps to NM_002711.3 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr7:113518008 A>G maps to NM_002711.3 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:113520086 C>A maps to NM_002711.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr7:113518580 G>A maps to NM_002711.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:113519436 G>C maps to NM_002711.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:113558400 T>C maps to NM_002711.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:8998906 C>G maps to NM_024607.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:93390349 A>T maps to NM_005398.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:58514536 G>A maps to NM_006242.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:49143231 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:49142648 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:49142833 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:49143152 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:49127235 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:49142325 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:49142719 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:49127100 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:49138526 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:242122201 C>T maps to NM_002712.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:242097240 G>T maps to NM_002712.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:94540576 T>A maps to NM_001166160.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr17:48226725 C>T maps to NM_032595.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:133541765 A>G maps to NM_002715.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:52729032 C>T maps to NM_014225.5 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:52709291 C>T maps to NM_014225.5 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:111622951 C>A maps to NM_181699.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr8:26212049 G>T maps to NM_001177591.1 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:26217797 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr8:26212073 G>T maps to NM_001177591.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:146070759 C>T maps to ENST00000394414 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:146070804 T>A did not map to a codon.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr5:146030241 G>A maps to ENST00000394414 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr5:146070756 T>A maps to ENST00000394414 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:146030284 C>A maps to ENST00000394414 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr5:146077623 C>T maps to ENST00000394414 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:6349666 C>T maps to NM_181876.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:6377596 C>T maps to NM_181876.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:6335429 G>A maps to NM_181876.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr4:6380271 C>A maps to NM_181876.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr4:6331041 G>A maps to NM_181876.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr4:6325219 G>T maps to NM_181876.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr10:133758919 G>A maps to ENST00000455566 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:135806730 C>G maps to NM_002718.4 S932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:135806728 A>G maps to NM_002718.4 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:135806770 A>G maps to NM_002718.4 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:135721206 G>A maps to NM_002718.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr3:135721503 A>G maps to NM_002718.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr3:135721989 C>G maps to NM_002718.4 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:135722316 G>A maps to NM_002718.4 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:347160 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:299401 T>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:299547 C>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:299416 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:302132 T>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:35554834 T>G maps to NM_017917.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:64697826 G>A maps to NM_006244.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:42957396 A>T maps to NM_006245.2 K26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:63920451 G>A maps to ENST00000422769 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr14:64006337 G>A maps to ENST00000422769 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:101961723 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:101947146 C>A maps to NM_000944.4 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr10:75230715 T>A maps to NM_001142353.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:22333112 G>T maps to ENST00000397775 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:104357037 G>T maps to NM_147180.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:104357089 C>T maps to NM_147180.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr9:104356918 C>T maps to NM_147180.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:104356938 C>A maps to NM_147180.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr16:30094791 C>T maps to NM_002720.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr16:30087725 C>T maps to NM_002720.1 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr16:30094152 G>T maps to NM_002720.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr18:9550048 C>A did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr3:73047267 G>C maps to NM_174907.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr14:94708735 C>T maps to NM_058237.1 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94731754 G>T maps to NM_058237.1 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr14:94733328 C>G maps to NM_058237.1 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:94700009 C>T maps to NM_058237.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr19:46890675 G>A maps to NM_006247.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:46857125 G>C maps to NM_006247.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:244855204 G>T maps to NM_016076.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:103906432 C>T maps to NM_015062.3 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:103898425 G>T maps to NM_015062.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:103898374 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr10:103906706 C>T maps to NM_015062.3 R1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:40558075 C>T maps to ENST00000372783 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:40539813 T>A maps to ENST00000372783 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:32130369 G>T maps to NM_138717.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:32123711 T>C maps to NM_138717.1 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:32130714 T>G maps to NM_138717.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:32122517 G>T maps to NM_138717.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:110989773 C>A did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr12:110983716 G>A maps to NM_139283.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:64875259 G>A maps to NM_015342.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:64872725 G>A maps to NM_015342.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr10:47087598 G>A maps to NM_005972.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:47087796 G>T maps to NM_005972.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:47087823 G>A maps to NM_005972.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:48759732 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:48758545 A>C did not map to a codon.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr18:77679236 C>A maps to NM_025078.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:11304380 G>T maps to NM_152391.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:46799745 G>T maps to NM_032391.2 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:48930131 G>A did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr19:8564619 G>C maps to NM_032152.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:8564439 C>A maps to NM_032152.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:22890695 A>G maps to NM_206954.1 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:22890545 C>A maps to NM_206954.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:22892503 C>T maps to NM_206954.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:22899245 G>A maps to NM_206954.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr22:22891031 T>A maps to NM_206954.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr22:22890728 G>T maps to NM_206954.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:22892422 G>T maps to NM_206954.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:22892502 T>A maps to NM_206954.1 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr22:22890890 G>A maps to NM_206954.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr22:22892595 C>A maps to NM_206954.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr22:22890899 C>T maps to NM_206954.1 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr22:22892467 C>T maps to NM_206954.1 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr22:22893241 G>A maps to NM_206954.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:12854068 G>A maps to NM_023013.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:12854180 A>G maps to NM_023013.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr1:12856093 T>G maps to NM_023013.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:12854357 T>A maps to NM_023013.2 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:12854399 A>G maps to NM_023013.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr1:12856111 G>A maps to NM_023013.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:12855850 C>A maps to NM_023013.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr1:12854345 G>A maps to NM_023013.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:12856012 C>A maps to NM_023013.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12952860 C>A maps to NM_001039361.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:12954976 C>A maps to NM_001039361.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr1:12954996 T>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:12887379 C>T maps to NM_001146344.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:12887652 G>A maps to NM_001146344.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:12885039 G>A maps to NM_001146344.1 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:12887538 G>C maps to NM_001146344.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:12837327 T>G maps to NM_001080830.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr1:12835252 G>T maps to NM_001080830.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:12837210 G>T maps to NM_001080830.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:12837588 G>T maps to NM_001080830.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:12837585 T>A maps to NM_001080830.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr1:12835748 T>C maps to NM_001080830.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:12835252 G>T maps to NM_001080830.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:13448265 C>A maps to NM_001024661.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:13695943 G>A maps to NM_001099850.1 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:12919587 G>T maps to NM_023014.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:12919841 T>C maps to NM_023014.1 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:12921529 C>T maps to NM_023014.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:12919946 G>A maps to NM_023014.1 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:12921354 C>T maps to NM_023014.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:12942114 T>C maps to ENST00000376192 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:12941865 T>C maps to ENST00000376192 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:12979698 C>G maps to NM_001012277.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr10:135163596 A>C maps to ENST00000368554 R1R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:135165618 T>C maps to ENST00000423766 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:135165540 G>A maps to ENST00000423766 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr12:11508472 C>A maps to NM_005039.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:11420915 G>T maps to NM_006249.4 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:11420642 C>T maps to NM_006249.4 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr12:11463271 C>A maps to NM_002723.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91512757 C>G maps to NM_003981.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr15:91522524 C>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:91510375 G>C maps to NM_003981.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:91527364 G>T maps to NM_003981.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:156770210 A>T maps to NM_005973.4 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:82560237 A>C maps to NM_199418.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr6:106554874 C>T maps to NM_001198.3 C664C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr6:106554874 C>T maps to NM_001198.3 C664C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:106555150 G>A maps to NM_001198.3 E756E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:106554880 C>A maps to NM_001198.3 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr11:129814845 C>G maps to NM_020228.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr11:129801995 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:129812524 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:129795004 C>A maps to NM_020228.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr11:129817145 C>T maps to NM_020228.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45117409 C>A maps to NM_020229.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:45117394 C>A maps to NM_020229.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:45204634 C>T maps to NM_020229.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr11:45204511 G>A maps to NM_020229.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:133553974 G>T maps to NM_021619.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr9:133553950 C>A maps to NM_021619.2 Y202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:100061800 C>A maps to ENST00000359773 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:100056666 G>T maps to ENST00000359773 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr8:70978617 T>C maps to NM_024504.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr21:43222982 C>G maps to NM_022115.3 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:43223077 C>A maps to NM_022115.3 E1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr21:43248627 G>A maps to NM_022115.3 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:43259795 C>A maps to NM_022115.3 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:43221630 G>A maps to NM_022115.3 P1431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr21:43256742 C>T maps to NM_022115.3 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:3321338 C>T maps to NM_022114.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:3328392 C>T maps to NM_022114.3 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:3328443 C>T maps to NM_022114.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:3319454 G>T maps to NM_022114.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:3342754 G>T maps to NM_022114.3 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:3328987 C>T maps to NM_022114.3 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr1:14107310 C>T maps to NM_012231.4 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr1:14107967 C>T maps to NM_012231.4 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:121737721 G>A maps to NM_018699.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr4:121774686 C>T maps to NM_018699.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr4:121706212 C>A maps to NM_018699.2 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:121732565 T>A maps to NM_018699.2 K302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr16:90128520 C>T maps to NM_001098173.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr16:90141395 G>T maps to NM_001098173.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr16:90124747 A>T maps to NM_001098173.1 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:81124649 C>A maps to NM_001099403.1 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr4:81123236 C>T maps to NM_001099403.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr4:81123068 G>T maps to NM_001099403.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:23521226 G>A maps to NM_020227.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:23522994 G>T did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr5:23524601 C>A maps to NM_020227.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:23527707 T>A maps to NM_020227.2 C837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:23521199 G>A maps to NM_020227.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:23526759 T>A maps to NM_020227.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:23527713 G>T maps to NM_020227.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:23522765 C>G maps to NM_020227.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:23509207 C>A maps to NM_020227.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr5:23524577 C>A maps to NM_020227.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr5:23522506 T>C maps to NM_020227.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526568 G>T maps to NM_020227.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526585 G>A maps to NM_020227.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:23526600 G>A maps to NM_020227.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr5:23524523 C>T maps to NM_020227.2 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:23522756 C>T maps to NM_020227.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:23527017 C>T maps to NM_020227.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr5:23527794 G>A maps to NM_020227.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:23522774 C>A maps to NM_020227.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr5:23527642 A>T maps to NM_020227.2 K816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr5:23522422 G>A maps to NM_020227.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr5:23527498 A>C maps to NM_020227.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:23527464 C>A maps to NM_020227.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:23509631 A>T maps to NM_020227.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:23509632 G>T maps to NM_020227.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:23510027 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:23509159 C>T maps to NM_020227.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:23521205 A>C maps to NM_020227.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:23527618 G>T maps to NM_020227.2 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:23521213 C>A maps to NM_020227.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:23526942 C>T maps to NM_020227.2 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr5:23527509 A>T maps to NM_020227.2 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:23522514 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:23518017 G>T maps to NM_020227.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr5:23526426 T>C maps to NM_020227.2 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:23522435 A>T maps to NM_020227.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr5:23522915 G>C maps to NM_020227.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr5:23527394 C>A maps to NM_020227.2 S733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:23527005 A>C maps to NM_020227.2 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:23522893 G>A maps to NM_020227.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:23526978 C>A maps to NM_020227.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:23523397 A>T did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:45981408 G>A maps to NM_181697.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:12910717 G>A maps to NM_005809.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:23685883 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:23685896 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:23704415 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:23704430 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:23693131 A>C did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:27354693 G>A maps to NM_013388.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:27355222 C>G maps to NM_013388.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr5:145176110 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:203453034 C>A maps to NM_201348.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:203456002 C>A maps to NM_201348.1 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:203455882 C>T maps to NM_201348.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:203453286 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:203455888 C>A maps to NM_201348.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:44566423 C>A maps to NM_001171603.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:44553862 C>A maps to NM_001171603.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:47266654 G>A maps to NM_020820.3 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr20:47273726 C>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr20:47246138 G>A maps to NM_020820.3 A1538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:47342862 C>A maps to NM_020820.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:47269226 G>T maps to NM_020820.3 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr20:47256394 C>A maps to NM_020820.3 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr20:47296203 C>T maps to NM_020820.3 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr20:47266678 C>A maps to NM_020820.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr20:47276567 G>A maps to NM_020820.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:47248855 C>G maps to NM_020820.3 A1495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:47265956 C>A maps to NM_020820.3 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:47307503 G>T maps to NM_020820.3 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr8:69129862 C>T maps to NM_024870.2 S1539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:68993021 C>T maps to NM_024870.2 D609D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:69104733 C>T maps to NM_024870.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:68956758 C>A maps to NM_024870.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr8:68992816 A>G maps to NM_024870.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:68995473 G>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:68942817 C>T maps to NM_024870.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr8:68972958 T>G maps to NM_024870.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:69011922 G>T maps to NM_024870.2 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr8:68972946 G>A maps to NM_024870.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:68950479 G>A maps to NM_024870.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:69058477 G>T maps to NM_024870.2 R1374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:69020435 C>T maps to NM_024870.2 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr8:68992768 T>C maps to NM_024870.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:72358888 G>A maps to NM_005041.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:72360454 C>A maps to NM_005041.4 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:57156548 G>A maps to NM_002728.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:57146162 G>T maps to NM_006093.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:186266033 C>G maps to NM_005807.3 Y9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:186276758 C>A maps to NM_005807.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:186276707 C>A maps to NM_005807.3 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:186276446 C>A maps to NM_005807.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr1:186280655 G>T maps to NM_005807.3 G1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:186273947 A>G maps to NM_005807.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:186275957 C>G maps to NM_005807.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:186275894 G>A maps to NM_005807.3 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:186275544 A>T maps to NM_005807.3 K232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:186269343 G>T maps to NM_005807.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:62202176 G>T maps to NM_001037335.2 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:62198634 C>A maps to NM_001037335.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:62198670 C>A maps to NM_001037335.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:62192791 C>A maps to NM_001037335.2 R2288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr20:62198343 T>A maps to NM_001037335.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr20:62203651 C>A maps to NM_001037335.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr20:62198565 C>A maps to NM_001037335.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:42866306 C>T maps to NM_153026.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:64142981 G>T maps to NM_198859.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:64148736 C>A maps to NM_198859.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:64132743 C>A maps to NM_198859.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:49035626 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:49034419 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:49032613 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:49033385 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:49034396 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:49033263 C>G did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:49040252 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:49032081 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:49034492 G>T did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:49035673 G>A did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr12:57128023 T>A maps to NM_000946.2 K384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr12:57135351 G>A maps to NM_000946.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:57246879 G>T maps to NM_000947.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:57246827 G>T did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:57398164 C>T maps to NM_000947.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:57189078 G>A did not map to a codon.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr14:94187867 A>G maps to NM_178013.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:94203693 G>T maps to NM_178013.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr5:40771890 C>A maps to NM_206907.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:57140145 C>T maps to NM_006252.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:57171766 A>G maps to NM_006252.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr12:120106159 G>A maps to NM_006253.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:146639437 C>T maps to NM_005399.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:146634072 G>A maps to NM_005399.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:146639353 C>T maps to NM_005399.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:14208608 C>T maps to NM_002730.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr19:14208662 C>G maps to NM_002730.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:84610228 C>G maps to NM_182948.2 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:84662322 A>T maps to NM_182948.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:84668406 A>T maps to NM_182948.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:71628084 C>T maps to NM_002732.3 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:71628258 C>T maps to NM_002732.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:49396732 C>A maps to NM_002733.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:151573651 G>T maps to NM_016203.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:151372616 G>T maps to NM_016203.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:219695054 G>A maps to NM_017431.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:219691723 T>C maps to NM_017431.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:66518894 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr17:66518895 G>T did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr17:66521989 C>G maps to NM_212472.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:590207 C>A maps to NM_002735.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:106797628 A>T did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr7:106797680 G>A maps to NM_002736.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr17:64299088 C>A maps to NM_002737.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:64728939 A>G maps to NM_002737.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:64684431 T>C maps to NM_002737.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:64800139 A>G maps to NM_002737.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr17:64641606 T>C maps to NM_002737.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:24196863 G>A maps to NM_002738.6 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:24046866 C>A maps to NM_002738.6 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:24046815 C>T maps to NM_002738.6 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:23847513 G>T maps to NM_002738.6 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:23999853 G>T maps to NM_002738.6 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:23847558 C>A maps to NM_002738.6 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr16:24105516 G>C maps to NM_002738.6 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:24202490 G>T maps to NM_002738.6 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr16:23848701 C>T maps to NM_002738.6 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:53222798 G>A maps to NM_212539.1 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:53217200 G>T maps to NM_212539.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:53218941 C>T maps to NM_212539.1 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:46211688 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:46378244 G>A maps to NM_005400.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:46228648 A>C maps to NM_005400.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:54385768 C>G maps to NM_002739.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:54403972 C>T maps to NM_002739.3 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:54403551 G>C maps to NM_002739.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:54410139 C>T maps to NM_002739.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:54406349 G>A maps to NM_002739.3 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:54403521 G>T maps to NM_002739.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:54403578 G>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:54407996 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:54403678 C>A maps to NM_002739.3 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr19:54403951 C>T maps to NM_002739.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:61917612 C>T maps to NM_006255.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr14:62016506 G>A maps to NM_006255.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:62016467 A>T maps to NM_006255.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:169953138 G>T maps to NM_002740.5 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:170016829 G>T maps to NM_002740.5 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:169981183 G>T maps to NM_002740.5 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:6498719 C>A maps to NM_006257.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:6527123 C>T maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:6539206 C>T maps to NM_006257.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:11559929 C>T maps to ENST00000436195 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:11560100 A>G maps to ENST00000436195 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11552076 G>T maps to ENST00000436195 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:30095756 G>A maps to NM_002742.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr14:30100228 T>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr14:30194844 C>T maps to NM_002742.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr14:30100002 G>A maps to NM_002742.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:30103641 G>A maps to NM_002742.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:47181712 G>A maps to ENST00000449438 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:47207624 C>G maps to ENST00000449438 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:37487371 G>A maps to NM_005813.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr2:37505046 C>A maps to NM_005813.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr2:37487472 G>T maps to NM_005813.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:48777167 G>A maps to NM_006904.6 F1839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:48711843 C>G maps to NM_006904.6 G3407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:48866264 T>C maps to NM_006904.6 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:48772320 C>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr8:48689544 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:48767901 T>C maps to NM_006904.6 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:48798589 G>C maps to NM_006904.6 S1563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:48713446 G>A maps to NM_006904.6 L3340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48690419 C>A maps to NM_006904.6 E3956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:48762046 C>G maps to NM_006904.6 L2340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:48752728 T>C maps to NM_006904.6 V2433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:48771463 C>T maps to NM_006904.6 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:48845667 A>T maps to NM_006904.6 L563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:48826609 C>A maps to NM_006904.6 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:48746957 C>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:53822337 C>A maps to NM_001098512.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:54041978 G>T maps to NM_001098512.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr10:53227549 G>T maps to NM_001098512.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:53564426 C>A maps to NM_001098512.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr10:54048594 A>T maps to NM_001098512.1 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr10:52912932 T>C maps to NM_001098512.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:82125933 C>A maps to NM_006259.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:82031765 C>T did not map to a codon.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr4:82092952 G>A maps to NM_006259.1 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr4:82125781 A>T maps to NM_006259.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr4:82056431 G>T maps to NM_006259.1 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:179315751 G>T maps to NM_003690.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:179315098 C>T maps to NM_003690.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr7:102036966 C>A maps to NM_024653.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:102047916 G>A maps to NM_024653.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:76063341 A>G maps to NM_004705.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr23:3573372 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:3533908 G>C did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:3573367 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:3544473 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:3533930 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:22287777 C>G maps to ENST00000397199 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:238475748 G>A maps to NM_015893.1 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:238475664 C>T maps to NM_015893.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:120354231 G>T maps to NM_004248.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr10:120354354 G>T maps to NM_004248.2 C134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:120353853 C>A maps to NM_004248.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:120353646 G>T maps to NM_004248.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr10:120354366 G>A maps to NM_004248.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:120353835 G>T maps to NM_004248.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:120354546 C>A maps to NM_004248.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:35065406 C>A maps to NM_000949.4 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr5:35072751 C>A maps to NM_000949.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:35068323 C>T maps to NM_000949.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:35065589 C>G maps to NM_000949.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:11370154 C>A maps to ENST00000435245 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:50189880 G>T maps to NM_001536.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:148601523 C>A maps to NM_138364.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:148582161 G>T maps to NM_138364.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr21:48080770 C>G maps to NM_206962.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr21:48064291 G>T maps to NM_206962.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:20429515 G>T maps to NM_005788.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:20486091 G>T maps to NM_005788.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:20429455 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:20515789 A>G maps to NM_005788.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:23398555 C>A maps to NM_006109.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:23392301 G>T maps to NM_006109.3 Y481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr14:23394234 G>A maps to NM_006109.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:23395764 C>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:107600086 G>T maps to NM_018137.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:107599900 C>G maps to NM_018137.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:3677878 C>A maps to NM_019854.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr12:3662860 G>A maps to NM_019854.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:3686109 C>T maps to NM_019854.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:3702300 G>T maps to NM_019854.3 G380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:3702308 G>C maps to NM_019854.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:3692327 T>C maps to NM_019854.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:3677989 G>C maps to NM_019854.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:4705649 G>A maps to NM_012409.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:4705389 A>T maps to NM_012409.2 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:4705433 G>A maps to NM_012409.2 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr20:4705262 T>C maps to NM_012409.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:4705532 C>T maps to NM_012409.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:4705235 C>G maps to NM_012409.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:4705247 C>G maps to NM_012409.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:4680057 C>G maps to NM_001080123.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:128186269 C>T maps to ENST00000409048 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:128183673 T>A maps to ENST00000409048 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:128179007 C>T maps to ENST00000409048 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:128178937 C>T maps to ENST00000409048 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr2:128184757 C>A maps to ENST00000409048 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:33764040 C>T maps to NM_006404.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:18905887 C>T maps to NM_016335.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:36297720 G>T maps to NM_021232.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:36290956 G>T maps to NM_021232.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr19:36303779 C>A maps to NM_021232.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:36297411 A>T maps to NM_021232.1 Y383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:110996617 C>A maps to NM_032414.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:71830725 G>T maps to NM_001126128.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:68882116 C>T maps to NM_138964.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:68882356 C>G maps to NM_138964.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:68882464 G>T maps to NM_138964.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:68873387 T>C maps to NM_138964.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:68882017 G>T maps to NM_138964.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:5294853 G>A maps to NM_144773.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr20:5283096 C>A maps to NM_144773.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr20:5283318 G>A maps to NM_144773.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr20:5283144 G>A maps to NM_144773.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr20:5283044 G>T maps to NM_144773.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr20:5294817 G>T maps to NM_144773.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr20:5283179 T>A maps to NM_144773.2 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:5294628 G>T maps to NM_144773.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr20:5294751 G>A maps to NM_144773.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:5294625 G>A maps to NM_144773.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:71275485 C>G maps to NM_021225.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:16019963 G>A maps to NM_006017.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:16014961 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:15995666 G>T maps to NM_006017.2 Y570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr4:16025960 G>T maps to NM_006017.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:15987395 C>T maps to NM_006017.2 W756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:95941742 G>T maps to NM_144707.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:95941727 C>T maps to NM_144707.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:95952240 G>T maps to NM_144707.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:95952273 C>T maps to NM_144707.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:95940351 C>T maps to NM_144707.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:177421210 G>A maps to NM_006261.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:177419796 C>T maps to NM_006261.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:93605238 C>A maps to NM_000313.3 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:93605239 C>T maps to NM_000313.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:93593250 T>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:93624697 A>G maps to NM_000313.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:93643108 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:93617413 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr3:93615520 G>A maps to NM_000313.3 C288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:93595822 C>A maps to NM_000313.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:93646189 A>T maps to NM_000313.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:93624898 A>G maps to NM_000313.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:37620233 G>T maps to NM_007198.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:214171497 A>G maps to NM_002763.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:214170993 G>T maps to NM_002763.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:214171197 C>A maps to NM_002763.3 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:214169982 T>C maps to NM_002763.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:75330423 G>T maps to ENST00000445876 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr13:113826115 C>T maps to ENST00000342783 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:13647725 C>T maps to NM_003675.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr10:13656034 A>G maps to NM_003675.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:60658700 C>G maps to NM_014502.4 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr11:60666722 G>A maps to NM_014502.4 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:150315815 A>G maps to NM_004698.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr1:150312942 C>G maps to NM_004698.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:54634743 G>T maps to NM_015629.3 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:54629928 G>T maps to NM_015629.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr1:52878239 G>T maps to NM_032864.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:52874342 G>A maps to NM_032864.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:109241224 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:116044940 C>G maps to NM_004697.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr9:116053822 G>A maps to NM_004697.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:153512878 C>A maps to ENST00000410080 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:153535965 G>T maps to ENST00000410080 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:153519185 T>C maps to ENST00000410080 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:50027764 C>T maps to NM_001031698.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:62664297 C>T maps to NM_012469.3 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr20:62642702 G>C maps to NM_012469.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:1578502 C>A maps to NM_006445.3 V1001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:1557162 G>A maps to NM_006445.3 R2045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:1583006 T>A maps to NM_006445.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:1554420 C>A maps to NM_006445.3 S2278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:1577911 C>T maps to NM_006445.3 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:49690769 C>T maps to ENST00000451891 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:49691153 C>T maps to ENST00000451891 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:49689411 G>A maps to ENST00000451891 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr6:42689565 G>A maps to NM_000322.4 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:42690065 G>A maps to NM_000322.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:42672192 C>T maps to NM_000322.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:106890893 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:106884175 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:106882645 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:106884133 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:18067063 A>G maps to NM_175886.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:18066952 G>T maps to NM_175886.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:12817485 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:12828214 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:12817344 G>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:12838874 A>G did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:12817441 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:12817466 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:74328467 C>T maps to NM_002766.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:74328493 C>A maps to NM_002766.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:74324813 T>A maps to NM_002766.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:57247239 A>T maps to NM_018304.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:57275119 G>A maps to NM_018304.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:57272165 C>T maps to NM_018304.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:50102992 C>T maps to NM_020719.1 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:50099341 G>T maps to NM_020719.1 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:50099832 C>T maps to NM_020719.1 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:50098434 C>T maps to NM_020719.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:50098207 G>T maps to NM_020719.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:50099886 G>T maps to NM_020719.1 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:50099514 C>T maps to NM_020719.1 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:50100114 G>T maps to NM_020719.1 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:120021731 T>C maps to NM_016644.1 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:120022253 C>A maps to NM_016644.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:120022157 G>T maps to NM_016644.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr5:120021827 C>T maps to NM_016644.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:42814212 G>A maps to NM_199285.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:240982153 G>C maps to NM_001080835.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:5783135 G>A maps to NM_001134316.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:138724870 C>T maps to NM_001134659.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:138724773 C>A maps to NM_001134659.1 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:138724633 G>A maps to NM_001134659.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:138724539 G>T maps to NM_001134659.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:138738864 G>T maps to NM_001013650.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:138739044 C>T maps to NM_001013650.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:138739119 C>A maps to NM_001013650.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:138739308 C>A maps to NM_001013650.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:138738888 A>G maps to NM_001013650.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:138762811 C>A maps to NM_001134657.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:138762886 G>T maps to NM_001134657.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:138763050 C>A maps to NM_001134657.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr3:138763204 C>G maps to NM_001134657.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr6:30525207 G>A maps to NM_025263.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr12:10999790 T>C maps to NM_007244.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr22:45132763 G>A maps to NM_001198721.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr22:45122458 C>T maps to ENST00000352766 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:45121159 G>A maps to ENST00000352766 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36424880 G>C maps to NM_001160167.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr11:36484284 G>T maps to NM_001160167.1 *369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:36422704 G>T maps to NM_001160167.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:36483952 C>T maps to NM_001160167.1 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:126860328 A>G maps to ENST00000330542 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:37312648 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:37312669 T>C did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:37285102 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:37312722 C>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:150869181 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:150869016 G>C did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr23:150869296 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:150869327 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:150867285 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:150868584 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:150869058 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:32117103 G>T maps to NM_030651.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr16:29825754 C>A maps to NM_145239.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr3:9991565 G>A maps to NM_207351.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:170695467 G>T maps to NM_022716.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:170695455 C>T maps to NM_022716.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr1:170705308 G>A maps to NM_022716.2 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:170695527 A>G maps to NM_022716.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:170699422 C>A maps to NM_006902.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr1:170633562 G>C maps to NM_022716.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:170695476 C>A maps to NM_022716.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:132484546 C>T maps to NM_016307.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr9:132481636 C>T maps to NM_016307.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:132483044 C>A maps to NM_016307.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:142460822 C>T maps to ENST00000486171 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:142460762 A>C maps to ENST00000486171 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:142459837 G>A maps to ENST00000486171 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr7:142458514 C>T maps to ENST00000486171 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:142458433 G>A maps to ENST00000486171 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:142459765 C>A maps to ENST00000486171 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:142459840 C>A maps to ENST00000486171 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:142459633 G>A maps to ENST00000486171 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:142459756 C>T maps to ENST00000486171 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:142458451 C>T maps to ENST00000486171 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:142460861 C>G maps to ENST00000486171 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:119259401 A>T maps to NM_003619.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:119216984 T>A maps to NM_003619.3 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:119220094 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:119234374 C>T maps to NM_003619.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:119252905 G>T maps to NM_003619.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:27216633 G>A maps to NM_005865.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:27223043 C>T maps to NM_005865.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:27222622 T>C maps to NM_005865.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:2871422 A>G maps to NM_006799.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:2868929 C>T maps to NM_006799.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr16:2906185 C>A maps to NM_022119.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2766519 C>T maps to NM_031948.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:2764225 G>T maps to NM_031948.3 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr6:84233709 C>T maps to NM_153362.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr6:84233831 G>T maps to NM_153362.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:84233348 C>T maps to NM_153362.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:84234206 G>T maps to NM_153362.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr6:84233921 C>A maps to NM_153362.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:31157276 C>G did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:31157190 G>A maps to NM_173502.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr16:31159899 G>T maps to NM_173502.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:141537762 G>T maps to NM_001008270.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:141536909 A>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:141539163 C>A maps to NM_001008270.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:141537688 G>C maps to NM_001008270.2 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:141537798 C>T maps to NM_001008270.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr7:141537819 G>A maps to NM_001008270.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:141536287 G>A maps to NM_001008270.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:228033665 G>C maps to NM_183062.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:228003798 C>A maps to NM_183062.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:152212364 T>G maps to NM_183375.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:46757059 G>A maps to NM_013270.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:31095548 G>A maps to NM_001039503.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr16:58318598 G>T maps to NM_001080492.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr16:58314361 C>T maps to NM_001080492.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:58314358 G>T maps to NM_001080492.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:58314661 C>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:58314604 C>T maps to NM_001080492.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:10396301 G>C maps to NM_198464.3 *353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10387191 A>G maps to NM_198464.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:10383136 G>T maps to NM_198464.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:10388885 T>A maps to NM_198464.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr8:10388828 G>T maps to NM_198464.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr8:10383151 T>G maps to NM_198464.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10387129 G>T maps to NM_198464.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:10383103 G>C maps to NM_198464.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:55970088 G>T maps to NM_173814.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:55964742 A>T maps to NM_173814.4 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:150997257 A>T maps to NM_021222.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:151006439 C>T maps to NM_021222.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:151006392 A>T maps to NM_021222.1 K349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:79325635 T>G maps to NM_015225.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:79323714 C>A maps to NM_015225.2 E1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:79328502 T>C maps to NM_015225.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr9:79324792 G>C maps to NM_015225.2 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:79325371 C>T maps to NM_015225.2 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr9:79461572 T>C maps to NM_015225.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr9:79461593 A>G maps to NM_015225.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:79318980 T>C maps to NM_015225.2 E2516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr9:79322392 C>T maps to NM_015225.2 V1599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:79320640 G>T maps to NM_015225.2 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:79322623 A>T maps to NM_015225.2 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr9:79323991 G>A maps to NM_015225.2 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr9:79318530 G>T maps to NM_015225.2 L2666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:79323682 C>T maps to NM_015225.2 V1169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr9:79441544 T>G maps to NM_015225.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:79320502 T>C maps to NM_015225.2 E2229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:79320106 G>T maps to NM_015225.2 I2361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr9:79323520 G>T maps to NM_015225.2 V1223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr9:79441494 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:40900085 C>A maps to NM_181882.2 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40902380 G>T maps to NM_181882.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:40900894 G>A maps to NM_181882.2 Q1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:40902281 G>A maps to NM_181882.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:40903048 G>T maps to NM_181882.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:40901738 C>T maps to NM_181882.2 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr19:40901332 C>A maps to NM_181882.2 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr19:40904688 C>T maps to NM_181882.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr19:40904709 C>T maps to NM_181882.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:73579615 C>A maps to ENST00000373120 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:73591638 G>A maps to ENST00000373120 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:73579245 G>A maps to ENST00000373120 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr9:80943084 T>C maps to ENST00000421149 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:143763501 G>T maps to ENST00000301258 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:143763483 G>T maps to ENST00000301258 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:104171929 C>G maps to NM_002779.3 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr10:104173680 C>T maps to NM_002779.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr10:104176510 C>A maps to NM_002779.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:104163111 C>A maps to NM_002779.3 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr10:104164426 G>A maps to NM_002779.3 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:104165178 A>G maps to NM_002779.3 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr10:104174960 G>A maps to NM_002779.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:139216518 C>G maps to NM_032289.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:139216786 C>T maps to NM_032289.2 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:139216500 G>T maps to NM_032289.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:139221971 C>T maps to NM_032289.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:139218302 C>G maps to NM_032289.2 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:139193932 C>A maps to NM_032289.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:139193007 C>T maps to NM_032289.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:18393414 T>C maps to ENST00000440756 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr8:18490288 G>T maps to ENST00000440756 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:18729562 C>A maps to ENST00000440756 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:18658840 T>C maps to ENST00000440756 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:113955141 G>A maps to NM_012455.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:113950016 A>T maps to NM_012455.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113955198 C>T maps to NM_012455.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:113950026 G>T maps to NM_012455.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:113943727 A>G maps to NM_012455.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:73653562 C>T maps to NM_000021.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:73664736 A>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:227073238 C>T maps to ENST00000391872 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:227076673 G>T maps to ENST00000391872 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:43382203 T>A maps to NM_006905.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:43375969 G>T maps to NM_006905.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:43373184 C>T maps to NM_006905.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:43382251 T>C maps to NM_006905.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:43373166 G>C maps to NM_006905.2 Y243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:43519393 G>A maps to ENST00000306308 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:43519364 A>T maps to ENST00000306308 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:43514151 A>T maps to ENST00000306308 *342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:43519522 C>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr19:43519514 T>A maps to ENST00000306308 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:43529170 G>C maps to ENST00000306308 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:43523024 G>C maps to ENST00000306308 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:43528954 G>A maps to ENST00000306308 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr19:43523197 C>A maps to ENST00000449000 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:43528894 C>T maps to ENST00000306308 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:43576106 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43575864 T>C maps to NM_031246.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr19:43576026 C>A maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43575947 G>A maps to NM_031246.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:43579539 G>A maps to NM_031246.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr19:43575999 A>G maps to NM_031246.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr19:43579758 G>A maps to NM_031246.3 S152S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MN-A4N4-01A-12D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:43236999 A>T maps to NM_021016.3 Y215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:43236969 G>T maps to NM_021016.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr19:43233395 T>G maps to NM_021016.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:43698708 G>C maps to NM_002780.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:43702179 G>A maps to NM_002780.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:43708128 C>T maps to NM_002780.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:43680271 G>T maps to ENST00000270059 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr19:43689117 A>C maps to ENST00000270059 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:43680280 G>A maps to ENST00000270059 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:43680049 G>C maps to ENST00000270059 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:43679556 G>A maps to ENST00000270059 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:43679577 G>A maps to ENST00000270059 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:43679577 G>C maps to ENST00000270059 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:43679574 A>C maps to ENST00000270059 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:43679523 T>C maps to ENST00000270059 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:43420610 G>A maps to NM_002782.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:43414765 G>T maps to NM_002782.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:43414783 T>A maps to NM_002782.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:43411794 G>T maps to NM_002782.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr19:43411106 C>A maps to NM_002782.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:43430162 G>C maps to NM_002783.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:43439664 C>A maps to NM_002783.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:43430043 G>C maps to NM_002783.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:43429934 G>T maps to NM_002783.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:43433837 A>G maps to NM_002783.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:43439787 G>T maps to NM_002783.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:43439646 G>T maps to NM_002783.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:43258470 T>G maps to NM_182707.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:43268341 A>C maps to NM_182707.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43258603 G>C maps to NM_182707.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43268389 G>C maps to NM_182707.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr19:43262415 G>A maps to NM_182707.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:43262388 G>T maps to NM_182707.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr19:43258605 T>A maps to NM_182707.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:43268067 G>A maps to NM_182707.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:43262241 G>T maps to NM_182707.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr19:43259217 C>A maps to NM_182707.2 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:43259170 G>T maps to NM_182707.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:43763021 G>T maps to NM_002784.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:43762591 G>T maps to NM_002784.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:43763168 G>A maps to NM_002784.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:43762450 G>T maps to NM_002784.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:43762510 T>A maps to NM_002784.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:43773547 G>A maps to NM_002784.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:43772239 T>A maps to NM_002784.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:43763009 G>A maps to NM_002784.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:43773565 G>T maps to NM_002784.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr19:43762357 G>C maps to NM_002784.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:43763036 G>C maps to NM_002784.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:43763164 G>A maps to NM_002784.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:43772200 G>T maps to NM_002784.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:43773565 G>T maps to NM_002784.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:15469011 A>C maps to NM_001128217.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr9:15466853 G>C maps to NM_001128217.1 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr9:15486912 G>C maps to NM_001128217.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr9:15506584 G>A maps to NM_001128217.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr9:15486864 G>C maps to NM_001128217.1 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:67943485 G>T maps to NM_006742.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:67943053 G>T maps to NM_006742.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:67943518 C>T maps to NM_006742.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:67943519 C>T maps to NM_006742.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:67943582 A>C maps to NM_006742.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:67943599 C>T maps to NM_006742.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:87076622 G>T maps to ENST00000276616 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:87076325 G>A maps to ENST00000276616 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:87060978 G>A maps to ENST00000276616 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:87076730 G>T maps to ENST00000276616 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr8:87076573 G>T maps to ENST00000276616 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:87081722 C>A maps to ENST00000276616 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:87076712 G>T maps to ENST00000276616 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:60715997 A>T maps to NM_002792.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:23713961 C>A maps to NM_144662.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:23738083 A>T did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr18:23724602 G>A maps to NM_144662.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:170846375 G>A maps to NM_002793.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:23512072 C>A maps to NM_001099780.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:23512147 C>T maps to NM_001099780.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:23512118 C>A maps to NM_001099780.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr14:23511886 C>A maps to NM_001099780.1 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr14:23511730 C>A maps to NM_001099780.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr17:36916716 C>T maps to NM_002795.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr14:23503985 G>A maps to NM_002797.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:127167674 C>A maps to NM_002799.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:32827218 G>C maps to NM_002800.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr6:32825851 C>A maps to NM_002800.4 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:40478060 C>T maps to NM_006503.2 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:40478343 G>A maps to NM_006503.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40478081 G>T maps to NM_006503.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:40487097 G>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:61907257 C>A maps to NM_002805.5 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr17:61907816 A>T maps to NM_002805.5 K170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:53173933 C>T maps to NM_002806.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:53178229 G>T maps to NM_002806.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:53194257 G>T maps to NM_002806.3 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:53180597 G>T did not map to a codon.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:231926009 G>T maps to NM_002807.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:231941752 A>T maps to NM_002807.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:107330999 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:107330986 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:107328311 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:30807571 G>T maps to NM_002815.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr17:65343327 C>A maps to NM_002816.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:248957 G>C maps to NM_002817.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:162242024 A>C maps to NM_005805.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr3:184026273 G>A maps to NM_002808.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:184024550 C>T maps to NM_002808.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:38144946 C>T maps to NM_002809.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr17:38146345 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr17:38146392 G>A maps to NM_002809.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:151236485 G>T maps to ENST00000368881 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:151237982 C>T maps to ENST00000368881 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:151237895 C>T maps to ENST00000368881 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:151234660 G>C maps to ENST00000368881 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr9:123593719 T>C maps to NM_005047.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:24615757 C>A maps to ENST00000429021 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr14:24614334 C>A maps to ENST00000429021 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:24614454 C>A maps to ENST00000429021 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:54125015 T>A maps to NM_014614.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:54125135 C>A maps to NM_014614.2 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:54122796 A>T maps to NM_014614.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:54114546 T>A maps to NM_014614.2 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:54161846 C>T maps to NM_014614.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:54147454 C>A maps to NM_014614.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:54114394 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr21:40550483 G>A maps to NM_003720.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr18:12718550 C>G maps to NM_020232.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:1608936 C>A maps to NM_001134340.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:31107663 G>T maps to NM_014068.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:31105977 C>T maps to NM_014069.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:31106772 G>A maps to NM_014069.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr13:20279941 G>A maps to NM_001042414.1 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr13:20346443 T>C maps to NM_001042414.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:56079562 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:109824315 G>A maps to ENST00000409138 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:124740201 G>A maps to NM_153336.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:77317630 G>A maps to NM_003978.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr15:77325275 C>A maps to NM_003978.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr18:43577777 C>G maps to NM_024430.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:28477076 G>A maps to NM_001164721.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:72347216 C>G maps to NM_001099666.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:803636 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:804557 G>T maps to NM_002819.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:97243151 A>G maps to ENST00000370197 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:97236292 A>G maps to ENST00000370197 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr1:97278355 G>A maps to ENST00000370197 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:99031020 C>A maps to NM_001198879.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:99022693 G>A maps to NM_001198879.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:99017595 G>A maps to NM_001198879.1 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:99032514 C>G maps to NM_001198879.1 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:99022729 C>G maps to NM_001198879.1 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:99032693 C>A maps to NM_001198879.1 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr7:99022876 G>A maps to NM_001198879.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:71654148 C>T maps to NM_024754.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:86361964 C>T maps to NM_017952.5 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:86346106 C>T maps to NM_017952.5 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:98242851 C>A maps to NM_000264.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:98229461 G>T maps to NM_000264.3 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:98240357 C>A maps to NM_000264.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:98209231 C>A maps to NM_000264.3 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr9:98244474 A>G maps to NM_000264.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:98270445 G>T maps to NM_000264.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:23412153 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:23397856 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:23353296 A>T did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:23412132 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:23412215 A>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:23412272 C>A did not map to a codon.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr23:23412155 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:23397799 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:23411684 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:23353285 C>G did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:23411589 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:23412034 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:23411991 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:23398253 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:23397898 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:23412124 A>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:23412248 G>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:23353198 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:23411705 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:23411071 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr23:23397974 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr23:23411311 C>G did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11591677 G>T maps to NM_020780.1 E1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:11596646 T>G maps to NM_020780.1 G1361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:11594436 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:11577527 C>A maps to NM_020780.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr1:11596418 C>T maps to NM_020780.1 A1285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:11576055 A>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:11562026 G>T maps to NM_020780.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:11589657 C>T maps to NM_020780.1 R948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:11576118 A>T maps to NM_020780.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:11579513 C>A maps to NM_020780.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:11562936 G>T maps to NM_020780.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:11562885 G>A maps to NM_020780.1 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:11561120 G>T maps to NM_020780.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:11562002 C>T maps to NM_020780.1 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:27703131 G>T maps to NM_001034842.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:27703038 G>T maps to NM_001034842.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr10:27702212 G>T maps to NM_001034842.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:27702942 C>A maps to NM_001034842.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:27703026 C>T maps to NM_001034842.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr10:27702549 C>A maps to NM_001034842.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr10:27703116 C>A maps to NM_001034842.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:42883812 C>A maps to NM_138296.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:42893098 C>T maps to NM_138296.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:42883860 C>G maps to NM_138296.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:97312031 C>T maps to NM_014754.1 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr8:97321847 T>C maps to NM_014754.1 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr8:97311923 C>A maps to NM_014754.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr8:97296349 A>T maps to NM_014754.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr8:97345787 G>A maps to NM_014754.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:89685268 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:89653807 G>T maps to NM_000314.4 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr10:89717707 C>T maps to NM_000314.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:16528529 G>A maps to NM_030664.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:16528616 G>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:16526804 C>G maps to NM_030664.3 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr10:16547036 A>G maps to NM_030664.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:23482675 A>G maps to NM_178161.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr10:23482714 C>G maps to NM_178161.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr10:23482774 C>G maps to NM_178161.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:52735297 C>T maps to NM_000953.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:52735014 G>T maps to NM_000953.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:52734662 C>A maps to NM_000953.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:52734990 C>A maps to NM_000953.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr14:52734789 C>T maps to NM_000953.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:52735242 C>A maps to NM_000953.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr14:52781373 G>T maps to NM_000956.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr14:52781430 G>T maps to NM_000956.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:71418622 C>T maps to NM_198718.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:71512942 G>A maps to ENST00000354608 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:71512420 C>A maps to ENST00000354608 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:40681205 G>T maps to NM_000958.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:40681529 G>A maps to NM_000958.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:40681389 C>T maps to NM_000958.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:40692197 C>T maps to NM_000958.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:40681160 C>T maps to NM_000958.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:40681211 C>T maps to NM_000958.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:40692159 C>A maps to NM_000958.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:57066594 T>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr12:57058274 T>A maps to NM_006601.5 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:79002131 G>T maps to NM_000959.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:78959093 C>A maps to NM_000959.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:78959225 G>T maps to NM_000959.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:78959226 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:78959096 A>G maps to NM_000959.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:117504135 A>G maps to NM_020440.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr1:117491976 G>A maps to NM_020440.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:47127353 C>T maps to NM_000960.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr19:47124818 G>T maps to NM_000960.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:47124809 G>T maps to NM_000960.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr20:48124471 G>T maps to NM_000961.3 Y496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr20:48129703 T>A maps to NM_000961.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr14:74343731 C>A maps to NM_152444.2 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:125141115 G>T maps to NM_000962.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:125154486 A>G maps to NM_000962.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr9:125145834 G>T maps to NM_000962.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:125148819 C>T maps to NM_000962.2 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr9:125154702 G>T maps to NM_000962.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr9:125148923 C>T maps to NM_000962.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:125154702 G>T maps to NM_000962.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:125145815 C>A maps to NM_000962.2 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:125154552 G>A maps to NM_000962.2 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:125140710 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:186648544 A>G maps to NM_000963.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:46945139 C>A maps to NM_000316.2 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr3:46945069 C>G maps to NM_000316.2 S569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr3:46944039 G>T maps to NM_000316.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:46935438 C>T maps to NM_000316.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:49925834 G>A maps to NM_178449.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:209353826 C>T maps to NM_005048.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:209309586 G>A maps to NM_005048.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr2:209358032 C>T maps to NM_005048.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:209355383 C>T maps to NM_005048.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:209358128 G>T maps to NM_005048.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr2:209302579 C>T maps to NM_005048.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:209302550 G>A maps to NM_005048.2 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:209315507 G>C maps to NM_005048.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr12:28116577 G>T maps to ENST00000354417 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:141669762 C>T maps to NM_005607.4 Q1009Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:27287916 G>A maps to NM_004103.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr8:27277479 G>T maps to NM_004103.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:27294636 A>C did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:27288391 G>T did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr8:27311714 G>T maps to NM_004103.3 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr8:27289811 C>T maps to NM_004103.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr20:62164020 C>T maps to NM_005975.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43096871 C>T maps to NM_002821.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:43114420 C>G maps to NM_002821.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr6:43109430 G>A maps to NM_002821.3 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:43109958 G>T maps to NM_002821.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:232577178 G>T maps to ENST00000409321 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:136939604 C>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:136938253 G>T maps to NM_002825.5 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:50360332 C>T maps to NM_017432.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr19:50360329 C>G maps to NM_017432.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:64288801 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:142435182 T>C maps to NM_032611.1 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr9:96860222 C>T maps to ENST00000434261 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr9:96827071 G>A maps to NM_177995.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:96860848 A>T maps to ENST00000434261 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr9:96859841 G>T maps to ENST00000434261 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:65847231 A>T maps to NM_016395.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:21011690 G>T maps to NM_001010915.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:21026605 T>G maps to NM_001010915.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:112915755 G>A maps to ENST00000392596 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:112891115 T>C maps to ENST00000392596 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:112915663 G>T maps to ENST00000392596 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr12:112926930 G>T maps to ENST00000392596 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:77256163 A>T maps to NM_002835.3 K390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr7:77256456 C>G maps to NM_002835.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:77256327 A>G maps to NM_002835.3 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:87679885 C>T maps to NM_080685.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:87643511 G>T maps to NM_080685.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr4:87687591 C>T maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:87703390 C>T maps to NM_080685.2 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:87656019 C>T maps to NM_080685.2 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:87687591 C>G maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:87696608 G>T maps to NM_080685.2 G1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:87680173 A>G maps to NM_080685.2 A1167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:87655901 G>A maps to NM_080685.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:87691036 G>A maps to NM_080685.2 K1540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:87701590 T>G maps to NM_080685.2 S1981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:214568285 G>A maps to NM_005401.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:214557496 C>G maps to NM_005401.4 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:214557589 C>A maps to NM_005401.4 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:214557622 T>A maps to NM_005401.4 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:214575099 T>C maps to NM_005401.4 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:214625224 G>A maps to NM_005401.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:214557042 C>A maps to NM_005401.4 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:214560258 G>A maps to NM_005401.4 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:131127757 C>T maps to NM_014369.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:12817223 C>T maps to NM_002828.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr18:12836857 C>A maps to NM_002828.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr14:88945911 G>A maps to NM_007039.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr14:89016692 C>A maps to NM_007039.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:88945515 C>T maps to NM_007039.3 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:88945334 G>A maps to NM_007039.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:114380718 C>A maps to NM_015967.5 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:114402055 G>T maps to NM_015967.5 Y38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr3:47451186 C>T maps to NM_015466.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:47449256 C>T maps to NM_015466.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr3:47447461 C>A maps to NM_015466.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr9:112141904 G>C maps to NM_002829.3 Y891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:112151515 C>A maps to NM_002829.3 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr9:112168852 A>G maps to NM_002829.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:112199250 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:18754823 C>A maps to NM_032781.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:18765646 G>T maps to NM_032781.3 S66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr11:18754792 C>A maps to NM_032781.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:18763816 C>A maps to NM_032781.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:18765576 G>T maps to NM_032781.3 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:18763888 A>T maps to NM_032781.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:18755102 C>A maps to NM_032781.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:202128593 G>T maps to NM_080588.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr15:75798091 T>G maps to NM_002833.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:75815559 G>A maps to NM_002833.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:2968982 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:3018721 C>T maps to NM_002836.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:3016325 C>A maps to NM_002836.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr20:3005233 G>A maps to NM_002836.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:2998537 C>T maps to NM_002836.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr20:3016329 C>T maps to NM_002836.3 R674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr20:3003398 G>T maps to NM_002836.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:2955859 G>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70974891 G>A maps to NM_001109754.1 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:70983909 G>T maps to NM_001109754.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:71016247 G>A maps to NM_001109754.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr12:70963485 C>T maps to NM_001109754.1 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:70963526 C>A maps to NM_001109754.1 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:71029627 G>A maps to NM_001109754.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr12:70974894 G>T maps to NM_001109754.1 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr12:70970273 C>T maps to NM_001109754.1 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:70989841 G>A maps to NM_001109754.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:70949881 C>A maps to NM_001109754.1 T1587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:70949648 C>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr12:71029808 A>G maps to NM_001109754.1 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:70956858 G>A maps to NM_001109754.1 I1311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:71029520 G>T maps to NM_001109754.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr12:71002894 G>A maps to NM_001109754.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr12:70931985 G>T maps to NM_001109754.1 S1965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr12:70956765 C>A maps to NM_001109754.1 G1342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:70974879 G>T maps to NM_001109754.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:70964821 G>A maps to NM_001109754.1 F1118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:70928311 G>T maps to NM_001109754.1 Y2108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr12:70956687 G>T maps to NM_001109754.1 Y1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr12:70964878 G>T maps to NM_001109754.1 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:70965067 A>T maps to NM_001109754.1 I1036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:70965814 A>G maps to NM_001109754.1 Y965Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:70929816 A>C maps to NM_001109754.1 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:71029487 C>T maps to NM_001109754.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:71016261 C>A maps to NM_001109754.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:70965796 C>A maps to NM_001109754.1 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:70938334 A>T did not map to a codon.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr12:70953186 G>C maps to NM_001109754.1 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:70918372 T>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:71029449 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:70963563 G>A maps to NM_001109754.1 H1175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:70974915 G>C maps to NM_001109754.1 Y826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:70954615 C>A maps to NM_001109754.1 E1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:198675923 A>T maps to ENST00000271610 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:198668830 C>A maps to ENST00000271610 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:198665955 C>A maps to ENST00000271610 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:198691571 G>T maps to ENST00000271610 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:198703511 C>A maps to ENST00000271610 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:198675956 T>C maps to ENST00000271610 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:198721884 C>T maps to ENST00000271610 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:198687427 T>C maps to ENST00000271610 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:198703529 C>A maps to ENST00000271610 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:198721820 C>A maps to ENST00000271610 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:198719619 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:198691559 G>T maps to ENST00000271610 G559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:198668739 C>T maps to ENST00000271610 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:198697541 C>G maps to ENST00000271610 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:198711390 C>A maps to ENST00000271610 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:198721721 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:198718599 G>A maps to ENST00000271610 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:67203496 C>A maps to NM_005608.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:8376608 T>A maps to NM_002839.3 K1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:8524976 G>T maps to NM_002839.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:8518098 G>T maps to NM_002839.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr9:8504366 C>G maps to NM_002839.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:8499799 G>T maps to NM_002839.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:8485783 G>A maps to NM_002839.3 F1011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr9:8528596 G>T maps to NM_002839.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:8500763 G>T maps to NM_002839.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:8636818 G>C maps to NM_002839.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:8485849 T>C maps to NM_002839.3 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr9:8340468 T>C maps to NM_002839.3 R1709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:8465464 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:8518297 C>A maps to NM_002839.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:8528592 G>T maps to NM_002839.3 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr9:8518127 C>G maps to NM_002839.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr9:8484342 C>A maps to NM_002839.3 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr9:8340381 G>T maps to NM_002839.3 T1738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:8319890 T>A maps to NM_002839.3 V1870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr9:8500943 G>A maps to NM_002839.3 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:8340447 A>T maps to NM_002839.3 A1716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr9:8492980 T>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8499763 G>T maps to NM_002839.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:8518230 G>T maps to NM_002839.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:8319938 G>A maps to NM_002839.3 F1854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:8341974 C>A maps to NM_002839.3 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:8339046 C>A maps to NM_002839.3 E1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:8507348 G>A maps to NM_002839.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:8518091 G>A maps to NM_002839.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr9:8389317 C>A maps to NM_002839.3 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:8525009 T>C maps to NM_002839.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr9:8486233 G>C maps to NM_002839.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:8507429 T>C maps to NM_002839.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:8528596 G>T maps to NM_002839.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:8517920 G>A maps to NM_002839.3 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:8521337 G>T maps to NM_002839.3 Y300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:8471057 C>T maps to NM_002839.3 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:8492931 G>A maps to NM_002839.3 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:8521486 C>A maps to NM_002839.3 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:8526625 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr9:8518385 T>A maps to NM_002839.3 T335T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5930-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:44058192 C>T maps to NM_002840.3 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:44085867 G>A maps to NM_002840.3 L1738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr1:44070992 C>T maps to NM_002840.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:44010766 A>T maps to NM_002840.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr1:44086228 G>A maps to NM_002840.3 E1781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:44064416 G>T maps to NM_002840.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr1:44058141 C>T maps to NM_002840.3 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:61975454 G>A maps to NM_002841.3 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr3:62262671 A>C maps to NM_002841.3 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr3:62180800 G>C maps to NM_002841.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:61734633 C>T maps to NM_002841.3 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:62253427 G>A maps to NM_002841.3 W936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:55697268 C>G maps to NM_002842.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:55710185 G>T maps to NM_002842.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr19:55697830 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:55713546 G>T maps to NM_002842.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:55715188 C>A maps to NM_002842.3 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr19:55693404 C>A maps to NM_002842.3 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr19:55711856 C>A maps to NM_002842.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:55698959 C>G maps to NM_002842.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:48142703 C>T maps to NM_002843.3 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:48157810 C>T maps to NM_002843.3 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr6:128312531 G>A maps to ENST00000368210 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr6:128306975 C>A maps to ENST00000368210 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:128294834 C>A maps to ENST00000368210 G1387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr6:128403660 C>A maps to ENST00000368210 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr6:128297828 C>T maps to ENST00000368210 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr6:128643393 C>A maps to ENST00000368210 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:128297927 C>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:8376570 G>A maps to NM_001105244.1 R1146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr18:7888242 G>A maps to NM_001105244.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220162804 G>A maps to NM_002846.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:220164858 G>C maps to NM_002846.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr2:220167069 G>A maps to NM_002846.3 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220162047 G>T maps to NM_002846.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:220161969 C>A maps to NM_002846.3 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:157414081 G>T maps to NM_002847.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157414102 G>A maps to NM_002847.3 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157691363 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:157985048 G>C maps to NM_002847.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:157959950 G>T maps to NM_002847.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr7:157691364 C>A maps to NM_002847.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:157926394 C>G maps to NM_002847.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr7:157997860 A>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:157959944 C>A maps to NM_002847.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:157959833 C>T maps to NM_002847.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:157387989 C>T maps to NM_002847.3 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:157387959 C>T maps to NM_002847.3 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:157926751 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:157931117 C>A maps to NM_002847.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:157475566 C>A maps to NM_002847.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:157931163 C>A maps to NM_002847.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr7:157926402 C>A maps to NM_002847.3 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:157926439 G>C maps to NM_002847.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr7:157926481 C>A maps to NM_002847.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr7:157396738 C>T maps to NM_002847.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:15704554 G>T maps to NM_030667.1 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:15669859 A>T maps to NM_030667.1 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr12:15654854 C>G maps to NM_030667.1 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:15733635 C>T maps to NM_030667.1 Y1001Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:15699626 G>A maps to NM_030667.1 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:15637128 G>T maps to NM_030667.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:15742394 C>A maps to NM_030667.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:15677802 C>T maps to NM_030667.1 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:71286584 G>T maps to NM_002849.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:71139814 C>A maps to NM_002849.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr12:71054796 G>T maps to NM_002849.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:71050593 T>A maps to NM_002849.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:5220015 G>A maps to NM_002850.3 N1233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr19:5274328 T>A maps to NM_002850.3 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:5273531 C>G maps to NM_002850.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:40747084 G>T maps to ENST00000373198 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:40770553 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40864876 G>A maps to ENST00000373198 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:40877403 C>T maps to ENST00000373198 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:40980817 C>G maps to ENST00000373198 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr20:40733346 C>A maps to ENST00000373198 V1156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:41076865 G>T maps to ENST00000373198 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:40748572 A>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:41306575 G>C maps to ENST00000373198 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:40748599 T>A maps to ENST00000373198 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:40911126 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:40979283 G>T maps to ENST00000373198 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:40980790 G>T maps to ENST00000373198 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr20:40739109 G>T maps to ENST00000373198 I1061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr20:40739001 C>T maps to ENST00000373198 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr20:41408900 G>T maps to ENST00000373198 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:40713346 C>A maps to ENST00000373198 E1393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:40730904 G>T maps to ENST00000373198 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:41419855 A>T maps to ENST00000373198 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr20:40747109 C>T maps to ENST00000373198 W994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr20:41306788 C>T maps to ENST00000373198 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr20:40790052 A>T maps to ENST00000373198 L896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:40714454 G>T maps to ENST00000373198 C1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr20:40730910 C>A maps to ENST00000373198 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr20:41101002 G>C maps to ENST00000373198 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:40714397 G>A maps to ENST00000373198 H1336H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-97-7546-01A-11D-2036-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr20:40714436 C>T maps to ENST00000373198 V1323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr20:40827934 G>A maps to ENST00000373198 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr20:41306758 C>A maps to ENST00000373198 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:40743856 G>A maps to ENST00000373198 R1049R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:40944617 G>C maps to ENST00000373198 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:40739000 C>A maps to ENST00000373198 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:41419996 G>T maps to ENST00000373198 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:40730871 G>A maps to ENST00000373198 N1224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr20:41306788 C>A maps to ENST00000373198 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:29609212 G>T maps to NM_005704.4 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:29609186 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:29587413 A>C maps to NM_005704.4 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:121651805 G>T maps to NM_002851.2 T902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr7:121651439 C>A maps to NM_002851.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr7:121684622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:121674343 G>A maps to NM_002851.2 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr7:121659301 G>T maps to NM_002851.2 V1656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:121651280 T>A maps to NM_002851.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:121637944 C>A maps to NM_002851.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:121653038 T>A maps to NM_002851.2 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:121652033 C>A maps to NM_002851.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121652108 T>C maps to NM_002851.2 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr7:121653455 G>A maps to NM_002851.2 Q1452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:121653413 C>A maps to NM_002851.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:121676737 T>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr7:121699857 C>T maps to NM_002851.2 H2241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr7:121651530 C>T maps to NM_002851.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:121652033 C>G maps to NM_002851.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:121682659 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:121680904 C>A maps to NM_002851.2 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr7:121659223 G>T maps to NM_002851.2 G1630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:121651241 T>C maps to NM_002851.2 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:121644666 G>C did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:121624101 G>T maps to NM_002851.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:121650419 C>T maps to NM_002851.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:121650941 A>T maps to NM_002851.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr17:40556905 G>A maps to NM_012232.5 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:130476515 C>A maps to NM_001002913.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:37962213 A>G maps to NM_006607.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr3:157155311 C>T maps to NM_002852.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr16:1537677 G>T maps to NM_001013658.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr16:1536428 G>A maps to NM_001013658.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr16:1538360 G>T maps to NM_001013658.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:1536527 C>A maps to NM_001013658.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:1538420 C>A maps to NM_001013658.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr16:1537674 C>T maps to NM_001013658.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:144902886 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:31426787 A>G maps to ENST00000373741 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr1:31447620 A>G maps to ENST00000373741 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:31425211 T>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:31501677 G>A maps to ENST00000373741 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:31406156 G>A maps to ENST00000373741 Y1192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr2:20455931 C>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:20455915 C>A maps to ENST00000361078 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:30889712 G>A maps to NM_013357.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:30890169 C>T maps to NM_013357.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr8:30889895 G>T maps to NM_013357.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr11:125765570 G>C maps to NM_031307.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:105148817 G>A maps to NM_019042.3 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:44124505 C>T did not map to a codon.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:44148625 G>A maps to NM_031292.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr12:44124205 C>T maps to NM_031292.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr19:45161042 C>T maps to NM_006505.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:99818585 C>A maps to NM_024070.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:99818868 C>T maps to NM_024070.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:119547915 T>C maps to NM_002855.4 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:119548514 C>T maps to NM_002855.4 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:119549167 G>A maps to NM_002855.4 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr11:119508808 T>C maps to NM_203285.1 *459W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:45381861 G>A maps to NM_002856.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:45375314 G>A maps to NM_001042724.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:45389235 G>A maps to NM_001042724.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:45391413 A>G maps to NM_001042724.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:110852593 G>A maps to NM_015480.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:110845180 A>G maps to NM_015480.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:110852791 A>G maps to NM_015480.1 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:110830887 G>T maps to NM_015480.1 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:161049710 G>T maps to NM_030916.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:161049470 G>A maps to NM_030916.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:108086636 G>T maps to NM_007062.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr21:45547948 C>T maps to NM_005049.2 F759F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr21:45544508 G>A maps to NM_005049.2 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr21:45544481 C>T maps to NM_005049.2 Y613Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:45540640 G>A maps to NM_005049.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr21:45540972 G>A maps to NM_005049.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr10:134219611 G>T maps to NM_138499.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:134218990 G>A maps to NM_138499.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:1652005 T>A maps to NM_012293.1 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:1667443 G>A maps to NM_012293.1 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:1652347 C>A maps to NM_012293.1 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:1691402 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:1653261 C>A maps to NM_012293.1 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:1670166 C>T maps to NM_012293.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:1652104 C>T maps to NM_012293.1 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:1652104 C>A maps to NM_012293.1 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:1651959 G>T maps to NM_012293.1 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:1668736 G>T maps to NM_012293.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:1657493 A>G maps to NM_012293.1 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:1652674 G>A maps to NM_012293.1 C959C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:1652062 C>G maps to NM_012293.1 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:1652139 C>A maps to NM_012293.1 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:1652878 C>T maps to NM_012293.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:1653190 G>T maps to NM_012293.1 Y787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:1670115 C>A maps to NM_012293.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:1653208 G>T maps to NM_012293.1 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:1652371 G>T maps to NM_012293.1 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:1652932 G>T maps to NM_012293.1 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:52232510 T>A maps to NM_144651.4 G1444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:52233379 G>C maps to NM_144651.4 R1408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr8:52321348 C>T maps to NM_144651.4 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:52284604 T>G maps to NM_144651.4 A1243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:52258449 G>T maps to NM_144651.4 S1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:52320773 G>T maps to NM_144651.4 S1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:52323921 C>A maps to NM_144651.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:52387682 G>A maps to NM_144651.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:52321963 G>A maps to NM_144651.4 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:52370124 G>T maps to NM_144651.4 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:52366283 A>T maps to NM_144651.4 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:52320838 G>C maps to NM_144651.4 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:52366223 T>A maps to NM_144651.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:52366196 C>A maps to NM_144651.4 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:52366325 G>T maps to NM_144651.4 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr8:52325774 G>T maps to NM_144651.4 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:52567303 T>A maps to NM_144651.4 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr8:52384802 G>T maps to NM_144651.4 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:52387648 C>A maps to NM_144651.4 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:52336216 C>G maps to NM_144651.4 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:52359672 A>G maps to NM_144651.4 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:52366214 C>A maps to NM_144651.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:52323921 C>A maps to NM_144651.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr8:52321927 C>G maps to NM_144651.4 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:52232504 G>T maps to NM_144651.4 C1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:52359576 A>G maps to NM_144651.4 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:52321387 G>A maps to NM_144651.4 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:52321470 G>T maps to NM_144651.4 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:58380796 G>T maps to NM_017771.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:58368427 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:58381405 C>T maps to NM_017771.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:58381435 C>T maps to NM_017771.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:32302523 C>A maps to NM_007238.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:32302523 C>A maps to NM_007238.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr12:120651680 G>A maps to NM_001080855.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:120650308 G>A maps to NM_001080855.1 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr12:120650260 G>A maps to NM_001080855.1 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr6:36368311 A>G maps to NM_152990.3 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr8:144689206 G>C maps to NM_023078.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr3:191179073 C>T maps to NM_001083308.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:191179034 T>A maps to NM_001083308.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:25276278 C>T maps to NM_002862.3 C784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr20:25257280 G>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr20:25239871 G>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr14:51401904 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:64518938 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:64521741 G>T maps to NM_005609.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr11:64522997 C>T maps to NM_005609.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:64519429 G>C maps to NM_005609.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:64514709 G>T maps to NM_005609.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:158906732 G>T maps to NM_152501.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:158913668 C>T maps to NM_152501.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158912011 C>T maps to NM_152501.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:158913590 T>C maps to NM_152501.3 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr1:158908868 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:21620470 T>A maps to NM_024854.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:100157239 C>A maps to NM_032709.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr10:100146993 T>C maps to NM_032709.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:9355208 G>A maps to NM_002864.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:9316323 C>T maps to NM_002864.2 E892E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:9317844 G>T maps to NM_002864.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:9344804 A>T maps to NM_002864.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:9333632 A>T maps to NM_002864.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:9349606 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:9312561 G>A maps to NM_002864.2 R1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:9310389 G>T maps to NM_002864.2 A1114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr12:9305843 C>T maps to NM_002864.2 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:9354947 G>T maps to NM_002864.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:9322028 G>C maps to NM_002864.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:9322070 A>G maps to NM_002864.2 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr12:9333617 C>A maps to NM_002864.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:49135439 G>A maps to NM_005051.1 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:49138786 C>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:17510914 C>A maps to NM_000320.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:17492368 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:163956144 A>G maps to ENST00000361752 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:163956051 A>G maps to ENST00000361752 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr19:46202150 G>A maps to NM_017659.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr19:46196732 A>T maps to NM_017659.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:122250566 A>G maps to NM_198179.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr4:122254112 G>A maps to NM_198179.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:49083997 G>A maps to NM_198880.1 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:49095082 C>A maps to NM_198880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74288677 C>T maps to NM_032134.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr17:74274092 G>A maps to NM_032134.1 C1532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74288491 G>T maps to NM_032134.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr17:74288465 A>T maps to NM_032134.1 L615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:74274101 G>A maps to NM_032134.1 H1529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:74283960 C>T maps to NM_032134.1 R1106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:74301007 C>A maps to NM_032134.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:107100453 A>G maps to NM_018292.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:107111059 G>T maps to NM_018292.4 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr6:107100348 G>T maps to NM_018292.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr6:107100090 G>T maps to NM_018292.4 G189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:32954591 A>G maps to NM_001076786.1 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:32956352 A>T maps to NM_001076786.1 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:32979467 C>G maps to NM_001076786.1 S1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:180166084 G>T maps to NM_002826.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:180158766 T>C maps to NM_002826.4 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:139137424 G>A maps to NM_181701.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr9:139100582 C>A maps to NM_181701.3 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr9:139103179 C>A maps to NM_181701.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr19:10823270 C>T maps to NM_031209.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:113784145 A>G maps to ENST00000485050 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:136393710 A>G maps to ENST00000409606 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr2:136403031 G>T maps to ENST00000409606 G520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:136389478 A>G maps to ENST00000409606 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:136467771 G>T maps to ENST00000409606 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr12:57648585 C>A maps to ENST00000438036 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:57663633 C>G maps to ENST00000438036 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr12:57648756 A>C maps to ENST00000438036 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:42969876 C>A maps to NM_178491.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:42965886 C>G maps to NM_178491.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr20:42973946 C>A maps to NM_178491.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:8468396 G>T maps to NM_004218.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr8:37734786 C>T maps to NM_001002814.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:37735014 A>T maps to NM_001002814.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:37734902 T>A maps to NM_001002814.2 K180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:37732511 G>C maps to NM_001002814.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:37729732 C>A maps to NM_001002814.2 E863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:37730440 C>A maps to NM_001002814.2 G627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:119805398 C>A maps to ENST00000369199 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:119805662 G>T maps to ENST00000369199 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr16:532598 G>A maps to NM_014700.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr16:570479 C>T maps to NM_014700.3 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:29855756 C>A maps to NM_032932.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:29854857 A>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:29857402 C>T maps to NM_032932.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:73303310 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr2:73316440 C>T maps to NM_015470.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:73316166 G>C maps to NM_015470.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:65419248 G>A maps to NM_198686.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr14:65417041 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:238483688 C>T maps to NM_022449.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:140125718 G>T maps to ENST00000275874 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:66043552 G>T maps to NM_030981.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:66039309 G>T maps to NM_030981.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:156039537 G>A maps to NM_020387.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr15:55516088 A>G maps to NM_183235.1 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr8:61533285 A>T maps to NM_002865.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:61471409 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:82693359 G>T maps to NM_014488.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:82708264 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:82705137 G>A maps to NM_014488.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:82693370 C>A maps to NM_014488.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:82693305 G>A maps to NM_014488.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr18:9792204 C>A maps to NM_006868.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:129318488 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:129318305 G>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:129306261 A>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:129306209 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:140375376 G>T maps to NM_031296.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:27044006 C>G maps to NM_001144943.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:27042266 C>T maps to NM_001144943.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:23495306 C>T maps to NM_004914.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:72741178 C>A maps to NM_001006638.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:87883019 T>A maps to NM_022337.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:87847299 T>A maps to NM_022337.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:154493531 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:154493560 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:154490315 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:154490324 G>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:154490295 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:154493453 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:154490215 A>G did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:154490292 C>A did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:154490502 C>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:154490357 C>A did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr1:52442780 T>C maps to NM_002867.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:52442606 C>A maps to NM_002867.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:58120940 G>T maps to NM_138453.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr5:57913474 C>A maps to NM_138453.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:58147018 G>A maps to NM_138453.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:11436211 C>T maps to NM_004283.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr19:11447856 C>G maps to NM_004283.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:135870741 G>T maps to NM_001172435.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:135888249 G>T maps to NM_001172435.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:135848565 A>G did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr2:135892885 A>T maps to NM_001172435.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:135893294 A>T maps to NM_001172435.1 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:135890496 A>T maps to NM_001172435.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:135883795 C>T maps to NM_001172435.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:220406194 T>C maps to ENST00000358951 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:220332760 A>T maps to ENST00000358951 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:220406154 C>A maps to ENST00000358951 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:102755238 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:102755545 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:102755632 G>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:102755507 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:102193079 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:102192278 C>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:102192641 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:102192748 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:102192260 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:80622415 C>A maps to NM_006822.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:69502145 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:69504488 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:69502703 T>G did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:69502666 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:128813856 C>A maps to NM_198490.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr3:20019839 C>T maps to NM_004162.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr12:56380776 G>T maps to NM_002868.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:56383882 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:40280323 C>A maps to NM_201434.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:73429730 T>C maps to NM_198896.1 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:133557008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:130738128 G>A maps to NM_032144.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr2:130738128 G>A maps to NM_032144.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:130738065 T>C maps to NM_032144.2 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:63547707 C>T maps to NM_016530.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr15:63481945 C>T maps to NM_016530.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:63547783 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:103080188 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:103080665 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:103080374 G>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:103080684 G>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:103080377 C>T did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:5286436 G>A maps to NM_004703.4 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:5264820 C>T maps to NM_004703.4 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:5250192 G>T maps to NM_004703.4 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr16:28926031 C>A maps to NM_024816.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:28920048 C>A maps to NM_024816.2 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:28916338 A>G maps to NM_024816.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr16:28922244 G>A maps to NM_024816.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:28920081 C>A maps to NM_024816.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr9:127982815 A>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:125751574 G>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:125751588 C>T maps to NM_012197.3 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:125782612 A>T maps to NM_012197.3 K557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:174200394 A>G maps to NM_014857.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:174190136 G>T maps to NM_014857.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:174190249 C>T maps to NM_014857.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:174781080 C>T maps to NM_014857.3 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:174363162 G>A maps to NM_014857.3 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:174219770 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:66270235 G>A maps to ENST00000451741 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:66260521 G>T maps to ENST00000451741 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:66274042 C>T maps to ENST00000451741 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr7:66274075 C>T maps to ENST00000451741 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr7:66264339 G>T maps to ENST00000451741 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:24735663 C>T maps to NM_182836.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:76253195 G>A maps to NM_004582.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100958529 G>C maps to NM_022777.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr7:100962286 A>G maps to NM_022777.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr22:37627428 C>T maps to NM_002872.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr12:50393003 C>A maps to NM_013277.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr12:50394957 G>A maps to NM_013277.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr5:68670477 G>A maps to NM_133339.1 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:68695996 G>A did not map to a codon.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr5:68709951 G>T maps to NM_133339.1 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:117874087 A>G maps to NM_006265.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:13059013 A>T maps to NM_005053.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:13063561 G>C maps to NM_005053.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:13059349 C>T maps to NM_005053.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:131923746 C>A maps to NM_005732.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr5:131973866 G>A maps to NM_005732.3 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:4665603 T>C maps to NM_001130862.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:17699574 G>T maps to NM_001099218.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:17697659 G>A maps to NM_001099218.2 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:17697104 C>A maps to NM_001099218.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:17698791 G>T maps to NM_001099218.2 Y297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:17699058 A>T maps to NM_001099218.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56774180 C>T maps to NM_058216.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:56774051 A>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr14:68878243 G>A maps to NM_133509.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:33443894 A>T maps to NM_001142571.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr8:95390438 G>A maps to NM_012415.2 D828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:95412525 C>T maps to NM_012415.2 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:95399222 T>A maps to NM_012415.2 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46727023 G>A maps to NM_003579.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:46725741 G>T maps to NM_003579.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:46740344 C>A maps to NM_003579.3 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:51679121 C>T maps to NM_015106.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr3:51679625 A>G maps to NM_015106.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:51696596 C>A maps to NM_015106.2 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:51663463 T>C maps to NM_015106.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:51671499 C>T maps to NM_015106.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:67164942 A>C maps to NM_004584.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:110944490 C>T maps to NM_152442.3 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:4917650 G>A maps to NM_018059.4 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:4917271 C>A maps to NM_018059.4 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:4917467 G>A maps to NM_018059.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:4917239 C>A maps to NM_018059.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:4917440 G>T maps to NM_018059.4 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:4839262 C>A maps to NM_018059.4 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr7:4917449 G>A maps to NM_018059.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:4841356 G>A maps to NM_018059.4 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:4874741 C>A maps to NM_018059.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:4874507 G>T maps to NM_018059.4 C382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:4862061 G>C maps to NM_018059.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:4874543 C>T maps to NM_018059.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:4862022 A>T did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr7:4839053 G>A maps to NM_018059.4 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr7:4862169 C>A maps to NM_018059.4 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:55929847 T>A maps to NM_001015885.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:150240365 G>A maps to NM_001001788.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:36597179 C>A maps to NM_000448.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:36596038 C>A maps to NM_000448.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:36597067 G>C maps to NM_000448.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr11:36597478 C>T maps to NM_000448.2 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr11:36597776 C>A maps to NM_000448.2 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:36595045 A>T maps to NM_000448.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:36597394 A>G maps to NM_000448.2 K847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:36614950 G>T maps to NM_000536.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:36614773 C>T maps to NM_000536.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:36615025 G>T maps to NM_000536.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr11:36614886 G>A maps to NM_000536.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr14:102717267 C>A maps to NM_014226.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:102732200 C>G maps to NM_014226.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:17701268 G>A maps to ENST00000395776 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr17:17698451 G>T maps to ENST00000395776 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:17701460 G>T maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:17699744 G>A maps to ENST00000395776 R1161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr17:17697978 C>T maps to ENST00000395776 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr17:17707135 T>A maps to ENST00000395776 P1921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:17699939 G>C maps to ENST00000395776 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:17700137 C>T maps to ENST00000395776 L1292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:34807957 T>C maps to NM_001145521.1 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:34823527 C>T maps to NM_001145521.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:34757652 C>A maps to NM_001145521.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:34803878 C>T maps to NM_001145521.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:17818873 G>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:17818840 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:17818841 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:17818976 G>C did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:17819004 C>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:17818600 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:17819690 G>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:17819427 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:17819709 G>T did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:17820043 C>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:17820120 G>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:17818711 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:121043512 G>T maps to NM_002881.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:9517287 C>T maps to NM_006788.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:36190906 C>T maps to NM_194301.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:36154335 C>A maps to NM_194301.2 G859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:36217804 C>A maps to NM_194301.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:36159113 C>A maps to NM_194301.2 E788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:36159050 G>A maps to NM_194301.2 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:20563736 A>C maps to NM_020343.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:20486179 T>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr20:20475778 C>A maps to NM_020343.3 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:20493371 T>A maps to NM_020343.3 L1547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:37187035 T>C maps to NM_020336.2 C1157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:37177414 A>T maps to NM_020336.2 R996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr20:37144832 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr20:37126102 T>G maps to NM_020336.2 L166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr9:135974059 T>A maps to NM_006266.2 K887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr9:135982591 G>A maps to NM_006266.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:135985806 C>A maps to NM_006266.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:178753641 A>G maps to NM_152663.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:178854253 G>C maps to NM_152663.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:178780463 T>A maps to NM_152663.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:178861442 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:178745931 C>G maps to NM_152663.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr1:178790799 A>G maps to NM_152663.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:178846672 C>T maps to NM_152663.3 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:85799895 C>A maps to NM_001100391.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr8:85441675 C>A maps to NM_001100391.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:85686826 A>T maps to NM_001100391.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:238820226 C>T maps to NM_005855.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:238785924 G>T maps to NM_005855.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:40914376 G>A maps to ENST00000456272 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:131357650 G>A maps to ENST00000392369 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:170341169 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:170305132 T>C maps to NM_022897.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:170346492 C>T maps to NM_022897.3 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:109352660 G>T maps to NM_006267.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:109380883 A>T maps to NM_006267.4 K1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:109380141 A>G maps to NM_006267.4 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr2:109381161 A>T maps to NM_006267.4 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr2:109365554 G>T maps to NM_006267.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:109367851 C>G maps to NM_006267.4 S469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:109365488 C>T maps to NM_006267.4 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:109352196 G>T maps to NM_006267.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:109381701 G>T maps to NM_006267.4 P1569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:109383270 G>T maps to NM_006267.4 T2092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:5925685 C>A maps to NM_007322.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:36269489 A>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:36255668 G>A maps to NM_001161429.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:36249756 C>A maps to NM_001161429.1 *491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:36253825 G>A maps to NM_001161429.1 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:6015238 C>G maps to NM_012416.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr9:6013938 C>A maps to NM_012416.2 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr9:6015087 C>A maps to NM_012416.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr9:6015049 G>A maps to NM_012416.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:13697084 C>T maps to NM_005493.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr6:13644814 G>A maps to NM_005493.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr22:41670683 G>A maps to NM_002883.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:69044229 A>T maps to NM_015646.4 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:21940150 G>A maps to NM_001145658.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:21936133 A>G maps to NM_001145658.1 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:21929358 C>A maps to NM_001145658.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:21940119 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:21928223 C>T maps to NM_001145658.1 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:2908735 T>C did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:99342457 G>T maps to NM_001100426.1 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr4:99358196 G>A maps to NM_001100426.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:99325713 G>T maps to NM_001100426.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:99273624 A>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:99337938 T>C maps to NM_001100426.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr4:99214553 A>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr13:98086960 C>T maps to NM_021033.6 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:152880647 C>T maps to NM_002886.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr3:152880658 G>A maps to NM_002886.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:152880853 C>T maps to NM_002886.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:152880553 G>A maps to NM_002886.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr23:131351167 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:131351091 C>G did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:131351114 G>C did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr9:134501636 G>A maps to NM_198679.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:134525548 G>A maps to NM_198679.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:134459979 G>A maps to NM_198679.1 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:134504532 C>T maps to NM_198679.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:160277143 G>T maps to NM_014247.2 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr4:160277128 C>G maps to NM_014247.2 A1431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr4:160259585 A>T maps to NM_014247.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:160264502 C>T maps to NM_014247.2 H906H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:160244633 C>T maps to NM_014247.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:160252978 G>T maps to NM_014247.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:160253822 C>T maps to NM_014247.2 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr4:160273950 C>A maps to NM_014247.2 S1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr4:160273835 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:160275016 C>T maps to NM_014247.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:48134465 G>C maps to NM_001098531.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:48141560 G>A maps to NM_001098531.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173855581 T>C maps to NM_007023.3 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:173891807 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr2:173894895 A>T maps to NM_007023.3 K855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr2:173853500 C>T maps to NM_007023.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:173891409 C>T maps to NM_007023.3 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:173825956 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:22184816 G>A maps to ENST00000344041 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:130897669 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr5:130799843 G>A maps to ENST00000514667 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr5:130766993 C>A maps to ENST00000514667 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:130831344 C>T maps to ENST00000514667 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38345516 C>A maps to ENST00000456989 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr17:38349643 C>A maps to ENST00000456989 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:38349914 G>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr2:204305194 G>A maps to ENST00000374493 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr2:204304405 G>C maps to ENST00000374493 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:204305089 T>C maps to ENST00000374493 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:38487574 C>G maps to NM_001145301.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:38506136 C>T maps to NM_001145301.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:25622074 C>G maps to NM_000965.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:25542752 C>T maps to NM_000965.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:25611291 G>A maps to NM_000965.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:25622194 C>A maps to NM_000965.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:53607013 C>T maps to NM_000966.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr5:86642486 A>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:86685289 C>T maps to NM_002890.1 C1002C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr5:86627280 C>A maps to NM_002890.1 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:86564540 T>C maps to NM_002890.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr5:86676331 G>A maps to NM_002890.1 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr5:86676332 A>C maps to NM_002890.1 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr5:86672757 C>T maps to NM_002890.1 R749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:141327426 C>T maps to ENST00000452898 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:141299243 C>G maps to ENST00000452898 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:141328869 T>C maps to ENST00000452898 Y828Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:141304929 C>T maps to ENST00000452898 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:114786935 C>A maps to ENST00000389544 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr13:114773055 C>A maps to ENST00000389544 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr13:114792863 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr13:114748769 A>T maps to ENST00000389544 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr13:114784247 C>A maps to ENST00000389544 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr13:114839283 C>A maps to ENST00000389544 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:114782826 C>T maps to ENST00000389544 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:114817631 T>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:113557021 C>A maps to NM_001193520.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:113553488 C>T maps to NM_001193520.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr12:113559398 C>A maps to NM_001193520.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:113565662 G>A maps to NM_001193520.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:178426889 G>T maps to ENST00000263528 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:178425833 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:178421648 C>G maps to ENST00000263528 S606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:178420781 G>C maps to ENST00000263528 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:15572098 T>C maps to NM_022904.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr22:35947785 G>T maps to NM_014310.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:85619414 G>A maps to NM_152573.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:85597693 T>C maps to NM_152573.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:85619413 T>G maps to NM_152573.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr9:85615132 G>A maps to NM_152573.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:85615104 C>A maps to NM_152573.2 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:43696228 C>T maps to ENST00000374459 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:43701429 G>T maps to ENST00000374459 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr10:43692502 C>T maps to ENST00000374459 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr10:43697255 C>T maps to ENST00000374459 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:82366677 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:82366731 T>A maps to NM_152545.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:179538538 G>C maps to NM_175062.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr5:179555603 G>T maps to NM_175062.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr5:179555604 G>T maps to NM_175062.3 Y148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr15:79298769 G>A maps to NM_002891.4 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:79292244 G>C maps to NM_002891.4 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr15:79327545 G>T maps to NM_002891.4 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:79294031 G>C maps to NM_002891.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr15:79323749 C>T maps to NM_002891.4 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr5:80369241 C>T maps to NM_006909.1 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:80409611 T>C maps to NM_006909.1 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr5:80408497 G>T maps to NM_006909.1 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr5:80382674 C>T maps to NM_006909.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:80409605 A>G maps to NM_006909.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr5:80408503 G>A maps to NM_006909.1 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:80338745 G>T maps to NM_006909.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:80338784 G>A maps to NM_006909.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:80497208 C>T maps to NM_006909.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:38791142 G>A maps to NM_005739.3 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr15:38805043 G>A maps to NM_005739.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:38793415 G>A maps to NM_005739.3 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:64497270 C>A did not map to a codon.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr11:64504338 G>C maps to ENST00000320253 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:64507484 C>A maps to ENST00000320253 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:64508453 G>A maps to ENST00000320253 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr11:64496352 G>A maps to ENST00000320253 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:64504476 C>A maps to ENST00000320253 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:33774800 G>T maps to NM_170672.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:33747027 C>T maps to NM_170672.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:38903628 G>T maps to ENST00000405332 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:38910547 C>T maps to ENST00000405332 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:38903680 G>A maps to ENST00000405332 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:38903602 G>T maps to ENST00000405332 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:49243434 C>T maps to NM_017805.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr19:49243512 G>T maps to NM_017805.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:49225108 A>C did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:53731602 T>C maps to NM_023940.2 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:65351718 C>T maps to NM_016563.2 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:65350889 G>T maps to NM_016563.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:65347377 G>A maps to NM_016563.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr15:65357603 G>A maps to NM_016563.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:50368056 G>A maps to NM_170714.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:50369287 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:4770301 G>T maps to NM_014737.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:4768347 C>T maps to NM_014737.2 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:4776564 G>T maps to NM_014737.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:4764981 G>T maps to NM_014737.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:206681282 G>A maps to NM_182663.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:74447532 C>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:86199739 T>C maps to NM_005447.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:10433904 G>A maps to NM_133452.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:10444192 C>T maps to NM_133452.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:10439671 C>T maps to NM_133452.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:65278515 C>T maps to ENST00000294428 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:65243705 C>T maps to ENST00000294428 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:48916811 G>T maps to NM_000321.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:49039353 C>G maps to NM_000321.2 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:48916850 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr13:48954376 A>T maps to NM_000321.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr13:49027248 T>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr13:48947628 G>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:48951165 C>G maps to NM_000321.2 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr13:48919289 T>A maps to NM_000321.2 L152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr13:48941628 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:48947604 G>T maps to NM_000321.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr13:48941719 C>T maps to NM_000321.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr13:48951074 G>T maps to NM_000321.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr13:49037877 T>A maps to NM_000321.2 C706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr13:48937093 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:53573762 C>A maps to NM_014781.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:53569133 C>T maps to NM_014781.4 Q1085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:53547494 A>G maps to NM_014781.4 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr8:53588990 C>T maps to NM_014781.4 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:53558270 C>A maps to NM_014781.4 A1326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr8:53558356 C>A maps to NM_014781.4 E1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:53555276 T>C maps to NM_014781.4 Q1361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:33133871 C>A maps to NM_005610.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr1:33138266 A>G maps to NM_005610.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:205065902 C>A maps to NM_005057.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:205090983 C>A maps to NM_005057.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:205064007 G>A maps to NM_005057.3 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:205070792 G>A maps to NM_005057.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr16:24582365 G>T maps to NM_006910.4 E1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr16:24564862 G>T maps to NM_006910.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:24582308 G>T maps to NM_006910.4 E1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:24580931 T>A maps to NM_006910.4 L974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:24573245 G>A maps to NM_006910.4 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:24583298 G>T maps to NM_006910.4 E1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:24551982 C>T maps to NM_006910.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr23:16875780 T>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:16870188 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr23:16867403 G>C did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr18:20572759 C>T maps to ENST00000360790 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:20577614 A>G maps to ENST00000360790 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:18470620 G>A maps to NM_006606.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr20:18470626 G>A maps to NM_006606.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:35693825 C>G did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr20:35684009 T>A maps to NM_002895.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:53524046 G>C maps to NM_005611.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr16:53515617 A>T maps to NM_005611.3 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr16:53503960 A>G maps to NM_005611.3 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr16:53487409 C>T maps to NM_005611.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:53501043 G>T maps to NM_005611.3 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:47044475 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr23:47044476 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:47032556 C>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:47041246 G>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:47034443 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:47039330 G>T did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:47044522 C>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:47044699 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:47034491 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:47045726 G>T did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:47039903 A>T did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:47040922 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:47044594 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:47038782 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:47041371 C>A did not map to a codon.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr23:47028897 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:47032550 G>T did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr23:47045016 A>G did not map to a codon.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr23:47045190 T>A did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:47039815 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:47034416 G>C did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:47034416 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:47045156 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47028840 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47045891 G>T did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:47028897 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:47045015 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:47041006 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr23:47045186 G>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr21:15596756 A>C did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr20:34240589 T>A maps to NM_001198838.1 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr8:94747018 G>A maps to NM_203390.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:94746532 G>A maps to NM_203390.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:94745755 C>T maps to NM_203390.2 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:94746576 G>A maps to NM_203390.2 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr8:94747221 T>A maps to NM_203390.2 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr8:94748572 G>A maps to NM_203390.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:94746109 G>A maps to NM_203390.2 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:66392645 G>T maps to NM_006328.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:66391824 C>T maps to NM_006328.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:110888218 G>A maps to NM_022768.4 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr1:110882746 C>T maps to NM_022768.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr1:110882200 C>T maps to NM_022768.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:110882410 C>T maps to NM_022768.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:110882320 C>G maps to NM_022768.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:110884205 C>T maps to NM_022768.4 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:155129872 A>G maps to NM_014892.3 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr6:155123282 T>C did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:155129904 C>G maps to NM_014892.3 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:6154178 G>T maps to NM_001145547.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr10:6157422 T>G maps to NM_001145547.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:125004273 C>G maps to NM_033117.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr9:125007556 C>A maps to NM_033117.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr12:114358413 A>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:114374916 C>A maps to NM_016196.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:114364966 C>T maps to NM_016196.3 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr12:114362516 T>A maps to NM_016196.3 K764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:114386709 C>A maps to NM_016196.3 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr12:114392971 G>A maps to NM_016196.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:114352883 G>C maps to NM_016196.3 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:114386692 C>A maps to NM_016196.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:114400174 C>T maps to NM_016196.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:17292271 C>T maps to NM_001143942.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:73554748 C>T maps to NM_021239.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:73566131 C>G maps to NM_021239.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:79929483 G>A maps to ENST00000438737 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr13:79943015 T>C maps to ENST00000438737 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr13:79933804 T>C maps to ENST00000438737 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:145613127 G>T maps to NM_018989.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr5:145610328 A>G maps to NM_018989.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr7:127964663 C>A maps to NM_018077.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:48435467 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:155538131 G>T maps to NM_053043.2 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:235299085 C>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr1:235318411 C>T maps to NM_015014.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:55982703 G>T maps to NM_017495.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr20:34309757 T>C maps to NM_184234.1 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:34302143 T>A maps to NM_184234.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:66411053 C>T maps to NM_001198845.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:66411600 T>A maps to NM_001198845.1 *340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:106310850 T>C did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:106310823 G>C did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:106331703 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:106310784 C>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:106359172 G>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:106331910 C>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:106310851 C>G did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:106359106 A>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:106310790 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:238725844 C>T maps to NM_001080504.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:178988948 G>T maps to ENST00000456670 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:155749035 C>A maps to NM_144979.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr4:155720681 G>A maps to NM_144979.3 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:155719111 C>A maps to NM_144979.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:155720325 G>T maps to NM_144979.3 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:155719994 G>T maps to NM_144979.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr4:40427926 T>C maps to NM_001098634.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:66444352 G>A maps to NM_031492.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr11:66444487 G>C maps to NM_031492.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr3:50145580 G>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr3:50147084 G>A maps to NM_005778.2 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50085712 G>T maps to NM_005777.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:50103766 C>T maps to NM_005777.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:50114545 C>A maps to NM_005777.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr3:50095895 G>A maps to NM_005777.2 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr3:50112757 G>T maps to NM_005777.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr3:50102540 G>A maps to NM_005777.2 K888K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr22:36177703 C>G maps to NM_001082578.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:36141975 G>A maps to NM_001082578.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr2:161223814 C>A maps to NM_016836.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:29941230 C>T maps to NM_001003793.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr23:135958802 A>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:135956612 T>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:135956514 C>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:135960087 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:135956384 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:135957248 A>C did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:135960159 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:135961218 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:135956316 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:129546492 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:129546547 C>G did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:129545488 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:129546814 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr1:89448432 T>A maps to NM_019610.5 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:89449151 T>G maps to NM_019610.5 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:7111241 G>T maps to NM_014469.4 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:7111184 C>A maps to NM_014469.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:139237322 C>T maps to NM_002899.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:139172009 T>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:139173633 C>A maps to NM_004164.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:48389940 G>A maps to NM_002900.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:48390445 C>A maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr10:48389203 C>G maps to NM_002900.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr10:48383952 G>T maps to NM_002900.2 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr10:48381909 G>A maps to NM_002900.2 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:48389677 C>A maps to NM_002900.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:48388537 G>T maps to NM_002900.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:48388048 C>A maps to NM_002900.2 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:48389715 G>T maps to NM_002900.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr10:48388285 C>A maps to NM_002900.2 R864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:48382045 C>A maps to NM_002900.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:48388042 C>T maps to NM_002900.2 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:95360225 G>C maps to NM_006744.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:95353736 G>T maps to NM_006744.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:10068243 G>A maps to ENST00000377192 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:43944982 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:43936879 C>G maps to NM_014276.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr20:43945346 C>A maps to NM_014276.2 C434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:30332326 G>T maps to NM_001008712.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:65041693 T>A did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:173931108 G>A maps to NM_172071.2 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:173930919 G>A maps to NM_172071.2 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:173953757 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:125620204 C>A maps to NM_001100588.1 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:125643033 T>A maps to NM_001100588.1 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:125621031 C>A maps to NM_001100588.1 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr21:35898978 G>A maps to NM_203418.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr21:35890402 G>A maps to NM_004414.5 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:46214581 C>A maps to ENST00000405162 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:50141334 G>A maps to NM_018191.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr13:50123717 C>A maps to NM_018191.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:50115947 T>A maps to NM_018191.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr13:49084907 C>A did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr13:49076858 C>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr13:49089380 G>A maps to NM_001268.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr13:49089419 C>G maps to NM_001268.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:28858387 G>T maps to NM_001048194.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:28861842 A>G maps to NM_001048194.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr1:28863367 G>T maps to NM_001048194.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:17755623 T>A maps to NM_018715.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr1:17735596 G>A maps to NM_018715.2 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:17742996 C>A maps to NM_018715.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:17735585 T>A maps to NM_018715.2 *523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:17743062 G>A maps to NM_018715.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:91504944 C>A maps to NM_033544.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr4:76416959 G>A maps to NM_015436.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:76434497 G>A maps to NM_015436.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:4833224 G>A maps to NM_005772.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr19:50045898 A>T maps to NM_020650.2 K257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:63681628 G>T maps to NM_173587.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:211486134 G>A maps to NM_001136223.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:211452577 A>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:167659283 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:167654677 C>A maps to NM_052862.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:9801521 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:9801521 C>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:211654670 A>G maps to NM_183059.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:68191237 C>A maps to NM_152443.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr14:68191903 G>T maps to NM_152443.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:55568078 C>A maps to NM_001145971.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:18736477 C>T maps to NM_020905.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:57351180 C>T maps to NM_003708.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:57351014 C>A maps to NM_003708.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr12:57346752 C>A maps to NM_003708.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:57346019 T>A maps to NM_003708.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:57346649 C>A maps to NM_003708.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:10132254 C>T maps to NM_015725.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:10129491 C>T maps to NM_015725.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:10132086 G>C maps to NM_015725.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:34251769 C>A maps to NM_145654.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110106874 T>A maps to ENST00000405097 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:24642161 G>T maps to NM_005132.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:36117029 A>T maps to NM_021111.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:36105138 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:36118893 C>G maps to NM_021111.2 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:36122951 G>T maps to NM_021111.2 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:21636327 C>A maps to NM_032941.2 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr12:21644596 G>A maps to NM_032941.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr12:21636333 G>A maps to NM_032941.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:21643160 A>T maps to NM_032941.2 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr8:145742149 T>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:145742845 G>A maps to ENST00000428558 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:73657141 C>T maps to NM_004259.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:73627304 G>A maps to NM_004259.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:73662538 T>C maps to NM_004259.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:73659001 T>A maps to NM_004259.5 K110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:73624500 G>A maps to NM_004259.5 Q868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr17:73658963 C>T maps to NM_004259.5 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:86479159 G>A maps to NM_022912.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:21996975 G>T maps to NM_025232.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:79349995 C>T maps to NM_002909.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:79349190 G>A maps to NM_002909.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:79349964 A>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79348007 C>A maps to NM_002909.4 Y7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:79349205 C>A maps to NM_002909.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:79348037 G>T maps to NM_002909.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:79348686 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:79348028 G>T maps to NM_002909.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:79349998 G>A maps to NM_002909.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:79350028 C>A maps to NM_002909.4 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:79313966 C>A maps to NM_006507.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:79313627 G>T maps to NM_006507.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:79314056 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:79313982 G>T maps to NM_006507.3 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:79314023 G>T maps to NM_006507.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:79384812 G>T maps to NM_138937.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:79385791 G>T maps to NM_138937.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:79386483 G>T maps to NM_138937.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:79385589 C>T did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:79384740 G>C maps to NM_138937.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:79384419 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:79385589 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:79384821 G>A maps to NM_138937.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:79385457 G>A maps to NM_138937.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:79386510 C>T maps to NM_138937.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:79384746 G>T maps to NM_138937.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:79254298 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:79253248 G>A maps to NM_001008387.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:79254991 T>C maps to NM_001008387.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:79253843 G>T maps to NM_001008387.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:79253236 C>A maps to NM_001008387.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:79255045 G>C maps to NM_001008387.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr2:79253908 C>A maps to NM_001008387.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:79255030 C>A maps to NM_001008387.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:79254996 G>A maps to NM_001008387.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr2:79253885 A>T maps to NM_001008387.1 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:120345519 A>G maps to NM_001159353.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:61149450 C>A maps to NM_002908.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:61144152 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:61149603 A>T maps to NM_002908.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:61118821 G>A maps to NM_002908.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr11:65422433 G>A maps to NM_021975.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:45541023 A>G maps to ENST00000221452 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr19:45540759 C>G maps to ENST00000221452 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:45515473 G>T maps to ENST00000221452 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr7:103126852 G>T maps to ENST00000428762 C3258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:103138648 C>T maps to ENST00000428762 W2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:103276758 G>T maps to ENST00000428762 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:103185751 G>A maps to ENST00000428762 A2114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr7:103180649 G>T maps to ENST00000428762 I2308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:103141203 G>T maps to ENST00000428762 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:103294652 C>G did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr7:103207174 C>T maps to ENST00000428762 G1540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:103275909 G>T maps to ENST00000428762 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:103193922 G>A maps to ENST00000428762 T2019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:103214660 G>T maps to ENST00000428762 Y1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:103207068 G>A maps to ENST00000428762 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:103138671 C>A maps to ENST00000428762 E2899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:103205756 C>T maps to ENST00000428762 K1726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr7:103159822 G>T maps to ENST00000428762 G2603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:103338530 G>T maps to ENST00000428762 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr7:103293131 C>T maps to ENST00000428762 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:103131116 A>G maps to ENST00000428762 S3201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:103180649 G>T maps to ENST00000428762 I2308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:103368629 A>T maps to ENST00000428762 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr7:103191668 C>G maps to ENST00000428762 A2049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:103341403 T>C maps to ENST00000428762 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:103191725 C>G maps to ENST00000428762 S2030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:103251194 G>T maps to ENST00000428762 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:103130345 A>G maps to ENST00000428762 S3202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:103292157 A>T maps to ENST00000428762 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:103163866 G>T maps to ENST00000428762 G2487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr7:103202291 T>G maps to ENST00000428762 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:103237093 C>T maps to ENST00000428762 Q1116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:103629664 C>A maps to ENST00000428762 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr7:103275984 C>A maps to ENST00000428762 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103194237 G>T maps to ENST00000428762 I1946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:103363605 A>G maps to ENST00000428762 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr7:103155857 A>G maps to ENST00000428762 A2631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:103341379 G>A maps to ENST00000428762 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr7:103138288 C>A maps to ENST00000428762 L2976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:103126780 G>A maps to ENST00000428762 N3282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:103293173 A>G maps to ENST00000428762 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr7:103202008 G>T maps to ENST00000428762 I1833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:103270623 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:103202351 C>A maps to ENST00000428762 G1753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr7:103163847 C>A maps to ENST00000428762 G2494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:103368614 G>A maps to ENST00000428762 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:103234146 T>A maps to ENST00000428762 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:103180697 G>A maps to ENST00000428762 R2292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:103338515 G>A maps to ENST00000428762 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:103197601 G>T maps to ENST00000428762 T1873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr7:103270610 T>C maps to ENST00000428762 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:73103418 G>T maps to NM_152222.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:30064325 G>T maps to NM_014012.4 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:30064328 C>A maps to NM_014012.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr20:30065682 G>A maps to NM_014012.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:23355421 C>A maps to NM_173527.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr14:23354156 C>A maps to NM_173527.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:204124179 C>A maps to NM_000537.3 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:204130498 G>T maps to NM_000537.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:204131251 C>T maps to NM_000537.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr1:204128651 G>A maps to NM_000537.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:204128681 C>G maps to NM_000537.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:204135376 C>A maps to NM_000537.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153209094 C>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153209530 C>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:153209787 A>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:153205580 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153208330 G>A did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr23:153209151 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:153209827 G>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:153208436 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:27849503 G>A maps to NM_001029874.1 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:150069073 G>A maps to NM_001099695.1 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:150069331 C>A maps to NM_001099695.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:139233925 G>A maps to ENST00000367663 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr6:139241421 C>A maps to ENST00000367663 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr6:139251119 G>A maps to ENST00000367663 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr6:139229863 T>C maps to ENST00000367663 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr6:139251134 A>C maps to ENST00000367663 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:139226203 T>C maps to ENST00000367663 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:17152021 G>C did not map to a codon.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr23:17073015 G>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:17095396 T>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:17095414 A>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:17047677 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:2328560 C>T maps to NM_007033.4 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:2334553 C>T maps to NM_007033.4 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:2334560 T>A maps to NM_007033.4 *197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:8425870 C>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:8716295 G>A maps to NM_012102.3 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:8425881 G>A maps to NM_012102.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:8426007 A>G maps to NM_012102.3 Y437Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr12:15262208 G>A maps to NM_032918.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:18234244 G>A maps to NM_024730.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:18234394 T>A maps to NM_024730.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:57796223 G>A maps to NM_005612.4 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr10:43615592 C>A maps to NM_020975.4 S891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:43610003 G>C maps to NM_020975.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:43601831 G>A maps to NM_020975.4 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:43615060 C>A maps to NM_020975.4 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:43609931 A>G maps to NM_020975.4 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:43622126 C>T maps to NM_020975.4 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr10:43596170 G>T did not map to a codon.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr10:43596057 G>A maps to NM_020975.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:43612111 C>A maps to NM_020975.4 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:108474669 G>T maps to NM_032579.2 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:108476011 G>T maps to NM_032579.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:85576585 C>T maps to NM_017750.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:85581605 G>A maps to NM_017750.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:85570767 G>A maps to NM_017750.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:85578965 C>A maps to NM_017750.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:100052326 T>A maps to NM_016316.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:100038093 A>G maps to NM_016316.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr2:100079004 G>T maps to NM_016316.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:100020218 C>T maps to NM_016316.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:111695224 C>A maps to NM_002912.3 G1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:111694253 T>C maps to NM_002912.3 E1768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:1827785 C>A maps to NM_020695.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:1818717 C>T maps to NM_020695.3 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr4:39291650 T>C maps to ENST00000381897 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr4:39291517 G>A maps to ENST00000381897 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73668692 A>G maps to NM_181471.1 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr7:73663379 G>C maps to NM_181471.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:34404009 T>C maps to NM_002915.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:34404942 A>T maps to NM_002915.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:186515343 T>A maps to NM_181573.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:186507929 C>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:186512498 G>A maps to NM_181573.2 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:118457467 A>G maps to NM_007370.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:33339090 C>A maps to NM_001017368.1 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:33348593 C>G maps to NM_001017368.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:80007651 G>A maps to NM_002917.1 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr22:29834950 C>T maps to NM_021026.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr22:29837624 G>A maps to NM_021026.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr22:29837588 C>A maps to NM_021026.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr22:29835025 C>A maps to NM_021026.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr22:32590413 T>C maps to NM_001098527.2 K61K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-7995-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr22:32754214 C>T maps to NM_001098535.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:112671605 T>C maps to NM_001013734.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:53137993 T>A maps to NM_052859.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:53156536 G>T maps to NM_052859.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:53145849 T>C maps to NM_052859.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:53156497 G>A maps to NM_052859.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:53160011 T>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:53145858 C>T maps to NM_052859.3 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:16399486 G>A maps to NM_015150.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:16411655 T>C maps to NM_015150.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:198498577 A>T maps to NM_144629.2 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:198436806 A>G maps to NM_144629.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:176105680 T>C maps to NM_022457.5 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:176153824 G>A maps to NM_022457.5 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:175956198 A>T maps to NM_022457.5 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:175956123 T>A maps to NM_022457.5 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:176012320 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:175957453 G>A maps to NM_022457.5 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:176132087 C>A maps to NM_022457.5 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:176153797 T>C maps to NM_022457.5 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr16:74660378 G>A maps to NM_018124.3 I681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:14080873 G>A maps to NM_002918.4 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:14073960 G>A maps to NM_002918.4 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:14083596 G>A maps to NM_002918.4 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:14077444 C>T maps to NM_002918.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:6026249 T>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr19:6016243 A>C maps to NM_000635.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:6007125 C>A maps to NM_000635.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:5997190 G>A maps to NM_000635.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:5997178 G>A maps to NM_000635.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr9:3257076 C>A maps to NM_134428.1 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:3270425 C>A maps to NM_134428.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:3248067 C>T maps to NM_134428.1 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr9:3247923 G>A maps to NM_002919.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr9:3288186 C>A maps to NM_134428.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:107080805 C>T maps to ENST00000357881 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:107048011 G>A maps to ENST00000357881 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr12:107080751 G>A maps to ENST00000357881 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:107114571 G>T maps to ENST00000357881 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:107109317 C>A maps to ENST00000357881 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:151316172 C>T maps to NM_000449.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:151316754 C>G did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:151316208 G>A maps to NM_000449.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:151314766 C>T maps to NM_000449.3 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:117250117 T>A maps to NM_173560.3 C865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:117248702 G>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:117249928 T>C maps to NM_173560.3 Y802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr6:117232174 T>A maps to NM_173560.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:117244364 C>A maps to NM_173560.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr6:117199103 C>A maps to NM_173560.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:117237178 G>T maps to NM_173560.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr6:117248301 A>C maps to NM_173560.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:117203553 C>T maps to NM_173560.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr6:117243314 G>T did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:56393596 C>T maps to NM_022841.5 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:56390278 C>A maps to NM_022841.5 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:19312473 G>A maps to NM_003721.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M2-01A-12D-A24P-08 chr19:19304810 C>G maps to NM_003721.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:101283639 C>G maps to NM_017819.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:101283657 C>T maps to NM_017819.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:109695409 C>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:109693956 G>C did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr23:109696065 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:109695217 C>A did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:109696442 A>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:109694213 T>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:109698545 G>T did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:109694087 A>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:109696972 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:109696887 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:109694147 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:109697403 G>T did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:109694399 A>T did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:109697656 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:109695631 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:109695398 A>G did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:109697337 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:109695254 C>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:109693869 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:109695042 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:109694745 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:109695604 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:109695656 A>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:109695610 C>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:109698492 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:109694074 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:109697113 G>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:109697857 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:109694721 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:109696447 C>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:109697784 G>A did not map to a codon.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr23:109694676 T>C did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr23:109695637 C>G did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:109694852 A>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:109695253 C>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:109697788 A>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:109696966 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:109694115 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:109697874 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:109697061 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:71350438 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:71350871 G>A did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:71351248 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:71349931 C>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:71349705 G>T did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr23:71350579 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:71350435 G>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:71349989 C>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:71351062 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:71351063 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:71351059 G>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:71350844 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:71351283 A>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:183885735 G>T maps to NM_015149.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:183869310 C>T maps to NM_015149.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:183885585 T>G maps to NM_015149.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:183881335 G>C maps to NM_015149.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:33263948 G>A maps to NM_004761.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr6:33263524 G>C maps to NM_004761.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:33264241 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:11505190 G>A maps to NM_001161616.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:11516003 C>T maps to NM_001161616.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr19:11508234 G>A maps to NM_001161616.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:24034689 G>A maps to ENST00000382833 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:98115291 C>T maps to NM_001012761.2 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr23:46949283 T>G did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:46949271 C>T did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:46951082 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:73165951 A>T maps to NM_001080479.2 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr5:73048995 G>A maps to NM_001080479.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:73153601 A>T maps to NM_001080479.2 K638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:73168827 A>T maps to NM_001080479.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:35752768 A>G maps to ENST00000456972 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:35752110 C>T maps to ENST00000456972 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr2:88082470 T>A maps to NM_001078170.2 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:107040986 G>A maps to ENST00000304514 R1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr2:107052702 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:107040315 T>C maps to ENST00000304514 K1369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:107040327 G>T maps to ENST00000304514 Y1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr2:107040264 C>T maps to ENST00000304514 Q1386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr2:107041236 T>A maps to ENST00000304514 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:107040264 C>T maps to ENST00000304514 Q1386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:107040795 C>T maps to ENST00000304514 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:107029669 G>A maps to ENST00000304514 H1712H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:107073497 C>A maps to ENST00000304514 G112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108487651 G>T maps to NM_182588.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:108487259 G>T maps to NM_182588.2 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:108496517 T>A maps to NM_182588.2 L1673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr2:108487765 A>G maps to NM_182588.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:108488461 C>A maps to NM_182588.2 Y1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:108488443 A>G maps to NM_182588.2 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:108475926 C>A maps to NM_182588.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr2:108487663 T>C maps to NM_182588.2 F1068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:86007431 G>T maps to ENST00000358110 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:86018322 C>A maps to ENST00000358110 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr10:86004866 G>T maps to ENST00000358110 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:86014177 G>T maps to ENST00000358110 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:192548397 A>G maps to NM_002922.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192545460 G>T maps to NM_002922.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:192547460 C>A maps to NM_002922.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:192548280 C>T maps to NM_002922.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:121275046 G>A maps to NM_001005339.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr16:321438 C>A maps to NM_183337.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:320550 G>A maps to NM_183337.1 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:3429844 A>T maps to NM_198229.2 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:3319585 C>T maps to NM_198229.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:3319633 C>A maps to NM_198229.2 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:3441278 G>C maps to NM_198229.2 A1404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:176799027 C>T maps to ENST00000398128 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr5:176793798 C>T maps to ENST00000398128 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:176798010 G>T maps to ENST00000398128 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182571202 C>T maps to NM_002928.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:182571617 T>A maps to NM_002928.3 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:192153500 T>A maps to NM_130782.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:192153461 A>T maps to NM_130782.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:192127883 C>A maps to NM_130782.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:192150507 A>T maps to NM_130782.2 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:192150555 G>T maps to NM_130782.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:192153518 T>A maps to NM_130782.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:192127877 C>A maps to NM_130782.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr1:192150434 T>A maps to NM_130782.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:192778312 T>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:192335235 A>G maps to NM_001039152.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:192335251 T>G maps to NM_001039152.3 *153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr8:101065028 C>A did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr8:101078437 T>C maps to NM_015668.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:101076250 C>A maps to NM_015668.3 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:101075954 A>G maps to NM_015668.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:101014540 G>T maps to NM_015668.3 Y893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr8:100994287 A>G maps to NM_015668.3 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:101065077 G>C maps to NM_015668.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:101054144 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:101076133 G>A maps to NM_015668.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:101020742 G>A maps to NM_015668.3 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr9:116269564 A>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:116276912 G>T maps to NM_144488.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr9:116246509 C>T maps to NM_144488.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:116279873 G>C maps to NM_144488.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:163044229 C>G maps to NM_001102445.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:163043249 G>C maps to NM_001102445.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:163043366 C>A maps to NM_001102445.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:163122408 G>T maps to NM_003617.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr14:72932466 C>A maps to NM_004296.4 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:72818843 G>C maps to NM_004296.4 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr14:72939586 C>A maps to NM_004296.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:72943467 G>T maps to NM_004296.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:72431519 A>T maps to NM_004296.4 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:72961949 T>A maps to NM_004296.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:241262062 C>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:240969526 G>C maps to ENST00000407727 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr1:240979706 A>G maps to ENST00000407727 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:241094037 C>A maps to ENST00000407727 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:240978030 G>T maps to ENST00000407727 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:240969626 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:241261964 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:240975229 G>T maps to ENST00000407727 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:63905071 C>A maps to NM_001029875.1 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:63803605 G>T maps to NM_001029875.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr5:63871618 C>A maps to NM_001029875.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:182617328 C>A maps to NM_033345.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:63221337 C>A maps to NM_003835.3 C542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:63204047 T>A maps to NM_003835.3 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:63221181 G>A maps to NM_003835.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:63221181 G>A maps to NM_003835.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr17:63221550 C>A maps to NM_003835.3 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:63189699 C>T maps to NM_003835.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr17:63221241 C>G maps to NM_003835.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:63221361 G>A maps to NM_003835.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:63221302 G>T maps to NM_003835.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:49578804 G>T maps to NM_000324.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:49578831 G>T maps to NM_000324.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:49604437 G>A maps to NM_000324.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr6:49582477 C>A maps to NM_000324.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:49587019 G>A maps to NM_000324.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:49578777 G>T maps to NM_000324.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:49574908 T>A maps to NM_000324.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:49585843 G>T maps to NM_000324.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:49585779 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:49585864 C>T maps to NM_000324.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:49580219 C>A maps to NM_000324.2 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr6:49587007 A>T maps to NM_000324.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:49585801 G>T maps to NM_000324.2 Y157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:49580202 G>T maps to NM_000324.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:227729705 G>T maps to NM_001167608.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:75517555 G>A maps to NM_001040456.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:75511504 C>T maps to NM_001040456.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:75511147 T>G maps to NM_001040456.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:75511471 G>T maps to NM_001040456.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:113012 C>A maps to NM_022450.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:111615 G>A maps to NM_022450.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:111902 C>T maps to NM_022450.3 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr17:74473846 G>A maps to NM_024599.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr17:74472970 G>A maps to NM_024599.5 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr17:74473272 C>T maps to NM_024599.5 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr17:74473791 C>A maps to NM_024599.5 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr16:728015 C>T maps to NM_003961.1 Y427Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr17:30611730 G>A maps to NM_138328.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:30648076 C>A maps to NM_138328.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:156347137 C>T maps to NM_020407.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:156351616 G>A maps to NM_020407.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:156352643 G>T maps to NM_020407.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:156351712 G>C maps to NM_020407.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:156339066 G>T maps to NM_020407.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:156352640 T>C maps to NM_020407.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:156354616 G>T maps to NM_020407.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:25701838 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:25718551 C>T maps to NM_020485.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:25701855 C>A maps to NM_020485.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:25729149 C>A maps to NM_020485.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:25717279 G>T maps to NM_020485.4 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:90021157 G>T maps to NM_016321.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:90020391 G>C maps to NM_016321.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr15:90022630 G>A maps to NM_016321.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr15:90020806 G>T maps to NM_016321.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr15:90020438 T>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:90021103 G>A maps to NM_016321.1 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:151174501 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:151167734 C>A maps to NM_005614.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:49459155 C>A maps to NM_144593.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:129251249 C>A maps to NM_000539.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:129252497 G>A maps to NM_000539.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:129247827 C>G maps to NM_000539.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr3:129251192 C>T maps to NM_000539.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:129251192 C>A maps to NM_000539.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr3:49412904 C>A maps to NM_001664.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:20647420 C>T maps to NM_004040.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:20647702 C>A maps to NM_004040.2 C159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:20647631 C>T maps to NM_004040.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:62634765 G>A maps to NM_014836.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:62652602 C>A maps to NM_014836.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:22873256 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:22868121 C>T maps to NM_001160036.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:22864675 G>T maps to NM_001160036.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:22874894 G>T maps to NM_001160036.1 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:95067574 C>T maps to NM_014899.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:95091259 C>T maps to NM_014899.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:66834239 G>T maps to NM_014578.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:66834275 C>T maps to NM_014578.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:66833437 C>T maps to NM_014578.3 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:122217460 G>C maps to NM_019034.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:40245053 G>C maps to NM_004310.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:40245026 C>A maps to NM_004310.3 C7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr14:63735887 T>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr14:63747807 C>A maps to NM_020663.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:63747783 C>T maps to NM_020663.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:63757699 G>A maps to NM_020663.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:63735880 G>T maps to NM_020663.3 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:46770307 C>T maps to NM_012249.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:46808132 G>T maps to NM_012249.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr17:30526551 A>G maps to NM_001033568.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:720760 C>T maps to NM_138769.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr16:722737 A>T maps to NM_138769.1 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:228879187 G>T maps to NM_021205.4 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:228871752 T>A did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:119249423 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:119249648 G>T did not map to a codon.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr23:119249756 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:119243217 T>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:119249585 C>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:119246801 C>T did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr23:119249499 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:119293089 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:119293137 C>A did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr23:119210982 T>C did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr23:119210983 G>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:119293263 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:119211064 A>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:33493810 G>A maps to NM_033103.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:33517468 C>T maps to NM_033103.4 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:33490546 T>A maps to NM_033103.4 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:33486995 G>A maps to NM_033103.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:33490579 C>T maps to NM_033103.4 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:53453248 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:53456804 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:53455230 G>C did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:53457341 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:53457658 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:8132301 G>A maps to ENST00000309737 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr11:8161741 T>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:8161579 C>A maps to ENST00000309737 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:8158922 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:8159831 G>T maps to ENST00000309737 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:8161561 T>C maps to ENST00000309737 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:8158961 C>A maps to ENST00000309737 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:209513 G>C maps to NM_021932.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:212637 G>A maps to NM_021932.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:107209054 G>C maps to ENST00000392837 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:12844440 G>T maps to NM_014859.4 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:38953091 G>A maps to ENST00000296782 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:38959969 G>A maps to ENST00000296782 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:38963015 G>A maps to ENST00000296782 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:38950334 T>C maps to ENST00000296782 V1205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr5:39021180 G>T maps to ENST00000296782 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr5:38950544 C>T maps to ENST00000296782 T1135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:38964891 A>C did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr5:38950136 C>T maps to ENST00000296782 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:152300041 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:152273318 A>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:152291975 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:152319894 A>C maps to NM_018151.4 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr2:152331515 T>C maps to NM_018151.4 C2450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:152314447 G>T maps to NM_018151.4 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:1551211 G>A maps to NM_031430.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:123983147 C>T maps to NM_178314.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr12:123900452 C>T maps to NM_145058.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:130912819 G>A maps to NM_015347.4 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:130941232 C>A maps to NM_015347.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:130963549 C>T maps to NM_015347.4 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:130926813 G>A maps to NM_015347.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:130898774 C>T maps to NM_015347.4 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr12:130921587 G>A maps to NM_015347.4 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:130898707 C>A maps to NM_015347.4 E872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr12:130898839 G>A maps to NM_015347.4 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:130926750 G>T maps to NM_015347.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr12:130934761 G>A maps to NM_015347.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:130892269 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr12:130927173 C>T maps to NM_015347.4 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr22:20458190 G>T maps to NM_015672.1 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:42880470 A>G maps to NM_173642.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:8906615 C>T maps to NM_020734.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:72960916 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:73110205 C>T maps to NM_014989.4 V1623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:73110292 G>A maps to NM_014989.4 V1652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:73110195 A>G did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:72889468 C>A maps to NM_014989.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:72806747 G>T maps to NM_014989.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:73023351 T>G maps to NM_014989.4 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:72889553 C>T maps to NM_014989.4 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:104513164 C>A maps to NM_001100117.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:105025732 C>A maps to NM_001100117.2 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr8:104898360 T>C maps to NM_001100117.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105261775 C>G maps to NM_001100117.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:104930686 T>C maps to NM_001100117.2 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr8:105026763 A>T maps to NM_001100117.2 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:104897841 T>C maps to NM_001100117.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:104897786 C>G maps to NM_001100117.2 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:105025750 C>A maps to NM_001100117.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr8:105001616 C>T maps to NM_001100117.2 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:104513212 G>A maps to NM_001100117.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr8:104897786 C>G maps to NM_001100117.2 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:104955026 A>G maps to NM_001100117.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:105001559 G>T maps to NM_001100117.2 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr8:104955057 C>T maps to NM_001100117.2 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:105263928 G>T maps to NM_001100117.2 G1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:104928672 A>T maps to NM_001100117.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:104831843 C>T maps to ENST00000262231 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:104973291 G>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:105260982 G>A maps to NM_001100117.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr8:105261042 T>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:104955076 C>A maps to NM_001100117.2 S875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:105257205 G>T maps to NM_001100117.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:104922392 G>T maps to NM_001100117.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:104922380 G>A maps to NM_001100117.2 W548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:104943520 C>T maps to NM_001100117.2 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:41092229 G>A maps to NM_014747.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:43385673 G>A maps to NM_182970.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:43399959 G>A maps to NM_182970.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr11:66099815 A>T maps to NM_004292.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:66103127 G>C maps to NM_004292.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:19955659 C>T maps to ENST00000255006 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr20:19955754 G>A maps to ENST00000255006 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:19970731 C>T maps to ENST00000255006 H664H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:19955397 C>G maps to ENST00000255006 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr14:93118140 C>T maps to NM_024832.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:93022233 G>A maps to NM_024832.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:93118098 G>T maps to NM_024832.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:93125680 G>T maps to NM_024832.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr14:93142835 G>A maps to NM_024832.3 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:93043769 G>A maps to NM_024832.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr14:93118854 G>T maps to NM_024832.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:33179628 C>T maps to NM_002931.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:33179099 C>T maps to NM_002931.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:39359958 G>A maps to NM_001195833.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr7:105195642 C>G maps to NM_021930.4 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:105187512 C>G maps to NM_021930.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr6:7410648 G>T maps to NM_031480.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:96513553 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr5:96503331 A>G maps to NM_018343.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:21053584 C>T maps to NM_003831.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:21059324 A>G maps to NM_003831.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:3111187 T>C maps to NM_003804.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr6:3111055 C>T maps to NM_003804.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:90775203 A>T maps to NM_003821.5 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr8:90777627 C>T maps to NM_003821.5 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr8:90777657 T>C maps to NM_003821.5 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:24807127 T>C maps to NM_006871.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:24808682 C>A maps to NM_006871.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43161677 G>A maps to ENST00000352483 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:106145411 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:106144711 G>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:106144761 C>G did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:106144007 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:84563491 G>T maps to NM_001009994.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:84563412 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:155880280 G>A maps to ENST00000368322 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:155870378 G>A maps to ENST00000368322 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:40503706 C>A maps to NM_002930.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:40554089 G>C maps to NM_002930.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr18:40503614 G>A maps to NM_002930.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr18:40503686 C>T maps to NM_002930.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:40695436 G>T maps to NM_002930.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:89760549 C>T maps to NM_000326.4 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr15:89758398 G>A maps to NM_000326.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:89761918 G>T maps to NM_000326.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:40627277 A>T maps to NM_012421.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40697320 A>T maps to NM_012421.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:40701711 G>A maps to NM_012421.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:40627274 C>G maps to NM_012421.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:40705941 C>T maps to NM_012421.3 S1856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:40661419 A>C maps to NM_012421.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:73812541 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:73812089 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:73811611 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:73812217 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:73812446 T>C did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:73811821 C>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:73811919 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:73812468 T>A did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:73811605 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:73811801 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:73812085 G>T did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:73811942 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:73812769 C>T did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:73815766 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:73811406 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:5339539 C>A maps to NM_006911.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:5335487 T>A maps to NM_006911.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr9:5304439 G>A maps to NM_134441.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr9:5300118 T>C maps to NM_134441.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr16:67686372 A>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:67685585 A>G did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr16:67681060 G>A maps to NM_001013838.1 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr16:67682106 C>T maps to NM_001013838.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr16:67686424 G>T maps to NM_001013838.1 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:67681431 C>A maps to NM_001013838.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr9:86616176 G>A maps to NM_024945.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:86617751 G>A maps to NM_024945.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr9:86616725 A>T maps to NM_024945.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr2:86992311 A>G maps to NM_022780.3 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr14:21269840 C>T maps to NM_198235.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:20978752 C>T maps to ENST00000430083 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:20978830 G>T maps to ENST00000430083 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:20979088 C>T maps to ENST00000430083 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr14:20979112 C>G maps to ENST00000430083 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:21052267 G>T maps to NM_145250.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:21052126 G>T maps to NM_145250.3 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:21052078 T>A maps to NM_145250.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:21058503 C>A maps to NM_001024822.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:21058510 G>A maps to NM_001024822.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr14:21501985 C>G maps to NM_001012264.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr14:21501991 G>A maps to NM_001012264.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:21502327 G>T maps to NM_001012264.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr14:21502072 G>T maps to NM_001012264.3 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:21424253 C>A maps to NM_002934.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:21424286 T>C maps to NM_002934.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:21423972 C>T maps to NM_002934.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr14:21424019 A>G maps to NM_002934.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr14:21360129 C>G maps to NM_002935.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr14:21511198 G>T maps to NM_032572.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:21526350 C>T maps to NM_138331.1 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:21025066 T>C maps to NM_001110361.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr14:21025048 A>T maps to NM_001110361.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:21024739 G>C maps to NM_001110361.1 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr14:21025060 G>T maps to NM_001110361.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:3596228 C>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:3598003 C>A maps to NM_002936.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr13:51501613 G>T maps to NM_024570.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:51517455 G>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:51528087 T>C maps to NM_024570.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:182554507 G>A maps to NM_021133.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr1:182553257 G>T maps to NM_021133.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:31483735 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:31410942 C>A maps to NM_013235.4 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:31448685 T>C maps to NM_013235.4 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr5:31464413 T>A maps to NM_013235.4 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:31495407 C>A maps to NM_013235.4 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:31464399 C>A maps to NM_013235.4 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:167344530 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:49255800 T>A maps to NM_014470.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:151326542 C>A maps to NM_005168.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:121001250 G>A maps to ENST00000458409 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr12:121001394 C>A maps to ENST00000458409 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:86847580 C>A maps to NM_005667.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:86831034 C>G maps to NM_005667.3 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:59323898 C>G maps to ENST00000434298 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:19318605 C>G maps to NM_007148.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr17:19317897 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr17:19316282 G>T maps to NM_007148.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:119004597 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:119004823 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:119005294 C>G did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:119005191 C>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:119005488 G>A did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:119005282 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:119005496 G>T did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:119005321 G>A did not map to a codon.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr23:119005002 T>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:119005483 T>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:98829157 G>T maps to NM_178861.4 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:145611283 A>T maps to NM_014455.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:145663205 C>G maps to NM_014455.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:33416287 C>A maps to NM_024787.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:49758499 C>T maps to NM_022064.2 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:49750009 C>T maps to NM_022064.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr18:29648258 A>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr18:29648259 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:106016174 A>C did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:106038879 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:106034404 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:105937353 G>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:106016272 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:105970442 G>C did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:105970358 C>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:106033447 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:105970513 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:105970489 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:106033442 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:105970234 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:179467603 G>A maps to NM_018434.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr7:122338651 C>A maps to NM_139175.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:122338252 T>A maps to NM_139175.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:122338096 T>A maps to NM_139175.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122338099 C>A maps to NM_139175.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:29325908 G>A maps to NM_032322.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:125498687 C>T maps to NM_007218.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:125487416 G>T maps to NM_007218.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr8:125498171 G>A maps to NM_007218.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:125498768 C>T maps to NM_007218.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr8:125498477 G>A maps to NM_007218.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr8:125499536 C>T maps to NM_007218.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:10540597 C>T maps to NM_016422.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:7164553 C>T maps to NM_014746.3 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:7170333 G>A maps to NM_014746.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:7164643 G>T maps to NM_014746.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:18463604 A>T maps to NM_182757.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:158589948 G>A maps to NM_144726.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr5:158585761 T>A maps to NM_144726.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:158596029 C>A maps to NM_144726.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr7:122342642 C>T maps to NM_198085.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr7:122342158 T>A maps to NM_198085.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:101924612 G>T maps to NM_173647.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:101911638 T>A maps to NM_173647.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:141847163 G>A maps to NM_020724.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:141832457 C>A maps to NM_020724.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:59483459 G>A maps to NM_173557.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:59483516 C>A maps to NM_173557.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:59483585 C>T maps to NM_173557.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr18:59483392 G>A maps to NM_173557.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr18:59483687 C>A maps to NM_173557.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:74150403 A>G maps to NM_052916.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74157642 G>T maps to NM_052916.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr17:74158668 A>G maps to NM_052916.2 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:74155588 G>A maps to NM_052916.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr21:30353439 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:30319882 T>A maps to NM_015565.2 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:30315658 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr21:30324586 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr21:30304986 C>A did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr21:30359173 G>A maps to NM_015565.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr18:44013279 C>A maps to NM_152470.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr3:196229918 C>A maps to NM_152617.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:196229810 C>A maps to NM_152617.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:196210726 G>A maps to NM_152617.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr11:74547637 C>T maps to NM_001098638.1 Q664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:25442835 C>T maps to ENST00000381927 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr13:25356049 G>A maps to ENST00000381927 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr13:25428046 C>T maps to ENST00000381927 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:25362200 C>T maps to ENST00000381927 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr13:25404637 G>A maps to ENST00000381927 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:25406055 G>T maps to ENST00000381927 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:25419097 G>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr13:25370317 C>A maps to ENST00000381927 C428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr13:25370275 T>C maps to ENST00000381927 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr13:25353860 C>T maps to ENST00000381927 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr13:25433214 G>A maps to ENST00000381927 W1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:42725240 G>A maps to NM_030954.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:154669892 G>T maps to ENST00000274068 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr5:63510243 C>A maps to NM_001113561.1 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr6:13977460 G>T maps to NM_001165033.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:116060425 G>A maps to NM_145051.3 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:116060188 G>A maps to NM_145051.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:20141126 G>C maps to NM_019062.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:101276265 A>C maps to NM_183419.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr8:101287226 A>G maps to NM_183419.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr1:33402415 G>C maps to NM_153341.2 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr9:104314691 C>T maps to NM_019592.5 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr9:104303257 G>C did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:104307161 C>T maps to NM_019592.5 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr9:104314735 G>A maps to NM_019592.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:104324193 G>A maps to NM_019592.5 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:104314666 A>G maps to NM_019592.5 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:6267531 G>C maps to NM_207396.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:6279358 G>A maps to NM_207396.2 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:6269997 G>A maps to NM_207396.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:140115058 G>A maps to NM_031297.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:78319271 G>T maps to NM_020914.4 L2428L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-05-4427-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:78272183 G>T maps to NM_020914.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:78320201 C>T maps to NM_020914.4 I2738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:78321356 C>T maps to NM_020914.4 F3123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:78318884 C>T maps to NM_020914.4 F2299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:78359383 C>G maps to NM_020914.4 S4883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr17:78318845 G>T maps to NM_020914.4 P2286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:78293204 C>G maps to NM_020954.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:78280205 C>T maps to NM_020914.4 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:78318929 A>G maps to NM_020914.4 P2314P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-55-A490-01A-11D-A24D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:78262110 C>T maps to NM_020914.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:78327865 C>T maps to NM_020914.4 S3591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr17:78286893 G>A maps to NM_020914.4 W962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:78265622 G>T maps to NM_020914.4 G539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:78349666 A>T maps to NM_020914.4 P4443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr17:78357709 C>G maps to NM_020914.4 L4817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:78360640 C>A maps to NM_020914.4 R5007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr17:78261709 C>T maps to NM_020914.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:78262065 C>T maps to NM_020914.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr11:117152668 C>T maps to NM_207343.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:30782715 T>A maps to NM_001017981.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr22:30782130 C>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:5792596 G>A maps to NM_207111.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:5662682 C>G maps to NM_207111.2 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:5752386 G>A maps to NM_207111.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr6:125397804 C>A maps to NM_152553.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:125404009 G>T maps to NM_152553.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:45088459 G>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:219529493 C>A maps to NM_022453.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:119207085 C>T maps to NM_032015.3 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:119206044 C>T maps to NM_032015.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr14:24619312 C>T maps to NM_017999.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr14:24620761 A>T maps to NM_017999.4 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr14:24621035 C>T maps to NM_017999.4 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr14:24624870 C>T maps to NM_017999.4 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr7:156450896 C>A maps to NM_001184997.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr12:121854011 C>T maps to NM_194271.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:2515394 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:30776580 G>A maps to NM_014771.2 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr16:30777536 T>A maps to NM_014771.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:30778075 G>T maps to NM_014771.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:56439903 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:56492902 G>C maps to NM_017763.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:56435162 C>A maps to NM_017763.4 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:56438272 G>A maps to NM_017763.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:175956381 C>T maps to NM_014901.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:32148054 C>T maps to NM_006913.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr13:26789729 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:37336423 T>C maps to NM_003958.3 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr6:37358600 C>T maps to NM_183078.2 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr17:58035663 A>G maps to NM_016125.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:117191858 A>C maps to NM_001109903.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:117217092 C>A maps to NM_001109903.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:117290462 G>A maps to NM_032814.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:117271634 G>C maps to NM_001109903.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:89324033 C>T maps to NM_003800.3 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:500625 G>T maps to NM_203389.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr11:498909 G>C maps to NM_203389.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:90074240 T>C maps to NM_001031709.2 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr18:13742485 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr18:13737098 G>A maps to NM_003799.1 W215*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-17-Z022-01A-01W-0746-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-86-8074-01A-11D-2238-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr17:686376 C>T maps to NM_018146.2 I123I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MP-A4SV-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:2312758 G>A maps to NM_080594.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2313104 G>A maps to NM_080594.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:2314332 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:78666911 G>A maps to NM_002941.3 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:78795961 G>T maps to NM_002941.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:79174642 G>T maps to NM_002941.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr3:78649340 A>G maps to NM_002941.3 N1621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:78656192 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:78656105 C>T maps to NM_002941.3 V1507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:78717673 G>A maps to NM_002941.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:78766948 C>A maps to NM_002941.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr3:78666887 C>T maps to NM_002941.3 S1393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:78667097 A>G maps to NM_002941.3 D1323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:78708957 C>G did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:78766911 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:78766912 C>A maps to NM_002941.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr3:78685052 T>C maps to NM_002941.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:79638971 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:78667115 G>A maps to NM_002941.3 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr3:77612381 G>T maps to ENST00000332191 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:77147282 C>T maps to ENST00000332191 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr3:77626671 A>C maps to ENST00000332191 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77623726 G>A maps to ENST00000332191 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:77666735 G>T maps to ENST00000332191 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:77147289 G>T maps to ENST00000332191 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:77651553 T>G maps to ENST00000332191 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr3:77571937 A>G maps to ENST00000332191 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:77612411 C>T maps to ENST00000332191 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:77651499 C>A maps to ENST00000332191 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr3:77666735 G>T maps to ENST00000332191 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr3:77612378 A>G maps to ENST00000332191 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr3:77651358 A>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:77657048 C>G maps to ENST00000332191 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:77147252 G>T maps to ENST00000332191 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr3:77089947 G>A maps to ENST00000332191 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr3:77607126 C>T maps to ENST00000332191 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:77623697 C>T maps to ENST00000332191 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:77638084 G>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:124743983 A>T maps to NM_022370.3 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:124735485 C>T maps to NM_022370.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:124748656 C>A maps to NM_022370.3 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:124742392 G>A maps to NM_022370.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:124745496 G>A maps to NM_022370.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr11:124744062 C>T maps to NM_022370.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr11:124765506 T>C maps to NM_019055.5 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr11:124756660 G>A maps to NM_019055.5 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:124767119 G>A maps to NM_019055.5 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:124763627 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:124755026 G>T maps to NM_019055.5 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:124757054 G>T maps to NM_019055.5 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:124763798 C>G maps to NM_019055.5 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:124766429 G>T maps to NM_019055.5 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:124766981 G>T maps to NM_019055.5 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:124765731 C>A maps to NM_019055.5 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr11:124766981 G>T maps to NM_019055.5 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:124765722 T>A maps to NM_019055.5 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:124757284 C>A maps to NM_019055.5 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:124765389 A>T maps to NM_019055.5 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr18:18690843 G>A maps to NM_005406.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:18548809 C>A maps to NM_005406.2 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:18567065 C>A maps to NM_005406.2 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr18:18534822 G>C maps to NM_005406.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr18:18600167 C>A maps to NM_005406.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:11375868 G>A maps to NM_004850.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr2:11355772 T>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:11332365 A>G maps to NM_004850.3 P1357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:114994495 A>T maps to NM_001163790.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr9:115060192 C>A maps to NM_001163790.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:114989794 A>C maps to NM_001163790.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:4848119 G>T maps to NM_024589.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:62380968 G>A maps to NM_000327.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:62381160 C>A maps to NM_000327.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr5:10442326 C>T maps to NM_031916.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:10461346 G>T maps to NM_031916.3 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:64624701 C>T maps to NM_005012.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:64605915 T>C maps to NM_005012.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:64608316 T>A maps to NM_005012.2 C386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:64644309 G>A maps to NM_005012.2 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:64624662 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr9:94487167 G>A maps to NM_004560.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:94486258 C>T maps to NM_004560.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:94486198 G>A maps to NM_004560.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr9:94519680 C>G maps to NM_004560.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr9:94487236 C>A maps to NM_004560.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:94485994 C>T maps to NM_004560.2 G927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:60970878 G>C maps to NM_134261.2 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:60795031 A>C maps to NM_134260.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77257433 G>T maps to ENST00000396204 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr9:77275584 C>T maps to ENST00000396204 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:77282815 A>G maps to ENST00000396204 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77275591 G>T maps to ENST00000396204 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:77300495 G>T maps to ENST00000396204 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:117706998 G>C maps to NM_002944.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:117658333 C>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr6:117647510 G>A maps to NM_002944.2 C1811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:117710576 C>A maps to NM_002944.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr6:117609681 G>A maps to NM_002944.2 H2339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr6:117687260 C>T maps to NM_002944.2 Q930Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:55541511 A>T maps to NM_006269.1 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:55540659 A>G maps to NM_006269.1 K1406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:55533649 A>T maps to NM_006269.1 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr8:55540347 C>G maps to NM_006269.1 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr8:55538035 G>T maps to NM_006269.1 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:55537554 A>T maps to NM_006269.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:55534107 T>A maps to NM_006269.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:10470213 G>T maps to NM_178857.5 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:10465813 C>A maps to NM_178857.5 E1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:10473974 C>A maps to NM_178857.5 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:10466150 C>A maps to NM_178857.5 A1819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr8:10465304 T>C maps to NM_178857.5 V2101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:10469635 G>T maps to NM_178857.5 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:10468595 C>A maps to NM_178857.5 G1004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10466377 C>A maps to NM_178857.5 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:10469885 G>T maps to NM_178857.5 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:10468145 C>A maps to NM_178857.5 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr8:10468154 G>C maps to NM_178857.5 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:10470477 G>C maps to NM_178857.5 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:10480174 G>T maps to NM_178857.5 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:10465552 C>A maps to NM_178857.5 E2019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:10469309 C>A maps to NM_178857.5 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:10468634 C>T maps to NM_178857.5 E991E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr8:10469744 C>T maps to NM_178857.5 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:10480504 G>T maps to NM_178857.5 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:10468136 C>T maps to NM_178857.5 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:10468340 C>T maps to NM_178857.5 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:10470188 G>C maps to NM_178857.5 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:10470794 C>G maps to NM_178857.5 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr8:10470340 G>T maps to NM_178857.5 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:10469060 A>G maps to NM_178857.5 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr8:10465805 C>T maps to NM_178857.5 E1934E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:10466456 G>A maps to NM_178857.5 P1717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr8:10468679 C>T maps to NM_178857.5 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:10480578 G>T maps to NM_178857.5 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:10465880 C>A maps to NM_178857.5 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:10466663 G>T maps to NM_178857.5 G1648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:10466662 C>A maps to NM_178857.5 E1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr8:10470311 G>C maps to NM_178857.5 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:10470494 G>T maps to NM_178857.5 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:10468893 G>T maps to NM_178857.5 S905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:10469813 G>T maps to NM_178857.5 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:46713295 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:46713149 C>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:46713150 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:46712937 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:46719489 G>C did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:46713256 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:46713480 C>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:33134962 C>T maps to NM_203288.1 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:33134983 G>T maps to NM_203288.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:1798346 A>G maps to NM_002945.3 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:28223633 T>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:96139802 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:96139495 G>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:96139774 G>A did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:96139764 C>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:96139655 T>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:96139981 G>T did not map to a codon.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr23:96139809 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:96139887 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:96139984 C>G did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr23:96139560 G>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:5335887 C>G maps to NM_001033002.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr15:41823326 C>T maps to NM_015540.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:41810248 C>A maps to NM_015540.2 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:41829176 C>G maps to NM_015540.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:41822099 G>A maps to NM_015540.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:41823308 G>A maps to NM_015540.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:41823358 G>A maps to NM_015540.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr1:92789823 C>T maps to NM_024813.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:68895599 C>T maps to NM_000329.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68895517 G>T maps to NM_000329.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:68904917 C>A maps to NM_000329.2 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:68915576 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:68910478 G>T maps to NM_000329.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:68895526 C>A maps to NM_000329.2 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:84955399 A>C maps to NM_025065.6 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:84955386 C>T maps to NM_025065.6 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:84956126 T>A maps to NM_025065.6 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:38132680 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:38129065 A>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:38132699 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:38169931 C>A did not map to a codon.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr23:38132727 A>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:38146245 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:38150671 C>T did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:38176669 C>G did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:38144876 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:38146131 C>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:38158227 C>G did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:38146126 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:38160618 C>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:38145169 C>G did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:38146136 C>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:21790023 G>A maps to NM_020366.3 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:21795867 G>T maps to NM_020366.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:21796744 G>T maps to NM_020366.3 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr14:21788335 G>A maps to NM_020366.3 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:21779996 G>A maps to NM_020366.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21771690 T>A maps to NM_020366.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr14:21793122 A>T maps to NM_020366.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:21796580 A>T did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr14:21795872 C>T maps to NM_020366.3 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:21793436 G>C maps to NM_020366.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:53670418 C>A maps to NM_015272.2 E1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr16:53653060 G>T maps to NM_015272.2 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr16:53726276 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:53679815 G>A maps to NM_015272.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr16:53686794 G>T maps to NM_015272.2 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:113307818 T>A maps to NM_001143854.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:113307696 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:113319614 C>A maps to NM_001143854.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:113325607 C>A maps to NM_001143854.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:113314633 G>A maps to NM_001143854.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:113285518 C>A maps to NM_001143854.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:96917 C>A maps to NM_006987.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:153628873 A>G did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:153628149 A>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:153627736 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153627910 G>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:35438058 C>G maps to NM_007104.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr14:47120506 C>A maps to NM_080746.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr14:47120852 G>T maps to NM_080746.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr14:47120735 G>C maps to NM_080746.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:47120295 C>A maps to NM_080746.2 *215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:47120342 G>C maps to NM_080746.2 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:24021208 G>T maps to NM_000975.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr16:89628077 C>T maps to NM_033251.1 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:49993732 G>A maps to NM_012423.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr3:40503437 A>G maps to NM_001034996.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr3:23960892 T>A maps to NM_002948.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:17973772 G>A maps to NM_000980.2 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr17:37357504 C>T maps to NM_000981.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr13:27830438 G>T maps to NM_000982.3 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr3:170587947 C>T maps to NM_001099645.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:170587947 C>A maps to NM_001099645.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr17:27047845 G>A maps to ENST00000394938 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:55899328 G>T maps to NM_001136135.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr22:39709668 T>A maps to NM_000967.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr22:39713539 T>A maps to NM_000967.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:101619265 G>T maps to NM_000993.4 G35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:100646033 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr5:40834630 G>C maps to NM_000997.4 Y27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:186838965 C>T maps to NM_052969.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr16:1994858 C>T maps to NM_005061.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:1996682 C>T maps to NM_005061.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:1995910 C>T maps to NM_005061.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:2004080 C>A maps to NM_005061.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:93306113 G>T maps to NM_000969.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7030-01A-11D-1945-08 chr1:93306106 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:74203859 G>C maps to ENST00000396470 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr8:74204484 G>A maps to ENST00000396470 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:136217158 C>T maps to NM_000972.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:42851244 C>T maps to NM_198486.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:146017269 C>A maps to NM_000973.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:146017400 G>A maps to NM_000973.3 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr4:39458035 C>A maps to NM_000661.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr3:128356926 C>T maps to NM_002950.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr3:128356932 T>G maps to NM_002950.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:35860772 G>T maps to NM_002951.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr20:35826892 G>T maps to NM_002951.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:35812691 G>T maps to NM_002951.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:58296073 C>T maps to NM_007042.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:92660373 C>A maps to ENST00000458617 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr10:92656111 G>A maps to ENST00000458617 A242A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-91-6848-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:5002425 C>T maps to NM_006638.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:33606994 C>G maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:33610791 T>G maps to NM_018170.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr18:33610848 C>T maps to NM_018170.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr20:36718246 C>G maps to NM_021215.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:36694588 G>A maps to NM_021215.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:150444485 C>G maps to NM_015203.3 S1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:150443310 G>A maps to NM_015203.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:150337288 G>T maps to NM_015203.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:150444441 G>C maps to NM_015203.3 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr2:154335040 G>T maps to NM_019845.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:17097026 G>A maps to NM_001017.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:149826405 G>A maps to NM_005617.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:39924008 A>T maps to NM_001020.4 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:33243777 C>T maps to NM_022551.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:55462634 T>C maps to NM_001177413.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr11:75115887 C>T maps to NM_001005.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:75115246 A>G maps to NM_001005.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:75115251 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:152025385 C>T maps to NM_001006.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:71493197 T>C did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:71496037 T>C did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr24:2712265 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr24:22921813 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr24:22921761 T>C did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:58904808 G>A maps to NM_001009.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr9:19378871 G>A maps to NM_001010.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:26887236 G>T maps to NM_001006665.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:166845887 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:20173623 A>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr23:20195193 A>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:20185762 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:20185763 C>A did not map to a codon.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr23:20181106 C>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:20187546 C>G did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:20212339 C>A did not map to a codon.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr23:20222212 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:64135650 G>T maps to NM_003942.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:91360852 G>A maps to NM_004755.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:91526736 G>T maps to NM_004755.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr14:91360903 T>C maps to NM_004755.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:83374965 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:83372408 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:83319978 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:83362700 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:83320045 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:83390110 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:83361408 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr23:83359664 C>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:83403091 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:83320108 G>A did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:83403064 T>C did not map to a codon.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr23:83402033 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:83371265 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:83411146 T>A did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:83360848 C>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr23:83352824 C>T did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:83372086 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:58011873 C>T maps to NM_003161.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:58024112 C>T maps to NM_003161.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:67200237 G>T maps to NM_003952.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:213414787 C>T maps to NM_012424.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:213445952 G>C maps to NM_012424.3 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:213445952 G>T maps to NM_012424.3 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:213277907 C>T maps to NM_012424.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr1:213414360 A>G maps to NM_012424.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:213303051 G>T maps to NM_012424.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:213415083 C>G maps to NM_012424.3 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:75388085 C>A maps to NM_031464.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr14:75388073 G>T maps to NM_031464.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:75376449 G>A maps to NM_031464.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:3623450 C>G maps to NM_001011.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr2:3627798 G>C maps to NM_001011.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:54711355 G>T maps to NM_001013.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr3:39449254 C>T maps to ENST00000443003 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:39453810 C>T maps to ENST00000443003 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:152128581 G>T maps to NM_001122965.1 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:152128886 G>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:152127333 G>T maps to NM_001122965.1 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:152127444 G>T maps to NM_001122965.1 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr17:78811790 G>A maps to NM_020761.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr17:78919497 G>A maps to NM_020761.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:78704505 G>A maps to NM_020761.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:78617594 G>A maps to NM_020761.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr15:40866102 G>A maps to NM_152260.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:126081367 C>A maps to NM_032795.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:219452360 A>C maps to NM_005444.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:219458846 A>T maps to NM_005444.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr9:19050307 C>T maps to NM_006570.4 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:55777610 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:55784733 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:55744766 G>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:55755772 G>C did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:55755792 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:55779872 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:55757833 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:55784771 G>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:39321546 G>A maps to NM_022157.2 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:90077867 C>G maps to NM_021244.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr6:90077867 C>T maps to NM_021244.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr6:90097286 G>A maps to NM_021244.4 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:17600358 C>T maps to ENST00000377813 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:17602406 C>T maps to ENST00000377813 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr20:17640863 G>A maps to ENST00000377813 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr20:17622537 C>T maps to ENST00000377813 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr6:7231085 C>A maps to NM_001003699.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:7231128 G>T maps to NM_001003699.3 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:7231532 C>T maps to NM_001003699.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:7230138 G>T maps to NM_001003699.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr6:7211109 C>T maps to NM_001003699.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:7229348 G>A maps to NM_001003699.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:7230980 G>T maps to NM_001003699.3 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:7231253 A>T maps to NM_001003699.3 A974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr6:7230035 G>T maps to NM_001003699.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:7230731 G>T maps to NM_001003699.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr11:4133142 A>T maps to NM_001033.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:4156358 G>T maps to NM_001033.3 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:10263557 G>A maps to NM_001165931.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:103244532 C>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:45220426 G>T maps to NM_003683.5 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr21:45217389 C>A maps to NM_003683.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr21:45220444 C>T maps to NM_003683.5 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:99130005 C>A maps to NM_015179.3 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:99144969 C>A maps to NM_015179.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:99150224 C>T maps to NM_015179.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:99126614 G>C maps to NM_015179.3 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr10:99125988 G>A maps to NM_015179.3 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:99139473 C>A maps to NM_015179.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:45106769 G>A maps to NM_015056.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr21:45113110 G>C maps to NM_015056.2 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr21:45107883 T>G maps to NM_015056.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr21:45103217 C>T maps to NM_015056.2 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:6621897 C>A did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr11:6622683 T>A maps to NM_015324.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:6622512 C>A maps to NM_015324.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:51971705 C>A maps to NM_004704.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:51969220 C>T maps to NM_004704.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:18660248 A>T did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:18665333 G>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:18675775 C>A did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:48560833 G>A maps to NM_018346.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:48560017 C>T maps to NM_018346.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:7035937 G>T maps to NM_080657.4 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:7036000 T>C maps to NM_080657.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:114309075 C>T did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:114354884 A>C maps to NM_018364.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:114354881 C>A maps to NM_018364.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:114308934 C>A maps to NM_018364.3 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:114308766 T>A maps to NM_018364.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:77402526 C>G maps to NM_198467.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr7:77378975 T>C maps to NM_198467.2 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr7:77408136 C>T maps to NM_198467.2 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr1:15986767 C>T maps to NM_006511.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:77413234 C>A maps to NM_016578.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr11:77378461 G>A maps to NM_016578.3 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:77412086 C>T maps to NM_016578.3 Q729Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:11931799 C>A maps to NM_015659.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr16:11933608 G>A maps to NM_015659.2 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr15:55489022 G>A maps to NM_016304.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:43896061 G>T maps to NM_080860.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr21:43896055 C>A maps to NM_080860.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr7:6797500 C>T maps to NM_173565.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:5966162 A>G maps to NM_173565.3 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:116949478 C>T maps to NM_001010892.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46318260 T>A maps to NM_030785.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:46299363 T>C maps to NM_030785.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:43638550 G>A maps to NM_152732.4 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr1:38082222 G>A maps to NM_001038633.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:38082183 G>T maps to NM_001038633.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:38079495 G>T maps to NM_001038633.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:38078563 G>T maps to NM_001038633.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr8:109001376 G>A maps to NM_178565.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr6:127440427 C>A maps to ENST00000368317 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:948682 G>T maps to NM_001029871.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr20:948617 G>A maps to NM_001029871.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr20:944659 G>T maps to NM_001029871.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr16:57265199 C>T maps to NM_133368.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:57243044 A>T maps to NM_133368.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr16:57261317 G>A maps to NM_133368.1 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:157920996 A>T maps to NM_016625.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:158072674 A>G maps to NM_016625.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:122992896 G>A maps to NM_023012.5 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:122990162 G>A maps to NM_023012.5 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:122990163 A>G maps to NM_023012.5 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:16859038 C>T maps to NM_012425.3 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:12940752 C>T maps to NM_031429.1 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:12936645 C>A maps to NM_031429.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:100757054 C>T maps to NM_001130841.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:100732077 A>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr22:23404055 T>A maps to NM_014433.2 K241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr22:23401804 C>T maps to NM_014433.2 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62312041 C>T maps to ENST00000482936 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:62292694 G>C maps to ENST00000482936 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr20:62298881 G>T maps to ENST00000482936 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:62319325 C>T maps to ENST00000482936 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:41750014 G>A maps to NM_015138.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:41762492 G>T maps to NM_015138.4 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr10:64000898 A>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr14:101348392 G>T maps to NM_001134888.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:101350918 C>T maps to NM_001134888.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr14:101349286 G>A maps to NM_001134888.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:60074058 G>A maps to NM_021136.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:60213092 A>G maps to NM_021136.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr14:60072160 C>A maps to NM_021136.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:60193879 C>A maps to NM_021136.2 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr14:60213199 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr14:60074097 G>A maps to NM_021136.2 Y626Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:60337147 G>A maps to NM_021136.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr14:60194213 G>A maps to NM_021136.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:60193682 T>C maps to NM_021136.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:60072180 G>A maps to NM_021136.2 Q673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr14:60212834 G>T maps to NM_021136.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:45998024 G>T maps to NM_005619.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:45992752 C>T maps to NM_005619.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr19:45989341 C>T maps to NM_005619.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:63486519 A>G maps to ENST00000377819 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:55253824 T>C maps to NM_020532.4 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:55253784 C>A maps to NM_020532.4 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:55253341 C>T maps to NM_020532.4 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:107035615 G>A maps to NM_032730.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:20229974 G>A maps to ENST00000425986 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:1840377 G>A maps to NM_178568.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:1840533 C>A maps to NM_178568.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr3:186917761 A>T maps to NM_153708.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:186915362 C>T maps to NM_153708.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:186917743 G>T maps to NM_153708.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:187416723 G>T maps to NM_001004312.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:187416441 C>T maps to NM_001004312.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:46542094 G>A maps to NM_031440.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:187088746 T>C maps to NM_022147.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr18:67801778 T>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr18:67697256 C>T maps to NM_173630.3 L1912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:67718784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr18:67809533 C>A maps to NM_173630.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr18:67794906 G>A maps to NM_173630.3 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:67733104 T>A maps to NM_173630.3 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr18:67863749 G>A maps to NM_173630.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:67794892 G>A maps to NM_173630.3 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr18:67781804 G>A maps to NM_173630.3 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:67802463 T>C maps to NM_173630.3 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr18:67718689 C>A maps to NM_173630.3 P1760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr18:67753921 T>G did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr18:67688030 T>A maps to NM_173630.3 S1991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:67860645 T>A maps to NM_173630.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr18:67872873 G>A maps to NM_173630.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr18:67698115 C>T maps to NM_173630.3 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr18:67812964 C>A maps to NM_173630.3 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:70154088 G>C maps to NM_017987.4 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:70156547 C>T maps to NM_017987.4 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:71588304 G>T maps to NM_001037442.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr4:71660565 C>T maps to NM_001037442.2 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:218954037 G>T maps to NM_198483.3 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:41143702 C>T maps to NM_173079.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr16:12145986 C>T maps to NM_032167.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:12142250 G>T maps to NM_032167.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr16:12145857 C>T maps to NM_032167.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr17:42386247 C>T maps to NM_001144825.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:42390610 C>A maps to NM_001144825.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr21:36265260 C>T did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:92998349 A>T did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:92982957 C>A maps to NM_175634.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr8:93088223 G>A maps to NM_175634.2 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:93026809 T>A maps to NM_175634.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr8:92999138 T>G maps to NM_175634.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr8:92998433 G>T maps to NM_175634.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr8:92982939 C>A maps to NM_175634.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:93004038 G>T maps to NM_175634.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr8:93003957 G>T maps to NM_175634.2 Y300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:93088268 G>C maps to NM_175634.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr8:93023227 A>G did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr8:92988172 A>T maps to NM_175634.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:45514705 C>A maps to ENST00000359524 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:25228822 C>A maps to NM_001031680.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:25256083 G>T maps to NM_001031680.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:25291041 G>A maps to NM_001031680.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:25229131 G>C maps to NM_001031680.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:25245809 A>T maps to NM_001031680.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:155292330 G>A maps to NM_001105203.1 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:155292199 C>G maps to NM_001105203.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:155296854 C>G maps to NM_001105203.1 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr9:35547522 T>A maps to NM_001135999.1 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:35547963 G>A maps to NM_001135999.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:127842453 C>T maps to NM_003707.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:127806629 G>A maps to NM_003707.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr3:127842495 C>T maps to NM_003707.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:127820452 T>A maps to NM_003707.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:127816234 G>A maps to NM_003707.2 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:49506545 C>G maps to NM_006666.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:49519072 G>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr6:83905765 C>T maps to NM_033411.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr21:30380094 C>A maps to NM_016940.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr4:159533308 C>T maps to ENST00000440678 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:159568168 A>C maps to ENST00000440678 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:159572981 G>T maps to ENST00000440678 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr4:159493973 T>C maps to ENST00000440678 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr4:159572993 A>T maps to ENST00000440678 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:159520481 C>A maps to ENST00000440678 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr13:32339228 A>C maps to NM_130806.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:32360702 G>C maps to NM_130806.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:32376334 G>A maps to NM_130806.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:32356836 T>C maps to NM_130806.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr13:32352716 G>A maps to NM_130806.3 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:32355866 C>A maps to NM_130806.3 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr13:32376301 A>T maps to NM_130806.3 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:33937207 C>A maps to NM_016568.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:33937261 G>A maps to NM_016568.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:33937085 C>A maps to NM_016568.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr5:33937387 C>A maps to NM_016568.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:33937436 C>A maps to NM_016568.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr5:33937450 C>T maps to NM_016568.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:33937058 G>T maps to NM_016568.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr5:33937684 G>T maps to NM_016568.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:33937000 G>T maps to NM_016568.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:33936955 G>A maps to NM_016568.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:155911748 G>A maps to NM_181885.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr1:155912576 C>T maps to NM_181885.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:33165611 C>T maps to ENST00000374685 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:165378823 G>A maps to NM_006917.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:165378912 G>A maps to NM_006917.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:165397988 T>A maps to NM_006917.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:165398198 G>T maps to NM_006917.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:165397964 G>T maps to NM_006917.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:165380319 G>A maps to NM_006917.4 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:165380218 T>C maps to NM_006917.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133913962 C>G maps to ENST00000296084 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:133910782 T>G maps to ENST00000296084 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:38995660 G>A maps to NM_000540.2 K2750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:38934436 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:39013885 G>T maps to NM_000540.2 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:39037099 G>T maps to NM_000540.2 E4010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:38954166 G>C maps to NM_000540.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:39025445 C>T maps to NM_000540.2 I3782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:38986923 G>A maps to NM_000540.2 T2206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:39075605 G>T maps to NM_000540.2 V4890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:39019688 G>C maps to NM_000540.2 T3711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:38960150 G>T maps to NM_000540.2 E1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr19:38949876 C>G maps to NM_000540.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38997148 G>T maps to NM_000540.2 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:38980056 A>T maps to NM_000540.2 K1930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:39008032 T>C maps to NM_000540.2 C3240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:38951173 C>T maps to NM_000540.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr19:38995478 C>G maps to NM_000540.2 S2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:38984998 G>A maps to NM_000540.2 L2094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr19:39018977 G>T maps to NM_000540.2 V3619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:39023366 C>G maps to NM_000540.2 V3750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:39009872 G>A maps to NM_000540.2 V3346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:39034011 G>A maps to NM_000540.2 Q3905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:38959648 G>A maps to NM_000540.2 W1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:38969089 C>T maps to NM_000540.2 N1490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:38946364 C>T maps to NM_000540.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:38980786 G>T maps to NM_000540.2 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:38966065 C>A maps to NM_000540.2 P1423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:38931491 T>C maps to NM_000540.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:39052026 C>G maps to NM_000540.2 S4186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:38939428 G>A maps to NM_000540.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr19:38951197 C>T maps to NM_000540.2 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr19:38939305 C>A maps to NM_000540.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:39002947 C>T maps to NM_000540.2 A3099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:38974003 G>T maps to NM_000540.2 L1594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:38993319 C>T maps to NM_000540.2 T2596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:38964324 G>C maps to NM_000540.2 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr19:38983276 G>A did not map to a codon.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:38933074 G>C maps to NM_000540.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr19:38976775 C>T maps to NM_000540.2 R1827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:38948828 C>A maps to NM_000540.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:39013724 C>T maps to NM_000540.2 G3439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr19:38951107 G>A maps to NM_000540.2 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr19:38951108 C>A maps to NM_000540.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:38993164 G>T maps to NM_000540.2 E2545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:39026032 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:237791357 A>T maps to NM_001035.2 K2140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:237947326 C>A maps to NM_001035.2 L4105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:237774249 T>A maps to NM_001035.2 P1624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr1:237791245 G>T maps to NM_001035.2 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:237948091 C>A maps to NM_001035.2 S4360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:237948032 G>T maps to NM_001035.2 E4341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:237608810 T>C maps to NM_001035.2 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:237947500 C>A maps to NM_001035.2 P4163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:237819146 G>A maps to NM_001035.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237765335 T>C maps to NM_001035.2 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:237872293 G>T maps to NM_001035.2 G3346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237756931 G>T maps to NM_001035.2 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:237791134 C>T maps to NM_001035.2 T2065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:237777470 T>C maps to NM_001035.2 D1681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237617850 C>A maps to NM_001035.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237620012 G>T maps to NM_001035.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:237995919 G>T maps to NM_001035.2 R4959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:237886546 T>C maps to NM_001035.2 L3558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:237895399 C>T maps to NM_001035.2 L3664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:237789018 G>T maps to NM_001035.2 G2027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:237947041 G>C maps to NM_001035.2 V4010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237881822 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:237936817 A>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:237711772 G>A maps to NM_001035.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:237758926 C>A maps to NM_001035.2 A1522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237729942 G>A maps to NM_001035.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237798279 G>A maps to NM_001035.2 P2260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:237955445 G>T maps to NM_001035.2 T4535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:237993831 C>T maps to NM_001035.2 T4886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:237777894 A>T maps to NM_001035.2 K1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237777446 C>A maps to NM_001035.2 A1673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:237780584 G>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr1:237947675 G>T maps to NM_001035.2 E4222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:237947957 G>T maps to NM_001035.2 G4316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:237947773 C>A maps to NM_001035.2 T4254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:237813175 G>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:237608789 G>T maps to NM_001035.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:237948019 C>T maps to NM_001035.2 D4336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:237837441 C>A maps to NM_001035.2 A2879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:237944869 C>A maps to NM_001035.2 S3962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237538082 G>T maps to NM_001035.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:237580396 T>A maps to NM_001035.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:237777542 G>T maps to NM_001035.2 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:237620006 C>G maps to NM_001035.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:237948082 C>A maps to NM_001035.2 A4357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237666759 C>A maps to NM_001035.2 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237780725 C>T maps to NM_001035.2 N1952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:237886430 G>T maps to NM_001035.2 E3520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:237813178 A>G maps to NM_001035.2 A2505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:237732577 C>A maps to NM_001035.2 S1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:237872778 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237802405 G>A maps to NM_001035.2 G2340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:237948113 G>T maps to NM_001035.2 E4368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:237617732 C>A maps to NM_001035.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:237947743 C>A maps to NM_001035.2 A4244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:237777350 C>T maps to NM_001035.2 I1641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:237777908 C>A maps to NM_001035.2 T1827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:237965170 T>C maps to NM_001035.2 D4702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:237777521 G>A maps to NM_001035.2 L1698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:237756789 G>T maps to NM_001035.2 V1430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:237659885 G>T maps to NM_001035.2 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:237777746 T>C maps to NM_001035.2 N1773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:237947704 G>T maps to NM_001035.2 P4231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:237777743 T>C maps to NM_001035.2 S1772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:237955550 C>A maps to NM_001035.2 P4570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:237777542 G>C maps to NM_001035.2 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:237791260 G>T maps to NM_001035.2 T2107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:237632443 C>T maps to NM_001035.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:237798187 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:237580423 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:237666753 A>G maps to NM_001035.2 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:237664095 C>A maps to NM_001035.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:237870339 C>A maps to NM_001035.2 S3224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:237947053 C>G maps to NM_001035.2 L4014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:237837453 C>A maps to NM_001035.2 A2883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr1:237754008 C>T maps to NM_001035.2 Q1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:237923131 C>T maps to NM_001035.2 A3794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:237895441 G>T maps to NM_001035.2 E3678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:237666651 T>A maps to NM_001035.2 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:237753162 C>A maps to NM_001035.2 T1223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:237777704 A>T maps to NM_001035.2 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:237886465 C>T maps to NM_001035.2 Y3531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237754043 G>A maps to NM_001035.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:237947111 G>T maps to NM_001035.2 E4034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237604626 G>A maps to NM_001035.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:237870569 G>T did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:237886563 T>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:237580398 G>A maps to NM_001035.2 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:237965164 C>A maps to NM_001035.2 S4700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:237660044 C>G maps to NM_001035.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:237955568 T>A maps to NM_001035.2 A4576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr1:237947591 G>T maps to NM_001035.2 E4194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:237540733 T>A maps to NM_001035.2 L192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:237753237 C>A maps to NM_001035.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:237791242 C>A maps to NM_001035.2 A2101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:237794802 G>T maps to NM_001035.2 E2173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:237753195 G>A maps to NM_001035.2 E1234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:237941997 A>G maps to NM_001035.2 A3936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:237777788 C>G maps to NM_001035.2 L1787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:237947221 G>T maps to NM_001035.2 A4070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr1:237948061 G>A maps to NM_001035.2 E4350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr1:237551424 G>T maps to NM_001035.2 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:237895413 C>A maps to NM_001035.2 I3668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:237947485 C>A maps to NM_001035.2 T4158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:237947599 C>A maps to NM_001035.2 T4196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:237948049 G>A maps to NM_001035.2 G4346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:237789030 C>A maps to NM_001035.2 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:237947923 C>A maps to NM_001035.2 G4304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:237823341 T>C maps to NM_001035.2 L2756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:237972325 T>C maps to NM_001035.2 D4808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:237993828 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:237666693 G>A maps to NM_001035.2 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:237777401 C>A maps to NM_001035.2 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:237813349 C>A maps to NM_001035.2 T2562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:237780641 C>A maps to NM_001035.2 A1924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:237729894 C>A maps to NM_001035.2 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:237880545 C>A maps to NM_001035.2 R3458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:237729936 A>T maps to NM_001035.2 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:237732487 G>A maps to NM_001035.2 W1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:237580372 T>C maps to NM_001035.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:237841399 G>A maps to NM_001035.2 K2961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:237713890 G>T maps to NM_001035.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:237947836 C>A maps to NM_001035.2 T4275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:237620025 G>T maps to NM_001035.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:237729922 G>T maps to NM_001035.2 E1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:237778121 G>T maps to NM_001035.2 L1898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:237951286 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr1:237659945 C>A maps to NM_001035.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:237777860 A>C maps to NM_001035.2 G1811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr1:237729882 G>A maps to NM_001035.2 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:237823307 A>T maps to NM_001035.2 G2744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:237948055 G>A maps to NM_001035.2 E4348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr1:237893640 G>A maps to NM_001035.2 L3640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:34102735 C>G maps to NM_001036.3 S3361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:33962734 G>A maps to NM_001036.3 T1946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:34146974 C>A maps to NM_001036.3 L4623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr15:34157384 C>A maps to NM_001036.3 A4857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:33945071 C>A maps to NM_001036.3 G1432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:33936548 C>T maps to NM_001036.3 I1198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr15:33878259 G>A maps to NM_001036.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:33955862 C>A maps to NM_001036.3 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:33855183 T>G maps to NM_001036.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:33954734 C>A maps to NM_001036.3 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:33926870 C>A maps to NM_001036.3 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:33895563 A>G maps to NM_001036.3 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:33895565 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr15:33941302 G>T maps to NM_001036.3 G1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:33878305 C>A maps to NM_001036.3 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr15:34078112 G>C maps to NM_001036.3 L3173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr15:34145787 A>G maps to NM_001036.3 A4568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr15:33988554 G>A maps to NM_001036.3 A1999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:33990136 G>T maps to NM_001036.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr15:34015045 C>A maps to NM_001036.3 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33895446 G>T maps to NM_001036.3 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:33962752 C>T maps to NM_001036.3 C1952C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:34130390 T>C maps to NM_001036.3 F4070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:34030760 C>T maps to NM_001036.3 F2542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr15:33936677 C>T maps to NM_001036.3 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr15:34016316 A>T maps to NM_001036.3 A2284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr15:33955874 G>A maps to NM_001036.3 L1852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr15:33765619 G>T maps to NM_001036.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr15:34064228 G>A maps to NM_001036.3 K2975K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6984-01A-11D-1945-08 chr15:33833065 G>A maps to NM_001036.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:34110876 G>A maps to NM_001036.3 T3566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:33895365 C>G maps to NM_001036.3 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr15:33895371 C>A maps to NM_001036.3 Y657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr15:33925182 T>A maps to NM_001036.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:33936680 G>A maps to NM_001036.3 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr15:34151795 C>A maps to NM_001036.3 Y4721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:34080452 C>T maps to NM_001036.3 P3208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr15:34018621 C>T maps to NM_001036.3 I2316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:33905393 C>A maps to NM_001036.3 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr15:33991969 G>C maps to NM_001036.3 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr15:34123252 C>T maps to NM_001036.3 V3808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr15:33603290 G>T maps to NM_001036.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr15:33962743 G>A maps to NM_001036.3 E1949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:33822818 C>A maps to NM_001036.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr15:34018588 C>A maps to NM_001036.3 L2305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr15:33954851 G>T maps to NM_001036.3 G1707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:33955907 C>G maps to NM_001036.3 T1863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:33916006 G>C did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:34135717 G>A maps to NM_001036.3 L4413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:33939622 A>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr15:33962734 G>C maps to NM_001036.3 T1946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:34072492 C>A maps to NM_001036.3 R3073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr15:34077908 C>A maps to NM_001036.3 P3105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:34078112 G>A maps to NM_001036.3 L3173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:33954941 G>T maps to NM_001036.3 V1737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr15:34102753 C>T maps to NM_001036.3 I3367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr15:33955103 C>G maps to NM_001036.3 V1791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr15:33872314 C>A maps to NM_001036.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:151955701 C>G maps to NM_002966.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:153346388 G>A maps to NM_005621.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:153346430 T>A maps to NM_005621.1 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:153346374 G>T maps to NM_005621.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:153598846 G>A maps to NM_001024210.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:153520865 C>A maps to NM_002960.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:153512580 C>G maps to ENST00000359215 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:153430322 G>A maps to NM_002963.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:153390626 T>A maps to NM_176823.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr1:153410769 G>A maps to NM_001045479.1 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:153409560 C>A maps to NM_001045479.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:153362655 G>A maps to NM_002964.4 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:153362695 G>A maps to NM_002964.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:153333231 G>A maps to NM_002965.3 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr21:48019356 G>A maps to NM_006272.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:16672562 G>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:33292038 C>G maps to NM_022753.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:33292343 C>G maps to NM_022753.2 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:33292200 G>A maps to NM_022753.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:101705385 C>T maps to NM_001400.4 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:101705130 C>A maps to NM_001400.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr1:101705214 C>A maps to NM_001400.4 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:101705001 G>A maps to NM_001400.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:101704716 C>A maps to NM_001400.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:101704644 G>A maps to NM_001400.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:101704875 C>A maps to NM_001400.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:10334756 G>A maps to NM_004230.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:10335473 G>T maps to NM_004230.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:10334603 C>A maps to NM_004230.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:10334520 C>G maps to NM_004230.3 *354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr9:91616189 G>A maps to NM_005226.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:3179348 C>T maps to NM_003775.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:10625537 G>A maps to NM_001166215.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:10625651 G>A maps to NM_001166215.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr11:18267007 C>A maps to NM_030754.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:18269489 C>A maps to NM_030754.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:18269516 C>G maps to NM_030754.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:18108505 G>A maps to NM_138421.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:18103034 C>A maps to NM_138421.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr3:45776856 C>T maps to NM_014016.3 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:23915307 G>A maps to NM_014363.4 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr13:23913457 T>C maps to NM_014363.4 G1519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr13:23904721 C>T maps to NM_014363.4 R4431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr13:23907940 G>A maps to NM_014363.4 P3358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr13:23913372 C>A maps to NM_014363.4 G1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr13:23914775 G>T maps to NM_014363.4 S1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr13:23928788 C>A maps to NM_014363.4 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:23913316 G>A maps to NM_014363.4 I1566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:23909310 C>A maps to NM_014363.4 G2902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr13:23907730 T>A maps to NM_014363.4 T3428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr13:23905742 G>C maps to NM_014363.4 S4091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr13:23913576 C>A maps to NM_014363.4 E1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr13:23906878 T>A maps to NM_014363.4 T3712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr19:5621404 C>G maps to NM_014649.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:5616187 C>A maps to NM_014649.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:234224722 G>T maps to NM_000541.4 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:234238161 C>A maps to NM_000541.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:134988656 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:134994547 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:134990726 T>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:134990673 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:134993769 G>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr23:134987533 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:134983833 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:134993791 C>T did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:134983715 A>T did not map to a codon.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr23:134983833 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:134990364 C>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:134989507 T>C did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:134992284 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:134989481 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:134987497 A>C did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:134992255 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:134990303 C>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:134991897 G>C did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:134989089 A>C did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:134990730 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:134991834 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:134993979 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:134983780 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:134990678 T>C did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:134988264 C>G did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:134994063 G>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:134990363 C>A did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr23:134989500 G>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:134993944 C>G did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:134991032 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:134994544 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:134989561 T>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174164 G>T maps to ENST00000251020 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:51174491 G>T maps to ENST00000251020 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:51174773 G>A maps to ENST00000251020 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:51174868 A>G maps to ENST00000251020 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:51175400 C>G maps to ENST00000251020 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:51171411 G>T maps to ENST00000251020 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr16:51174344 C>G maps to ENST00000251020 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:51175295 G>T maps to ENST00000251020 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr16:51174770 G>A maps to ENST00000251020 C454C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr16:51173591 G>A maps to ENST00000251020 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:51173941 C>A maps to ENST00000251020 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:51171226 G>A maps to ENST00000251020 N1257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr16:51174944 G>A maps to ENST00000251020 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr16:51175079 C>T maps to ENST00000251020 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr16:51171262 C>T maps to ENST00000251020 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr16:51175457 G>A maps to ENST00000251020 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr16:51175049 C>T maps to ENST00000251020 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:51174422 G>A maps to ENST00000251020 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr16:51174545 G>T maps to ENST00000251020 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr16:51172739 G>A maps to ENST00000251020 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:51171109 G>C maps to ENST00000251020 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:51174188 G>A maps to ENST00000251020 D648D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr16:51174347 G>T maps to ENST00000251020 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr16:51175559 G>T maps to ENST00000251020 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:21992358 C>T maps to NM_005407.1 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:76755312 C>A maps to NM_171999.2 R1108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:76757282 G>T maps to NM_171999.2 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:76753742 A>G maps to NM_171999.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr18:76753601 G>T maps to NM_171999.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:76754520 G>T maps to NM_171999.2 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr18:76754642 C>T maps to NM_171999.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr18:76754903 G>T maps to NM_171999.2 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:76755281 C>A maps to NM_171999.2 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr18:76754096 G>C maps to NM_171999.2 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr18:76754438 C>A maps to NM_171999.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr18:76753877 G>A maps to NM_171999.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:50407374 C>T maps to NM_020436.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr20:50408808 C>A maps to NM_020436.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:50408103 C>A maps to NM_020436.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr20:50407791 G>A maps to NM_020436.3 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr20:50418833 G>T maps to NM_020436.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr20:50400994 G>A maps to NM_020436.3 Q991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:50408064 C>A maps to NM_020436.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:50406858 C>G maps to NM_020436.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr20:50407326 G>A maps to NM_020436.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr20:50406960 G>A maps to NM_020436.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:50401129 C>A maps to NM_020436.3 G946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:50407047 C>A maps to NM_020436.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr20:62608327 G>A maps to NM_080621.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:877626 C>A maps to ENST00000443100 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:874453 C>A maps to ENST00000443100 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr8:119391928 C>A maps to NM_207506.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr8:119391763 C>T maps to NM_207506.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:48192997 G>T maps to NM_174920.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:48190268 G>T maps to NM_174920.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr17:48193254 G>T maps to NM_174920.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr17:48195542 C>A maps to NM_174920.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr17:48195634 G>T maps to NM_174920.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:130530638 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:130505332 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:130465705 C>A maps to ENST00000457563 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:130535489 T>A maps to ENST00000457563 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:130535666 T>C maps to ENST00000457563 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:130467242 T>A maps to ENST00000457563 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:130505705 A>T maps to ENST00000457563 L173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:55231179 A>G maps to NM_015589.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr14:55243226 C>G maps to NM_015589.4 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:55203961 C>A maps to NM_015589.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr19:39870703 G>A maps to NM_018028.2 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:147830240 G>A maps to NM_001030060.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:147830477 C>G maps to NM_001030060.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:169642918 T>C maps to NM_182610.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:169637305 T>A maps to NM_182610.2 L7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr10:76910336 A>G maps to ENST00000372690 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr10:76924414 C>T maps to ENST00000372690 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:92733058 C>A maps to NM_017654.3 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:92735074 T>C maps to NM_017654.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:92731290 C>A maps to NM_017654.3 E1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:92731108 T>C maps to NM_017654.3 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:92731660 G>T maps to NM_017654.3 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:92734861 A>G maps to NM_017654.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:92732037 G>A maps to NM_017654.3 Q1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:92763289 T>C maps to NM_152703.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr7:92763766 G>A maps to NM_152703.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr7:92762500 G>A maps to NM_152703.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:92764150 T>C maps to NM_152703.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:92763403 C>A maps to NM_152703.2 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:92761057 T>C maps to NM_152703.2 Q1409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:92765059 C>T maps to NM_152703.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr7:92761810 T>C maps to NM_152703.2 K1158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:92762521 G>A maps to NM_152703.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:92762731 C>T maps to NM_152703.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:92760660 C>A maps to NM_152703.2 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:92762905 C>T maps to NM_152703.2 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:35521454 T>G maps to NM_015474.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:35540892 T>C maps to NM_015474.3 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:44368854 A>G maps to NM_015380.4 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr21:15872984 C>A maps to ENST00000285670 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr21:15882675 C>T maps to ENST00000285670 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr21:15884834 G>T maps to ENST00000285670 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr21:15884769 G>T maps to ENST00000285670 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr21:15870822 C>A maps to ENST00000285670 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:128757333 G>A maps to NM_001145928.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:128712557 A>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:128754024 C>A maps to NM_001145928.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr4:174292578 C>T maps to NM_003864.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:73663475 G>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:153835468 C>A maps to NM_024632.5 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:55753603 C>A maps to ENST00000443936 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:55748125 C>A maps to ENST00000443936 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr19:55753856 C>G did not map to a codon.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr22:50832507 G>A maps to ENST00000216061 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:68337295 T>C maps to NM_001164160.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr11:68305258 A>T maps to NM_001164160.1 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr10:71913617 C>G maps to NM_020150.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:71912270 G>A maps to NM_020150.4 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:133942681 A>C maps to NM_016103.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:136573444 C>A maps to NM_007101.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr9:136529010 T>C maps to NM_007101.3 *919W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:136595227 G>A maps to NM_007101.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:136599097 C>T maps to NM_007101.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:136555518 A>G maps to NM_007101.3 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:136597661 C>G maps to NM_007101.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:26711500 C>A maps to ENST00000379061 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:26712193 G>A maps to ENST00000379061 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr12:56211461 G>A maps to NM_033082.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr1:109773540 A>T maps to ENST00000369923 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr19:39421115 G>A maps to NM_017827.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr11:65745040 G>T maps to NM_005146.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr11:65733925 C>A maps to NM_005146.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:65734947 G>T maps to NM_005146.4 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:65746352 C>T maps to NM_005146.4 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:108954774 C>A maps to NM_014706.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr12:108918235 A>C maps to NM_014706.3 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:148795358 G>T did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:148869468 C>T maps to NM_015278.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:148761493 G>T maps to NM_015278.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr6:148664268 G>A maps to NM_015278.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:128926648 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:128922015 G>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:128926691 C>G did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:128925026 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:128926601 G>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:100598310 C>T maps to NM_194292.1 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:100572477 A>G maps to NM_194292.1 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:23801931 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:23803930 G>A did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:23803527 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:18436361 A>G maps to ENST00000332610 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:18393627 C>A maps to ENST00000332610 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:18419676 T>G maps to ENST00000332610 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:200173680 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:200137208 C>A maps to NM_001172509.1 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:200188558 G>T maps to NM_001172509.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:200246528 C>A maps to NM_001172509.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:200137221 C>A maps to NM_001172509.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:200213480 C>T maps to NM_001172509.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:200246415 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:200136963 C>T maps to NM_001172509.1 K724K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:200245204 G>T maps to NM_001172509.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:84362523 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:84363383 G>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:84363342 G>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:84363146 C>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:84362768 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:84363383 G>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:84362580 C>A did not map to a codon.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr23:84362762 T>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:84363130 T>G did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:84347562 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:84363343 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:84349160 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:84363298 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:84363239 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:84363391 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:84363865 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:84349179 G>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr14:51132058 C>A maps to NM_021818.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr7:66456123 G>A maps to NM_016038.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr22:50902832 G>A maps to ENST00000337034 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr22:50894716 T>A maps to ENST00000337034 P1408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:50905859 G>A maps to ENST00000337034 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:9990004 C>A maps to NM_030962.3 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:10011042 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr16:28331560 G>T maps to NM_001024401.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr16:28328789 T>A maps to NM_001024401.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:56042602 C>T maps to NM_001101401.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:56041234 C>A maps to NM_001101401.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr12:123780483 G>A maps to NM_001167856.1 Q1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr12:123801891 G>A maps to NM_001167856.1 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr19:36018820 G>A maps to NM_001166034.1 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr4:166258948 A>T maps to NM_006745.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:39967431 C>A maps to NM_006455.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr19:50161556 C>T maps to NM_021228.2 H1280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:50148297 T>C maps to NM_021228.2 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:50154155 C>T maps to NM_021228.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:50148668 G>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:50148390 G>A maps to NM_021228.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:50154182 G>T maps to NM_021228.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:50157970 T>G maps to NM_021228.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:127765391 C>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:127782984 G>C maps to NM_173690.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr9:127738466 T>G did not map to a codon.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr15:75143766 G>A maps to NM_005697.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr15:75137883 G>C maps to NM_005697.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:155226463 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr1:155230147 G>A maps to NM_005698.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:155230378 C>G maps to NM_005698.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr15:75310791 G>A maps to ENST00000361900 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr15:75310806 G>T maps to ENST00000361900 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr15:75309084 C>T maps to ENST00000361900 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:28541446 G>T maps to NM_052923.1 S740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:28554167 C>T maps to NM_052923.1 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:28540908 C>T maps to NM_052923.1 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr6:28554221 G>A maps to NM_052923.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:28539962 C>A maps to NM_052923.1 G1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:28543260 C>A maps to NM_052923.1 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:28539764 G>A maps to NM_052923.1 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:28547181 T>A maps to NM_052923.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:28554454 G>A maps to NM_052923.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr3:47456481 C>A maps to NM_012235.2 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:47465463 G>C maps to NM_012235.2 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:47469108 C>G maps to NM_012235.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr3:47476593 T>A maps to NM_012235.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:47460979 G>T maps to NM_012235.2 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:47470145 C>A maps to NM_012235.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:76763648 G>A maps to ENST00000324767 Y994Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:77057678 T>A maps to ENST00000324767 R538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:27516181 A>G maps to NM_016240.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:27516098 G>T maps to NM_016240.2 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:27764704 C>T maps to NM_173833.5 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr8:27823929 C>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr4:77089566 T>C maps to NM_005506.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:77091112 T>C maps to NM_005506.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:1543282 G>C maps to NM_003693.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr17:1538813 C>T maps to NM_003693.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:1548985 C>A maps to NM_003693.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:1540331 C>A maps to NM_003693.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr22:20785161 C>T maps to NM_153334.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:20786092 C>A maps to NM_153334.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr1:246930494 A>G did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:83602053 G>A maps to NM_001037582.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:83602008 C>T maps to NM_001037582.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:78173883 G>T did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr13:78176220 G>A maps to NM_144777.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr13:78130759 C>A maps to NM_144777.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:78167669 C>T maps to NM_144777.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:78188088 G>T maps to NM_144777.2 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr14:31191117 C>T maps to ENST00000311943 Q597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:54179818 T>A maps to NM_152540.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:54232057 C>A maps to NM_152540.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr4:54218829 G>A maps to NM_152540.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr4:53786889 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:54231378 G>A maps to NM_152540.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr2:224462308 C>T maps to NM_003469.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:224463261 C>A maps to NM_003469.4 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr2:224462974 A>T maps to NM_003469.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:224463547 A>G maps to NM_003469.4 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:224463276 C>A maps to NM_003469.4 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr15:51975581 G>T maps to NM_013243.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr15:52011671 C>A maps to NM_013243.3 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:62189753 C>T maps to NM_003357.4 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:62186608 C>G maps to NM_003357.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr11:61957767 G>A maps to NM_006552.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:62037699 G>T maps to NM_002411.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr6:25689708 T>C maps to NM_006998.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr7:12684299 C>T maps to NM_001112706.2 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr7:12664767 G>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr7:12683869 G>A maps to NM_001112706.2 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:129867261 C>A maps to NM_144643.2 E447*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-5644-01A-21D-2036-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:238973024 G>T maps to NM_016510.4 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:238990699 C>T maps to NM_016510.4 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:41536267 T>A maps to NM_001031694.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:17771463 A>G did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:17762332 C>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:17768021 T>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:17768270 C>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:17768289 C>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:17768239 G>A did not map to a codon.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr23:18278316 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:18264764 A>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:18278316 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:18278383 T>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:18276281 C>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:18275118 C>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:18323336 T>C did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:18264731 T>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:18276193 G>C did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr23:18348706 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:18323299 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:18260585 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:18260586 C>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:18283768 G>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:18259464 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:18276332 G>A did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr23:18275063 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:18342066 T>G did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:18265996 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr23:18342107 C>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:108042039 C>A maps to NM_198081.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:38802749 G>C maps to NM_006514.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr3:38835489 G>A maps to NM_006514.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:38830505 C>G maps to NM_006514.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr3:38739976 G>T maps to NM_006514.2 A1578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr3:38760173 G>A maps to NM_006514.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:38766751 G>A maps to NM_006514.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:38739997 G>T maps to NM_006514.2 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:38793718 G>A maps to NM_006514.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:38770044 T>C maps to NM_006514.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr3:38770308 C>G maps to NM_006514.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr3:38798589 G>C maps to NM_006514.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:38770074 G>T maps to NM_006514.2 C866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:38835285 T>A maps to NM_006514.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr3:38739793 G>A maps to NM_006514.2 D1639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr3:38738877 C>A maps to NM_006514.2 E1945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:38770227 G>A maps to NM_006514.2 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:38743501 C>T maps to NM_006514.2 V1495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:38739416 G>T maps to NM_006514.2 S1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:38797449 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:38908895 T>A maps to ENST00000302328 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:38951597 G>T maps to ENST00000302328 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:38888597 C>A maps to ENST00000302328 E1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr3:38938334 C>A did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr3:38988323 A>G maps to ENST00000302328 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr3:38908864 G>A maps to ENST00000302328 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr3:38938350 C>A maps to ENST00000302328 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:38913707 C>T maps to ENST00000302328 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:38938617 G>A maps to ENST00000302328 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:166903467 T>A maps to NM_001165963.1 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166850734 T>C maps to NM_001165963.1 K1591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:166901689 G>A maps to NM_001165963.1 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr2:166897827 G>T maps to NM_001165963.1 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:166900384 G>A maps to NM_001165963.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:166852588 C>T maps to NM_001165963.1 K1505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:166859122 A>T maps to NM_001165963.1 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:166900187 A>T maps to NM_001165963.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:166892599 C>T maps to NM_001165963.1 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:166897830 G>T maps to NM_001165963.1 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:166900550 C>T maps to NM_001165963.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:166898801 C>A maps to NM_001165963.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:166895986 T>A maps to NM_001165963.1 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:166866285 G>A maps to NM_001165963.1 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:166903432 G>A maps to NM_001165963.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:166856286 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:166848816 G>T maps to NM_001165963.1 I1656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:166903285 T>C maps to NM_001165963.1 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:166900520 C>T maps to NM_001165963.1 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:166896070 C>T maps to NM_001165963.1 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166183486 C>A maps to NM_001040142.1 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:166172033 G>T maps to NM_001040142.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166166887 C>T maps to NM_001040142.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:166245668 G>T maps to NM_001040142.1 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr2:166245808 A>T maps to NM_001040142.1 I1831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:166179955 C>A maps to NM_001040142.1 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:166172173 C>A maps to NM_001040142.1 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166245430 C>A maps to NM_001040142.1 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:166245866 C>A maps to NM_001040142.1 R1851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:166245832 C>G maps to NM_001040142.1 L1839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:166223865 G>T maps to NM_001040142.1 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr2:166245788 C>T maps to NM_001040142.1 L1825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr11:118038983 A>G maps to NM_004588.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:166018881 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:165994466 G>A maps to NM_006922.3 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:165986746 A>T maps to NM_006922.3 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:165952084 G>T maps to NM_006922.3 S1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:165956880 G>T maps to NM_006922.3 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:165953839 A>G maps to NM_006922.3 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:166011087 C>T maps to NM_006922.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:166003332 T>C maps to NM_006922.3 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:165970388 A>G maps to NM_006922.3 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr2:165970340 G>T maps to NM_006922.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr2:165987786 C>A maps to NM_006922.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:165946872 C>T maps to NM_006922.3 E1930E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:165956927 A>G maps to NM_006922.3 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr2:165984434 C>T maps to NM_006922.3 K1033K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:123509018 G>A maps to NM_018400.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:123513204 G>T maps to NM_018400.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr11:123508976 G>T maps to NM_018400.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:62025294 C>A maps to NM_000334.4 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:62025345 G>T maps to NM_000334.4 Y1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:62034575 G>A maps to NM_000334.4 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr17:62049173 G>C maps to NM_000334.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:62018709 C>G maps to NM_000334.4 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr17:62049512 G>C maps to NM_000334.4 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:62022923 C>A maps to NM_000334.4 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr17:62024443 C>A maps to NM_000334.4 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr17:62026870 G>A maps to NM_000334.4 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:62018355 C>A maps to NM_000334.4 G1762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:62020279 C>T maps to NM_000334.4 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:62034785 C>T maps to NM_000334.4 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:62018184 G>C maps to NM_000334.4 P1819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr17:62019060 G>T maps to NM_000334.4 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:62045710 C>T maps to NM_000334.4 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:38592977 G>T maps to NM_001099404.1 R1629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:38622505 G>A maps to NM_001099404.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr3:38639327 A>G maps to NM_001099404.1 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:38622697 G>T maps to NM_001099404.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr3:38592972 T>A maps to NM_001099404.1 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:38592216 G>T maps to NM_001099404.1 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr3:38674693 G>A maps to NM_001099404.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:38595896 C>T maps to NM_001099404.1 K1562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr3:38622763 G>T maps to NM_001099404.1 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:38639234 C>T maps to NM_001099404.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:38622837 G>A maps to NM_001099404.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:38592195 G>A maps to NM_001099404.1 Y1889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:38592066 C>A maps to NM_001099404.1 A1932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr3:38628929 G>T maps to NM_001099404.1 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:38592469 C>T maps to NM_001099404.1 W1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:38622673 G>C maps to NM_001099404.1 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr3:38603944 G>T maps to NM_001099404.1 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr3:38645253 G>T maps to NM_001099404.1 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:167330311 A>T maps to NM_002976.2 L147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167262665 G>T maps to NM_002976.2 Y1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:167262818 A>G maps to NM_002976.2 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:167262211 G>A maps to NM_002976.2 R1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:167328883 G>T maps to NM_002976.2 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:167262795 C>T maps to NM_002976.2 W1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr2:167298208 C>T maps to NM_002976.2 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:167301480 A>G maps to NM_002976.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:167262929 G>T maps to NM_002976.2 A1403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:167262274 G>A maps to NM_002976.2 R1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:167279813 G>T maps to NM_002976.2 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:52163070 C>T maps to NM_014191.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:52162773 C>A maps to NM_014191.2 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:52180405 C>T maps to NM_014191.2 F1341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:52156454 C>A maps to NM_014191.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:52182531 G>A maps to NM_014191.2 K1427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:52200402 G>T maps to NM_014191.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:52164460 C>A maps to NM_014191.2 G1213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:52159489 C>A maps to NM_014191.2 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr2:167141097 C>T maps to ENST00000303354 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:167168244 C>A maps to ENST00000303354 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:167145087 A>G maps to ENST00000303354 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr2:167085245 C>T maps to ENST00000303354 V1388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:167138187 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:167055685 G>C maps to ENST00000303354 V1822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:167168068 A>T maps to ENST00000303354 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:6457407 G>C maps to NM_001159576.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:6483727 C>A maps to NM_001159576.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr12:6457371 G>A maps to NM_001159576.1 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:23366786 C>T maps to ENST00000307331 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:23388519 G>T maps to ENST00000307331 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:1222559 C>A maps to NM_001130413.2 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:1226737 C>T maps to NM_001130413.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:1221508 G>T maps to NM_001130413.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr1:1225875 C>T maps to NM_001130413.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:23197657 G>C maps to NM_001039.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr22:50962831 C>T maps to NM_001169111.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:50962675 A>G maps to NM_001169111.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:141302137 A>T maps to NM_001153484.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:53480679 A>C maps to NM_002979.4 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:55058572 C>A maps to NM_021626.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:55072971 G>T maps to NM_021626.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr17:55083593 T>C maps to NM_021626.2 *453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:55083531 A>T did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:174312421 C>T maps to NM_007281.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr8:144890967 G>C maps to NM_182706.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr8:144887127 C>A maps to NM_182706.3 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:144874230 C>A maps to NM_182706.3 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr8:144876105 C>T maps to NM_182706.3 K1291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:29983639 C>T maps to NM_001145514.1 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:45915650 C>T maps to NM_138355.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:45917624 G>A maps to NM_138355.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:175268853 C>T maps to NM_024583.4 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr8:145557005 C>T maps to NM_031309.4 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr20:644540 G>T maps to NM_033129.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:120197693 C>T maps to NM_002980.2 *441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr22:43614411 G>T maps to NM_173050.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr22:43627881 C>G did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr22:43617206 T>C maps to NM_173050.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:43715945 G>A maps to NM_173050.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:43619124 C>G maps to NM_173050.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr22:43619184 G>A maps to NM_173050.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:9052303 C>A did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr11:9051429 C>G did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:35210035 A>G maps to ENST00000394681 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:35212535 A>G maps to ENST00000394681 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:35199626 C>A maps to ENST00000394681 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:35209365 C>G maps to ENST00000394681 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:35211467 C>A maps to ENST00000394681 C685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:35210810 G>T maps to ENST00000394681 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr6:35210966 G>A maps to ENST00000394681 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:65304156 G>C maps to NM_020680.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:65300212 C>T maps to NM_020680.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr11:65293593 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:65303734 C>T maps to NM_020680.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:100717319 C>T maps to NM_017988.4 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr12:100729586 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:100732541 C>T maps to NM_017988.4 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:169823653 T>G maps to NM_181093.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:169831876 G>A maps to NM_181093.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:76882213 T>C maps to NM_018115.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr4:76877193 G>A maps to NM_018115.2 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:20403999 G>A maps to NM_001006946.1 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr8:97605769 A>T maps to NM_002998.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:31351583 G>A maps to NM_014654.3 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr14:50280704 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr14:50272776 G>T maps to NM_004713.3 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr14:50266230 T>C maps to NM_004713.3 K809K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr9:139304593 C>A maps to NM_001039707.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:139301806 G>A maps to NM_001039707.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:139301895 G>A maps to NM_001039707.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:243579076 G>T maps to NM_006642.3 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:243542084 G>A maps to NM_006642.3 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:243504396 A>T maps to NM_006642.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr1:243581330 A>G maps to NM_006642.3 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:26982418 T>A maps to NM_006923.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:26976079 C>T maps to NM_006923.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:1159281 C>A maps to NM_016176.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:1154296 G>T maps to NM_016176.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z019-01A-01W-0746-08 chr5:231089 A>C maps to NM_004168.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr5:236580 C>T maps to NM_004168.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:240506 G>T maps to NM_004168.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:236547 G>C maps to NM_004168.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:251217 G>T maps to NM_004168.2 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:224542 C>T maps to NM_004168.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:17354336 C>T maps to NM_003000.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:17349132 G>A maps to NM_003000.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr11:111959711 A>T maps to NM_003002.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr11:111958605 C>T maps to NM_003002.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:4116808 G>T maps to NM_152744.3 G1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:4281521 C>T maps to NM_152744.3 T2076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:4014039 G>T maps to NM_152744.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:4153880 G>T maps to NM_152744.3 V1266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr7:4169562 G>T maps to NM_152744.3 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:4249747 C>T maps to NM_152744.3 I1831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:4273010 G>A maps to NM_152744.3 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr7:3678651 T>C maps to NM_152744.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr7:4008953 C>T maps to NM_152744.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr7:4259738 A>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:4091274 G>T maps to NM_152744.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4116732 C>A maps to NM_152744.3 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:4198172 G>C maps to NM_152744.3 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:3991445 C>T maps to NM_152744.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr7:4167082 A>G maps to NM_152744.3 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:3991466 G>T maps to NM_152744.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr7:4006998 C>T maps to NM_152744.3 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:4249735 G>T maps to NM_152744.3 A1827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:4167058 G>A maps to NM_152744.3 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:4091283 G>T maps to NM_152744.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr17:71427795 A>T maps to NM_001144952.1 L442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:71334923 C>A maps to NM_001144952.1 S2107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr17:71354343 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:71410866 C>T maps to NM_001144952.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:71412115 C>T maps to NM_001144952.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:71397870 G>A maps to NM_001144952.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:71398168 C>A maps to NM_001144952.1 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:71394317 G>T maps to NM_001144952.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:71389875 C>A maps to NM_001144952.1 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:71415417 C>T maps to NM_001144952.1 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:71420155 G>C maps to NM_001144952.1 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:71419588 C>G maps to NM_001144952.1 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:71431625 G>T maps to NM_001144952.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:71427710 C>T maps to NM_001144952.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr17:71354287 G>A maps to NM_001144952.1 A1841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:71390437 C>A maps to NM_001144952.1 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:192700894 G>A maps to NM_004657.5 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:192700753 C>T maps to NM_004657.5 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:192701326 C>A maps to NM_004657.5 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:192700849 C>T maps to NM_004657.5 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:57324167 C>T maps to NM_148897.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:57327751 G>T maps to NM_148897.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:113837396 G>T maps to NM_006843.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr12:113830940 G>T maps to NM_006843.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:113834979 T>A maps to NM_006843.2 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:113873250 G>C maps to NM_138432.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:113873238 G>T maps to NM_138432.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr18:56819782 G>A maps to NM_033280.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:75208255 G>T maps to NM_001039573.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:75208129 G>A maps to NM_001039573.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr17:75187324 T>C maps to NM_001039573.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:30857303 G>A maps to NM_174975.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr22:30860809 C>A maps to NM_174975.4 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:30866237 C>A maps to NM_174975.4 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr22:30856094 G>T maps to NM_174975.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr22:30860828 G>T maps to NM_174975.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:30887626 G>A maps to NM_174977.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:5042017 G>T maps to NM_014692.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr9:139353684 T>C maps to NM_014866.1 P1770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:139358873 C>A maps to NM_014866.1 E1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:139357392 C>T maps to NM_014866.1 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:139370618 C>A maps to NM_014866.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr1:177909850 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:177929538 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:177911049 T>C maps to NM_033127.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:122942516 T>G maps to NM_012430.4 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:122942426 G>T maps to NM_012430.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:122928211 A>T maps to NM_012430.4 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:122944079 G>T maps to NM_012430.4 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:145096545 G>C did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:145109655 G>T maps to NM_004892.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:145115792 G>A maps to NM_004892.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr14:39556194 A>C maps to NM_006364.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:18529365 C>T maps to NM_001172745.1 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:18535780 A>C maps to NM_001172745.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:121671605 G>T maps to NM_007190.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr10:121691670 G>T maps to NM_007190.2 G867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:121652417 C>T maps to NM_007190.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr10:121662474 T>G maps to NM_007190.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:121662450 A>G maps to NM_007190.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:121657963 G>A maps to NM_007190.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr5:134022558 C>A maps to NM_021982.1 S524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:134023903 C>T maps to NM_021982.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr5:134010907 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr5:134044430 G>C maps to NM_021982.1 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:110394205 C>T maps to NM_006323.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:110431266 G>T maps to NM_006323.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:110394217 A>T maps to NM_006323.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:110434906 T>C maps to NM_006323.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr10:75526299 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:75525631 C>T maps to NM_198597.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:119745842 A>G maps to ENST00000379735 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr4:119659532 A>C maps to ENST00000379735 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:119678976 T>C maps to ENST00000379735 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr4:119674014 G>A maps to ENST00000379735 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:83795889 G>T maps to ENST00000505472 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr4:83748590 G>T maps to ENST00000505472 G1105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr4:83799971 T>A maps to ENST00000505472 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr10:102249903 C>G maps to NM_015490.3 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr10:102256137 C>G maps to NM_015490.3 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr10:102250469 T>C maps to NM_015490.3 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:127785969 G>T maps to ENST00000464451 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:54823476 G>A maps to NM_014302.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:91943572 A>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:91940393 C>T maps to NM_024077.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr9:91943788 A>T maps to NM_024077.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:49304864 G>A maps to NM_001193489.1 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr15:49301448 G>T maps to NM_001193489.1 S664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:49285067 A>G maps to NM_001193489.1 N893N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:80280234 G>A maps to NM_003004.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr14:81964259 A>G maps to NM_005065.4 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr14:81972489 T>G maps to NM_005065.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr20:13971162 C>G maps to NM_025229.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:13846070 A>T maps to NM_025229.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:13858198 G>T maps to NM_025229.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr20:13850152 G>C maps to NM_025229.1 Y417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr20:13847461 G>T maps to NM_025229.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:13894499 G>T maps to NM_025229.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr20:13971165 A>G maps to NM_025229.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr20:13830199 G>A maps to NM_025229.1 H666H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:13912363 T>A maps to NM_025229.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr20:13850182 G>C maps to NM_025229.1 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr20:13830887 G>T maps to NM_025229.1 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:25785870 C>T maps to NM_015187.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:169698389 C>A maps to NM_000450.2 G343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:169698390 C>T maps to NM_000450.2 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:169699708 G>T maps to NM_000450.2 C193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr1:169696957 C>A maps to NM_000450.2 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:169698743 G>A maps to NM_000450.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:151338043 C>A maps to ENST00000435071 G389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:53925794 A>G did not map to a codon.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:169677567 G>C maps to NM_000655.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr22:31501066 C>G maps to NM_080430.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:31501027 C>T maps to NM_080430.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr22:50655550 C>T maps to NM_031454.1 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr22:50655558 C>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr22:50649149 G>A maps to NM_031454.1 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:169572375 A>G maps to NM_003005.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:169582878 G>T maps to NM_003005.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:169581568 G>A maps to NM_003005.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:169572266 C>A maps to NM_003005.3 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:169566258 T>A maps to NM_003005.3 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:169565169 T>A maps to NM_003005.3 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:169581479 C>T maps to NM_003005.3 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:169564017 A>G maps to NM_003005.3 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:169562912 C>A maps to NM_003005.3 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:109017869 G>A maps to ENST00000228463 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr12:109017936 T>C maps to ENST00000228463 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr12:109017168 G>T maps to ENST00000228463 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:109017657 C>T maps to ENST00000228463 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:109016955 G>T maps to ENST00000228463 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:40009751 T>A maps to NM_182704.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:40009423 C>T maps to NM_182704.1 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:83739784 C>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:83590814 G>T maps to NM_006080.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:83606483 C>A maps to NM_006080.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr7:83640501 G>A maps to NM_006080.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:83590844 C>A maps to NM_006080.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr7:83739878 T>A maps to NM_006080.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:83610794 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:80418808 G>A maps to NM_006379.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr7:80427412 C>A maps to NM_006379.2 G376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:80546043 A>G maps to NM_006379.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr7:80433565 T>C did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr7:80374431 G>A maps to NM_006379.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:84751059 T>A maps to NM_152754.2 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:84697505 C>G did not map to a codon.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr7:84644481 G>A maps to NM_152754.2 H532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr7:84751072 G>T maps to NM_152754.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:84636207 A>G maps to NM_152754.2 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:84651815 T>A maps to NM_152754.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:84636135 C>A maps to NM_152754.2 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr7:84629151 C>A maps to NM_152754.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr7:84685052 G>T maps to NM_152754.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr7:84642104 G>T maps to NM_152754.2 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:84727237 T>C maps to NM_152754.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:84628805 G>A maps to NM_152754.2 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:84685071 G>A maps to NM_152754.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:83095860 C>A maps to NM_012431.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr7:83032092 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:83036448 A>G maps to NM_012431.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr7:82997012 C>T maps to NM_012431.2 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr7:83095803 A>G maps to NM_012431.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr3:50211517 G>T maps to NM_004186.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:50223737 G>T maps to NM_004186.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:50197158 C>A maps to NM_004186.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:50223756 C>T maps to NM_004186.3 Q597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:50220143 C>T maps to NM_004186.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:50223353 C>T maps to NM_004186.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:52469753 T>C maps to NM_020163.1 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:52476873 G>A maps to NM_020163.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr3:52469786 C>T maps to NM_020163.1 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:156131246 G>T maps to NM_022367.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:156144917 G>T maps to NM_022367.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:156146367 C>T maps to NM_022367.3 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6148-01A-11D-1753-08 chr1:156146628 A>T maps to NM_022367.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:156130744 C>T maps to NM_022367.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:156142756 C>A maps to NM_022367.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:156127865 G>A maps to NM_022367.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr1:156131273 A>C maps to NM_022367.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:90771571 C>G maps to NM_198925.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr15:90771739 C>T maps to NM_198925.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr15:90770875 T>C maps to ENST00000379122 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:97526584 C>A maps to NM_017789.4 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:97526513 G>C maps to NM_017789.4 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:92007406 C>A maps to NM_006378.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr9:91993999 G>T maps to NM_006378.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr9:91994485 C>G maps to NM_006378.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:92011693 G>A maps to NM_006378.3 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr9:91994041 C>A maps to NM_006378.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:74902761 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:74881607 C>A maps to NM_004263.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr10:102738134 C>T maps to NM_017893.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:102732997 C>G maps to NM_017893.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:9337871 C>A maps to NM_003966.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr5:9122841 G>A maps to NM_003966.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:9044622 G>C maps to NM_003966.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:9119213 G>A maps to NM_003966.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:9052121 G>T maps to NM_003966.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:9238003 T>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:9227080 T>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr5:9054199 T>G maps to NM_003966.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr5:9044560 G>C maps to NM_003966.2 S1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:9202173 G>A maps to NM_003966.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:9043068 G>C maps to NM_003966.2 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr5:9237963 G>T maps to NM_003966.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr5:9190394 G>A maps to NM_003966.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:9190543 C>A maps to NM_003966.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:9237948 G>T maps to NM_003966.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr5:9054286 A>T maps to NM_003966.2 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr5:9238002 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:9054241 C>A maps to NM_003966.2 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr5:9052012 C>T maps to NM_003966.2 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:9052128 C>A maps to NM_003966.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr5:9063107 G>A maps to NM_003966.2 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:9044613 G>T maps to NM_003966.2 Y992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:9063217 C>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:9227043 C>G maps to NM_003966.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:9136666 C>T maps to NM_003966.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:9044565 G>T maps to NM_003966.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:9197363 C>A maps to NM_003966.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:9197414 C>G maps to NM_003966.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:9119135 C>A maps to NM_003966.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:9063161 C>A maps to NM_003966.2 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:9119231 C>T maps to NM_003966.2 W601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr5:9054338 C>T maps to NM_003966.2 W850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:122632802 C>A maps to NM_001031702.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:122629685 C>G did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr3:122645243 G>T maps to NM_001031702.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:122642571 G>A maps to NM_001031702.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:122629684 A>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:122631816 G>T maps to NM_001031702.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:122645470 G>T maps to NM_001031702.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:122632427 G>T maps to NM_001031702.2 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:115782851 C>A maps to ENST00000257414 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:115838023 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr5:115783223 G>A maps to ENST00000257414 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:115822566 G>T maps to ENST00000257414 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr5:115782665 G>A maps to ENST00000257414 Y929Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:115782461 G>T maps to ENST00000257414 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:115783391 G>A maps to ENST00000257414 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:115827451 G>A maps to ENST00000257414 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:115782557 G>T maps to ENST00000257414 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:115783382 G>A maps to ENST00000257414 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:115803426 G>A maps to ENST00000257414 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr5:115827445 T>A maps to ENST00000257414 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:4556050 C>A maps to NM_032108.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr19:4558144 G>A maps to NM_032108.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4550173 G>T maps to NM_032108.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr19:4550271 G>T maps to NM_032108.3 C378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:4556014 C>A maps to NM_032108.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:151107785 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:151108131 T>C maps to NM_001178061.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:151109457 A>C maps to NM_001178061.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:151110863 C>A maps to NM_001178061.1 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:48062871 C>A maps to NM_153618.1 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:48063501 G>A maps to NM_153618.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:48056264 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:48058161 C>T maps to NM_153618.1 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr15:48053948 G>T did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr15:48063879 G>T maps to NM_153618.1 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr15:48063796 C>T maps to NM_153618.1 Q1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:48055265 C>A maps to NM_153618.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr15:48063981 G>T maps to NM_153618.1 *1074Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr15:48053418 T>C did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:48053407 C>A maps to NM_153618.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:48063496 G>T maps to NM_153618.1 G913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr15:48058842 C>T maps to NM_153618.1 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:48056987 C>A maps to NM_153618.1 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr15:48060805 C>A maps to NM_153618.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr15:48063678 T>C maps to NM_153618.1 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr15:74703901 G>A maps to NM_003612.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr15:74707190 C>T maps to NM_003612.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr15:74708158 A>T maps to NM_003612.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:43836132 T>C maps to NM_003007.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43851751 T>C maps to NM_003008.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:43850566 A>G maps to NM_003008.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:43851220 C>A maps to NM_003008.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr12:48490159 T>A maps to ENST00000004980 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr12:48457498 A>G maps to ENST00000004980 N467N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:185341816 A>T maps to ENST00000427465 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:185307916 A>G maps to ENST00000427465 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr17:7474714 C>T maps to ENST00000321337 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr17:7468081 C>T maps to ENST00000321337 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr3:196612171 G>T maps to NM_152699.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:196627253 G>T maps to NM_152699.4 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr3:196630481 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:76385183 G>T maps to NM_015571.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:101080668 C>A maps to NM_020654.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr3:101047371 T>A maps to NM_020654.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr3:101060530 A>G maps to NM_020654.3 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:101047390 C>A did not map to a codon.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr10:13378280 G>A maps to NM_012247.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:26140370 G>T did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr5:42800828 G>C maps to NM_001093726.1 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:42801361 C>A maps to NM_001093726.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:25160708 G>A maps to NM_016955.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:30391339 C>T maps to NM_052838.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:30392510 G>T maps to NM_052838.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:30393196 C>T maps to NM_052838.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:30390499 C>T maps to NM_052838.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr16:30391350 G>T maps to NM_052838.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:110310789 T>C maps to ENST00000356688 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:110325409 C>T maps to ENST00000356688 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:110325450 G>A maps to ENST00000356688 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:77917576 G>A did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr16:4829783 G>A maps to NM_144605.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr7:55910637 A>G maps to NM_207366.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr22:42388739 C>T maps to NM_145733.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:56599365 C>A maps to NM_004574.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:19707368 C>T maps to NM_002688.5 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:118774739 C>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:118771147 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:118771018 C>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:118783986 G>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:118767438 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:118771035 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:118763452 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:118797510 T>C did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:118771061 T>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:118797601 G>A did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:118771104 C>A did not map to a codon.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr23:118786863 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:118786855 C>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:35930322 T>C maps to NM_001788.4 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:132097247 G>A maps to NM_001098811.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:132099496 G>A maps to NM_001098811.1 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr17:75493406 C>T maps to NM_001113491.1 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:1990777 C>G did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:158549152 A>G maps to NM_032861.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:158534624 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:44085914 G>T maps to ENST00000409960 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr11:18028279 G>A maps to NM_012139.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr11:17809802 C>A maps to NM_012139.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:17981156 G>A maps to NM_012139.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:18017430 C>G maps to NM_012139.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr6:122768321 C>T maps to NM_020755.2 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr6:122777624 C>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:43142612 C>A maps to NM_006811.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:43142612 C>A maps to NM_006811.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr20:43132457 A>G maps to NM_006811.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:44087737 C>T maps to ENST00000319327 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:44088827 A>G maps to ENST00000319327 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr5:79498749 G>A maps to NM_001174072.1 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:79498703 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:79465218 T>A maps to NM_001174072.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr14:94847329 C>T maps to NM_001127707.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr14:94845920 C>A maps to NM_001127707.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr14:94848950 C>A maps to NM_001127707.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr14:94849307 G>A maps to NM_001127707.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:94756234 A>T maps to NM_001100607.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:94756525 G>T maps to NM_001100607.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:94756846 C>T maps to NM_001100607.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:94756522 G>T maps to NM_001100607.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:94914751 C>A maps to NM_001080451.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:94914952 G>T maps to NM_001080451.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr14:94914724 G>T maps to NM_001080451.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr14:94915054 A>T maps to NM_001080451.1 C19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:94908972 C>A maps to NM_001080451.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr14:94915006 G>T maps to NM_001080451.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr14:94914544 G>T maps to NM_001080451.1 Y189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:94914643 G>A maps to NM_001080451.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr14:94964440 G>T maps to NM_173850.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:94964158 C>A maps to NM_173850.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:94962978 G>T maps to NM_173850.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr14:94962939 C>T maps to NM_173850.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr14:94953738 G>T maps to NM_173850.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr14:95090003 C>T maps to ENST00000393080 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr14:95085718 C>T maps to ENST00000393080 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr14:95080976 A>T maps to ENST00000393080 K92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr14:95081407 C>T maps to ENST00000393080 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:95085763 C>A maps to ENST00000393080 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr14:95081182 G>A maps to ENST00000393080 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr14:95081326 C>A maps to ENST00000393080 Y208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr14:95081395 C>A maps to ENST00000393080 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr14:95033574 G>A maps to NM_006215.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:95030067 G>T maps to NM_006215.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr14:95029848 G>T maps to NM_006215.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:95030301 C>T maps to NM_006215.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:95030052 C>A maps to NM_006215.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:95058515 C>A maps to NM_000624.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:95053824 C>A maps to NM_000624.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr14:95053975 G>T maps to NM_000624.4 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr14:95053812 C>A maps to NM_000624.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:94772488 C>T maps to NM_001756.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr14:94780976 G>A maps to NM_001756.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr14:94780928 G>C maps to NM_001756.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:94776179 G>T maps to NM_001756.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr14:94776110 C>G maps to NM_001756.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:105277676 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:105280956 A>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:105278253 G>C did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:105280838 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:105280604 C>G did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:105280469 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:105279109 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:105280840 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:105278316 G>C did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:105277583 G>T did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr23:105280591 A>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:105278269 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:105277591 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:105278239 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:94933717 G>C maps to NM_175739.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:94935679 G>A maps to NM_175739.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:94936105 G>T maps to NM_175739.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61587110 C>T maps to NM_005024.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:61600404 C>T maps to NM_005024.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr18:61602376 C>T maps to NM_005024.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:61584736 T>C maps to NM_005024.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:61582863 C>A maps to ENST00000397996 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:61390291 A>T maps to NM_080475.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61379923 T>C maps to NM_080475.2 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:61388156 C>A maps to NM_080475.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:61231352 G>T maps to ENST00000382768 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:61231211 T>A maps to ENST00000382768 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr18:61223490 G>C maps to ENST00000382768 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr18:61232706 G>T maps to ENST00000382768 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr18:61232775 C>A maps to ENST00000382768 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:61256060 G>T maps to NM_012397.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr18:61262396 C>T maps to NM_012397.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:61259707 C>T maps to NM_012397.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr18:61264450 G>T maps to NM_012397.3 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr18:61261695 G>T maps to NM_012397.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:61264449 C>G maps to NM_012397.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr18:61261682 G>A maps to NM_012397.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:61256036 C>A maps to NM_012397.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61569690 A>T maps to NM_001143818.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr18:61569034 G>A maps to NM_001143818.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr18:61569720 A>T maps to NM_001143818.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr18:61565001 C>A maps to NM_001143818.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr18:61323002 G>T maps to NM_006919.2 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:61324184 G>T maps to NM_006919.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr18:61328408 G>A maps to NM_006919.2 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr18:61328385 G>T maps to NM_006919.2 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr18:61326665 C>T maps to NM_006919.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:61323256 C>T maps to NM_006919.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:61323257 C>T maps to NM_006919.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr18:61322929 G>T maps to NM_006919.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr18:61323160 G>C maps to NM_006919.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:61310739 C>T maps to NM_002974.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:61306951 A>T maps to NM_002974.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr18:61305339 A>G maps to NM_002974.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:61305165 G>A maps to NM_002974.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr18:61309035 G>T maps to NM_002974.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:61309071 T>C maps to NM_002974.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr18:61170714 C>A maps to NM_002639.4 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr18:61154282 G>T maps to NM_002639.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr18:61154261 C>A maps to NM_002639.4 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr18:61170561 G>C did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr6:2948735 G>A maps to ENST00000316782 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr6:2948600 G>A maps to ENST00000316782 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:61460396 A>T maps to NM_001040147.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:61468113 A>T maps to NM_001040147.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:61460402 C>T maps to NM_001040147.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr18:61471727 C>A maps to NM_001040147.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr18:61648984 C>T maps to NM_198833.1 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr6:2896337 C>A maps to NM_004155.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:2892183 G>A maps to NM_004155.4 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:173883689 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:173881079 G>A maps to NM_000488.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr22:21133941 C>A maps to NM_000185.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr7:100773739 G>T maps to NM_000602.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr7:100773717 C>A maps to NM_000602.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:100773861 C>A maps to NM_000602.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:100771709 G>A maps to NM_000602.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr13:51915466 G>A maps to NM_001101320.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr13:51922466 C>T maps to NM_001101320.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr13:51918463 G>T maps to NM_001101320.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr17:1680501 C>A maps to NM_002615.4 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr17:1675166 G>A maps to NM_002615.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:1675163 A>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:1673259 C>A maps to NM_002615.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:1657731 G>A maps to NM_000934.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr11:57382044 C>T maps to ENST00000403558 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:57367359 C>A maps to ENST00000403558 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:57367686 C>G maps to ENST00000403558 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:75277633 C>T maps to NM_001235.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr3:167506982 G>T maps to NM_005025.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:167525118 A>T maps to NM_005025.4 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:167159973 C>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:167183058 A>T maps to NM_006217.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:167189532 T>G maps to NM_006217.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:167189439 C>G maps to NM_006217.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:167183273 T>A maps to NM_006217.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:64863199 G>C maps to NM_014755.2 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:64863722 C>A maps to NM_014755.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:64863726 G>A maps to NM_014755.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:40947908 G>A maps to NM_203344.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:210415315 G>A maps to NM_019605.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:28599219 A>T maps to NM_031459.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:28598183 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:94924579 A>G maps to NM_144665.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:180014088 T>C maps to NM_178123.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr2:179974755 C>G did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr2:179997120 T>C maps to NM_178123.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr2:180008449 C>A maps to NM_178123.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:42618462 C>A maps to NM_015559.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr18:42532247 A>T maps to NM_015559.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:42643105 C>A maps to NM_015559.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:42533271 G>T maps to NM_015559.2 E1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr18:42529997 C>A maps to NM_015559.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:42531801 A>T maps to NM_015559.2 R833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr18:42531131 C>G maps to NM_015559.2 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:42531485 G>T maps to NM_015559.2 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:42530306 G>A maps to NM_015559.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:42531572 G>T maps to NM_015559.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr18:42281613 A>T maps to NM_015559.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr18:42531647 A>G maps to NM_015559.2 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:42281593 G>T maps to NM_015559.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr18:42531104 G>A maps to NM_015559.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:42530330 G>C maps to NM_015559.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr18:42643041 A>T did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr18:42530705 G>A maps to NM_015559.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr18:42531614 G>A maps to NM_015559.2 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:42530400 G>T maps to NM_015559.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr18:42530225 G>A maps to NM_015559.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr18:42530156 G>T maps to NM_015559.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr18:42530537 G>A maps to NM_015559.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr18:42532788 C>A maps to NM_015559.2 R1162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr18:42533123 G>A maps to NM_015559.2 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr18:42449193 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:42532739 T>G maps to NM_015559.2 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr16:30974842 A>T maps to NM_014712.1 K203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr16:30977307 C>T maps to NM_014712.1 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr16:30972796 C>T maps to NM_014712.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:30982945 G>C maps to NM_014712.1 T1088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:30991033 G>T maps to NM_014712.1 T1309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:30977497 G>T maps to NM_014712.1 G766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:30990547 C>T maps to NM_014712.1 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:30976133 T>C maps to NM_014712.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:47098502 C>T maps to NM_014159.6 L2257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:47164267 G>A maps to NM_014159.6 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr3:47158146 C>A maps to NM_014159.6 E1518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:47098322 T>G maps to NM_014159.6 P2317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:47162938 T>A maps to NM_014159.6 R1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr3:47142963 G>A maps to NM_014159.6 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr3:47058705 A>T maps to NM_014159.6 C2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr3:47103746 T>A maps to NM_014159.6 K2067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr3:47158224 G>A maps to NM_014159.6 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:47161675 C>A maps to NM_014159.6 E1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:47162370 G>C maps to NM_014159.6 S1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr3:47162474 C>T maps to NM_014159.6 W1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr3:47079268 T>A did not map to a codon.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr3:47103737 G>A maps to NM_014159.6 Q2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr3:47161669 A>C did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr3:47125820 C>A maps to NM_014159.6 E1817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:99876522 G>A maps to NM_199123.1 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr21:37418121 G>A maps to NM_017438.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr21:37429496 C>A maps to NM_017438.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr3:9517225 C>T maps to ENST00000407969 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr3:9488801 G>A maps to ENST00000407969 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr16:58552872 C>A maps to NM_001160305.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:140432852 C>T maps to NM_030648.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr12:123892160 C>A maps to NM_020382.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:150923356 A>T maps to NM_001145415.1 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:150913869 C>T maps to NM_001145415.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:150933450 T>G maps to NM_001145415.1 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:150936130 A>T maps to NM_001145415.1 K1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:150933235 G>T maps to NM_001145415.1 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr1:150933235 G>T maps to NM_001145415.1 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:135204106 T>A maps to ENST00000372169 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr9:135140264 G>T maps to ENST00000372169 L2494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:135139985 T>A maps to ENST00000372169 P2587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr9:135205013 C>T maps to ENST00000372169 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr9:135139694 C>T maps to ENST00000372169 R2684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:135147097 C>A maps to ENST00000372169 G2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:135158731 C>T maps to ENST00000372169 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr9:135139898 T>A maps to ENST00000372169 I2616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:135173643 C>T maps to ENST00000372169 P1868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr17:27308830 G>A maps to NM_178860.4 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:27306715 G>A maps to NM_178860.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:27284378 G>T maps to NM_178860.4 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr22:26706650 C>T maps to NM_021115.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr22:26688678 C>G maps to NM_021115.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26688934 G>T maps to NM_021115.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:26689002 G>A maps to NM_021115.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:26688943 G>T maps to NM_021115.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr22:26747057 C>A maps to NM_021115.4 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr22:26688867 C>G maps to NM_021115.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:26736428 G>A maps to NM_021115.4 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr22:26688382 G>T maps to NM_021115.4 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:26761425 C>A maps to NM_021115.4 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:26743760 G>A maps to NM_021115.4 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr22:26743880 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr22:26688795 C>A maps to NM_021115.4 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:26706659 C>T maps to NM_021115.4 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr22:26707785 T>C maps to NM_021115.4 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr22:26694959 G>C maps to NM_021115.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr22:26736410 G>T maps to NM_021115.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:29897070 C>T did not map to a codon.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr16:29883531 G>A maps to NM_201575.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:29889678 A>G maps to NM_201575.2 Y547Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:29884967 G>C maps to NM_201575.2 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:29909228 A>T maps to NM_201575.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:29896999 C>A maps to NM_201575.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:29900016 G>T maps to NM_201575.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr16:29891308 T>A maps to NM_201575.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:64534697 C>A maps to NM_201995.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr11:64533556 G>C maps to NM_201995.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:30738839 G>C maps to NM_005877.4 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr22:30738814 G>A maps to NM_005877.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:30735011 A>G maps to NM_005877.4 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr22:30737733 C>A maps to NM_005877.4 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr22:30740978 G>C maps to NM_005877.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:2247830 C>T maps to NM_007165.4 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:38435024 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:198273135 T>C maps to NM_012433.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:198260780 T>G maps to NM_012433.2 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:198281635 C>G did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:198273120 T>G maps to NM_012433.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:198274702 C>T maps to NM_012433.2 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:198257170 T>G maps to NM_012433.2 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:198274686 A>G maps to NM_012433.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr11:65819888 G>T maps to NM_006842.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:65819873 G>T maps to NM_006842.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:65829420 A>T maps to NM_006842.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:65828199 G>T maps to NM_006842.2 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:65823020 C>T maps to NM_006842.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr16:70573038 T>A maps to NM_012426.4 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:70599101 C>T maps to NM_012426.4 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr16:70602364 G>T maps to NM_012426.4 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:70599026 A>T maps to NM_012426.4 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:70605713 T>C maps to NM_012426.4 *1218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:70605714 G>T maps to NM_012426.4 *1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr16:70590925 G>T maps to NM_012426.4 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:149895598 C>A maps to NM_005850.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:149898366 G>A maps to NM_005850.3 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:144416465 C>A maps to NM_031287.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:19427360 C>A maps to NM_172231.2 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr22:31924784 C>T maps to NM_001007467.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr22:31985510 C>A maps to NM_001007467.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:7269846 C>A maps to NM_001018039.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:7290515 C>T maps to NM_001018039.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr10:7285574 C>A maps to NM_001018039.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr10:7230596 C>T maps to NM_001018039.1 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr10:7325986 G>A maps to NM_001018039.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr10:7214468 C>A maps to NM_001018039.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:7318907 C>A maps to NM_001018039.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:7214468 C>A maps to NM_001018039.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:7214463 G>T maps to NM_001018039.1 S715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:7423854 C>T maps to NM_001018039.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:7290521 C>A maps to NM_001018039.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:27189777 C>T maps to NM_006142.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:27190104 G>A maps to NM_006142.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:35652806 C>A maps to NM_005066.2 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:41122770 C>T maps to NM_003012.4 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:41166585 G>A maps to NM_003012.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr4:154702675 G>T maps to NM_003013.2 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:154709966 C>G maps to NM_003013.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:154707013 A>T did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr7:37953842 T>A maps to ENST00000223214 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr7:37953813 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr7:37956064 C>T maps to ENST00000223214 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:37955911 G>A maps to ENST00000223214 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:37953857 C>T maps to ENST00000223214 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:37949245 C>T maps to ENST00000223214 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:99531422 G>A maps to NM_003015.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:99531107 G>A maps to NM_003015.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:70716186 G>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:70715731 T>C did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:70715709 C>T maps to NM_004768.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:64020381 G>A maps to ENST00000513458 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr6:89808332 G>A maps to ENST00000452027 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr19:19115385 T>A maps to NM_001017392.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:19135689 C>T maps to NM_001017392.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:19115172 C>A maps to NM_001017392.3 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:19136772 C>T maps to NM_001017392.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:19136916 C>G maps to NM_001017392.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr21:33073367 T>C maps to NM_020706.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr21:33073387 G>A maps to NM_020706.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr21:33068518 A>G maps to NM_020706.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr21:33064700 G>A maps to NM_020706.2 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:45561076 G>A maps to NM_007056.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:45567458 C>T maps to NM_007056.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:45567404 A>G maps to NM_007056.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:45567305 C>G maps to NM_007056.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:45565453 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:1720178 G>T did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:1714285 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:1713003 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:1712955 G>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:1712781 G>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:1718146 G>T did not map to a codon.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr23:1719904 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:1719991 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr23:1712604 G>C did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:1712373 G>C did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:1714320 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr23:1720177 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:99857221 T>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr6:99848690 G>A maps to NM_032870.2 R715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr6:99848774 C>A maps to NM_032870.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:74733002 C>G maps to NM_003016.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr17:74733176 G>C maps to NM_003016.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr12:46355640 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr12:46315890 C>A maps to NM_004719.2 R1444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:29476679 G>T maps to NM_005626.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:29475665 G>A maps to NM_005626.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:29475145 C>A maps to NM_005626.4 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:42088435 G>C maps to NM_006275.5 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr20:42089579 G>C maps to NM_006275.5 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:38976797 G>T maps to NM_001031684.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:132199365 G>T did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:132198708 G>T maps to NM_004592.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr12:132262641 T>A maps to NM_004592.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr12:132281797 A>G maps to NM_004592.2 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:132195839 G>T maps to NM_004592.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:120901791 G>A maps to NM_003769.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:168211775 T>C maps to NM_199344.2 *161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:85894863 G>A maps to NM_198843.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:85893738 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr10:81697778 C>T maps to NM_003019.4 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr10:81700539 A>T maps to NM_003019.4 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr5:174936181 A>T maps to NM_022754.5 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr5:174938508 G>T maps to NM_022754.5 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:104488199 G>T maps to NM_178858.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:102796832 A>G maps to NM_030971.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr2:73172186 C>A maps to NM_144579.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr17:48244786 G>A maps to NM_000023.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:155771557 G>A maps to NM_000337.5 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:156186283 G>C maps to NM_000337.5 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:155935667 G>T maps to NM_000337.5 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:155935672 C>T maps to NM_000337.5 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:155935676 C>T maps to NM_000337.5 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr13:23808790 C>T maps to NM_000231.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr8:13948038 G>A maps to NM_139167.2 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:14412246 G>A maps to NM_139167.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr8:13948146 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:14181673 G>T maps to NM_139167.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr8:14095115 C>A maps to NM_139167.2 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr8:14412309 C>A maps to NM_139167.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:153909104 A>G maps to NM_015595.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr3:153909092 C>T maps to NM_015595.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr3:153839862 C>T maps to NM_015595.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:67199563 G>C did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:67155925 C>A maps to ENST00000237247 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:67155964 C>A maps to ENST00000237247 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:67148050 T>C maps to ENST00000237247 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:67147756 A>G maps to ENST00000237247 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:67154912 A>T maps to ENST00000237247 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr1:67101697 G>T maps to NM_032291.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:67147696 G>T maps to ENST00000237247 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:67148047 C>G maps to ENST00000237247 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:134491573 C>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr8:42977284 A>G maps to NM_032237.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr8:42977911 C>T maps to NM_032237.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr8:8185690 C>A maps to NM_001080826.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:8234235 T>A maps to NM_001080826.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:8234232 C>T maps to NM_001080826.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:8175843 C>A maps to NM_001080826.1 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr8:8197003 G>T maps to NM_001080826.1 C768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr8:8234169 G>T maps to NM_001080826.1 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr15:77471193 T>C maps to NM_024776.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr15:77471207 C>A maps to NM_024776.2 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:77406518 C>G maps to NM_024776.2 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77471963 G>A maps to NM_024776.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:77472166 G>C maps to NM_024776.2 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:77407466 G>A maps to NM_024776.2 D1424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:77406889 C>A maps to NM_024776.2 E1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:67734615 C>T maps to NM_013257.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:67763154 G>T maps to NM_013257.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:67740917 G>C maps to NM_013257.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:26938633 C>A maps to NM_001174103.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:52103483 C>A maps to ENST00000361543 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr4:108831633 T>G maps to NM_152621.5 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:108817002 A>T maps to NM_152621.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:20216188 T>C maps to NM_001012410.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr3:20225246 T>C maps to NM_001012410.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:20212683 C>A maps to NM_001012410.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr3:20216035 G>C maps to NM_001012410.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:201448174 G>A maps to NM_152524.5 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:201437198 G>A maps to NM_152524.5 K710K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:201436295 G>A maps to NM_152524.5 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:201400786 G>C did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:201436412 C>T maps to NM_152524.5 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:201437172 C>T maps to NM_152524.5 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:201438677 G>T maps to NM_152524.5 R1203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:72633342 C>G maps to NM_003901.3 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr14:64194056 G>A maps to NM_030791.2 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:64194139 G>A maps to NM_030791.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:78184802 C>A maps to NM_000199.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr22:25264767 G>T maps to NM_001039948.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:25280125 G>A maps to NM_001039948.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:2270676 C>T maps to NM_014853.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:2278841 C>T maps to NM_014853.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr22:40804796 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:40804843 C>A maps to NM_015705.4 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:64976347 C>T maps to NM_019072.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr16:28883955 C>T maps to NM_001145795.1 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:28883245 G>A maps to NM_001145795.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:28878263 G>T maps to NM_001145795.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:28880416 G>T maps to NM_001145795.1 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:28878162 G>T maps to NM_001145795.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:28884518 G>A maps to NM_015503.2 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr16:28884057 G>T maps to NM_001145797.1 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr7:101952176 C>T maps to ENST00000306803 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr7:101957802 C>T maps to ENST00000306803 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:101944559 C>T maps to ENST00000306803 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:123504057 G>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:123504070 C>G did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:123480600 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:123480537 G>T did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:162372582 A>G maps to NM_053282.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:162372570 T>G maps to NM_053282.4 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:162381776 C>T maps to NM_053282.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:156779566 G>A maps to NM_001161441.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:156784832 G>T maps to NM_001161441.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:156776987 G>A maps to NM_001161441.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr9:130502573 C>T maps to NM_170600.2 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr9:130502578 T>A maps to NM_170600.2 K720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:130511548 G>A maps to NM_170600.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:130513534 G>T maps to NM_170600.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:130511802 C>A maps to NM_170600.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr8:19218728 A>T maps to NM_022071.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr10:82329943 G>T maps to NM_207372.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:82363434 G>A maps to NM_207372.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:82363482 G>A maps to NM_207372.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:82403797 G>T maps to NM_207372.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:82403815 C>A maps to NM_207372.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:21050588 C>T maps to ENST00000444387 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr15:78390402 C>A maps to NM_001101404.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr21:40871810 G>T maps to NM_007341.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr21:40824018 C>G maps to NM_007341.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr21:40871828 C>T maps to NM_007341.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:80552721 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:80532612 C>A did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr22:38046678 G>T maps to NM_018957.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:2826360 G>A maps to NM_001145856.1 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:2829390 A>T maps to NM_001145856.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr4:2831499 C>T maps to NM_001145856.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:235950022 G>T maps to NM_014521.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:235949598 G>A maps to NM_014521.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:235951263 C>T maps to NM_014521.2 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:235951776 G>C maps to NM_014521.2 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:235949691 G>A maps to NM_014521.2 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:15298612 C>T maps to NM_004844.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:249110822 C>A maps to NM_030645.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:152069309 G>A maps to NM_001009555.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:152086801 T>A maps to NM_001009555.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:152043242 C>A maps to NM_001009555.3 *791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr4:152095960 C>A maps to NM_001009555.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr9:17795654 G>T maps to NM_003026.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:17795575 G>T maps to NM_003026.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:17793472 C>T maps to NM_003026.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:17791272 G>A maps to NM_003026.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:17791273 G>T maps to NM_003026.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr15:84286921 G>A maps to ENST00000434347 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:84257443 A>T maps to ENST00000434347 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr15:84237416 C>A maps to ENST00000434347 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr15:84286885 G>A maps to ENST00000434347 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:84245426 G>T maps to ENST00000434347 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:84237386 G>C maps to ENST00000434347 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:87181525 A>G maps to ENST00000482504 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:131784696 C>A maps to ENST00000372554 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:19650022 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:19817750 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:19555895 C>G did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr23:19560189 C>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:19560136 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:19554561 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:19564043 G>T did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:19649987 G>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:19854297 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:19555847 C>A did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:105365610 C>A maps to ENST00000369774 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr10:105365602 C>T maps to ENST00000369774 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr10:105362703 C>T maps to ENST00000369774 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:105362385 C>A maps to ENST00000369774 A863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:171765891 C>A maps to NM_001017995.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr5:171766496 C>A maps to NM_001017995.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:171766608 T>A maps to NM_001017995.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr5:171765852 C>T maps to NM_001017995.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr5:171849422 G>A maps to NM_001017995.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:171765621 G>A maps to NM_001017995.2 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:171849421 G>A maps to NM_001017995.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr5:171765672 C>T maps to NM_001017995.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:171765998 C>A maps to NM_001017995.2 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:171765969 C>A maps to NM_001017995.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:171777412 G>A maps to NM_001017995.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:170190189 C>G maps to NM_020870.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:170037776 T>A maps to NM_020870.3 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:145379835 C>T maps to NM_152550.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:145439753 G>A maps to NM_152550.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:145435702 C>G maps to NM_152550.3 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:145435759 G>T maps to NM_152550.3 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:110015185 G>T maps to NM_001099289.1 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:109988085 G>A maps to NM_001099289.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:110015056 C>A maps to NM_001099289.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:110048968 C>G maps to NM_001099289.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:110065635 T>A maps to NM_001099289.1 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:8220036 C>T maps to NM_018986.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:8224564 A>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:8230276 G>A maps to NM_018986.3 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:8224570 G>T maps to NM_018986.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr4:8229061 G>T maps to NM_018986.3 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr4:8233745 C>T maps to NM_018986.3 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr4:8242468 C>T maps to NM_018986.3 A1266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:148388513 G>T maps to NM_024577.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:148408067 C>T maps to NM_024577.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:148407764 G>A maps to NM_024577.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:148406268 C>T maps to NM_024577.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:233126 C>T maps to NM_015677.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:51220029 A>G maps to ENST00000391814 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:51217449 G>T maps to ENST00000391814 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:51205844 G>A maps to ENST00000391814 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:51191243 C>A maps to ENST00000391814 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:51217149 G>A maps to ENST00000391814 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:51217135 C>A maps to ENST00000391814 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:51215302 C>T maps to ENST00000391814 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr19:51169804 T>A maps to ENST00000391814 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:51219651 A>G maps to ENST00000391814 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:51171706 G>T maps to ENST00000391814 R1178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:51165488 C>T maps to ENST00000391814 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:51219609 G>A maps to ENST00000391814 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:51205826 C>T maps to ENST00000391814 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr19:51165361 G>A maps to ENST00000391814 R2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:51165452 G>A maps to ENST00000391814 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:70319291 T>A maps to ENST00000338508 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr11:70319333 G>A maps to ENST00000338508 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr11:70319438 G>A maps to ENST00000338508 P1689P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8506-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:70507782 A>G maps to ENST00000338508 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:70331738 C>T maps to ENST00000338508 K1547K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-86-8358-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr11:70505956 T>C maps to ENST00000338508 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr11:70335436 T>C maps to ENST00000338508 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:51143399 G>T maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr22:51159380 C>A maps to NM_001080420.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr22:51160826 G>T maps to NM_001080420.1 L1538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr22:51143399 G>C maps to NM_001080420.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr22:51123020 C>T maps to NM_001080420.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr22:51160715 G>T maps to NM_001080420.1 G1501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:145153864 G>A maps to NM_030974.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:37974622 C>G maps to NM_003028.2 L350L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-8507-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:38016129 T>G did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:37974718 G>A maps to NM_003028.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:7536068 G>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:154940997 G>A maps to NM_001130040.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr1:154940730 G>A maps to NM_001130040.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr1:154942830 G>A maps to NM_001130040.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:419035 C>G maps to NM_012435.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr19:436407 G>A maps to NM_012435.2 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:436422 C>T maps to NM_012435.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:422250 C>A maps to NM_012435.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:91656986 C>T maps to NM_016848.5 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:91690071 C>T maps to NM_016848.5 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:49149956 T>A maps to NM_203349.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr15:49118220 T>A maps to NM_203349.3 K614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr15:49255112 G>T maps to NM_203349.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:46615700 C>A maps to NM_024745.4 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr16:46633755 T>A maps to NM_024745.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr16:46638314 G>A maps to NM_024745.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:4290476 G>T maps to NM_020209.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:154471586 C>A did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:154458441 G>A maps to NM_001010846.2 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:45490968 C>G did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:96318268 T>C maps to NM_006304.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr13:26620731 C>T maps to NM_001007538.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr13:26621046 G>T maps to NM_001007538.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr4:42403322 C>A maps to NM_001080505.1 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:201860533 G>T maps to NM_198149.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr3:48510921 G>A maps to NM_016479.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41096893 C>A maps to NM_138392.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:41094611 A>G maps to NM_138392.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:112764371 A>G maps to NM_007373.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:112724820 T>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:112764362 G>T did not map to a codon.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr23:591834 T>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr23:591646 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:591679 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:591811 G>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:591668 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:591803 G>C did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:591846 A>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:591754 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:591663 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:591755 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:601755 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:591765 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:595518 G>T did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:595381 G>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:591818 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:595528 C>G did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:157823777 A>G maps to NM_003030.4 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:157820573 C>A maps to NM_003030.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:157820535 G>T maps to NM_003030.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:157820468 G>A maps to NM_003030.4 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr3:157817684 A>G maps to NM_003030.4 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:157817717 G>A maps to NM_003030.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:157815884 G>C maps to NM_003030.4 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:3539417 G>A maps to NM_013276.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:146247375 T>A maps to ENST00000367503 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr6:146276083 A>T maps to ENST00000367503 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:146269412 T>C maps to ENST00000367503 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:146266722 C>A maps to ENST00000367503 G458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr6:146262926 T>C maps to ENST00000367503 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:72890351 T>C did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:72890282 G>C maps to NM_018130.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr3:72897455 C>A maps to NM_018130.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:9862710 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:9864436 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:9862977 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:9863529 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:9900369 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:9862756 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:9864171 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:9905203 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:9900401 C>A did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:9863283 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:9864700 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:9905466 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:9863245 G>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:9862785 C>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:9863585 C>T did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:9864515 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:9900700 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:77660381 G>C maps to NM_020859.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr4:77680772 G>A maps to NM_020859.3 E1758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:77660855 G>A maps to NM_020859.3 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:50377001 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:50378520 G>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:50378102 T>C did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:50351110 C>A did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:50350457 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:50350575 C>T did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:50350570 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:50351177 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:50376445 T>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:50350710 T>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:50350925 G>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:50377002 C>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:50378221 T>A did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:50350943 C>A did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:50376204 A>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:50350667 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:50377605 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:50376864 T>C did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:164714403 T>C maps to NM_001041.3 S1537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:164758883 T>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:164700807 T>A maps to NM_001041.3 V1743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:164748532 T>C maps to NM_001041.3 Q953Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:164709181 G>A maps to NM_001041.3 H1689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:164735437 T>G maps to NM_001041.3 P1219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:164766994 G>T maps to NM_001041.3 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:164704959 C>T maps to NM_001041.3 Q1721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:164760930 T>C maps to NM_001041.3 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:164780196 C>A maps to NM_001041.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr3:164758795 G>A maps to NM_001041.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:164748523 T>A maps to NM_001041.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr3:164709250 G>T maps to NM_001041.3 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:164735353 C>A maps to NM_001041.3 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:164780172 G>A maps to NM_001041.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:164764689 C>T maps to NM_001041.3 W609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr3:164741355 A>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:164737504 G>T maps to NM_001041.3 S1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:164777758 G>T maps to NM_001041.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr3:164780203 G>T maps to NM_001041.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:164757710 C>T maps to NM_001041.3 W736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr3:164732922 A>G maps to NM_001041.3 I1329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:164793763 G>A maps to NM_001041.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:164737504 G>T maps to NM_001041.3 S1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:164714385 G>T maps to NM_001041.3 T1543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:164709250 G>C maps to NM_001041.3 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr3:164785183 C>T maps to NM_001041.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:164724631 C>A maps to NM_001041.3 G1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:164735452 G>T maps to NM_001041.3 G1214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:164737458 T>C maps to NM_001041.3 E1118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:164764800 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:164741564 C>A did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr3:164716430 C>G maps to NM_001041.3 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr3:164760959 C>A maps to NM_001041.3 G631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr3:150460020 G>A maps to NM_005067.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr13:46357676 C>T maps to NM_198849.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr13:46357744 G>A maps to NM_198849.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr13:46357952 G>T maps to NM_198849.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:113323795 G>T maps to ENST00000393830 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:113323789 G>A maps to ENST00000393830 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:117058368 T>A maps to NM_001040455.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr11:117062657 G>C maps to NM_001040455.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:117052223 C>A maps to NM_001040455.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr11:117050023 G>T maps to NM_001040455.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr11:117063022 C>T maps to NM_001040455.1 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:3675340 G>A maps to NM_023068.3 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr20:3682055 C>T maps to NM_023068.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr20:3669804 C>A maps to NM_023068.3 T1689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr20:3672023 C>A maps to NM_023068.3 G1518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr20:3674160 G>T maps to NM_023068.3 Y1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:3677377 G>T maps to NM_023068.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:3672715 C>A maps to NM_023068.3 T1388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr20:3682160 C>A maps to NM_023068.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr20:3680083 C>A maps to NM_023068.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr20:3687144 G>C maps to NM_023068.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:3673731 G>T maps to NM_023068.3 G1185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:3677795 G>C maps to NM_023068.3 Y772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:3680040 T>A maps to NM_023068.3 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:3677876 G>A maps to NM_023068.3 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr20:3675113 G>A maps to NM_023068.3 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:3684574 C>A maps to NM_023068.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:51918645 G>T maps to NM_033130.4 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:51914384 G>A maps to NM_033130.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:51919588 G>A maps to NM_033130.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:51914559 G>T maps to NM_033130.4 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:51916968 G>T maps to NM_033130.4 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:51919275 G>T maps to NM_033130.4 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:51920651 C>T maps to NM_033130.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51918204 G>T maps to NM_033130.4 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:51914472 G>T maps to NM_033130.4 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr19:51918537 G>T maps to NM_033130.4 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr19:51918585 G>A maps to NM_033130.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:50453298 T>A maps to NM_052884.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr19:50453256 C>T maps to NM_052884.2 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:50453286 C>T maps to NM_052884.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:52002707 G>T maps to NM_053003.2 V357V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-6590-01A-12D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:52003552 C>G maps to NM_053003.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr19:52003555 T>A maps to NM_033329.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:52002905 C>T maps to NM_053003.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr19:51994906 G>A maps to NM_053003.2 N592N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:52002433 T>G maps to NM_053003.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:52003341 C>A maps to ENST00000441969 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:52147103 C>A maps to NM_001098612.1 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52147181 G>T maps to NM_001098612.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:52146637 G>C maps to NM_001098612.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:52147284 C>A maps to NM_001098612.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:52146833 A>C maps to NM_001098612.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:43405707 C>T maps to NM_213602.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr18:43418872 G>T maps to NM_213602.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:43417012 A>G maps to NM_213602.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:52132707 G>A maps to ENST00000222107 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:52132674 G>T maps to ENST00000222107 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:52130811 G>A maps to ENST00000222107 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:52034720 C>A maps to NM_001245.5 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:52023449 G>T maps to NM_001245.5 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr19:52031474 C>A maps to NM_001245.5 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:52033170 G>T maps to NM_001245.5 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:52034549 C>T maps to NM_001245.5 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:52034178 C>T maps to NM_001245.5 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:52034211 G>T maps to NM_001245.5 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:51650071 C>A maps to NM_014385.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:51656417 C>T maps to NM_014385.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:51961203 C>G maps to NM_014442.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:51961290 C>T maps to NM_014442.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:51958852 A>C maps to NM_014442.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:51955751 G>A maps to NM_014442.2 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr19:51960928 C>A maps to NM_014442.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:51958819 G>T maps to NM_014442.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:51955812 C>G maps to NM_014442.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:51960827 G>T maps to NM_014442.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:51957990 C>A maps to NM_014442.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:51628389 T>G maps to NM_014441.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:51628629 C>T maps to NM_014441.2 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:51629007 C>T maps to NM_014441.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr19:51630512 T>A maps to NM_014441.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:51628302 G>A maps to NM_014441.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:51633159 G>T maps to NM_014441.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:44845962 G>T maps to NM_173354.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:111592582 C>T maps to NM_015191.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:116729003 T>C maps to ENST00000445177 Q1052Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:115323060 C>T maps to NM_001102396.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr6:100841681 C>T maps to ENST00000262901 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:100838548 C>T maps to ENST00000262901 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:100838542 G>T maps to ENST00000262901 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:100901720 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:100868680 A>T maps to ENST00000262901 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:100838701 G>T maps to ENST00000262901 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:100841690 C>T maps to ENST00000262901 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:100838302 C>G maps to ENST00000262901 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:100838746 C>A maps to ENST00000262901 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr6:100838763 G>A maps to ENST00000262901 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr6:100895208 C>T maps to ENST00000262901 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr21:38095421 C>T maps to NM_005069.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr21:38095363 C>A maps to NM_005069.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr15:75687133 C>A maps to NM_001145357.1 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:16973309 G>T maps to NM_015260.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:16977261 G>A maps to NM_015260.1 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:16942394 C>T maps to NM_015260.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:16980569 G>T maps to NM_015260.1 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:39597481 A>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:65409956 C>T maps to NM_153253.29 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:72176330 G>T maps to NM_015556.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr14:72139159 G>A maps to NM_015556.1 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr14:72117071 A>T maps to NM_015556.1 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:72165839 G>T maps to NM_015556.1 E1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr14:72055392 G>A maps to NM_015556.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:72191384 A>C did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr14:72055434 C>G maps to NM_015556.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr14:72055329 C>T maps to NM_015556.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:72054984 G>T maps to NM_015556.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:72176378 A>T maps to NM_015556.1 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr14:72138120 A>G maps to NM_015556.1 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:72139291 G>T maps to NM_015556.1 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:72196852 G>T maps to NM_015556.1 E1587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:72054813 G>T maps to NM_015556.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr14:72090865 G>T maps to NM_015556.1 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr14:72152330 G>C maps to NM_015556.1 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:232596805 C>A maps to NM_020808.3 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:232577114 G>A maps to NM_020808.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:232650755 G>A maps to NM_020808.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:232577114 G>C maps to NM_020808.3 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:232568020 C>A maps to NM_020808.3 E1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:232600609 G>A maps to NM_020808.3 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:232596703 G>A maps to NM_020808.3 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:232579371 C>T maps to NM_020808.3 W1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:232600633 C>A maps to NM_020808.3 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232538194 G>T maps to NM_020808.3 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:232601022 C>A maps to NM_020808.3 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:232539871 T>A maps to NM_020808.3 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:232650571 C>A maps to NM_020808.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:232539222 G>A maps to NM_020808.3 G1637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:232577107 G>A maps to NM_020808.3 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:232601162 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:232649717 G>C maps to NM_020808.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:232649636 C>A maps to NM_020808.3 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:38621382 C>A maps to NM_015073.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:38689107 C>G maps to NM_015073.1 P1640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:38572906 G>C maps to NM_015073.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:38600928 G>A maps to NM_015073.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:38590663 C>T maps to NM_015073.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:38610392 C>T maps to NM_015073.1 C913C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:38692559 G>T maps to NM_015073.1 P1681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr20:1905434 C>T maps to ENST00000400068 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:1902287 C>A maps to ENST00000400068 C228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:1592249 C>A maps to NM_001135844.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr20:1551450 C>A maps to NM_006065.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:1584723 G>T maps to NM_001135844.1 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr20:1559086 G>T maps to NM_006065.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr20:1600515 T>G maps to NM_006065.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:1552624 T>C maps to NM_006065.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:1559270 G>T maps to NM_006065.3 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:1600575 G>A maps to NM_006065.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:1458022 T>A maps to NM_001122962.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:1457983 T>A maps to NM_001122962.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:1460537 G>A maps to NM_001122962.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:1456859 G>A maps to NM_001122962.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr20:1532358 C>A maps to ENST00000381621 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:1616966 G>T maps to NM_018556.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr20:1617080 G>T maps to NM_018556.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:1617043 G>A maps to NM_018556.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:69666587 A>G maps to NM_012238.4 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:69648736 G>A maps to NM_012238.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr19:39379729 C>A maps to NM_012237.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr11:216719 T>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:120741789 C>T maps to NM_012240.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:79873369 C>T maps to NM_016538.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:79872367 C>A maps to NM_016538.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:61113222 C>A maps to NM_005982.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:61113210 G>A maps to NM_005982.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:45233557 T>C maps to NM_016932.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:45233521 C>A maps to NM_016932.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:45233521 C>T maps to NM_016932.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:45236243 G>A maps to NM_016932.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:45169953 C>T maps to NM_005413.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:45169935 C>A maps to NM_005413.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr2:45169548 G>T maps to NM_005413.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:61180535 T>A maps to NM_017420.4 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr14:60976496 C>T maps to ENST00000381716 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:57232318 G>A maps to NM_001100595.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr17:57232318 G>A maps to NM_001100595.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr17:46239859 G>T maps to NM_003726.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:46247979 G>A maps to NM_003726.3 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:46262149 G>A maps to NM_003726.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:26778483 C>A maps to NM_003930.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:26779577 G>A maps to NM_003930.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:26766625 C>A did not map to a codon.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:2234505 C>T maps to NM_003036.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr1:2160606 C>T maps to NM_003036.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170108877 C>T maps to NM_005414.3 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:170078702 C>G maps to NM_005414.3 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr3:170078421 G>A maps to NM_005414.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:170110111 C>G maps to NM_005414.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr6:31930284 G>C maps to NM_006929.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:31934830 G>A maps to NM_006929.4 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:31928517 G>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr5:54701405 G>T maps to NM_015360.4 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr5:54654398 A>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr5:54603852 A>G maps to NM_015360.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:54674314 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:54649009 G>T maps to NM_015360.4 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr5:133496683 G>T maps to NM_170679.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:36184064 T>C maps to ENST00000308927 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr5:36171761 G>T maps to NM_005983.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:36183977 C>T maps to ENST00000308927 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:134050793 G>T maps to NM_006748.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:35261996 G>C maps to NM_032214.2 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:48381722 A>G maps to NM_020846.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr4:48422151 A>T maps to NM_020846.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160604646 G>T maps to NM_003037.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:160604514 G>T maps to NM_003037.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:160465952 G>A maps to NM_001184714.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:160719713 G>T maps to NM_021181.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:160709144 A>T maps to NM_021181.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:160722918 C>G maps to NM_021181.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr1:160718245 G>T maps to NM_021181.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:160722019 T>A maps to NM_021181.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr1:159799980 C>A maps to NM_020125.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr1:159799709 C>A maps to NM_020125.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:159921657 T>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:159921479 C>A maps to NM_033438.3 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr1:159921513 C>T maps to NM_033438.3 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:159922324 C>G did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr4:1705369 T>A maps to ENST00000318386 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:70252969 G>C maps to NM_003049.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr14:70253008 G>A maps to NM_003049.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr14:70245095 G>T maps to NM_003049.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:103698484 A>C maps to NM_000452.2 *349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr13:103718409 G>T maps to NM_000452.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:103718365 G>T maps to NM_000452.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:103718338 C>A maps to NM_000452.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr13:103718242 G>T maps to NM_000452.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:153716928 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:153716007 C>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:153716543 T>A did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr23:153716612 G>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:153716439 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:153716656 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:153716385 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:48486984 C>A maps to NM_152679.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr8:82607047 G>T maps to NM_001010893.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:87770120 C>A maps to NM_197965.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:87770177 C>A maps to NM_197965.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:87746720 T>A maps to NM_197965.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:147438204 T>A maps to ENST00000507030 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:147215232 G>A maps to ENST00000507030 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219255991 C>G maps to NM_000578.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:51385986 G>A maps to NM_001174125.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:51390649 C>A maps to NM_001174125.1 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:48537079 C>A maps to NM_000338.2 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:48541793 C>T maps to NM_000338.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:48500072 G>T maps to NM_000338.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr15:48559801 G>A maps to NM_000338.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:48512829 G>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:48541778 G>A maps to NM_000338.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr15:48577388 C>A maps to NM_000338.2 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:48577446 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr15:48500059 C>T maps to NM_000338.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:48591462 C>G maps to NM_000338.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:127487035 A>T maps to NM_001046.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr5:127466873 A>T maps to NM_001046.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:127512818 T>A maps to NM_001046.2 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:127520533 T>C maps to NM_001046.2 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:127469952 G>T maps to NM_001046.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr5:127471498 A>G maps to NM_001046.2 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:127466898 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:127420128 G>T maps to NM_001046.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:56906303 C>A maps to NM_000339.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr16:56913527 G>T maps to NM_000339.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:56903737 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:56913483 C>T maps to NM_000339.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:56902267 G>A maps to NM_000339.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr16:56913479 G>A maps to NM_000339.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:56901118 G>A maps to NM_000339.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:56921835 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:56906649 C>T maps to NM_000339.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:56904029 C>T maps to NM_000339.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr16:56904080 C>T maps to NM_000339.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:56906694 C>A maps to NM_000339.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr16:56906649 C>A maps to NM_000339.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr16:67995579 C>G maps to NM_005072.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:44664167 G>T maps to NM_001134771.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:44665906 C>A maps to NM_001134771.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:44676137 C>T maps to NM_001134771.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr20:44664477 C>T maps to NM_001134771.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:44674596 C>A maps to NM_001134771.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44680366 G>T maps to NM_001134771.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:44676201 G>T maps to NM_001134771.1 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr20:44682332 C>A maps to NM_001134771.1 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:44684856 C>A maps to NM_001134771.1 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr20:44671915 C>A maps to NM_001134771.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:44682251 G>T maps to NM_001134771.1 V884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:44671909 T>C maps to NM_001134771.1 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:44670120 C>A maps to NM_001134771.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:44674635 G>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:44670121 C>A maps to NM_001134771.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:44678414 C>T maps to NM_001134771.1 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:44673769 C>A maps to NM_001134771.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr20:44685847 G>T maps to NM_001134771.1 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr15:34549905 T>C maps to NM_133647.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr5:1089170 G>A maps to NM_006598.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:1085384 G>T maps to NM_006598.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr5:1057692 C>T maps to NM_006598.2 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:100459432 G>T maps to NM_020246.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:100459384 C>T maps to NM_020246.2 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr7:100454718 C>T maps to NM_020246.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100457847 G>A maps to NM_020246.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr7:100452362 G>T maps to NM_020246.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr7:100463719 C>T maps to NM_020246.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:100459381 G>T maps to NM_020246.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:122809328 C>A maps to NM_022444.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:122768941 G>T maps to NM_022444.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:122774492 G>T maps to NM_022444.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:122787355 G>T maps to NM_022444.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:26817769 C>T maps to NM_001145975.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:26817754 G>A maps to NM_001145975.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:26821466 G>A maps to NM_001145975.1 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:26817354 G>T maps to NM_001145975.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr17:26821424 G>A maps to NM_001145975.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:26818828 G>T maps to NM_001145975.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:45194996 C>T maps to NM_022829.5 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:45224800 G>C maps to NM_022829.5 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr20:45188666 G>T maps to NM_022829.5 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:135376068 C>T maps to NM_012450.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:135384242 C>T maps to NM_012450.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:135406253 G>A maps to NM_012450.2 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:6597461 C>G maps to NM_177550.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:6606403 G>T maps to NM_177550.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:43319550 C>T maps to NM_001146037.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr18:43319535 C>G maps to NM_001146037.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr18:43316471 C>A maps to NM_001146037.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr18:43247834 C>A maps to NM_007163.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:43262342 G>C maps to NM_007163.3 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:43204723 C>A maps to NM_007163.3 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:43217059 C>T maps to NM_007163.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:43262321 A>T maps to NM_007163.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:43217146 G>T maps to NM_007163.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr18:43223095 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr18:43262477 C>T maps to NM_007163.3 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr18:43219805 G>A maps to NM_007163.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr18:43249420 C>A maps to NM_007163.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr18:43204730 C>T maps to NM_007163.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr18:43262345 G>T maps to NM_007163.3 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr18:43247046 G>T maps to NM_007163.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:99364134 T>A maps to NM_005073.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr13:99337124 A>G maps to NM_005073.3 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr13:99336993 G>C maps to NM_005073.3 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr13:99364188 G>T maps to NM_005073.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:99356686 T>C maps to NM_005073.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr13:99368130 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr13:99337070 G>T maps to NM_005073.3 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:99340561 A>T maps to NM_005073.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr13:99340767 G>A maps to NM_005073.3 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:121658293 T>C maps to NM_021082.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:121634150 A>G maps to NM_021082.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:121641149 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:60714086 G>C maps to NM_016582.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:60714149 C>A maps to NM_016582.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:60711283 C>T maps to NM_016582.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr12:129299351 G>A maps to ENST00000376744 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:113464669 A>T maps to NM_003051.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:113456701 G>A maps to NM_003051.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:113460445 G>A maps to NM_003051.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:111498612 C>T maps to NM_018593.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:91195874 C>T maps to NM_213606.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:230911412 C>A maps to NM_152527.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:230911223 C>T maps to NM_152527.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:230910509 G>T maps to NM_152527.4 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr2:230902170 G>A maps to NM_152527.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:230923852 G>A maps to NM_152527.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:73744217 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:73744384 A>C did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:73740832 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:73641729 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:73749080 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:73740855 C>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:80194623 C>A maps to NM_001042423.1 C81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:80195566 C>T maps to NM_001042423.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:110925480 G>A maps to NM_004696.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr17:73096183 G>T maps to ENST00000450736 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:73089907 C>T maps to ENST00000450736 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:66267478 G>T maps to NM_004694.4 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:66267220 G>T maps to NM_004694.4 Y360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:66267739 G>T maps to NM_004694.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr17:66274419 C>T maps to NM_004694.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:60168525 C>T maps to NM_004731.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr12:60168855 T>C maps to NM_004731.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:60169062 C>T maps to NM_004731.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:60168654 C>G maps to NM_004731.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr10:61424036 C>A maps to NM_194298.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:61413643 G>A maps to NM_194298.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr10:61413826 T>A maps to NM_194298.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:25799036 T>C maps to NM_005074.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr6:25811899 G>A maps to NM_005074.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:25813178 A>C maps to NM_005074.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:25820092 G>T maps to NM_005074.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:25813394 A>G maps to NM_005074.3 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr6:25819736 A>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:25917310 G>A maps to NM_005835.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr6:25914896 A>G maps to NM_005835.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr6:25921559 G>T maps to NM_005835.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr6:25921538 C>G maps to NM_005835.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr6:25921589 G>T maps to NM_005835.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr6:25921577 C>A maps to NM_005835.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:25921631 C>A maps to NM_005835.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr6:25924082 G>C maps to NM_005835.2 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr6:25850731 G>C maps to NM_001098486.1 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:25850351 C>A maps to NM_001098486.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:25861851 C>A maps to NM_001098486.1 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:25850031 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr6:25776839 C>T maps to NM_005495.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:25769243 C>A maps to NM_005495.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:25773865 G>C maps to NM_005495.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:25777187 G>T maps to ENST00000397076 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr6:25776914 C>A maps to NM_005495.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:25762210 C>G maps to NM_005495.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr6:25770377 C>A maps to NM_005495.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:74325055 T>A maps to NM_012434.4 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:22363283 C>G maps to NM_020346.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:22397613 G>T maps to NM_020346.2 G421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:22384369 C>T maps to NM_020346.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr11:22364897 C>T maps to NM_020346.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr11:22391655 C>A maps to NM_020346.2 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr11:22396357 G>T maps to NM_020346.2 G367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:22396309 C>T maps to NM_020346.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:22363193 C>A maps to NM_020346.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:22398218 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:22364833 C>T maps to NM_020346.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:22397612 G>A maps to NM_020346.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:22363100 G>C maps to NM_020346.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:22380973 C>A maps to NM_020346.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:22384321 T>A maps to NM_020346.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr11:22384372 T>C did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:22397582 G>T maps to NM_020346.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:22380973 C>A maps to NM_020346.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:22382441 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:49934328 C>A maps to NM_020309.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr19:49934331 G>A maps to NM_020309.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:49938489 A>G maps to NM_020309.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr19:49933856 G>T maps to NM_020309.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr19:49933994 G>A maps to NM_020309.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr12:100806590 G>A maps to NM_139319.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr12:100811934 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:100796414 G>T maps to NM_139319.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:100806633 G>T maps to NM_139319.2 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:61594721 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr20:61594047 C>T maps to NM_022082.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:20004894 G>T maps to NM_001135691.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:20003353 G>T maps to NM_001135691.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr8:20004767 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:20036724 A>T maps to NM_001135691.2 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr8:20036005 T>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr8:20022570 G>T maps to NM_001135691.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:119017344 G>T maps to NM_003054.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr10:119014860 G>T maps to NM_003054.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:119003683 C>A maps to NM_003054.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:119027182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:119026323 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:119015005 G>T maps to NM_003054.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:119013583 C>A maps to NM_003054.4 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr10:119029955 T>A maps to NM_003054.4 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr10:119015130 C>G maps to NM_003054.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:119017344 G>T maps to NM_003054.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr10:119017345 G>T maps to NM_003054.4 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:119015014 G>T maps to NM_003054.4 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:119015168 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:50819862 C>A maps to NM_003055.2 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:50819661 C>A maps to NM_003055.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:50819925 C>T maps to NM_003055.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr10:50818878 G>A maps to NM_003055.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:50819097 G>A maps to NM_003055.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr10:50819934 A>T maps to NM_003055.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr10:50820237 G>T maps to NM_003055.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:50819976 C>A maps to NM_003055.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr21:46951948 G>T maps to NM_194255.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:228552160 C>A maps to NM_025243.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr2:228552262 T>C maps to NM_025243.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:228563569 G>A maps to NM_025243.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:35336633 C>A maps to NM_004171.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:36608611 C>A maps to NM_004172.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:36679860 C>A maps to NM_004172.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr5:36671140 G>A maps to NM_004172.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:36686205 C>A maps to NM_004172.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:36608587 A>T maps to NM_004172.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr5:36680628 T>A maps to NM_004172.4 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:36677169 C>A maps to NM_004172.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:36677034 C>A maps to NM_004172.4 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr5:36608563 C>T maps to NM_004172.4 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:47290871 G>A maps to NM_005628.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr19:47281993 G>A maps to NM_005628.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:15061008 A>T maps to NM_005071.1 *565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:15072905 G>T maps to NM_005071.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr19:15072884 C>T maps to NM_005071.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:15064948 G>A maps to NM_005071.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:15082638 G>A maps to NM_005071.1 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:15083539 C>A maps to NM_005071.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:15079158 C>T maps to NM_005071.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:15073022 C>T maps to NM_005071.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:15064948 G>T maps to NM_005071.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:53553734 A>T maps to NM_006671.4 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:113417306 T>C maps to NM_005415.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:113420520 C>T maps to NM_005415.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr2:113420600 G>A maps to NM_005415.3 *680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:42302218 C>G maps to NM_006749.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:42302221 G>A maps to NM_006749.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:42287679 C>A maps to NM_006749.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:42329755 A>G maps to NM_006749.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:42296977 C>A maps to NM_006749.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr6:160575835 C>T maps to NM_003057.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr6:160560786 G>A maps to NM_003057.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:63057975 A>T maps to NM_001039752.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63067050 G>A maps to NM_001039752.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:63071685 C>A maps to NM_001039752.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:63057948 T>A maps to NM_001039752.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:63072193 G>A maps to NM_001039752.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:63069893 C>T maps to NM_001039752.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:63057852 C>G maps to NM_001039752.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:64329781 G>T maps to NM_018484.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:64323680 G>C maps to NM_018484.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr11:64329844 G>T maps to NM_018484.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:64366302 G>A maps to NM_144585.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr11:64359069 C>A maps to NM_144585.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:64361119 G>T maps to NM_144585.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr11:64359045 C>G maps to NM_144585.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr11:64359054 C>T maps to NM_144585.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:64359270 C>A maps to NM_144585.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr11:64360330 T>A maps to NM_144585.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:64360258 C>A maps to NM_144585.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr11:64367243 C>T maps to NM_144585.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:64359264 G>T maps to NM_144585.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:64361126 C>A maps to NM_144585.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:64366347 C>A maps to NM_144585.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr11:64368373 T>A maps to NM_144585.2 L521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr11:64361182 C>A maps to NM_144585.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:38316549 G>T maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr3:38307441 C>T maps to NM_004256.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr3:38355271 C>T maps to NM_004803.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:38348824 C>T maps to NM_004803.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:110778045 G>T maps to NM_033125.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:110752466 C>A maps to NM_033125.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:110763978 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:110763798 C>A maps to NM_033125.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:110746218 G>T maps to NM_033125.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr6:110752418 C>A maps to NM_033125.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:110763897 G>T maps to NM_033125.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:110777847 G>A maps to NM_033125.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:110746180 C>T maps to NM_033125.2 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr14:23816879 C>A maps to NM_020372.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr11:2943330 G>C did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:2929521 C>T maps to NM_002555.5 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:160679774 C>A maps to NM_003058.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:160679699 C>T maps to NM_003058.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr6:160679384 G>T maps to NM_003058.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr6:160668323 T>A maps to NM_003058.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:160679513 G>T maps to NM_003058.3 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:160666573 G>A maps to NM_003058.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr6:160671616 C>G maps to NM_003058.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:160662563 C>A maps to NM_003058.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:64990987 C>G maps to ENST00000438990 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr11:62997040 G>A maps to NM_199352.3 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:62933576 G>A maps to NM_199352.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:160858106 C>T maps to ENST00000392145 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr6:160868760 A>C maps to ENST00000392145 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:160819027 C>G maps to ENST00000392145 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr6:160831778 C>T maps to ENST00000392145 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr5:131630488 C>T maps to NM_003059.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr11:62744845 C>A maps to NM_004790.3 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:62751102 G>T maps to NM_004790.3 C178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:62751942 G>A maps to NM_004790.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:62744654 C>T maps to NM_004790.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:62751967 G>A maps to NM_004790.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:62744704 C>A maps to NM_004790.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr6:43270468 G>A maps to ENST00000372585 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:43267783 C>A maps to ENST00000372585 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:43268950 C>T maps to ENST00000372585 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr11:62760895 C>T maps to ENST00000430500 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:62782096 C>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr11:62782142 C>G maps to ENST00000430500 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr11:62760800 G>T maps to ENST00000430500 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr11:62782419 G>T maps to ENST00000430500 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr11:62763219 C>G maps to ENST00000430500 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:62766561 C>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:62760969 C>A maps to ENST00000430500 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:62782358 C>A maps to ENST00000430500 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr11:63137533 C>T maps to NM_080866.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:63137566 G>T maps to NM_080866.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:63141447 G>A maps to NM_080866.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr11:63141181 C>A maps to NM_080866.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:138714948 G>A maps to NM_152685.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:138713676 G>T maps to NM_152685.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr5:138718264 C>T maps to NM_152685.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:4837785 G>A maps to NM_203327.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:4864310 C>A maps to NM_203327.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:4864460 C>A maps to NM_203327.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:4880359 T>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:65946347 T>A maps to NM_004727.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr9:19786258 G>A maps to NM_020344.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr9:19786747 G>T maps to NM_020344.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:19786114 G>T maps to NM_020344.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr9:19550263 G>T maps to NM_020344.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr9:19516201 C>T maps to NM_020344.2 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:19261612 C>A maps to NM_020689.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:19674053 C>A maps to NM_020689.3 Y492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr20:19193608 G>T maps to NM_020689.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr20:19662597 C>T maps to NM_020689.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr20:19634776 C>T maps to NM_020689.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr20:19664973 C>T maps to NM_020689.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:92922950 G>A maps to NM_153646.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr14:92909096 C>A maps to NM_153646.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr14:92958096 C>T maps to NM_153646.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:92915519 C>T maps to NM_153646.3 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:92909075 G>A maps to NM_153646.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr14:92909769 G>T maps to NM_153646.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr14:92922776 T>A maps to NM_153646.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr14:92909796 C>T maps to NM_153646.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr15:48426632 T>C maps to NM_205850.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:48414086 C>A maps to NM_205850.2 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:48413258 C>A maps to NM_205850.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr15:48413259 C>T maps to NM_205850.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:113748058 G>A maps to NM_024959.2 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr12:113745550 C>A maps to NM_024959.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:79684439 C>A maps to ENST00000331531 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:4842371 C>G maps to NM_003562.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:172666786 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:172641897 G>A maps to NM_003705.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:95750583 C>A maps to NM_001160210.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:95813612 C>A maps to NM_001160210.1 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:95775920 G>A maps to NM_001160210.1 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:129492639 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:129499557 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:129484688 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:129499531 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:129506910 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:129474305 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:129492704 G>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:129492702 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:129498604 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr22:18066220 T>A maps to NM_031481.1 C110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr22:18064153 G>T maps to NM_031481.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:73273564 C>G did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:140683192 G>C maps to NM_031947.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:140683345 G>A maps to NM_031947.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:37641525 C>T maps to NM_030631.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:37198737 C>A maps to NM_030631.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:6454686 G>A maps to NM_024103.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:6458286 C>A maps to NM_024103.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108681710 C>T maps to NM_013386.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:108700188 T>C maps to NM_013386.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:108686308 T>C maps to NM_013386.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:108700152 T>G maps to NM_013386.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr9:130830760 C>T maps to ENST00000373069 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr9:130868087 C>A maps to ENST00000373069 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:101370758 C>A maps to NM_031212.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:98987860 G>A maps to NM_213611.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:98987788 G>T maps to NM_213611.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:128688335 G>T maps to NM_031291.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr8:104420012 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:104412680 G>A maps to NM_030780.3 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr1:16065837 C>G maps to NM_207348.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:16065192 A>G maps to NM_207348.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr3:140692806 C>T maps to NM_001104647.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:140692764 G>T maps to NM_001104647.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:140689814 T>A maps to NM_001104647.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:23425844 G>T maps to NM_016612.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:23429106 G>A maps to NM_016612.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr3:39432933 C>T maps to NM_017875.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42398531 C>A maps to NM_001143780.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:42398532 G>T maps to NM_001143780.1 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:186068040 C>T maps to NM_001151.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:87473178 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr7:87473179 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:6432092 C>A maps to NM_173637.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:19216419 C>T maps to NM_178526.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:118544215 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:118586087 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:118540464 G>A did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr11:65146933 G>C maps to NM_182556.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:65147340 C>T maps to NM_182556.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:110083919 A>C maps to NM_138773.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:118604334 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:118604440 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:118603884 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:1508206 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:1508328 C>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:1505552 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:1508154 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:1508295 C>A did not map to a codon.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr4:973208 C>T maps to NM_134425.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:58018914 A>T maps to NM_133489.2 K452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:58018650 C>G maps to NM_133489.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:78225180 C>T maps to NM_173626.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:149360181 A>T maps to NM_000112.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr5:149360469 A>T maps to NM_000112.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr5:149360118 C>T maps to NM_000112.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:107408246 C>T maps to NM_000111.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:107431675 C>T maps to NM_000111.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:107423709 C>A maps to NM_000111.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:107423682 G>T maps to NM_000111.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:107431531 C>A maps to NM_000111.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr7:107423730 G>A maps to NM_000111.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:107430025 G>T maps to NM_000111.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:107432290 G>T maps to NM_000111.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:107352991 C>T maps to NM_000441.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:107315472 C>A maps to NM_000441.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr7:107303797 G>A maps to NM_000441.1 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:107323739 G>T maps to NM_000441.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:103014986 T>C maps to ENST00000354356 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:103050879 C>A maps to ENST00000354356 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:103017306 A>T maps to ENST00000354356 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:103038451 C>A maps to ENST00000354356 G300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:103061305 T>A maps to ENST00000354356 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:103048297 C>T maps to ENST00000354356 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:48664410 T>G maps to NM_022911.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:92401581 C>A maps to NM_134266.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:92307882 A>G maps to NM_134266.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:92330586 C>A maps to NM_134266.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:92307873 T>C maps to NM_134266.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:92364057 C>A maps to NM_134266.1 C387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:92346638 G>A maps to NM_134266.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:92374657 C>T maps to NM_134266.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:92261893 G>A maps to NM_134266.1 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:92346558 C>A maps to NM_134266.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:92406161 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:92406192 G>T maps to NM_134266.1 G621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr8:92374657 C>G maps to NM_134266.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:35980028 G>A maps to NM_052961.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:35928846 T>G maps to NM_052961.3 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:205884138 G>T maps to NM_134325.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:205892742 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:17599847 C>T maps to NM_198580.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:17612121 C>T maps to NM_198580.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:17615393 C>A maps to NM_198580.1 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:17599677 C>T maps to NM_198580.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:50519375 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:153752299 A>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:131117962 C>T maps to NM_005094.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr9:131115779 G>T maps to NM_005094.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:59021274 C>A maps to NM_012254.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:59022758 C>G maps to NM_012254.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:59021367 G>A maps to NM_012254.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:59021372 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:128302063 C>T maps to NM_001017372.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:128302150 G>T maps to NM_001017372.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr5:128320946 T>A maps to NM_001017372.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:128321029 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:128324344 T>G maps to NM_001017372.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:128302219 C>T maps to NM_001017372.1 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr5:128324437 A>G maps to NM_001017372.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:128302076 C>T maps to NM_001017372.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:128362848 C>A maps to NM_001017372.1 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:128302194 G>A maps to NM_001017372.1 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:85488008 G>T maps to NM_004213.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr15:85438234 C>A maps to NM_004213.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:85486725 C>T maps to NM_004213.3 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr15:85487875 G>T maps to NM_004213.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr15:45557791 C>T maps to NM_004212.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr15:45555436 G>A maps to NM_004212.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr15:45560575 G>A maps to NM_004212.3 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr15:45545485 G>T maps to NM_004212.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr15:45555406 C>A maps to NM_004212.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:86912204 C>T maps to NM_022127.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:86894926 C>G maps to NM_022127.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr9:86914528 G>T maps to NM_022127.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:44200165 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:44197351 C>T maps to ENST00000313248 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr10:73121983 C>T maps to NM_018344.5 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr10:73122085 G>T maps to NM_018344.5 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr10:73122031 C>T maps to NM_018344.5 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr10:73082703 C>T maps to NM_018344.5 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:5338647 C>T maps to NM_153247.2 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:45353678 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:45362392 A>G did not map to a codon.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr20:45355557 C>T maps to NM_030777.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr20:45354079 G>T maps to NM_030777.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr20:45354607 C>T maps to NM_030777.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:134350263 A>G maps to NM_145176.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:134350375 C>T maps to NM_145176.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr6:134312436 C>T maps to NM_145176.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:40265663 T>C maps to NM_052885.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:7984357 G>T maps to NM_153449.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:7981411 T>C maps to NM_153449.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:170715880 T>C maps to NM_000340.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:170723753 A>G maps to NM_000340.1 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:8074209 G>C maps to NM_006931.2 Y430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:8078466 C>A maps to NM_006931.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr12:8084032 G>A maps to NM_006931.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:7189842 G>A maps to NM_001042.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:9097800 G>T maps to NM_003039.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:9097677 C>G maps to NM_003039.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr9:136339162 G>A maps to NM_017585.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr1:9064912 G>T maps to NM_207420.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:10027568 G>T maps to NM_001001290.1 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr4:9982332 G>T maps to NM_020041.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:10027562 C>A maps to NM_001001290.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:10022984 G>A maps to NM_020041.2 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:9909888 C>A maps to NM_020041.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:9828092 C>T maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:220089057 C>G maps to NM_018713.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:220101686 G>T maps to NM_018713.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:220100447 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:220091746 C>A maps to NM_018713.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:220088799 C>G maps to NM_018713.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr1:220088834 T>A maps to NM_018713.2 K472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:27480054 C>A maps to NM_003459.4 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:27481081 C>T maps to NM_003459.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:27479665 G>T maps to NM_003459.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:27481774 G>T maps to NM_003459.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:27479695 G>A maps to NM_003459.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr15:45803357 G>A maps to NM_013309.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:68396735 C>T maps to NM_022902.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:68425392 A>C maps to NM_022902.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:32445601 A>C maps to NM_001193513.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:32417449 G>A maps to NM_001193513.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:32445436 A>T maps to NM_001193513.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr1:101362156 C>T maps to NM_133496.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:118165312 T>C maps to NM_173851.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr8:118174009 C>A maps to NM_173851.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:118165222 T>A maps to NM_173851.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:42065119 A>C maps to NM_006345.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:42024920 A>G maps to NM_006345.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr4:42051438 C>T maps to NM_006345.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:41992737 C>T maps to NM_006345.3 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr9:115920022 C>G maps to ENST00000394724 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:37357065 G>T maps to NM_080552.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr20:37356235 G>T maps to NM_080552.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:37356226 G>T maps to NM_080552.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr20:37356873 G>T maps to NM_080552.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:37356414 C>A maps to NM_080552.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr3:155571729 G>A maps to NM_004733.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr3:155571624 C>A maps to NM_004733.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr3:155571258 C>A maps to NM_004733.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr3:155571390 G>A maps to NM_004733.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr5:176813015 C>A maps to NM_003052.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr5:176825193 G>A maps to NM_003052.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr4:25674766 C>G maps to NM_006424.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:25678019 C>G maps to NM_006424.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr4:25669598 G>A maps to NM_006424.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr4:25664325 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:140126578 C>A maps to NM_080877.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr9:140128970 C>T maps to NM_080877.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr9:140129077 G>C maps to NM_080877.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:140128934 C>T maps to NM_080877.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr9:140126204 G>A maps to NM_080877.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:88187119 G>A maps to NM_006416.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:88218205 C>T maps to NM_006416.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:48762072 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:48762038 C>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:48762435 G>C did not map to a codon.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr23:48762203 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48767186 A>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:48767202 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:139947245 C>T maps to NM_080670.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:112288108 A>T maps to NM_017945.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:112300106 G>A maps to NM_017945.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr3:112299880 C>A maps to NM_017945.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr3:112299905 A>G maps to NM_017945.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:47785105 G>A maps to ENST00000415270 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:44224129 G>A maps to NM_178148.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr6:44222604 G>A maps to NM_178148.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr6:44222571 G>T maps to NM_178148.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:8417115 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:8430377 G>A maps to NM_001142540.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:133979773 G>C maps to NM_032826.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr7:133984944 T>A maps to NM_032826.4 K186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:44980767 G>A maps to NM_173179.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:44986385 C>A maps to NM_173179.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr20:44986343 G>A maps to NM_173179.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:67513051 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:67470087 C>A maps to NM_015139.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:67518516 G>C maps to NM_015139.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:99083524 T>C maps to NM_007001.2 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:99126811 T>A maps to NM_007001.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:99114338 G>A maps to NM_007001.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr6:137245320 C>A maps to NM_001008783.1 C246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:16664606 G>A maps to NM_024881.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:16666163 G>A maps to NM_024881.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:69158621 G>A maps to NM_018656.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr12:69158526 G>T maps to NM_018656.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:118475608 G>T maps to NM_001029858.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:118596767 G>T maps to NM_001029858.3 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:118588222 C>A maps to NM_001029858.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:118635279 C>A maps to NM_001029858.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:118475640 G>T maps to NM_001029858.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:118635411 C>T maps to NM_001029858.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:118635340 C>T maps to NM_001029858.3 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:107663484 C>A maps to NM_017515.4 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:107676083 C>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:107676119 C>A maps to NM_017515.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr11:107663346 G>A maps to NM_017515.4 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:107677512 C>A maps to NM_017515.4 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:234454682 T>C maps to NM_173508.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:234367226 C>T maps to NM_173508.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:234367269 C>T maps to NM_173508.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:234367439 G>A maps to NM_173508.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:58036698 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr14:58056109 T>A maps to NM_001080455.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:114500280 A>G maps to NM_025181.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:114512771 C>G maps to NM_025181.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr5:150867730 G>T maps to NM_078483.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:150846758 G>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:150847345 C>T maps to NM_078483.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr5:150846810 C>G maps to NM_078483.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr5:150701673 G>T maps to NM_181776.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:150657177 G>A maps to NM_001145017.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:150682853 G>T maps to NM_001145017.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:150682910 G>T maps to NM_001145017.1 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr5:150657055 G>A maps to NM_001145017.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:92899089 T>A maps to NM_152313.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr21:43955580 G>C did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:124946727 C>A maps to NM_198277.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr11:124947409 C>T maps to NM_198277.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr7:140037108 C>T maps to NM_207113.1 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:46592512 G>A maps to NM_030674.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:46591783 G>C maps to NM_030674.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:79219673 C>T maps to NM_001037984.1 Q1014Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:79244795 C>A maps to NM_001037984.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:79244762 C>A maps to NM_001037984.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:79263599 G>A maps to NM_001037984.1 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:79219441 G>A maps to NM_001037984.1 Q1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr2:165768147 C>A maps to ENST00000409662 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:165771772 G>T maps to ENST00000409662 C177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:46758303 C>G maps to NM_018976.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:46760711 G>A maps to NM_018976.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:50256082 G>T maps to NM_006841.4 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:47182309 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:47186733 A>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:48319073 C>G did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:48324400 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:48320400 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:48317989 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:48318236 A>C did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:48318157 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:48326125 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:61451498 G>T maps to NM_001172702.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:61486287 G>A maps to NM_001172702.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:61517305 A>G maps to NM_001172702.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr16:58712723 G>A maps to NM_018231.1 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:58705098 C>A maps to NM_018231.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:58705099 C>T maps to NM_018231.1 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr16:84056377 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:54960596 C>A maps to NM_173514.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:54968509 C>A maps to NM_173514.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:153932915 G>A maps to NM_014437.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:196573496 C>T maps to NM_001127257.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:70845806 C>A maps to NM_001159770.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr17:70732858 C>G did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr17:71027787 C>A maps to NM_001159770.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:18331686 G>T maps to NM_001145195.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:18254566 T>C maps to NM_001145195.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:18292250 T>A maps to NM_001145195.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:18331728 C>G maps to NM_001145195.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:18270306 G>T maps to NM_001145195.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr10:18292256 G>T maps to NM_001145195.1 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr10:18289688 C>A maps to NM_001145195.1 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:18242214 C>A maps to NM_001145195.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:18276492 G>A maps to NM_001145195.1 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr10:18276534 C>A maps to NM_001145195.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr10:18276528 C>A maps to NM_001145195.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:18280166 G>T maps to NM_001145195.1 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr10:18331725 G>T maps to NM_001145195.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:18280100 G>T maps to NM_001145195.1 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr10:18280161 T>A maps to NM_001145195.1 L451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:18270267 G>T maps to NM_001145195.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:18280166 G>T maps to NM_001145195.1 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:18331737 A>T maps to NM_001145195.1 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:18289662 C>A maps to NM_001145195.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:18254431 G>T maps to NM_001145195.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr11:47431695 C>G maps to NM_001128225.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:22272313 G>T maps to NM_001135153.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr14:21469626 C>T maps to NM_014579.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:21467955 G>T maps to NM_014579.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr8:145638292 C>A maps to NM_130849.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:56629469 C>T maps to NM_001135195.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:56625201 C>A maps to NM_001135195.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:56629423 C>T maps to NM_001135195.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:56631421 C>T maps to NM_001135195.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:33706787 G>A maps to NM_012319.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr18:33694105 C>A maps to NM_012319.3 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr18:33706234 C>A maps to NM_012319.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr18:33706777 C>A maps to NM_012319.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr18:33706277 C>A maps to NM_012319.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr4:103226269 T>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:69908951 G>A maps to NM_018375.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:44502976 C>A maps to NM_000341.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr2:44547564 C>G maps to NM_000341.3 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:44502904 T>C maps to NM_000341.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:44508604 A>G maps to NM_000341.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:44508562 G>T maps to NM_000341.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:62656035 C>T maps to NM_001012661.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:62649387 C>T maps to NM_001012661.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:62656062 C>T maps to NM_001012661.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr11:62656119 G>A maps to NM_001012661.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:190439932 C>G maps to NM_014585.5 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:190439989 G>A maps to NM_014585.5 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:190428940 T>A maps to NM_014585.5 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:190428486 G>A maps to NM_014585.5 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:205764003 C>T maps to NM_173854.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:205779242 T>G maps to NM_173854.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:205779530 C>T maps to NM_173854.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:205767854 G>A maps to NM_173854.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr12:105199028 G>A maps to NM_032148.3 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr12:105198952 G>A maps to NM_032148.3 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr11:57258836 T>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:1479965 G>A maps to ENST00000382147 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:1520012 C>A maps to ENST00000382147 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:57177517 G>A maps to ENST00000428603 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:57175306 C>A maps to ENST00000428603 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr11:57184121 G>A maps to ENST00000428603 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr11:57193105 G>A maps to ENST00000428603 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:108136901 C>A maps to NM_080546.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr9:108097867 C>T maps to NM_080546.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr19:10747090 G>A maps to NM_020428.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:95311003 G>T maps to NM_001114106.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr1:95360465 C>T maps to NM_001114106.1 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:95357835 G>T did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:95311019 G>T maps to NM_001114106.1 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:31836985 G>A maps to NM_025257.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:31831478 G>A maps to NM_025257.2 Y686Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr6:31839279 G>A maps to NM_025257.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:31843869 C>A maps to NM_025257.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:31844848 G>C maps to NM_025257.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:75684359 C>T maps to NM_152697.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:75716950 G>A maps to NM_152697.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:75685014 G>T maps to NM_152697.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:75702720 C>A maps to NM_152697.4 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:75684240 C>T maps to NM_152697.4 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:75672393 C>A maps to NM_152697.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:75699725 T>G maps to NM_152697.4 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:75684272 G>T maps to NM_152697.4 C477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:75672357 G>A maps to NM_152697.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:75693543 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:8398029 C>T maps to ENST00000377479 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:8397903 C>T maps to ENST00000377479 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:8384595 G>T maps to ENST00000377479 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:8390299 C>T maps to ENST00000377479 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:8384415 G>T maps to ENST00000377479 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr5:33947360 C>A maps to NM_016180.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr5:33947449 C>A maps to NM_016180.3 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:33964061 C>A maps to NM_016180.3 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:33947282 G>A maps to NM_016180.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:33947414 C>G maps to NM_016180.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr5:33947402 C>G maps to NM_016180.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr5:33951713 G>T maps to NM_016180.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:33984643 G>T maps to NM_016180.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr5:33944854 C>T maps to NM_016180.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr5:33947354 C>A maps to NM_016180.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:33944821 C>G maps to NM_016180.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:33963843 A>G maps to NM_016180.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:33982416 G>T maps to NM_016180.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:205631991 C>G maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:205628457 G>A maps to NM_033102.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:142228514 C>A maps to NM_001080431.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:142228199 G>C maps to NM_001080431.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr9:115652022 G>A maps to NM_033051.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:115651959 G>A maps to NM_033051.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr17:19445803 C>A maps to ENST00000395585 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr17:19470428 G>A maps to ENST00000395585 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:19445752 G>T maps to ENST00000395585 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:19470124 C>T maps to ENST00000395585 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:42335507 G>T maps to NM_000342.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:42340031 G>T maps to NM_000342.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:42335047 C>T maps to NM_000342.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:42337251 C>T maps to NM_000342.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr17:42328948 G>C maps to NM_000342.3 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:42337805 C>A maps to NM_000342.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:42336629 C>A maps to NM_000342.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:42332000 C>G maps to NM_000342.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:42333190 C>T maps to NM_000342.3 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:42328857 G>A maps to NM_000342.3 Q804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr17:42336614 G>A maps to NM_000342.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:42330542 G>A maps to NM_000342.3 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:42338117 C>A maps to NM_000342.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:162821589 G>A maps to NM_001178015.1 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:162711523 G>A maps to NM_001178015.1 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:162735741 C>T maps to NM_001178015.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr2:162830769 T>C maps to NM_001178015.1 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:162751274 C>T maps to NM_001178015.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:162661083 G>T maps to NM_001178015.1 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:162751331 C>T maps to NM_001178015.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr2:162804197 C>A maps to NM_001178015.1 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:162799313 G>T maps to NM_001178015.1 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:3214909 T>G maps to NM_001174090.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:3211845 G>T maps to NM_001174090.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr20:3211996 G>T maps to NM_001174090.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr20:3209241 G>A maps to NM_001174090.1 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr20:3210253 G>C maps to NM_001174090.1 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:3211597 C>T maps to NM_001174090.1 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr20:3210839 C>A maps to NM_001174090.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr7:150773143 C>G maps to NM_003040.3 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr7:150767985 C>T maps to NM_003040.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr7:150761736 G>T maps to NM_003040.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:150761317 G>T maps to NM_003040.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:150768923 G>A maps to NM_003040.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:150767560 A>T maps to NM_003040.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:220497731 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:220505176 G>C maps to NM_201574.2 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr2:220500157 G>T maps to NM_201574.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:220503473 C>A maps to NM_201574.2 S996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:72332250 G>T maps to NM_001098484.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr4:72205151 C>T maps to NM_001098484.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr4:72332162 C>A maps to NM_001098484.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr4:72432730 A>G maps to NM_001098484.2 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:72432718 A>G did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr4:72316218 T>A maps to NM_001098484.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr4:72222800 C>G maps to NM_001098484.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:72222845 G>T maps to NM_001098484.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:72215655 A>G maps to NM_001098484.2 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr4:72205109 C>T maps to NM_001098484.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:74489279 T>C maps to NM_021196.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr2:74460690 C>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:74491382 T>A maps to NM_021196.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:74459672 G>A maps to NM_021196.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:27462237 G>A maps to ENST00000454389 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr3:27472894 G>A maps to ENST00000454389 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr3:27442271 T>A maps to ENST00000454389 R804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:51888799 G>C maps to NM_001039960.1 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51883653 G>T maps to NM_001039960.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:51863458 C>A maps to NM_001039960.1 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:51890824 G>T maps to NM_001039960.1 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr12:51863544 G>T maps to NM_001039960.1 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:51845944 C>A maps to NM_001039960.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr12:51890829 G>C maps to NM_001039960.1 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:139751894 G>A maps to ENST00000507527 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:139742047 G>T maps to ENST00000507527 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:139740436 C>A maps to ENST00000507527 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr22:32439310 C>A maps to NM_000343.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr22:32477865 C>A maps to NM_000343.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:32495172 G>A maps to NM_000343.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr22:32498214 G>A maps to NM_000343.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr22:32480561 A>G maps to NM_000343.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr22:32498112 C>T maps to NM_000343.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr22:32464547 C>T maps to NM_000343.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr22:32477941 C>A maps to NM_000343.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr22:32477881 C>A maps to NM_000343.3 I169I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4487-01A-21D-1855-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr17:18918398 G>T maps to NM_152351.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:18923704 C>T maps to NM_152351.3 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr17:18916756 G>A maps to NM_152351.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:26702708 G>T maps to NM_178498.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:26720039 C>A maps to NM_178498.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:26725437 C>A maps to NM_178498.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:26743177 A>G maps to NM_178498.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr16:31499013 T>C maps to ENST00000431354 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:31501657 C>T maps to ENST00000431354 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr16:31498857 C>T maps to ENST00000431354 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr21:35468162 C>T maps to NM_006933.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr21:35469089 T>A maps to NM_006933.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr22:32614703 C>A maps to NM_014227.2 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr22:32647852 G>T maps to NM_014227.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:32616904 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr22:32651307 A>G maps to NM_014227.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr22:32625227 G>A maps to NM_014227.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:17988771 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:17994524 C>T maps to NM_000453.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:17986909 C>A maps to NM_000453.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:17985509 C>T maps to NM_000453.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr19:18001743 C>A maps to NM_000453.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr19:17985494 G>A maps to NM_000453.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr19:18004571 C>A maps to NM_000453.2 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:27426161 C>T maps to NM_021095.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:27430329 G>A maps to NM_021095.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:108618377 C>A maps to NM_021815.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:108614426 C>A maps to NM_021815.2 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:108609530 T>A maps to NM_021815.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:108626707 T>A maps to NM_021815.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:108618432 G>A maps to NM_021815.2 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:108624948 A>T maps to NM_021815.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:108609539 G>T maps to NM_021815.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:108626770 G>A maps to NM_021815.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:108626830 C>A maps to NM_021815.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr12:101577934 G>A maps to NM_145913.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr12:101603518 C>A maps to NM_145913.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr12:101587470 C>T maps to NM_145913.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:101603527 G>T maps to NM_145913.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:101560422 C>A maps to NM_145913.3 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:101551059 C>T maps to NM_145913.3 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr12:101598295 G>A maps to NM_145913.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:101551146 T>G maps to NM_145913.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:48698139 C>A maps to NM_001135181.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:48713202 C>T maps to NM_001135181.1 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:48713139 C>T maps to NM_001135181.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr1:48703368 G>T maps to NM_001135181.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr1:48705145 C>T maps to NM_001135181.1 C563C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:11070433 G>A maps to NM_003042.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr3:11078612 C>A maps to NM_003042.3 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:11059649 T>A maps to NM_003042.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:11072885 C>G maps to NM_003042.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr3:10960100 C>G maps to NM_014229.1 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:10967705 T>C maps to NM_014229.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:10916776 C>A maps to NM_014229.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:301673 G>T maps to NM_003044.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:301808 A>G maps to NM_003044.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:310985 C>A maps to NM_003044.3 G174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr12:313793 C>T maps to NM_003044.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr23:115582709 C>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:115590105 C>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:115584234 G>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:115572133 G>T did not map to a codon.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr23:115574909 G>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:115584295 T>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:115578012 C>A did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:85264450 T>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:85255557 C>A maps to NM_182767.4 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:85285752 T>C maps to NM_182767.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr12:85260937 C>G maps to NM_182767.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr12:85277544 G>T maps to NM_018057.5 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr12:85285609 C>A did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:49793478 G>T maps to NM_014037.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:110738260 G>T maps to NM_001010898.2 G516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:110737301 C>T maps to NM_001010898.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:110738361 C>A maps to NM_001010898.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:110714730 C>A maps to NM_001010898.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:110717482 G>C maps to NM_001010898.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:110717483 G>T maps to NM_001010898.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:110716698 C>T maps to NM_001010898.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr1:110734688 C>A maps to NM_001010898.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:110709730 G>T maps to NM_001010898.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1240699 C>A maps to NM_182632.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:1235746 T>C maps to NM_182632.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:1232367 C>A maps to NM_182632.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:1212463 G>A maps to NM_001003841.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:1213591 C>A maps to NM_001003841.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:1208873 C>T maps to NM_001003841.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:1212451 G>T maps to NM_001003841.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:1219181 C>T maps to NM_001003841.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr5:1221361 C>T maps to NM_001003841.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:1217011 C>T maps to NM_001003841.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr5:1212556 C>A maps to NM_001003841.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:1219740 C>T maps to NM_001003841.2 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:55690764 G>A maps to NM_001043.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:55730215 C>T maps to NM_001043.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr16:55729201 G>T maps to NM_001043.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:55725891 C>T maps to NM_001043.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:55730143 C>A maps to NM_001043.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr16:55729297 G>A maps to NM_001043.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:55731843 A>T maps to NM_001043.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr16:55729222 C>T maps to NM_001043.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:55735779 G>A maps to NM_001043.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr16:55732406 G>T maps to NM_001043.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr16:55703492 G>A maps to NM_001043.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:1416253 G>T maps to NM_001044.4 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:1422085 G>A maps to NM_001044.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:1420755 G>A maps to NM_001044.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:28548790 A>G maps to ENST00000394821 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:28539836 C>T maps to ENST00000394821 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:28544216 G>A maps to ENST00000394821 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:28530213 G>A maps to ENST00000394821 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:28530256 G>T maps to ENST00000394821 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr17:28537619 G>A maps to ENST00000394821 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:28530282 G>A maps to ENST00000394821 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:28539755 A>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:20636270 G>T maps to NM_004211.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:20652350 G>C maps to NM_004211.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:20648267 G>A maps to NM_004211.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:20629073 C>A maps to NM_004211.3 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:20676398 G>T maps to NM_004211.3 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:20639366 C>T maps to NM_004211.3 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:20623036 C>A maps to NM_004211.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:20639363 C>G maps to NM_004211.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:20676383 G>A maps to NM_004211.3 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:20622672 A>T did not map to a codon.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr11:20658728 C>T maps to NM_004211.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:20628604 C>T maps to NM_004211.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:14489309 C>T maps to NM_001134367.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:14526391 G>T maps to NM_001134367.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:14489270 C>A maps to NM_001134367.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr5:149589042 G>T maps to NM_014228.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:149583540 G>C maps to NM_014228.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr5:149574474 G>T did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr5:149578886 C>A maps to NM_014228.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:149576354 C>A maps to NM_014228.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr5:149585023 C>A maps to NM_014228.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:152956966 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:152959806 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:152958580 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:152958789 A>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:152956880 G>A did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:152954184 C>G did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:152960250 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:152959709 C>G did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:152957556 G>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:44474185 G>C maps to NM_201649.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:44476398 T>A maps to NM_201649.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr1:44474143 G>A maps to NM_201649.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:30110069 C>A maps to NM_003045.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:30104756 C>A maps to NM_003045.4 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:33703292 C>A maps to NM_019849.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr19:33703453 G>T maps to NM_019849.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr19:33700334 G>A maps to NM_019849.2 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:139163142 C>A maps to ENST00000280612 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:87229890 T>A maps to NM_138817.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr8:87242188 C>A maps to NM_138817.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:87242401 G>T maps to NM_138817.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:87235240 G>A maps to NM_138817.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr8:87242274 C>A maps to NM_138817.2 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:87229782 G>A maps to NM_138817.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:87242215 G>T maps to NM_138817.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr8:87235285 A>T maps to NM_138817.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:170219102 G>A maps to NM_020949.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr3:170216487 C>A maps to NM_020949.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:170198078 C>A maps to NM_020949.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr3:170198378 C>A maps to NM_020949.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:170198681 A>T maps to NM_020949.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr3:170216671 C>A maps to NM_020949.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr3:170198531 G>C maps to NM_020949.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:170244420 C>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:170216536 C>A maps to NM_020949.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr3:170216596 C>A maps to NM_020949.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:17419519 C>A maps to NM_001164771.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr8:17412164 G>A maps to NM_001164771.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr8:17421113 T>C maps to NM_001164771.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:70146527 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:70148046 T>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:70146813 T>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:70148373 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:70146819 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:70147814 C>G did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:70147432 C>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:70148345 C>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:70148047 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:70145938 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:70145694 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr22:21384143 G>C maps to NM_004173.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr22:21384419 G>C maps to NM_004173.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr22:21385579 A>G maps to NM_004173.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr22:21385900 A>T maps to NM_004173.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr22:21385924 T>A maps to NM_004173.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr16:68309090 G>A maps to NM_003983.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:68337949 G>A maps to NM_032178.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr14:23243286 G>A maps to NM_001126106.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:23596442 G>A maps to NM_012244.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:23598915 C>A maps to NM_012244.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:23596403 C>T maps to NM_012244.2 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr14:23598873 G>A maps to NM_012244.2 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr14:23609765 G>A maps to NM_012244.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:33353073 C>A maps to NM_014270.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:33355670 G>A maps to NM_014270.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr19:33353472 G>A maps to NM_014270.4 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:33355538 C>T maps to NM_014270.4 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:40656955 T>C maps to NM_021097.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:40656142 G>T maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:40656448 T>A maps to NM_021097.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:40366802 G>A maps to NM_021097.2 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:40342530 C>A maps to NM_021097.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:40656136 G>T maps to NM_021097.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:40655728 A>G maps to NM_021097.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr2:40342548 C>A maps to NM_021097.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:40657384 G>T maps to NM_021097.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr2:40655755 G>T maps to NM_021097.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr2:40657345 G>A maps to NM_021097.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr2:40392002 A>G maps to NM_021097.2 Y720Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:40657159 G>T maps to NM_021097.2 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40397427 G>T maps to NM_021097.2 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:40656997 G>C maps to NM_021097.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr2:40657059 C>A maps to NM_021097.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr2:40657051 G>T maps to NM_021097.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:40397448 C>A maps to NM_021097.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:47940788 C>G maps to NM_015063.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:47935673 G>C maps to NM_015063.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:47969420 G>T maps to NM_015063.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:47969324 G>A maps to NM_015063.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:47969537 C>A maps to NM_015063.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr19:47935672 G>T maps to NM_015063.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:47951073 G>A maps to NM_015063.2 D585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:47940751 C>A maps to NM_015063.2 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:70634944 C>A maps to NM_183002.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:70515700 G>T maps to NM_183002.1 Y730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr14:70634692 G>T maps to NM_183002.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr14:70634686 A>G maps to NM_183002.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr14:70634959 C>A maps to NM_183002.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:70633726 G>A maps to NM_183002.1 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:70634869 C>T maps to NM_183002.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr14:70634698 C>T maps to NM_183002.1 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:70633579 T>C maps to NM_183002.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr14:70634869 C>T maps to NM_183002.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr14:70515700 G>T maps to NM_183002.1 Y730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr14:70634984 G>T maps to NM_183002.1 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:70530646 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr14:70633657 T>A maps to NM_183002.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr14:70515613 G>A maps to NM_183002.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr14:70634538 G>A maps to NM_183002.1 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr1:27436120 G>A maps to NM_003047.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:27426943 C>A maps to NM_003047.3 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:27426944 C>T maps to NM_003047.3 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:27480729 G>C maps to NM_003047.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr1:27432510 G>A maps to NM_003047.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:27440544 C>A maps to NM_003047.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:111950282 A>G maps to NM_183061.1 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr3:111887725 G>A maps to NM_183061.1 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:111983045 C>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:111993741 A>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:111923076 T>C maps to NM_183061.1 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:173502879 A>G maps to NM_178527.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:173486707 C>A maps to NM_178527.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr1:173472448 G>A maps to NM_178527.3 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:173493106 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:173569327 A>T maps to NM_178527.3 C52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr1:173569348 C>T maps to NM_178527.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:173569279 T>A maps to NM_178527.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr1:173523927 G>C maps to NM_178527.3 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:103300761 C>T maps to NM_003048.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr2:103324830 C>A maps to NM_003048.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:103317654 G>C maps to NM_003048.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:103299908 G>T maps to NM_003048.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:103299788 C>A maps to NM_003048.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:103299839 C>T maps to NM_003048.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:103274376 C>G maps to NM_003048.3 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:477529 G>A maps to NM_004174.2 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:479948 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:482773 G>T maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr17:72759558 C>T maps to NM_004252.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:103090301 T>A maps to NM_001011552.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:103119904 A>G did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:103136407 G>T maps to NM_001011552.3 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:103120016 G>C maps to NM_001011552.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:103148978 G>T maps to NM_001011552.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:103095466 C>A maps to NM_001011552.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:103095646 G>C maps to NM_001011552.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:103148808 G>T maps to NM_001011552.3 G687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:103128687 C>A maps to NM_001011552.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr2:103095544 C>T maps to NM_001011552.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:103124592 C>T maps to NM_001011552.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:135112294 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:135112300 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:135084372 G>T did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:135115593 A>G did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:135098823 C>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:135104853 C>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:135095588 C>A did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:135126718 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:135106566 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:135098851 A>G did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:135067821 A>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:135095107 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:135067911 C>T did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:135126814 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:135081018 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:135098877 G>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:135095149 A>G did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:135067900 G>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:135104822 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:135067799 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:135122278 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:135106601 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:46541866 T>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:46508188 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:46618329 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:46466491 C>T did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:46618197 C>G did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:46618392 C>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:46532013 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:46618269 C>G did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:46522079 T>G did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:46618217 G>C did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:48491356 T>A maps to ENST00000417961 C374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr20:48504416 G>T maps to ENST00000417961 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr3:143297459 T>A maps to NM_173653.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:142985597 C>A maps to NM_173653.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr3:143550931 C>A maps to NM_173653.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:142985725 C>A maps to NM_173653.3 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr3:143513850 G>A maps to NM_173653.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:143271263 G>T maps to NM_173653.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:21422687 C>A maps to NM_134431.3 G603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:21422676 T>A maps to NM_134431.3 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:21467595 T>G maps to NM_134431.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:21448709 A>T maps to NM_134431.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr12:21391918 C>A maps to NM_006446.4 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:21350114 T>C maps to NM_006446.4 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:21392038 C>A maps to NM_006446.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:21329799 C>T maps to NM_006446.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:21355453 G>T maps to NM_006446.4 G389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:21331588 C>A maps to NM_006446.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:21331657 T>G did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr12:21355422 A>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:21051393 A>T maps to NM_019844.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr12:21033900 C>T maps to NM_019844.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:21011460 A>C maps to NM_019844.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:21036414 T>C maps to NM_019844.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:21069085 G>T maps to NM_019844.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:21008062 C>T maps to NM_019844.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:21028236 G>T maps to NM_019844.2 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:20874894 C>A maps to NM_017435.4 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:20890124 C>A maps to NM_017435.4 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:20874970 G>T maps to NM_017435.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:20874845 T>A maps to NM_017435.4 L295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:20890205 T>C maps to NM_017435.4 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr12:20903756 T>C maps to NM_001145946.1 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr12:20890119 G>T maps to NM_017435.4 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:20885978 C>T maps to NM_017435.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:20885846 C>T maps to NM_017435.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:133692534 C>T maps to NM_005630.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:133663998 G>A maps to NM_005630.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr3:133653611 C>T maps to NM_005630.2 W626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:133667449 G>A maps to NM_005630.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:133664098 G>C maps to NM_005630.2 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:133654685 C>A maps to NM_005630.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:133672505 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:74880371 G>A maps to NM_007256.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:74880440 C>T maps to NM_007256.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:74915621 G>A maps to NM_007256.4 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:74915501 T>A maps to NM_007256.4 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:74880317 C>A maps to NM_007256.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr15:92459365 G>A maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:92690296 C>T maps to NM_013272.3 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr15:92459309 C>T maps to NM_013272.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:61296405 C>T maps to NM_016354.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr20:61299252 C>T maps to NM_016354.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr20:61288447 G>T maps to NM_016354.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:101599389 T>C maps to NM_180991.4 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:101606328 T>A maps to NM_180991.4 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:101631702 G>A maps to NM_180991.4 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:101585492 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585415 G>C maps to NM_030958.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:70585514 G>C maps to NM_030958.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:70617324 T>C maps to NM_030958.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr8:70617447 G>A maps to NM_030958.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:70674027 G>T maps to NM_030958.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr8:70744488 G>T maps to NM_030958.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:70585457 C>A maps to NM_030958.2 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:70744697 C>A maps to NM_030958.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr8:70585342 G>T maps to NM_030958.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:101755678 A>T maps to NM_173488.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr5:101795358 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:101755666 G>T maps to NM_173488.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:101774336 C>A maps to NM_173488.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:33679959 G>T maps to NM_152270.3 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr17:33690514 G>T maps to NM_152270.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr17:33687334 A>G maps to NM_152270.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:33687260 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:33690514 G>T maps to NM_152270.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:33679387 C>T maps to NM_152270.3 W898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:33680923 C>T maps to NM_152270.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33738842 G>A maps to NM_018042.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:33749698 G>A maps to NM_018042.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr17:33738770 G>A maps to NM_018042.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:33802073 T>C maps to ENST00000361112 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:33802109 C>A maps to ENST00000361112 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:33802348 G>A maps to ENST00000361112 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr17:33769260 C>A maps to NM_144682.5 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr17:33770903 G>A maps to NM_144682.5 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:33768258 C>T maps to NM_144682.5 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:33586311 G>A maps to NM_144975.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:33585708 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:41486065 C>G maps to NM_144990.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:41486212 G>C maps to NM_144990.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr1:41483476 C>A maps to NM_144990.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:98819863 G>T maps to NM_003061.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr10:98820416 C>A maps to NM_003061.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:98799742 A>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr10:98807523 A>T maps to NM_003061.2 C519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr10:98806496 G>T maps to NM_003061.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr10:98763930 G>A maps to NM_003061.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:98764457 G>T maps to NM_003061.2 A1234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr10:98770766 G>A maps to NM_003061.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr4:20568940 A>T maps to ENST00000273739 K932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:20618728 C>T maps to ENST00000273739 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr4:20618584 C>T maps to ENST00000273739 N1313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:20543081 C>T maps to ENST00000273739 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:20600009 C>T maps to ENST00000273739 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:20259526 A>G maps to ENST00000273739 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr4:20469407 A>T maps to ENST00000273739 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:20620523 G>T maps to ENST00000273739 P1507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:20555484 G>A maps to ENST00000273739 W877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:20525798 A>T maps to ENST00000273739 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr4:20543243 T>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:20591315 C>A maps to ENST00000273739 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:20535275 G>A maps to ENST00000273739 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:20487858 G>T maps to ENST00000273739 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr4:20591324 C>T maps to ENST00000273739 H1062H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr4:20570574 A>T maps to ENST00000273739 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:20533667 C>T maps to ENST00000273739 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:20569196 A>T maps to ENST00000273739 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:20541150 T>C maps to ENST00000273739 N644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr4:20530614 G>A maps to ENST00000273739 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:20619214 T>G maps to ENST00000273739 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168187940 C>T maps to NM_003062.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr5:168310298 C>T maps to NM_003062.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:168151446 C>G maps to NM_003062.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168093539 G>T maps to NM_003062.2 Y1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:168250305 G>T maps to NM_003062.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr5:168233476 G>T maps to NM_003062.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:168135052 C>T maps to NM_003062.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:168187880 G>T maps to NM_003062.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:168096806 G>A maps to NM_003062.2 S1439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:168149325 C>T maps to NM_003062.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr5:168100191 G>T maps to NM_003062.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr5:168310310 G>T maps to NM_003062.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:168098270 G>A maps to NM_003062.2 C1353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:168671773 C>A maps to NM_003062.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:168114057 G>T maps to NM_003062.2 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr5:168096926 C>A maps to NM_003062.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr5:168093530 C>T maps to NM_003062.2 Q1500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:168123327 G>A maps to NM_003062.2 N1017N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:168233554 G>C maps to NM_003062.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:168189656 G>A maps to NM_003062.2 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr5:168098300 G>T maps to NM_003062.2 C1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr5:168199813 C>T maps to NM_003062.2 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr5:168189548 G>A maps to NM_003062.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:168201289 C>T maps to NM_003062.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:168098471 G>T maps to NM_003062.2 T1286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:168098327 G>T maps to NM_003062.2 S1334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr5:168180867 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:84454288 G>A maps to NM_052910.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr13:84455263 G>A maps to NM_052910.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:84454949 G>C maps to NM_052910.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr13:84453706 G>T maps to NM_052910.1 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr13:84454310 C>A maps to NM_052910.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr13:84455573 A>T maps to NM_052910.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr13:84453665 G>T maps to NM_052910.1 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr13:84454622 G>T maps to NM_052910.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:84454367 G>C maps to NM_052910.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:84453890 C>T maps to NM_052910.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr13:84453916 C>A maps to NM_052910.1 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr13:84453904 G>A maps to NM_052910.1 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr13:84453977 G>A maps to NM_052910.1 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr13:84454112 C>T maps to NM_052910.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:84455165 G>T maps to NM_052910.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr23:144905578 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:144904793 G>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:144906016 G>T did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:144904083 G>T did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:144904509 G>C did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr23:144906365 G>T did not map to a codon.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr23:144904728 C>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:144906316 C>G did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:144904079 G>C did not map to a codon.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr23:144905794 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:144904348 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:144905648 T>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:144904452 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr23:144906229 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:144905635 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:144905725 A>T did not map to a codon.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr23:144905147 A>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:144904466 G>C did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:144905857 T>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:144904118 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:144904138 C>T did not map to a codon.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr23:144904435 C>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr23:144904873 C>A did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:144905762 G>T did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:144905190 A>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:144904396 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:144904397 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:144904884 A>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:144905487 G>C did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:144905985 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:144905683 A>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:144904873 C>G did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:144904122 C>A did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:144906139 C>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:144906314 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:144906013 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr23:144905996 A>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:144904002 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:144906400 C>T did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:144905066 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:144904771 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:144904646 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:144904398 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:144906010 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:144905082 C>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:144904062 C>T did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr23:144906247 G>T did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:144905708 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:144904366 G>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:144905669 C>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:144904291 C>G did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:144905476 A>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:144904764 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:144905062 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:144905167 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:144905555 T>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:144905907 G>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:144905433 C>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:144904662 G>A did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:144905809 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:144905526 G>T did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:144903953 G>A did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:144904471 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:144905598 C>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:144904666 G>A did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:144904116 G>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:144904177 C>T did not map to a codon.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr23:144905309 A>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:144905986 G>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:144905987 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:144904213 C>A did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:144904757 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:144906474 G>A did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr23:144904118 C>A did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:144905219 G>T did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr23:144905220 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:144905812 G>C did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:144905394 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:144904207 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:144906477 G>C did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:164906716 C>A maps to NM_014926.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:164906356 G>T maps to NM_014926.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr3:164907124 T>C maps to NM_014926.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:164907997 C>T maps to NM_014926.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr3:164906952 G>A maps to NM_014926.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:164907670 A>T maps to NM_014926.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:164908201 G>T maps to NM_014926.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr3:164907523 G>T maps to NM_014926.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:164906699 G>T maps to NM_014926.2 S640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:164907406 A>T maps to NM_014926.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:164906974 C>A maps to NM_014926.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:164906056 C>A maps to NM_014926.2 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:164906233 C>T maps to NM_014926.2 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr3:164906571 G>A maps to NM_014926.2 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr3:164906812 C>T maps to NM_014926.2 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:164907847 T>A maps to NM_014926.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr3:164906356 G>T maps to NM_014926.2 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr3:164906008 C>A maps to NM_014926.2 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr3:164905987 G>T maps to NM_014926.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:142717695 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:142718101 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:142718398 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:142718171 C>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:142717964 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:142717231 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:142716770 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:142718750 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:142717181 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:142717182 G>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:142716994 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:142716611 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:142717340 C>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:142716498 C>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:142717290 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:142718461 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr23:142716740 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:142718817 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:142716538 C>A did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:142716663 T>C did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:142718544 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:142718604 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:142718243 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:142717049 T>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:142716906 T>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:142717425 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:142718704 G>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:142718130 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:142716845 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:142717434 G>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:142717683 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:142717195 C>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:142716436 C>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:142716437 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:142717817 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:142716784 G>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:142716990 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:142716746 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:142718334 C>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:142717339 C>A did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:142718321 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:142717406 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:142717509 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:142718913 C>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:142717091 A>C did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:142717413 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:142718374 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:142717507 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr13:88328536 G>A maps to NM_015567.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr13:88328486 G>T maps to NM_015567.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr13:88327942 G>A maps to NM_015567.1 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr13:88327900 C>T maps to NM_015567.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr13:88329424 G>A maps to NM_015567.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr13:88328731 C>T maps to NM_015567.1 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:88330387 G>A maps to NM_015567.1 V915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:88327909 C>G maps to NM_015567.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr13:88328773 G>T maps to NM_015567.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:88328099 G>T maps to NM_015567.1 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:86368999 G>T maps to NM_032229.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:86368536 C>A maps to NM_032229.2 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr13:86369929 T>C maps to NM_032229.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr13:86369251 C>A maps to NM_032229.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:86368432 G>C maps to NM_032229.2 Y737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr10:105763285 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:105752384 A>T maps to NM_014720.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:57908710 T>A maps to ENST00000428312 C785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:57613682 C>A maps to NM_016045.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:57613526 C>T maps to NM_016045.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr11:107578640 G>T maps to NM_003063.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr15:59179172 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:59182578 T>C maps to NM_024755.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr15:59193470 C>A maps to NM_024755.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:59172238 C>A maps to NM_024755.2 G1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:159839520 T>C maps to NM_006425.4 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:146467853 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:45368311 C>A maps to NM_001003652.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr18:45394790 G>A maps to NM_001003652.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr18:45372172 T>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:67457256 G>T maps to NM_005902.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr15:67473636 G>A maps to NM_005902.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:48584797 G>T maps to NM_005359.5 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr18:48591908 G>T maps to NM_005359.5 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr18:48604732 A>T maps to NM_005359.5 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr18:48593466 G>T maps to NM_005359.5 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr18:48575057 G>T maps to NM_005359.5 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr18:48584592 C>T maps to NM_005359.5 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr18:48581197 G>T maps to NM_005359.5 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:135496713 C>T maps to NM_001001419.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr13:37427570 C>T maps to NM_001127217.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:37422951 C>T maps to NM_001127217.2 W422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:71566659 A>C maps to NM_001044305.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:71562316 G>T maps to NM_001044305.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:71566578 A>G maps to NM_001044305.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:40881912 G>T maps to NM_022733.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr1:40882768 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:40882506 C>T maps to NM_022733.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:128649711 C>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:128649930 G>C did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:128650468 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:128657271 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:128633752 C>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:128652374 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:128599537 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:128582329 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:128599499 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:128645818 G>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:128633731 C>A did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:128630741 C>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:128630844 G>C did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr23:128645930 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:128599690 G>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:128599909 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:128640125 C>T did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:128633818 C>G did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:128650464 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:128624152 A>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:128652415 A>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:128657241 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:128599873 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:128614690 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:128599831 G>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:2182166 G>C maps to NM_003070.3 R1462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr9:2056742 C>T maps to NM_003070.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr9:2123819 C>T maps to NM_003070.3 D1288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:11100014 C>T maps to NM_001128849.1 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:11170530 G>T maps to NM_001128849.1 E1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:11169546 C>T maps to NM_001128849.1 F1571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:11138490 G>T maps to NM_001128849.1 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:11145652 G>T maps to NM_001128849.1 E1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr19:11168982 G>T maps to NM_001128849.1 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:11105641 G>T maps to NM_001128849.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:11136096 G>T did not map to a codon.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:11100020 C>T maps to NM_001128849.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:11130299 C>T maps to NM_001128849.1 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:11097629 C>T maps to NM_001128849.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:11144030 C>G maps to NM_001128849.1 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr19:11144174 G>A maps to NM_001128849.1 E1252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:11121054 A>G did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:11129650 G>A maps to NM_001128849.1 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr19:11145655 G>T maps to NM_001128849.1 E1340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:11123788 G>T did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:11118586 G>T maps to NM_001128849.1 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr19:11105503 G>T maps to NM_001128849.1 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:11129630 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:11114067 G>T maps to NM_001128849.1 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:144469214 T>C maps to NM_003601.2 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:95162157 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:95206109 G>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:95198208 C>T maps to NM_001128429.1 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr4:95200143 A>G maps to NM_001128429.1 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:95171961 A>G maps to NM_001128429.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:217315566 A>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:217279573 C>T maps to NM_014140.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr3:47752262 G>A maps to NM_003074.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:50490682 C>T maps to NM_003076.4 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:50481192 T>C maps to NM_003076.4 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr12:50492535 C>T maps to NM_003076.4 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:50490688 G>A maps to NM_003076.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:61914379 G>A maps to NM_001098426.1 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr7:150936505 G>A maps to NM_003078.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:38785087 T>G maps to NM_003079.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr17:38787101 G>A maps to NM_003079.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:53423250 C>G did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:53409203 G>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:53432206 C>G did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:53439184 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:53436074 C>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:53423453 C>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:53409547 G>T did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:53432770 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:53409447 C>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr23:53440275 T>G did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:53432307 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr22:45802672 T>A maps to NM_148674.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr22:45795220 G>A maps to NM_148674.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr22:45802746 C>G did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr22:45795000 G>A maps to NM_148674.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr9:106889631 T>A maps to NM_001042550.1 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:112328694 G>T did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:160134079 C>A maps to NM_005496.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:160142722 A>C maps to NM_005496.3 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr9:72933455 G>A maps to NM_015110.3 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:72967156 C>T maps to NM_015110.3 Y1072Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:17896177 T>A maps to ENST00000381272 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr18:2698037 A>T maps to NM_015295.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr18:2763759 C>T maps to NM_015295.2 P1564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr18:2705693 C>T maps to NM_015295.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr18:2656196 G>T maps to NM_015295.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr18:2688675 T>G maps to NM_015295.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr18:2751312 C>T maps to NM_015295.2 I1401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr18:2775814 C>T maps to NM_015295.2 V1753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8397-01A-11D-2323-08 chr17:18167984 C>T maps to NM_148886.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr22:39910293 C>G maps to NM_019008.4 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:39908301 C>T maps to NM_019008.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr22:39909757 C>T maps to NM_019008.4 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:18226353 C>T maps to NM_144775.2 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:18219222 G>A maps to NM_144775.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:91948453 C>A maps to ENST00000417249 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr14:91928501 T>A maps to ENST00000417249 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:55844397 C>T maps to NM_001122964.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:18853096 C>T maps to ENST00000389467 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr16:18883651 G>A maps to ENST00000389467 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr16:18887483 G>A maps to ENST00000389467 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr16:18896865 A>G maps to ENST00000389467 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:18841078 T>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:18887445 C>G maps to ENST00000389467 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:18856972 T>C maps to ENST00000389467 K1999K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:18846338 C>A maps to ENST00000389467 V2735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:18896877 G>A maps to ENST00000389467 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:18826799 G>T maps to ENST00000389467 I3493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:18849509 C>A maps to ENST00000389467 L2413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:18882127 T>C maps to ENST00000389467 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr16:18823361 G>C maps to ENST00000389467 S3571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:156237396 C>G maps to NM_015327.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr1:156235926 A>G maps to NM_015327.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:156238163 G>C maps to NM_015327.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:156220780 G>A maps to NM_015327.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:2202975 T>C maps to NM_017575.4 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:183486888 G>A maps to ENST00000367537 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:128846354 C>A maps to NM_005631.4 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr14:70420143 C>T maps to NM_001034852.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr14:70480190 G>T maps to NM_001034852.1 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr14:70418905 C>T maps to NM_001034852.1 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr14:70490117 C>A maps to NM_001034852.1 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:70442475 G>T maps to NM_001034852.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168910592 A>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:168999540 C>A maps to NM_022138.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:168910740 G>A maps to NM_022138.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:169051406 C>T maps to NM_022138.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:4167987 G>C maps to ENST00000443211 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr20:4163479 C>T maps to ENST00000443211 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr20:4163118 C>T maps to ENST00000443211 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:4163346 G>A maps to ENST00000443211 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:6415524 A>T maps to NM_000543.4 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr6:109764083 C>T maps to NM_003080.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:68405826 G>T maps to NM_018667.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:68405508 G>A maps to NM_018667.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr16:68405583 G>T maps to NM_018667.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr16:68404941 G>C maps to NM_018667.3 Y381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr16:68397445 C>T maps to NM_018667.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:130912762 G>A maps to NM_017951.4 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:130910654 G>A maps to NM_017951.4 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:130931106 C>A maps to NM_017951.4 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:130910639 C>T maps to NM_017951.4 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:130911948 C>G maps to NM_017951.4 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:123126142 A>T maps to NM_006714.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:123116819 A>T did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:21755739 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:71232509 T>C maps to NM_012390.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr4:71232503 C>A maps to NM_012390.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr4:71227848 G>A maps to NM_012390.3 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr4:71232647 T>A maps to NM_012390.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:22010738 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:21996186 G>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:21990088 G>C did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr22:31486830 G>T maps to ENST00000454496 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:31484882 C>T maps to ENST00000454496 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr22:31487244 G>A maps to ENST00000454496 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr11:57309022 C>A maps to ENST00000457912 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr17:4500519 C>T maps to NM_001114974.1 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:33071821 G>A maps to NM_018225.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr9:33068869 G>A maps to NM_018225.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr9:33053210 G>C maps to NM_018225.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr12:54577463 T>A maps to NM_014311.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr12:54577565 G>A maps to NM_014311.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:54577481 G>A maps to NM_014311.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:98634710 A>G maps to NM_020429.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:98654859 G>C maps to NM_020429.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:62551056 T>C maps to NM_022739.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr17:62552035 G>A maps to NM_022739.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:62574680 C>T maps to NM_022739.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:88390655 T>C maps to NM_198274.3 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:88410029 G>A maps to NM_198274.3 *491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:88405917 G>T maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr2:88387494 G>A maps to NM_198274.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:88405947 C>T maps to NM_198274.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:214491479 C>G maps to NM_020197.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:245912967 T>A did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr1:246498677 G>A maps to NM_001167740.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr17:1686770 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:73449043 G>T maps to NM_006062.2 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:73450602 C>T maps to NM_006062.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:73441456 C>T maps to NM_006062.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr2:73441462 G>T maps to NM_006062.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:48604460 C>T maps to NM_005985.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:48600677 C>T maps to NM_005985.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:48600454 C>T maps to NM_005985.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr8:49831548 T>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:49832848 G>A maps to NM_003068.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:49832847 C>A maps to NM_003068.3 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr8:49832626 G>A maps to NM_003068.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr16:88744933 G>A maps to NM_178310.3 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:10273812 A>G maps to NM_130811.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr20:10286808 C>T maps to NM_130811.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr20:10277674 C>A maps to NM_130811.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr1:227954726 G>T maps to NM_053052.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:227935688 G>A maps to NM_053052.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:84311041 G>C maps to NM_014841.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:84350817 T>G maps to NM_014841.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:84290251 G>C maps to NM_014841.2 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr6:84310987 A>G did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:84269918 A>T maps to NM_014841.2 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:7986939 G>T maps to NM_003083.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr9:15423095 G>C maps to NM_001039697.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr9:139270915 A>T maps to NM_003086.2 G1434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:139291434 C>A maps to NM_003086.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:139272246 C>T maps to NM_003086.2 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:90743426 A>T maps to NM_001146055.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:90743474 T>C maps to NM_001146055.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:90743486 C>A maps to NM_001146055.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr5:121786346 C>A maps to ENST00000379533 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:121759049 A>T maps to ENST00000379533 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr10:88719863 C>T maps to NM_003087.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:127729611 G>T maps to NM_014390.2 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:127343308 C>T maps to NM_014390.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:127725832 G>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:127338951 G>T maps to NM_014390.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr2:242009518 G>A maps to NM_001080437.1 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:38019713 T>C maps to NM_024700.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr3:43381979 C>T maps to NM_017719.4 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:43389871 C>T maps to NM_017719.4 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956195 G>A maps to NM_014014.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:96956426 G>A maps to NM_014014.3 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:96943346 C>T maps to NM_014014.3 W1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr2:96957581 C>A maps to NM_014014.3 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:96963259 C>A maps to NM_014014.3 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:96951076 C>A maps to NM_014014.3 V1335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:96955716 C>A maps to NM_014014.3 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:96956499 T>C maps to NM_014014.3 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:96949017 C>T maps to NM_014014.3 T1612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:96950131 C>A maps to NM_014014.3 V1452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:96944366 G>A maps to NM_014014.3 I1802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:96955683 T>C maps to NM_014014.3 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:123950104 C>G maps to NM_180699.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:123950179 C>T maps to NM_180699.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:123950128 C>G maps to NM_180699.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:31762254 G>C maps to ENST00000446633 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:31769577 A>T maps to ENST00000446633 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:101825948 C>A maps to NM_003090.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr20:2446398 C>A maps to ENST00000339610 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr18:19203776 C>T maps to NM_006938.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:96259134 T>C maps to NM_003095.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr2:70516504 C>G did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:25222148 C>A maps to NM_022805.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:25222061 A>T maps to NM_022805.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr15:25221463 G>T maps to NM_022805.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr20:31998085 G>A maps to NM_003098.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr8:121706014 G>A maps to NM_021021.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:121823891 G>A maps to NM_021021.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:51362271 C>G maps to NM_018967.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:51415441 T>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:51705340 T>A maps to NM_018967.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:51569498 G>T maps to NM_018967.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:51571150 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:51617257 C>T maps to NM_018967.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:51705289 C>A maps to NM_018967.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:51705358 T>A maps to NM_018967.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:51314825 G>C maps to NM_018967.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr8:51306815 C>A maps to NM_018967.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:51621444 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:51306825 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr8:51363264 G>T maps to NM_018967.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr8:51465740 T>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr8:51363113 A>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:51465645 C>A maps to NM_018967.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:51617224 G>A maps to NM_018967.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr8:51351119 C>T maps to NM_018967.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:51705298 T>A maps to NM_018967.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr8:51442785 T>C maps to NM_018967.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:51617299 A>G maps to NM_018967.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:51617236 G>A maps to NM_018967.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:1093879 A>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:1168844 T>C maps to NM_018968.3 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr2:1241725 C>T maps to NM_018968.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:1263176 C>T maps to NM_018968.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:1251145 C>A maps to NM_018968.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:1241749 G>T maps to NM_018968.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:1251196 C>A maps to NM_018968.3 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr3:63645443 T>A maps to NM_001080537.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:75902272 G>A maps to ENST00000371091 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr14:78189552 C>G maps to NM_012245.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr14:78197466 A>T maps to NM_012245.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr15:64404770 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:26411518 T>A maps to ENST00000446848 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr17:46196132 C>T maps to NM_152244.1 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:70280927 G>A did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:70288109 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:70282789 G>A did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:17885293 T>A maps to ENST00000417048 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr7:17931174 G>A maps to ENST00000417048 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:86248582 C>G did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr6:86227557 G>A maps to NM_153816.3 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:86251734 T>C maps to NM_153816.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr6:86253018 C>A maps to NM_153816.3 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr6:86238080 C>T did not map to a codon.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr2:27598473 G>A maps to NM_014748.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:27597002 C>T maps to NM_014748.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr5:53814690 G>T maps to NM_052870.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:53814546 G>T maps to NM_052870.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:130785060 G>A maps to NM_014758.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:130781540 T>C maps to NM_014758.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:130773247 C>A maps to NM_014758.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:130785618 C>A maps to NM_014758.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:130785627 G>T maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr5:122130961 C>G maps to NM_003100.2 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:50707433 G>A maps to NM_182854.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:122337652 T>C maps to ENST00000395451 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:186231801 G>T maps to NM_031953.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr4:186185598 G>T maps to NM_031953.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:151638446 G>C maps to ENST00000458013 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:151630884 G>T maps to ENST00000458013 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:151634640 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr16:12662398 G>C maps to NM_001080530.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:12618638 C>T maps to NM_001080530.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:115600940 G>C maps to NM_001012994.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr9:115598636 C>G maps to NM_001012994.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:101625259 G>C maps to NM_152628.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:101589248 G>A maps to NM_152628.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:101586162 G>T maps to NM_152628.3 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr8:101629861 C>A maps to NM_152628.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:101601150 G>C maps to NM_152628.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:101648224 A>G maps to NM_152628.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr11:65618286 C>T maps to NM_152760.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:75942360 G>T maps to NM_153271.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr3:125208250 C>G did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:99161071 A>T did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr1:99156701 G>A maps to NM_015976.4 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:2297014 C>T maps to NM_013321.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr7:2296528 G>A maps to NM_013321.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:2303979 C>A maps to NM_013321.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:158288665 G>T did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr6:158330982 G>A maps to NM_016224.3 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:179304747 A>T maps to NM_003101.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:179320524 C>T maps to NM_003101.4 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:179306969 A>C did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:179304744 C>T maps to NM_003101.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr1:179312039 A>G maps to NM_003101.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:179316741 G>A maps to NM_003101.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:53514664 C>A maps to NM_003578.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:53514576 C>T maps to NM_003578.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:53497987 G>T maps to NM_003578.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr6:107956573 G>C maps to NM_018013.3 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:107954956 G>A maps to NM_018013.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr6:107955721 C>T maps to NM_018013.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr6:107854780 G>C maps to NM_018013.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:107955763 G>T maps to NM_018013.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr6:107955649 G>A maps to NM_018013.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:107955116 G>T maps to NM_018013.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:93968705 T>G maps to NM_003877.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr14:55510835 G>T maps to NM_199421.1 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:46986073 A>T maps to NM_144949.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:46986214 G>A maps to NM_144949.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:46986014 C>T maps to NM_144949.2 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr2:46986305 T>C maps to NM_144949.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr2:46986925 C>T maps to NM_144949.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:46986565 G>C maps to NM_144949.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:46986644 G>T maps to NM_144949.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr18:67992311 G>T maps to NM_004232.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr18:67992071 C>A maps to NM_004232.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr18:67992885 G>T maps to NM_004232.3 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr18:67992498 G>T maps to NM_004232.3 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr18:67992758 G>C maps to NM_004232.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr17:36521189 G>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr17:36520737 A>G maps to NM_014598.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:138589371 C>A maps to NM_001101677.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr9:138590207 G>A maps to NM_001101677.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:138588557 G>T maps to NM_001101677.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr9:138588530 C>G maps to NM_001101677.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:138590926 C>A maps to NM_001101677.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr9:138588635 C>T maps to NM_001101677.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr13:36748987 G>A maps to ENST00000511166 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr13:36748887 C>A maps to ENST00000511166 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr16:601520 G>T maps to NM_005632.2 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr16:601601 C>T maps to NM_005632.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr21:34918599 C>T maps to NM_138927.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:34923099 G>T maps to NM_138927.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr21:34924839 G>C maps to NM_138927.1 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:34923231 G>T maps to NM_138927.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr21:34926906 T>C maps to NM_138927.1 Y1790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr21:34924188 G>A maps to NM_138927.1 Q884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr21:34927180 G>T maps to NM_138927.1 G1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr10:97174267 C>A maps to NM_001034954.1 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:97144022 G>A maps to NM_001034954.1 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr10:97141462 G>A maps to NM_001034954.1 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:97174271 G>A maps to NM_001034954.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:97141440 C>T did not map to a codon.
Sequencing variant TCGA-17-Z054-01A-01W-0747-08 chr4:186539746 C>T maps to ENST00000355634 Q977Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:186515055 G>A maps to ENST00000355634 Q1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:186544287 G>A maps to ENST00000355634 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr4:186536068 C>T maps to ENST00000355634 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr4:186515085 G>A maps to ENST00000355634 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:22414372 G>A maps to NM_005775.4 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:22421800 C>T maps to NM_005775.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr8:22412383 G>C maps to NM_005775.4 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:22423980 C>T maps to NM_005775.4 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:108431125 C>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr10:108380224 G>A maps to NM_001013031.1 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:108447970 C>T maps to NM_001013031.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:108536423 A>G maps to NM_001013031.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr10:108439435 C>A maps to NM_001013031.1 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:108489871 C>T maps to NM_001013031.1 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:108366922 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:108371674 C>T maps to NM_001013031.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:108339227 G>T maps to NM_001013031.1 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:108427523 G>T maps to NM_001013031.1 C742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:108339199 C>A maps to NM_001013031.1 G1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr10:108427546 C>A maps to NM_001013031.1 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr10:108466320 C>G maps to NM_001013031.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:108338852 G>T maps to NM_001013031.1 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:108469078 G>T maps to NM_001013031.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108366971 A>G maps to NM_001013031.1 Y1039Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:108923869 C>A maps to NM_001013031.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr10:108716301 G>A maps to NM_001013031.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:108339170 C>A maps to NM_001013031.1 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr10:108459106 C>G maps to NM_001013031.1 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:108469028 G>A maps to NM_001013031.1 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr10:108412181 C>T maps to NM_001013031.1 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:108357184 C>A maps to NM_001013031.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr10:108412208 T>A maps to NM_001013031.1 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr10:108339230 G>T maps to NM_001013031.1 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:108439444 G>T maps to NM_001013031.1 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:108380254 C>T maps to NM_001013031.1 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr10:108466320 C>T maps to NM_001013031.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr10:108489814 C>T maps to NM_001013031.1 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:108377955 G>T maps to NM_001013031.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:7717038 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr4:7736086 C>G maps to NM_020777.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr4:7705099 T>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:7668858 A>C maps to NM_020777.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:7691292 C>T maps to NM_020777.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr4:7725440 C>G maps to NM_020777.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:106907475 G>A maps to NM_014978.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:106970933 C>T maps to NM_014978.1 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:106960942 C>T maps to NM_014978.1 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:106974203 C>A maps to NM_014978.1 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:107022241 G>T maps to NM_014978.1 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:106916949 A>T maps to NM_014978.1 K513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr10:106976821 A>T maps to NM_014978.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr10:106937931 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:107012558 C>A maps to NM_014978.1 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr10:106737226 G>T maps to NM_014978.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr10:106983007 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr10:106602617 G>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr10:106960960 A>G maps to NM_014978.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr10:106675690 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:106916928 A>T maps to NM_014978.1 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr10:106802862 C>G maps to NM_014978.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:106976692 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:106959841 G>T maps to NM_014978.1 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:106976795 A>T maps to NM_014978.1 K884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr10:107022217 G>T maps to NM_014978.1 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:106907445 G>A maps to NM_014978.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:107005407 G>T maps to NM_014978.1 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:107022153 C>G maps to NM_014978.1 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr10:106918721 G>T maps to NM_014978.1 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr10:106959755 G>A did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:45361250 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:121495846 G>T maps to NM_003105.5 G2075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:121429396 A>T maps to NM_003105.5 K921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:121360804 C>G maps to NM_003105.5 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:121429298 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:121428093 G>T maps to NM_003105.5 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:121348869 C>G maps to NM_003105.5 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr11:121477962 C>T maps to NM_003105.5 I1710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr11:121429317 C>T maps to NM_003105.5 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:121383743 C>T maps to NM_003105.5 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:39222288 G>A maps to NM_005633.3 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr2:39214706 A>G maps to NM_005633.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:39234201 T>C maps to NM_005633.3 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr2:39240607 T>A maps to NM_005633.3 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:39250367 T>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr14:50600929 C>A maps to NM_006939.2 G996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr14:50587103 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr14:50671079 G>A maps to NM_006939.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:50585439 T>C maps to NM_006939.2 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr14:50667676 C>A maps to NM_006939.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:41835994 C>A maps to NM_025237.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:16502316 T>A maps to ENST00000396652 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr13:112722332 C>A maps to NM_005986.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr22:38373946 C>T maps to NM_006941.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:38374018 G>C maps to NM_006941.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr22:38369658 G>T maps to NM_006941.3 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr22:38374041 G>T maps to NM_006941.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:5833047 G>A maps to NM_003108.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:137483967 C>T maps to NM_004189.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:137483919 C>A maps to NM_004189.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:137483857 C>A maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:137483992 G>T maps to NM_004189.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:137483964 G>T maps to NM_004189.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr3:137484279 C>A maps to NM_004189.2 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr8:55371726 G>C maps to NM_022454.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr20:62680581 T>C maps to NM_018419.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr13:95364146 C>A maps to NM_007084.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr23:139586818 T>C did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:139586816 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:139586817 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:139586875 G>C did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:139586802 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:139586679 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:139586650 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:139586864 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:139586843 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:139587103 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:157073777 T>C maps to NM_178424.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:21596141 G>T maps to NM_003107.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr12:23893821 C>A maps to NM_006940.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:23716277 C>A maps to NM_006940.4 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:23818488 G>A maps to NM_006940.4 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:23728773 T>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:23793748 C>A maps to NM_006940.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr12:23687281 A>G maps to NM_006940.4 H721H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr11:15994630 T>A maps to NM_001145819.1 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:16208412 C>T maps to NM_001145819.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr11:16010774 T>G maps to NM_001145819.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:16077357 C>A maps to NM_001145819.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:10583457 G>A maps to ENST00000354846 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:10584168 C>T maps to ENST00000354846 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:10583682 C>A maps to ENST00000354846 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:1035262 C>A maps to NM_014587.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:1035160 C>A maps to NM_014587.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr16:1035112 C>G maps to NM_014587.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr17:70117603 C>G maps to NM_000346.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr17:70117636 C>A maps to NM_000346.3 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:70119771 C>A maps to NM_000346.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:53775907 C>T maps to NM_138473.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:53777320 G>A maps to NM_138473.2 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr12:53777372 C>T maps to NM_138473.2 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:53803151 G>A maps to NM_138473.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr12:53805022 G>A maps to NM_138473.2 *786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:53777108 G>T maps to NM_138473.2 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr12:53776244 C>T maps to NM_138473.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:53800366 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:231311580 G>T maps to NM_001080391.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:231371123 A>T maps to NM_001080391.1 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:231327147 A>T did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr2:231338155 G>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:231065681 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:231067328 C>T maps to NM_080424.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:231067406 G>C maps to NM_080424.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:231050815 C>A maps to NM_080424.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr2:231036808 C>T maps to NM_080424.2 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:231135346 G>A maps to NM_007237.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:231120198 G>T maps to NM_007237.4 G398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:231135313 T>C maps to NM_007237.4 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:231174739 T>A maps to NM_007237.4 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:231090582 G>T maps to NM_007237.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr2:231150521 T>C maps to NM_007237.4 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:231103064 T>C maps to NM_007237.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:231157403 C>T maps to NM_007237.4 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr2:231222645 C>T maps to NM_138402.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:231264873 G>T maps to NM_138402.4 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:45993739 G>C maps to NM_003110.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:45994183 G>A maps to NM_003110.5 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:174820399 C>A maps to NM_003111.4 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:174828612 T>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:174820237 G>C maps to NM_003111.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:21469848 G>T maps to NM_003112.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:21521556 A>T maps to NM_003112.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:21469526 T>C maps to NM_003112.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:21516847 T>A maps to NM_003112.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:21516764 G>T maps to NM_003112.3 G583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr7:21469829 C>T maps to NM_003112.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr17:45925439 G>T maps to NM_199262.2 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:53722568 C>G maps to NM_001173467.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:53722172 C>T maps to NM_001173467.1 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:53722322 G>A maps to NM_001173467.1 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr12:53722856 G>T maps to NM_001173467.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:20824766 G>A maps to NM_182700.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr11:124564340 G>A maps to NM_017425.3 *152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:88773938 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:88775996 C>T maps to NM_030960.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:88773892 C>T maps to NM_030960.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:88773814 A>G did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:31324728 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:31318968 C>T maps to NM_173847.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr17:31322460 G>T maps to NM_173847.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:49110447 C>A maps to NM_133498.2 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:101178125 G>A maps to NM_003114.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:101252648 G>T maps to NM_003114.3 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:7308655 T>A maps to NM_016512.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr8:7308422 C>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr2:214878755 C>A maps to NM_024532.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:215274945 C>A maps to NM_024532.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr2:215013862 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:214215335 G>T maps to NM_024532.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr2:214239764 A>T maps to NM_024532.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:118558769 T>A maps to NM_206996.2 K1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:118550774 T>C maps to NM_206996.2 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:118539079 G>A maps to NM_206996.2 R1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:118570993 A>T maps to NM_206996.2 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:118567935 G>T maps to NM_206996.2 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:118581913 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:118548156 T>C maps to NM_206996.2 S1552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:118558665 G>T maps to NM_206996.2 I1403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr1:118568008 C>T maps to NM_206996.2 W1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr20:34207179 G>A maps to NM_003116.1 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:34205715 C>A maps to NM_003116.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr20:34207126 C>A maps to NM_003116.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:26907093 G>T maps to NM_006461.3 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:26925629 A>T maps to NM_006461.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:26906190 T>A maps to NM_006461.3 K1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr17:26905477 G>A maps to NM_006461.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:22680765 C>A maps to ENST00000376603 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:22653939 G>T maps to ENST00000376603 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:22678129 G>T maps to ENST00000376603 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:22700084 T>C maps to ENST00000376603 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:22680713 T>A maps to ENST00000376603 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:4863163 C>A maps to NM_004890.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:4862939 T>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr17:49098726 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:49156968 T>A maps to ENST00000376407 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr17:49197816 C>T maps to ENST00000376407 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:49198013 C>A maps to ENST00000376407 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:123594226 A>G maps to NM_001174046.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:123594256 G>A maps to NM_001174046.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:123594319 C>T maps to NM_001174046.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:123594223 G>T maps to NM_001174046.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:123594166 C>G maps to NM_001174046.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr7:123594451 C>A maps to NM_001174046.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:123594253 T>A maps to NM_001174046.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:123594063 G>A maps to NM_001174046.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:140336550 C>A did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:140335790 T>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:140336541 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:140335803 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:140336565 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:140336570 G>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr23:140785626 T>C did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:140785754 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:140785679 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:144337244 A>C did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:144329155 G>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr23:144337279 C>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:142795403 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:142795436 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:142803689 C>A did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:142795246 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:142795593 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:142795253 C>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:142795331 C>A did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:142795253 C>A did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:142795240 C>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:142795579 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:142795380 G>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:142795343 C>G did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:142596805 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:142596909 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:142596920 G>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:142596946 C>G did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:142596969 C>G did not map to a codon.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr23:142605205 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:142605182 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:142596805 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:142596701 T>C did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:142596979 T>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:142596928 T>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:142605141 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:142596719 G>C did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:52825630 C>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:151054175 A>T maps to NM_003118.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151046004 G>T maps to NM_003118.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:151049240 G>A maps to NM_003118.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr4:88401603 C>T maps to NM_004684.4 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:32289088 G>T maps to NM_014946.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:32289028 G>A maps to NM_014946.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:57107824 A>T maps to NM_181727.1 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr13:24864908 G>T maps to ENST00000424834 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr3:172835416 C>G maps to NM_031955.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr3:172835182 A>G maps to NM_031955.5 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:172634253 G>T maps to NM_031955.5 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:217822222 G>C did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr1:217856608 C>A maps to NM_138796.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr1:217915383 G>T maps to NM_138796.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:217856597 A>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:52944958 C>A maps to NM_145263.2 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr4:52938290 C>T maps to NM_145263.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr4:52944930 A>C maps to NM_145263.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr4:52948664 A>T maps to NM_145263.2 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:133715329 C>A maps to NM_174927.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr11:133712378 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:133714516 G>T maps to NM_174927.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr20:48523253 C>T maps to NM_006038.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr20:48522884 A>G maps to NM_006038.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:48522818 G>A maps to NM_006038.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:48629013 C>A maps to NM_022827.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:48627385 A>G maps to NM_022827.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr17:48625106 G>A maps to NM_022827.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:16727320 C>T maps to NM_198546.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:16735643 G>A maps to NM_198546.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:3343455 C>T maps to NM_001170695.1 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:89764599 C>A maps to NM_152339.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:177116676 G>A maps to NM_144644.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr4:177116674 C>T maps to NM_144644.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr4:123859322 T>A maps to NM_145207.2 C459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:48865226 C>T maps to NM_019073.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:48865285 C>A maps to NM_019073.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr14:88904618 G>A maps to NM_018418.4 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr14:88895775 A>T maps to NM_018418.4 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr15:97327388 G>A maps to NM_173499.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:97326908 G>T maps to NM_173499.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr15:97326890 C>A maps to NM_173499.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr5:95011343 C>G did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr5:95011207 G>A maps to NM_031952.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:94999695 A>T maps to NM_031952.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr5:95018281 C>A maps to NM_031952.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr8:145095242 C>G maps to NM_198572.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:145101811 C>A maps to NM_198572.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:44329628 C>T maps to NM_145026.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr6:44328185 C>A maps to NM_145026.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr6:44336164 A>G maps to NM_145026.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:44336232 C>G maps to NM_145026.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:44336232 C>A maps to NM_145026.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:44310867 G>A maps to NM_145026.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:44310903 C>T maps to NM_145026.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:49916601 G>A maps to NM_023071.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:11258791 G>A maps to NM_182513.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr11:74676881 C>T maps to NM_014752.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:34508805 G>A maps to NM_012391.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr6:34506077 G>A maps to NM_012391.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:29052091 G>A maps to NM_182756.3 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:64940261 C>A maps to NM_001008778.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:64938908 G>T maps to NM_001008778.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr11:64939426 C>A maps to NM_001008778.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:64938796 G>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr7:44046938 G>A maps to NM_175064.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr5:35691154 G>A maps to NM_024867.3 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:35779449 T>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:35793322 G>T maps to NM_024867.3 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr5:35753775 G>T maps to NM_024867.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:35776362 A>T maps to NM_024867.3 I1361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr5:35649460 A>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr5:35771818 G>T maps to NM_024867.3 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:35644576 G>T maps to NM_024867.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:35727903 T>C maps to NM_024867.3 Y1014Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:35691317 A>G maps to NM_024867.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr5:35709092 A>T maps to NM_024867.3 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:35795803 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr5:35800099 A>T maps to NM_024867.3 K1621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr5:35659119 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:35644536 C>T maps to NM_024867.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:220336961 C>A maps to NM_005876.4 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220309868 G>T maps to NM_005876.4 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:220354244 C>G maps to NM_005876.4 L2835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr2:220342496 G>T maps to NM_005876.4 E1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr2:220354240 C>A maps to NM_005876.4 S2834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:220336997 G>T maps to NM_005876.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:220333961 G>T maps to NM_005876.4 R1192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr2:220348587 G>T maps to NM_005876.4 E2135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:220353373 C>A maps to NM_005876.4 T2671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:220353802 C>G maps to NM_005876.4 S2726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:220355149 C>T maps to NM_005876.4 R2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:220336994 G>T maps to NM_005876.4 V1294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr2:220346371 A>T maps to NM_005876.4 A1845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:220313112 G>C maps to NM_005876.4 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:220309427 G>T maps to NM_005876.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr2:220354241 G>A maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:220344770 G>T maps to NM_005876.4 G1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:220354241 G>T maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220344799 A>T maps to NM_005876.4 T1760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:220354289 G>A maps to NM_005876.4 R2850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:220309589 G>A maps to NM_005876.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:220337807 G>A maps to NM_005876.4 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:220327060 C>T maps to NM_005876.4 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:220354190 C>G maps to NM_005876.4 V2817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:220313107 C>T maps to NM_005876.4 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:220312958 C>A maps to NM_005876.4 S360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7324722 G>T maps to NM_199339.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr17:7323953 C>T maps to NM_199339.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr17:7324311 G>A maps to NM_199339.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:16257948 C>G maps to NM_015001.2 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:16265828 C>T maps to NM_015001.2 F3634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:16255644 A>T maps to NM_015001.2 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr1:16258746 G>A maps to NM_015001.2 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr1:16256409 C>T maps to NM_015001.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:16263821 G>T maps to NM_015001.2 T3397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:16259229 A>G maps to NM_015001.2 L2165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:16260738 G>A maps to NM_015001.2 L2668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr1:16258563 G>A maps to NM_015001.2 A1943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr13:46287783 C>A maps to NM_152719.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr13:46287684 G>A maps to NM_152719.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr15:44914529 C>A maps to NM_025137.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr15:44955626 C>A maps to NM_025137.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44862812 C>T maps to NM_025137.3 T2129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:44903123 G>A maps to NM_025137.3 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr15:44900769 T>A maps to NM_025137.3 K1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr15:44914077 G>A maps to NM_025137.3 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:44865870 G>A maps to NM_025137.3 Q2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:44887651 G>C maps to NM_025137.3 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr15:44859691 G>A maps to NM_025137.3 C2228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:44890970 T>A maps to NM_025137.3 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr15:44952722 C>A maps to NM_025137.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr15:44876525 G>A maps to NM_025137.3 A1784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr15:44955722 G>C maps to NM_025137.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:44876468 C>G maps to NM_025137.3 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:44943788 G>A maps to NM_025137.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:36909549 C>A maps to NM_001142294.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:89603222 G>T maps to NM_199367.1 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:89611125 G>A maps to NM_003119.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr16:89611152 C>T maps to NM_003119.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:89620292 C>T maps to NM_003119.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:74382928 G>A maps to NM_182965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:74383159 A>T maps to NM_182965.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:74383633 C>G maps to NM_182965.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr17:74383480 C>T maps to NM_182965.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:228973592 G>T maps to NM_001142644.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:228881212 G>A maps to NM_001142644.1 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:228886676 A>G maps to NM_001142644.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228855714 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:228882761 C>A maps to NM_001142644.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:228881495 A>G maps to NM_001142644.1 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:228883384 G>T maps to NM_001142644.1 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:228881510 C>T maps to NM_001142644.1 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:228882689 A>G maps to NM_001142644.1 C960C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr2:228855801 G>A maps to NM_001142644.1 R1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:228884870 A>G maps to NM_001142644.1 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:228855801 G>T maps to NM_001142644.1 R1625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:229046290 C>T maps to NM_001142644.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228882329 G>T maps to NM_001142644.1 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr2:228884753 G>T maps to NM_001142644.1 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:228881687 C>G maps to NM_001142644.1 R1294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:228996710 G>A maps to NM_001142644.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:228882197 G>A maps to NM_001142644.1 S1124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:228882608 C>A maps to NM_001142644.1 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:228996757 G>A maps to NM_001142644.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:228881859 G>T maps to NM_001142644.1 S1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr2:228846465 C>T maps to NM_001142644.1 L1690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:228884711 A>T maps to NM_001142644.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:228882593 C>G maps to NM_001142644.1 V992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:228881837 G>T maps to NM_001142644.1 S1244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:228881738 G>C maps to NM_001142644.1 V1277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr19:50926965 G>A maps to NM_003121.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr12:101880200 A>T maps to ENST00000299272 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:101880254 C>A maps to ENST00000299272 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr12:101880375 C>T maps to ENST00000299272 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:91083323 A>T maps to NM_006717.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:57162257 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:57146384 G>C did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:57146617 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:57021109 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:57021330 C>T did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:57020668 C>G did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:62570190 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:62570684 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:62570086 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:62570541 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr5:147209173 G>A maps to NM_003122.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:147549354 A>G maps to NM_001001325.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:57686701 C>G maps to ENST00000506738 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr4:57686700 C>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr4:57677864 C>T maps to ENST00000506738 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr9:33248441 C>A maps to ENST00000379725 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr9:33248467 G>A maps to ENST00000379725 *110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:147493974 C>A maps to NM_001127698.1 C646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr5:147450010 A>C maps to NM_001127698.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:147693700 C>A maps to NM_032566.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr5:147693706 C>A maps to NM_032566.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:44170793 C>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:41149043 C>T maps to NM_181642.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr15:41146706 T>A maps to NM_181642.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr19:38774437 G>T did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:44352522 C>A maps to NM_178455.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:89920945 A>T maps to NM_032451.1 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr16:89922094 G>C did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:29675183 C>A maps to NM_003123.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr16:29675720 T>C maps to NM_003123.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr16:28993751 C>G maps to NM_032038.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28995568 G>T maps to NM_032038.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:4436618 G>A maps to NM_001124758.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:4352682 G>T did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:4349455 C>T maps to NM_182538.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr17:4337384 G>T maps to NM_182538.4 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr20:55906983 C>G maps to ENST00000371258 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:32259394 T>C maps to NM_144569.4 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:32267263 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:32280166 G>T maps to NM_144569.4 C256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:32265011 G>A maps to NM_144569.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:32257999 G>A maps to NM_144569.4 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:136448122 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:136314450 C>A maps to NM_004598.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:136324288 G>T maps to NM_004598.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:136328287 G>T maps to NM_004598.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr10:73826771 G>A maps to NM_014767.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr4:167656176 C>T maps to NM_016950.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:167675842 T>A maps to NM_016950.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr4:167675785 T>A maps to NM_016950.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:14282210 C>A maps to NM_006108.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:14282263 G>T maps to NM_006108.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr11:14063147 G>C maps to NM_006108.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:14157005 C>T maps to NM_006108.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:1161316 C>T maps to NM_012445.3 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr4:1165769 C>T maps to NM_012445.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:139316702 A>T maps to NM_001001664.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:139318415 A>G maps to NM_001001664.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr4:88903957 G>T maps to NM_001040058.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:88902884 C>A maps to NM_001040058.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr4:88901271 C>A maps to NM_001040058.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:234975187 G>T maps to NM_006944.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:2340934 G>A maps to NM_152988.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr19:2337524 C>A maps to NM_152988.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:2337593 C>G maps to NM_152988.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:65540931 C>T maps to NM_181784.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:65571930 C>A maps to NM_181784.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:65541009 C>G maps to NM_181784.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:152957792 C>A maps to NM_005987.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:153005015 C>A maps to NM_003125.2 C65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:153004833 C>T maps to NM_003125.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:153012668 G>A maps to NM_006945.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:153012672 G>T maps to NM_006945.4 C50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:153066038 G>A maps to NM_001024209.2 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:153122508 T>A maps to NM_001014291.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:152975690 C>T maps to NM_005416.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:152975696 C>A maps to NM_005416.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:152975720 C>A maps to NM_005416.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:155004395 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:155003544 G>C did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:155003661 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:155004222 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:155004004 T>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:155003883 T>A did not map to a codon.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:155003792 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:155003732 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:155003583 G>C did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr23:155003946 G>C did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr23:155003947 C>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:155004045 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:155004197 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:155003851 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:155003852 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:56863237 G>A maps to NM_207344.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55653023 C>G maps to NM_032681.3 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:55657474 G>T maps to NM_032681.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:55653041 G>A maps to NM_032681.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:55655698 G>T maps to NM_032681.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:55655666 A>C maps to NM_032681.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr11:55658696 A>G maps to NM_032681.3 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:55658999 T>C maps to NM_032681.3 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:55655603 C>A maps to NM_032681.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:55653314 G>T maps to NM_032681.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:55658921 C>A maps to NM_032681.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:55658648 C>A maps to NM_032681.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr11:55653014 C>A maps to NM_032681.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr11:55658654 G>C maps to NM_032681.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:55659077 C>A maps to NM_032681.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:9416201 G>T maps to NM_025106.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:9416180 G>A maps to NM_025106.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:9416303 G>C maps to NM_025106.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:6981811 G>T maps to NM_032641.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:1828308 G>A maps to NM_080861.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr16:1828176 G>A maps to NM_080861.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:1827142 A>G maps to NM_080861.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:140785431 G>T maps to NM_080862.1 P162P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-55-6968-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:158615030 C>A maps to NM_003126.2 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:158596790 G>A maps to NM_003126.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:158644205 A>T maps to NM_003126.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:158584067 G>A maps to NM_003126.2 L2273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:158644337 G>A maps to NM_003126.2 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:158618418 C>T maps to NM_003126.2 Q1198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158596724 G>A maps to NM_003126.2 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:158647624 C>A did not map to a codon.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:158596752 T>A maps to NM_003126.2 I1903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158612254 C>A maps to NM_003126.2 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:158623068 C>T maps to NM_003126.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr1:158627412 G>A maps to NM_003126.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:158585142 C>A maps to NM_003126.2 V2217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:158618310 G>C maps to NM_003126.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622333 C>A maps to NM_003126.2 E1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:158622400 A>T maps to NM_003126.2 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158612233 A>G maps to NM_003126.2 C1568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158632542 C>A maps to NM_003126.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:158653252 C>A maps to NM_003126.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:158583599 C>T maps to NM_003126.2 L2300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158624418 C>G maps to NM_003126.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:158636288 T>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:158617447 G>A maps to NM_003126.2 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr1:158592829 C>A maps to NM_003126.2 L2021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:158606520 G>A maps to NM_003126.2 D1740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:158613133 G>T maps to NM_003126.2 R1474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:158606532 C>A maps to NM_003126.2 V1736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158612762 C>T maps to NM_003126.2 W1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:158648303 G>T maps to NM_003126.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:158654954 G>T maps to NM_003126.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:158645962 G>T maps to NM_003126.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr1:158609779 C>A maps to NM_003126.2 L1585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:158606552 T>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr1:158615300 A>T maps to NM_003126.2 L1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:158609403 G>A maps to NM_003126.2 Q1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:158646019 G>T maps to NM_003126.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:158632635 G>T maps to NM_003126.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:158581116 C>A maps to NM_003126.2 R2399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:158639265 C>A maps to NM_003126.2 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:158604465 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:158624490 G>T maps to NM_003126.2 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:158644416 G>A maps to NM_003126.2 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:158639314 G>A maps to NM_003126.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:158651411 G>A maps to NM_003126.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:158621213 T>C maps to NM_003126.2 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:158648312 A>T maps to NM_003126.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:158644392 A>T maps to NM_003126.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr1:158605806 T>A maps to NM_003126.2 A1776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158627269 A>T maps to NM_003126.2 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158637795 C>T maps to NM_003126.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:158648219 G>T maps to NM_003126.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:158613151 T>A maps to NM_003126.2 K1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158648265 C>T maps to NM_003126.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:158654918 A>G maps to NM_003126.2 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:158653172 G>A maps to NM_003126.2 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:158622409 G>T maps to NM_003126.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:158622423 G>T maps to NM_003126.2 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:158590151 C>T maps to NM_003126.2 L2075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:158632513 G>A maps to NM_003126.2 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:158590118 C>T maps to NM_003126.2 E2086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:158639546 A>T maps to NM_003126.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr1:158592982 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:158609779 C>G maps to NM_003126.2 L1585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:158590066 C>A maps to NM_003126.2 E2104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr1:158581059 G>T maps to NM_003126.2 G2418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:158612332 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131356465 G>T maps to NM_001130438.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr9:131395179 C>T maps to NM_001130438.2 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:131371398 A>G did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr9:131371196 C>T maps to NM_001130438.2 I1512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:131371235 G>T maps to NM_001130438.2 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr14:65216152 G>T maps to ENST00000389723 A2290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr14:65239967 C>A maps to ENST00000389723 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:65289695 G>T maps to ENST00000389723 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr14:65263396 C>A maps to ENST00000389723 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:65266573 C>A maps to ENST00000389723 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr14:65268072 C>T maps to ENST00000389723 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr14:65245929 G>C maps to ENST00000389723 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:54852018 G>T maps to NM_003128.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54853247 C>T maps to NM_003128.2 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:54856192 G>A maps to NM_003128.2 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:54839362 C>T maps to NM_003128.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:54872431 C>T maps to NM_003128.2 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:54852006 C>T maps to NM_003128.2 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:54858127 C>T maps to NM_003128.2 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:54880792 G>T maps to NM_003128.2 A1875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:54872491 A>T maps to NM_003128.2 K1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr2:54872457 C>T maps to NM_003128.2 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:54872391 G>T maps to NM_003128.2 R1432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr2:54871599 C>T maps to NM_003128.2 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:66475713 C>T maps to NM_006946.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr11:66460087 C>T maps to NM_006946.2 L1703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:66455338 C>A maps to NM_006946.2 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:66453365 G>A maps to NM_006946.2 F2383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr11:66458922 C>T maps to NM_006946.2 A1799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr11:66455641 G>A maps to NM_006946.2 D2124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:66475181 G>A maps to NM_006946.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:66478174 C>G maps to NM_006946.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:41019338 C>T maps to NM_020971.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:41081360 G>A maps to NM_020971.2 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:41071433 T>A maps to NM_020971.2 S2007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:40996037 G>T maps to NM_020971.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:41019461 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:40993634 C>T maps to NM_020971.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:41078080 G>A maps to NM_020971.2 K2492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:41078029 C>G maps to NM_020971.2 L2475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:41009786 C>T maps to NM_020971.2 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:41063309 G>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:40996130 C>A maps to NM_020971.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:40996001 C>A maps to NM_020971.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr15:42166579 G>A maps to ENST00000320955 L1533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr15:42151128 C>A maps to ENST00000320955 E2680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr15:42169381 G>A maps to ENST00000320955 R1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr15:42168844 C>A maps to ENST00000320955 T1284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:94877643 G>A maps to NM_006415.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr9:94794785 C>G maps to NM_006415.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr20:13145411 T>G maps to NM_018327.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr20:13074219 C>T maps to NM_018327.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr11:18637495 G>A maps to NM_194285.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr11:18637459 G>A maps to NM_194285.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr5:79616339 T>A maps to NM_032567.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr5:79617069 C>T maps to NM_032567.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:79617266 T>C maps to NM_032567.3 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:79616983 T>A maps to NM_032567.3 L317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr15:45981367 C>G maps to NM_021199.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179250037 C>T maps to NM_003900.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr5:179251242 G>A maps to NM_003900.4 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr3:142769828 A>T maps to NM_001080415.1 K865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr3:142742814 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:142745999 C>T maps to NM_001080415.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr3:142772594 C>T maps to NM_001080415.1 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr2:45616529 G>A maps to NM_018079.4 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr2:45646958 C>T maps to NM_018079.4 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:45800476 G>A maps to NM_018079.4 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:45774722 G>A maps to NM_018079.4 Y568Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr20:36031655 C>T maps to ENST00000373558 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr20:36022654 C>T maps to ENST00000373558 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:30724539 G>A maps to NM_006662.2 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:30748500 G>T maps to NM_006662.2 R2380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr16:30722384 G>T maps to NM_006662.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr16:30732558 G>T maps to NM_006662.2 T1101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr16:30732534 G>A maps to NM_006662.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr16:30732645 C>G maps to NM_006662.2 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:30734043 C>T maps to NM_006662.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:30735391 G>T maps to NM_006662.2 L1549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:30748386 C>T maps to NM_006662.2 A2342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr16:30736201 G>A maps to NM_006662.2 Q1819Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr16:30749477 C>A maps to NM_006662.2 S2706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr16:30740306 G>T maps to NM_006662.2 R1893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr16:30750546 C>A maps to NM_006662.2 P3062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:30747678 C>T maps to NM_006662.2 S2296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr16:30735523 A>C maps to NM_006662.2 P1593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:30715382 A>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:30747667 G>T maps to NM_006662.2 E2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:36708819 C>A maps to NM_025248.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:36709060 C>T maps to NM_025248.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:36714511 C>A maps to NM_025248.2 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:36714550 C>A maps to NM_025248.2 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:76026892 G>A maps to NM_080744.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:76033705 G>T maps to NM_080744.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr2:31805945 G>A maps to NM_000348.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:31805786 C>T maps to NM_000348.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr4:56212691 C>T maps to NM_024592.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr4:56212670 G>A maps to NM_024592.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr4:56230250 G>A maps to NM_024592.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr4:56236182 C>G maps to NM_024592.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:56233824 C>T maps to NM_024592.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:17720654 C>A maps to NM_001005291.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr17:17718179 G>A maps to NM_001005291.2 F887F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:42276883 C>T maps to NM_004599.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr5:121355924 C>T maps to NM_152546.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr5:121355963 G>A maps to NM_152546.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:121311045 G>T maps to NM_152546.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:121355029 C>T maps to NM_152546.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:121356023 G>T maps to NM_152546.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr5:121356345 G>T maps to NM_152546.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:64536283 C>T maps to NM_020762.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:64377776 G>T maps to NM_020762.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:64472703 G>A maps to NM_020762.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr12:64437228 A>G maps to NM_020762.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:64509624 G>T maps to NM_020762.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr12:64491114 C>T maps to NM_020762.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:206566978 C>T maps to ENST00000414359 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:206566146 A>G maps to ENST00000414359 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:9106198 C>A maps to NM_014850.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr3:9102044 T>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr3:9100090 G>C maps to NM_014850.2 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:9055494 C>T maps to NM_014850.2 Q615Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:9121753 C>A maps to NM_014850.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:87837824 A>G maps to NM_003130.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:87838652 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:11115021 G>T maps to NM_003132.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr20:62174735 C>T maps to NM_080823.2 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr20:62172565 G>C maps to NM_080823.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr20:62172700 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:35470160 G>T maps to NM_003136.3 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr17:74035837 G>A maps to NM_014230.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr17:74046603 C>A maps to NM_014230.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr17:74068494 A>C maps to NM_014230.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:57349351 G>T maps to NM_006947.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:57335834 A>G maps to NM_006947.3 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:57344755 A>T did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:35837333 G>A maps to ENST00000361690 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr7:104782520 C>A maps to ENST00000336613 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:153048469 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:153047619 C>A did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:153048493 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:153048561 C>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:153049511 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:153048508 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:153047045 G>C did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:153047239 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:153049524 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:153046801 G>T did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:153049583 G>T did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:153049527 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:153046699 C>T did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr11:126135201 G>A maps to NM_003139.3 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:133525471 G>T maps to NM_021203.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:38033549 G>A did not map to a codon.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr23:38024105 C>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:38016191 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:38019324 A>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:38033567 C>A did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:38020260 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:38031231 C>A did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr23:38024094 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:99921830 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:99920562 T>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:99917178 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:99920553 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:99921879 G>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:99924326 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:99924307 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:99921851 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:99925896 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:99901369 A>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:99920542 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:26887614 G>T maps to NM_001013694.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr22:26886155 T>C maps to NM_001013694.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:24996712 C>T maps to NM_005839.3 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr16:2814827 A>G maps to NM_016333.3 R1433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:2818262 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:2813640 G>T maps to NM_016333.3 G1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr16:2813699 G>C maps to NM_016333.3 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:2814773 G>A maps to NM_016333.3 S1415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:2812487 T>C maps to NM_016333.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr16:2809139 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:2811926 A>T maps to NM_016333.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr7:75894094 C>T maps to ENST00000388802 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr12:119563200 C>A maps to NM_194286.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:119568488 C>A maps to NM_194286.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:119563200 C>A maps to NM_194286.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6543-01A-11D-1753-08 chr7:100478962 G>A maps to NM_015908.5 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr7:100483531 A>G maps to NM_015908.5 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr7:100481744 G>C maps to NM_015908.5 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:629552 T>A maps to NM_080725.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:23612425 T>C maps to ENST00000415083 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr20:60736499 G>T maps to NM_198935.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr20:60737877 G>T maps to NM_198935.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:60738587 C>T maps to NM_198935.1 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr5:80724478 C>A maps to ENST00000380182 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:80809458 T>A maps to ENST00000380182 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:80946158 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:54722798 C>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:18545054 G>A maps to NM_032627.3 *386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr2:182767108 T>C maps to NM_001130445.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:182779941 G>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:182780277 G>T maps to NM_001130445.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr2:182774636 G>A maps to NM_001130445.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:182783513 G>T maps to NM_001130445.1 R966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr2:182786886 A>G maps to NM_001130445.1 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:109186490 C>A maps to NM_018984.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:109210908 C>T maps to NM_018984.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr12:109182546 C>T maps to NM_018984.3 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr12:109182462 C>T maps to NM_018984.3 Q817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr17:28004719 G>A maps to NM_033389.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:27999143 A>G maps to NM_033389.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:27958697 C>A maps to NM_033389.2 E1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr17:27999014 T>C maps to NM_033389.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27959178 C>T maps to NM_033389.2 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:27958223 C>A maps to NM_033389.2 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:27993911 A>T maps to NM_033389.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:27994189 C>T maps to NM_033389.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:67075136 G>A maps to NM_017857.3 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:67074510 A>T did not map to a codon.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr9:140083650 A>G maps to NM_003731.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:26383939 C>A maps to NM_005086.4 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr7:149502580 C>G maps to NM_198455.2 R2799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:149492317 G>T maps to NM_198455.2 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr7:149492428 A>T maps to NM_198455.2 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:149485869 G>T maps to NM_198455.2 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:149526083 G>A maps to NM_198455.2 P5052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:149483225 C>A maps to NM_198455.2 Y1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149523229 C>A maps to NM_198455.2 A4777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr7:149525061 G>T maps to NM_198455.2 G4996G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:149503132 G>T maps to NM_198455.2 T2880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:149515768 C>T maps to NM_198455.2 S3894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr7:149528278 G>T maps to NM_198455.2 G5071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr7:149477085 C>G maps to NM_198455.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:149519662 C>T maps to NM_198455.2 Q4389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:149515066 G>A maps to NM_198455.2 P3822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:149486457 G>T maps to NM_198455.2 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:149509062 G>A maps to NM_198455.2 R3206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:149520901 C>A maps to NM_198455.2 A4497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:149518043 G>A maps to NM_198455.2 P4133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:149522469 C>T maps to NM_198455.2 L4706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:149519224 C>T maps to NM_198455.2 P4347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr7:149502626 G>T maps to NM_198455.2 G2815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr7:149494419 C>T maps to NM_198455.2 H2298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:149480301 G>A maps to NM_198455.2 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr7:149512269 G>T maps to NM_198455.2 G3533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:149522429 G>C maps to NM_198455.2 L4692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8496-01A-11D-2393-08 chr7:149493796 G>T maps to NM_198455.2 E2266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:149490412 C>A maps to NM_198455.2 P1964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr7:149495213 G>T did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr7:149493700 C>T maps to NM_198455.2 L2234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr7:149523301 G>T maps to NM_198455.2 G4801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:149499005 G>T maps to NM_198455.2 R2487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:149486407 G>T maps to NM_198455.2 G1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr7:149529906 G>A maps to NM_198455.2 P5113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:149493711 G>C maps to NM_198455.2 G2237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:149502644 G>T maps to NM_198455.2 E2821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr6:7301602 T>C maps to ENST00000474597 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:7301602 T>C maps to ENST00000474597 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:156271451 G>C maps to ENST00000467789 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:153062963 G>T did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr23:153060160 C>G did not map to a codon.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr23:153062933 G>T did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr11:57095847 G>T maps to NM_003146.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:65338162 G>A maps to NM_006396.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:187387014 C>T maps to NM_001048.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:38679166 C>A maps to NM_001049.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr14:38679154 C>T maps to NM_001049.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:38678881 C>A maps to NM_001049.2 Y96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:38678665 C>A maps to NM_001049.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:38679752 C>A maps to NM_001049.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr14:38679679 C>A maps to NM_001049.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:38678809 G>A maps to NM_001049.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:38679166 C>G maps to NM_001049.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr14:38679638 G>T maps to NM_001049.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr17:71165802 C>T maps to NM_001050.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:71166223 C>T maps to NM_001050.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:71166525 C>A maps to NM_001050.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr22:37603665 C>A maps to NM_001051.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr22:37602591 G>T maps to NM_001051.2 Y417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr20:23016905 G>T maps to NM_001052.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr20:23016842 G>T maps to NM_001052.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr20:23016251 G>T maps to NM_001052.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr20:23016605 G>T maps to NM_001052.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr20:23016608 C>A maps to NM_001052.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:23016323 C>G maps to NM_001052.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:23016572 T>A maps to NM_001052.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr20:23016433 C>A maps to NM_001052.2 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:1129560 G>A maps to NM_001053.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr16:1129686 C>T maps to NM_001053.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr16:1129518 C>T maps to NM_001053.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:1500187 C>T maps to NM_014188.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:48121244 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:48121246 G>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:48125746 G>C did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:85124124 G>A maps to NM_001166417.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr1:85136872 T>C maps to NM_001166417.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr1:85127997 G>A maps to NM_001166417.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:85135576 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr1:85113116 T>C maps to NM_001166417.1 *615W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:48211538 G>T did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:48213499 G>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:48209005 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:48047125 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:48053612 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:48054769 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:48054774 A>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:52677374 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:52681929 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:52681968 T>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:52682022 A>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:52682476 G>C did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr23:52682497 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr11:130064042 G>T did not map to a codon.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:130068227 G>T maps to NM_021978.3 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:130064079 C>T maps to NM_021978.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:130064106 C>G maps to NM_021978.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:53045645 G>T maps to NM_014682.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:53045815 G>A maps to NM_014682.2 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr8:53079508 C>A maps to NM_014682.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:53062519 C>A maps to NM_014682.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:53084628 T>C maps to NM_014682.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:53084451 G>T maps to NM_014682.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:53126805 C>T maps to NM_014682.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:53085143 C>G did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr8:53044593 G>A maps to NM_014682.2 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr8:53079546 C>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:53085050 C>A maps to NM_014682.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:53085022 A>T maps to NM_014682.2 L133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:53076547 G>A maps to NM_014682.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:53079445 C>T maps to NM_014682.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr8:53045623 C>A maps to NM_014682.2 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:53079523 C>T maps to NM_014682.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:53084451 G>T maps to NM_014682.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:53071669 C>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:53044585 T>A maps to NM_014682.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr8:53062468 G>A maps to NM_014682.2 D625D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr8:53085060 A>T maps to NM_014682.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:53071529 G>T maps to NM_014682.2 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr8:53074100 G>A maps to NM_014682.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:134472024 C>A maps to NM_173344.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr8:134472054 C>A maps to NM_173344.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:134472090 C>A maps to NM_173344.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:134478231 C>A maps to NM_173344.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:134474190 C>T maps to NM_173344.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:134474237 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:134472090 C>T maps to NM_173344.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr8:134488117 C>G maps to NM_173344.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:70415729 G>T maps to NM_006927.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr16:70432337 G>A maps to NM_006927.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr16:70415747 G>A maps to NM_006927.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:44364920 T>C maps to NM_174963.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr11:126276876 C>G maps to ENST00000356132 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr11:126279242 C>T maps to ENST00000356132 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:86067446 C>G maps to NM_003896.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:8732779 T>A did not map to a codon.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr11:8751567 G>A maps to NM_005418.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:186760865 C>G maps to NM_003032.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:107460147 G>A maps to NM_001142351.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr2:107460325 A>G maps to NM_001142351.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr2:107459839 G>T maps to NM_001142351.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:107423226 C>T maps to NM_001142351.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr2:107460223 C>A maps to NM_001142351.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:107423250 C>G maps to NM_001142351.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:107459731 G>A maps to NM_001142351.1 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:107460127 G>T maps to NM_001142351.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr2:107423241 G>T maps to NM_001142351.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr2:107459707 C>A maps to NM_001142351.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:74623575 G>T maps to NM_018414.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr17:74625693 T>A maps to NM_018414.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr17:74570504 G>C maps to NM_006456.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:74570456 G>C maps to NM_006456.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:77093235 C>A maps to NM_152996.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:76877814 C>A maps to NM_152996.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:76779641 C>A maps to NM_152996.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:77510142 C>A maps to NM_030965.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:77510082 C>A maps to NM_030965.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:77515963 C>T maps to NM_030965.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr1:77510124 C>T maps to NM_030965.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr1:77509890 C>A maps to NM_030965.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:77510181 C>A maps to NM_030965.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:130648895 G>A maps to NM_013443.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr7:116769844 A>T did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:113098588 G>T maps to NM_017744.4 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:22408290 G>A maps to NM_003034.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:22402032 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:22402022 G>A maps to NM_003034.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr12:22354577 C>A maps to NM_003034.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr12:22354962 G>A maps to NM_003034.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr12:22487121 G>T maps to NM_003034.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr15:92988093 C>A maps to NM_006011.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr15:92988033 G>A maps to NM_006011.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:44260274 G>T maps to NM_013305.4 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr18:44260078 C>A maps to NM_013305.4 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr18:44268882 C>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr18:44260238 G>A maps to NM_013305.4 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:44260187 C>A maps to NM_013305.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:17373457 T>C maps to NM_001004470.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr10:17363107 G>T maps to NM_001004470.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:17365137 G>T maps to NM_001004470.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:17362879 G>T maps to NM_001004470.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:17363208 C>A maps to NM_001004470.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr10:17362962 G>A maps to NM_001004470.1 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:17369044 T>A maps to NM_001004470.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr10:17363073 G>A maps to NM_001004470.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:52558143 C>A maps to NM_015136.2 S2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr3:52529464 C>T maps to NM_015136.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:52553398 T>C maps to NM_015136.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr3:52536034 C>T maps to NM_015136.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:52556664 C>T maps to NM_015136.2 A2235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:52546616 G>T maps to NM_015136.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:52553344 C>A maps to NM_015136.2 I1700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr3:52544510 G>C maps to NM_015136.2 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr3:52536020 G>A did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr3:52544402 C>T maps to NM_015136.2 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr3:52554260 C>A maps to NM_015136.2 T1818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr3:52538855 C>T maps to NM_015136.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:52543236 G>C maps to NM_015136.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:104125388 C>T maps to NM_017564.9 Y1753Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:104031839 T>A maps to NM_017564.9 C252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr12:104100637 C>G maps to NM_017564.9 V1355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:104046428 A>T maps to NM_017564.9 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:104149121 C>A maps to NM_017564.9 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:103984724 A>C maps to NM_017564.9 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr12:104099501 C>T maps to NM_017564.9 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr12:104077047 C>A maps to NM_017564.9 C957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:104081981 C>A maps to NM_017564.9 R1012R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:104144427 C>A maps to NM_017564.9 P2170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:104089374 C>T maps to NM_017564.9 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr12:104089427 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:104067778 C>A maps to NM_017564.9 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:104031792 G>T did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr12:104067700 C>T maps to NM_017564.9 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:104054471 C>T maps to NM_017564.9 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:104138962 C>A maps to NM_017564.9 S2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr12:104096984 C>A maps to NM_017564.9 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:104063374 C>A maps to NM_017564.9 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:104078814 G>T maps to NM_017564.9 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:104025457 C>T maps to NM_017564.9 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:104049081 A>G maps to NM_017564.9 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:104152922 C>A maps to NM_017564.9 R2374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:104129312 G>A maps to NM_017564.9 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr12:104133197 T>C maps to NM_017564.9 C1902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr12:104054516 C>A maps to NM_017564.9 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr12:104054149 C>A maps to NM_017564.9 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:104129322 G>T maps to NM_017564.9 E1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr12:103988208 C>T maps to NM_017564.9 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:104149162 C>G maps to NM_017564.9 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:104106153 C>A maps to NM_017564.9 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:104056697 G>A maps to NM_017564.9 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:104100718 C>A maps to NM_017564.9 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr3:36545949 G>T did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:36527654 G>T maps to NM_003149.1 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr3:36485097 C>A maps to NM_003149.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:37369268 G>A maps to NM_198993.3 Y370Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:57642486 A>G did not map to a codon.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr3:136342080 A>G maps to NM_005862.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:136170966 G>A maps to NM_005862.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:136078060 C>T maps to NM_005862.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr3:136062771 T>C maps to NM_005862.2 Q1116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:123217336 G>C did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:123229239 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:123217306 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:123220442 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:123156494 A>T did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:123190029 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:123191803 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:123202494 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:123200236 A>G did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:123210220 T>C did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:123211827 A>G did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:123179211 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:123217269 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:123224762 A>G did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:123224614 G>A did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:123227889 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:123190074 C>G did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:123195707 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:123191728 A>G did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:123197898 G>C did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:123164821 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:123197786 T>A did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:99786547 T>C maps to NM_012447.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:99795498 G>A maps to NM_012447.2 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr7:99802329 C>A maps to NM_012447.2 A961A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:99792987 C>G maps to NM_012447.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:99795435 G>C maps to NM_012447.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr7:99798717 C>A maps to NM_012447.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:99798417 C>A maps to NM_012447.2 L629L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MP-A4TC-01A-11D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:17737165 A>T maps to NM_003473.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:17750818 G>A maps to NM_003473.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr10:17756751 A>G maps to NM_003473.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:152977147 T>A maps to NM_005843.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr10:90670737 C>T maps to NM_020799.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:68447162 T>A maps to NM_012108.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:68436839 T>A maps to NM_012108.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr4:68456638 G>T maps to NM_012108.2 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr4:68442940 G>A maps to NM_012108.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:4338666 C>T maps to ENST00000314714 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:4327148 C>A maps to ENST00000314714 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:4325282 G>A maps to ENST00000314714 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:72469604 G>C maps to NM_006645.2 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:33684071 C>T maps to NM_178007.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr13:33700247 C>A maps to NM_178007.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr13:33703904 G>A maps to NM_178007.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr13:33760023 G>A maps to NM_178007.2 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:37817239 C>T maps to NM_006804.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:37809960 C>T maps to NM_006804.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:37818597 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:81615290 T>C did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:81615244 C>T maps to NM_181900.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr18:51863545 A>G maps to NM_139171.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr18:51858175 G>C maps to NM_139171.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr18:51858171 G>T maps to NM_139171.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:96853020 G>A maps to NM_020151.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:67937279 C>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:67937332 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:67937355 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:67941412 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:67940831 T>A did not map to a codon.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr23:67937209 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:67939191 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:67938332 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:67937570 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:67940174 A>C did not map to a codon.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr23:67937284 C>T did not map to a codon.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr23:67940174 A>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:67938320 C>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:67938389 G>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:67939097 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:67940174 A>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:67943858 G>A did not map to a codon.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr2:191873762 G>A maps to NM_007315.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:191855976 C>G maps to NM_007315.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:191845378 G>C maps to NM_007315.3 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:191859799 G>A maps to NM_007315.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:191856009 C>A maps to NM_007315.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:56748642 C>T maps to NM_005419.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:56750050 C>A maps to NM_005419.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:56737840 C>A maps to NM_005419.3 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:56750037 T>A maps to NM_005419.3 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr17:40475148 G>T maps to NM_139276.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr17:40476747 T>A maps to NM_139276.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:40468915 C>G maps to NM_139276.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr17:40485907 C>G did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr17:40474405 G>A maps to NM_139276.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:191926453 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:191926495 C>A maps to NM_003151.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:191898688 C>A maps to NM_003151.2 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:40452732 G>A maps to NM_003152.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:40459419 G>T maps to NM_003152.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr17:40453373 C>T maps to NM_003152.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:40460322 C>T maps to NM_003152.3 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:40364012 G>A maps to NM_012448.3 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:40376832 C>T maps to NM_012448.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr12:57501399 G>A maps to NM_003153.4 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:57501992 G>A maps to NM_003153.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:70865519 A>G maps to NM_003154.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr20:47768129 C>A maps to NM_017453.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr20:47734481 G>C maps to NM_017453.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr20:47768229 C>A maps to NM_017453.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:74585456 C>A maps to NM_001164380.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr8:74585457 C>A maps to NM_001164380.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:74464372 G>A maps to NM_001164380.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:74515975 T>C maps to NM_001164380.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr8:74529687 T>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:77227933 C>G maps to NM_003943.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:23711940 G>T maps to NM_003155.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:172753011 C>T maps to NM_003714.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr5:172755181 C>A maps to NM_003714.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr5:172745170 C>T maps to NM_003714.2 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr5:172752927 C>A maps to NM_003714.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr5:172745122 G>T maps to NM_003714.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr5:172750394 G>A maps to NM_003714.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:89790486 A>G maps to ENST00000433102 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:89790156 T>C maps to ENST00000433102 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr7:89793972 G>A maps to ENST00000433102 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr7:89856809 C>T maps to NM_152999.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr7:87912285 A>G maps to NM_024636.2 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:47716839 T>A maps to NM_001048166.1 K1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:47746263 T>A maps to NM_001048166.1 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr1:47746005 C>T maps to NM_001048166.1 K708K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr1:47746581 G>A maps to NM_001048166.1 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:47746500 A>G maps to NM_001048166.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr1:47726106 G>A maps to NM_001048166.1 Y978Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:47746386 T>A maps to NM_001048166.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:4103449 G>T maps to NM_003156.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr11:4076783 A>T maps to NM_003156.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:4104571 C>T maps to NM_003156.3 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:4104600 A>T maps to NM_003156.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr11:3988912 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:27019333 G>T maps to ENST00000382009 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr4:27004687 T>C maps to ENST00000382009 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:27010419 G>T maps to ENST00000382009 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:27010601 C>G maps to ENST00000382009 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr11:63967503 G>A maps to ENST00000358794 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr11:63965324 G>C did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr11:63967651 C>T maps to ENST00000358794 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:171488230 C>G maps to NM_005990.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr5:171533718 G>C maps to NM_005990.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:171488251 C>T maps to NM_005990.3 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr5:171520787 T>G maps to NM_005990.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:171583630 C>A maps to NM_005990.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr5:171482779 C>A maps to NM_005990.3 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:1219359 G>T maps to NM_000455.4 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:1221339 G>T did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:1218446 A>T maps to NM_000455.4 K108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:1220684 A>T maps to NM_000455.4 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr19:1221260 A>T maps to NM_000455.4 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:1220501 G>T maps to NM_000455.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:1207161 A>T maps to NM_000455.4 K84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:1207119 G>T maps to NM_000455.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:1218414 G>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr19:1220716 G>T did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr19:1220485 C>A maps to NM_000455.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:1218414 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr19:1220429 A>T maps to NM_000455.4 K175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:1220648 G>T maps to NM_000455.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:1207119 G>T maps to NM_000455.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr19:1207167 C>T maps to NM_000455.4 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:1220369 A>T did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr19:1221210 G>T did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr19:1207095 A>T maps to NM_000455.4 K62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr19:1207008 G>T maps to NM_000455.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:1223130 C>T maps to NM_000455.4 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr19:1221945 A>T did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:1220577 A>G did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr19:1219383 A>T maps to NM_000455.4 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:1220578 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr19:1219412 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:1219335 G>T maps to NM_000455.4 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr19:1207117 C>A maps to NM_000455.4 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:1220648 G>T maps to NM_000455.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:220473844 C>T maps to NM_052902.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr2:220476446 C>T maps to NM_052902.2 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:220473359 G>C maps to NM_052902.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:220465955 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr2:220477902 G>T maps to NM_052902.2 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:220473348 G>T maps to NM_052902.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:220479831 C>T maps to NM_052902.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:220112226 G>T maps to ENST00000409260 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:197004483 T>C maps to NM_004226.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr6:31940148 C>G maps to NM_032454.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:31939952 C>A maps to NM_032454.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr13:99127077 C>T maps to NM_003576.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:242441096 G>C maps to NM_006374.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:242438130 G>C maps to NM_006374.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:99560299 C>A maps to ENST00000354930 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:23793961 A>T maps to NM_031414.3 K388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:23827749 T>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:23811830 G>A maps to NM_031414.3 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr7:23802538 G>A maps to NM_031414.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr7:23793981 A>T maps to NM_031414.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:23871910 G>T maps to NM_031414.3 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:23811863 A>G maps to NM_031414.3 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:23823237 G>T maps to NM_031414.3 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr7:23871858 A>G maps to NM_031414.3 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:23830441 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:23823248 G>A maps to NM_031414.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:146658823 G>A maps to NM_001112724.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:5170039 G>A maps to NM_018401.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:5461930 A>G maps to NM_018401.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr4:5461852 C>T maps to NM_018401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr4:5332965 G>T maps to NM_018401.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:134040417 G>T maps to NM_173575.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr10:134040456 G>A maps to NM_173575.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr10:134040357 C>A maps to NM_173575.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr11:8486360 A>G maps to NM_030906.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr11:8479027 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr20:2097420 A>T maps to NM_080836.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr20:2097994 A>T maps to NM_080836.3 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr2:219553475 G>T maps to NM_015690.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:219561778 A>T maps to NM_015690.3 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr2:219563695 G>T maps to NM_015690.3 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:219563773 G>T maps to NM_015690.3 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr6:36467710 G>A maps to NM_007271.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr6:36507864 C>A maps to NM_007271.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:27475315 T>C maps to NM_015000.3 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:168931720 T>A maps to NM_013233.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168997236 C>G maps to NM_013233.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:168873605 C>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:43623832 C>T maps to NM_006282.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:36826828 G>A maps to ENST00000373130 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:36807505 G>A maps to ENST00000373130 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr1:26228094 C>A maps to NM_203399.1 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:80553736 C>A maps to NM_007029.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:80567104 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:80577087 C>T maps to NM_007029.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:80553736 C>A maps to NM_007029.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr8:80553718 A>G maps to NM_007029.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:62275216 A>C maps to NM_015894.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr8:27098675 G>T maps to NM_030795.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr8:27098600 C>T maps to NM_030795.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr8:27097514 G>T maps to NM_030795.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:27097616 G>T maps to NM_030795.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:124103596 G>T maps to NM_004099.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr9:124116914 A>G maps to NM_004099.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr9:35102813 G>A maps to NM_013442.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:39564833 C>A maps to NM_145286.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr13:39544447 C>A maps to NM_145286.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr13:39541062 C>A maps to NM_145286.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:39542625 G>T maps to NM_145286.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:39544408 C>A maps to NM_145286.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:48807909 C>A maps to NM_172311.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr2:48822395 C>T maps to NM_001198595.1 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr14:81744685 T>C maps to NM_033104.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr14:81743749 G>T maps to NM_033104.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:81744277 C>A maps to NM_033104.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:81743599 G>C maps to NM_033104.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:81864699 G>T maps to NM_033104.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr14:81743578 C>T maps to NM_033104.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:81744457 T>C maps to NM_033104.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:70645519 T>C maps to NM_001130161.2 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:184930347 G>C maps to NM_020225.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:184938370 G>T maps to NM_020225.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:184931700 C>T maps to NM_020225.1 C570C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr15:74481498 C>T maps to ENST00000449139 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr15:74486212 G>A maps to ENST00000449139 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:74476206 A>G maps to ENST00000449139 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr15:74473634 C>T did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:134925342 C>T maps to NM_182489.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:134925269 G>A did not map to a codon.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr17:61781921 G>A maps to NM_001003787.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr9:125920381 G>C maps to NM_018387.4 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr15:43892286 G>A maps to NM_153700.2 Q1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:43910165 C>G maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr15:43893140 C>A maps to NM_153700.2 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr15:43893701 A>G maps to NM_153700.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:37143294 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:37096800 G>C maps to NM_003162.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:37132761 C>A did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:31374708 T>A maps to NM_001083893.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr14:31416469 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:31416423 C>A maps to NM_001083893.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:31381008 C>T maps to NM_001083893.1 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:47240081 T>C maps to NM_001039877.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:47230792 G>A maps to NM_001039877.1 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr19:47228788 G>A maps to NM_001039877.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr23:7177622 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:7243483 A>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:7177472 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:7223213 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:7252073 A>T did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr23:7267978 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:7175601 G>T did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:7267982 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:7171272 G>T did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:7177622 G>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:125482927 C>G maps to NM_152713.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:125483986 G>A maps to NM_152713.3 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr3:31641904 A>T maps to NM_178862.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:31638348 C>T maps to NM_178862.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr6:144507901 A>T maps to NM_003764.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:144508474 G>A maps to NM_003764.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr6:144508469 G>T maps to NM_003764.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:144508447 C>T maps to NM_003764.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:28144411 C>T maps to ENST00000373939 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:28148838 G>A maps to ENST00000373939 *300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr20:57245565 A>C did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr20:57244381 G>T maps to NM_001001433.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr20:57242592 A>G maps to NM_001001433.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr20:57246220 G>A maps to NM_001001433.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr4:4543582 C>A maps to NM_016930.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:93734017 C>T maps to NM_001001850.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:73115083 G>C maps to NM_004603.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr16:31008313 G>T maps to NM_052874.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:31008296 G>A maps to NM_052874.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:31004141 C>A maps to NM_052874.3 *289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr16:31008057 G>A maps to NM_052874.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:131293250 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr12:131286001 T>C maps to NM_194356.1 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:31046342 A>C maps to NM_004604.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr11:62595031 C>A did not map to a codon.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132785214 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:132781940 C>A maps to NM_003569.2 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:9460846 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:9395239 T>A did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr17:9281902 C>A maps to NM_004853.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr9:130420711 C>T maps to NM_003165.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:7705870 C>T maps to ENST00000441779 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:7712287 G>T maps to ENST00000441779 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:7707909 G>A maps to ENST00000441779 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:109315284 A>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr17:53084904 G>T maps to NM_178509.5 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:53150367 G>T maps to NM_178509.5 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr17:53218669 G>C did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr17:53084898 C>T maps to NM_178509.5 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:147680250 G>T maps to NM_001127715.1 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:147684480 G>A maps to NM_001127715.1 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:147646093 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr6:147680373 G>T maps to NM_001127715.1 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:147588245 A>C maps to NM_001127715.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr6:147581766 C>T maps to NM_001127715.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr6:147581749 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:147685200 A>C maps to NM_001127715.1 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:120957868 T>A maps to NM_014980.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr3:120976174 C>A maps to NM_014980.2 C609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:25288400 C>A maps to ENST00000445298 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:25326364 T>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:25288389 G>A maps to NM_014178.6 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr12:10782262 C>T maps to NM_018423.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr7:75634593 G>A maps to NM_016086.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr7:75630222 G>A maps to NM_016086.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr13:48575317 G>A maps to NM_003850.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr2:84670518 G>A maps to NM_003849.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:84660551 C>A maps to NM_003849.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:84668442 T>C maps to NM_003849.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr3:67451167 C>T maps to NM_003848.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr3:67578633 C>A maps to NM_003848.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:151598717 A>T maps to NM_033050.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr10:104263971 T>A maps to NM_016169.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr13:53250390 G>A maps to NM_001130912.1 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr8:70533430 C>G maps to NM_001128206.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:70512969 G>T maps to NM_001128206.1 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:70551058 G>A maps to NM_001128206.1 K839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:46365537 G>T maps to NM_001161841.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:46305850 G>T maps to NM_001161841.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:46305828 C>A maps to NM_001161841.1 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr20:46365591 G>A maps to NM_001161841.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:46313321 C>A maps to NM_001161841.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:46318955 G>C maps to NM_001161841.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:46331301 C>A maps to NM_001161841.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr20:46290571 C>T maps to NM_001161841.1 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr20:46313261 G>T maps to NM_001161841.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:28619880 A>G maps to NM_177529.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr16:28620116 G>A maps to NM_177529.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr16:28619800 G>C maps to NM_177529.1 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:28617478 G>A maps to NM_177529.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr16:28606783 C>T maps to NM_001054.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:70599958 G>C maps to NM_014465.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr2:108863676 C>A maps to NM_001008743.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:108863676 C>A maps to NM_001008743.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:108868890 C>A maps to NM_001008743.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:108994906 C>T maps to NM_006588.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:70723320 G>C maps to NM_005420.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:70715266 G>T maps to NM_005420.2 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:48382313 C>T maps to NM_003167.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:44237717 G>T maps to NM_014351.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr22:44237699 C>T maps to NM_014351.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:37406599 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:37398720 C>A maps to NM_001032377.1 G175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:56131997 A>G maps to ENST00000395437 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr7:901101 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:883153 A>T maps to ENST00000456758 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:881654 C>A maps to ENST00000456758 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:891584 A>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:909027 C>T maps to ENST00000456758 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:39135816 C>A maps to ENST00000405018 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr22:39146304 G>A maps to ENST00000405018 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:48046854 C>A maps to NM_152782.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:48046872 G>A maps to NM_152782.3 I127I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-17-Z031-01A-01W-0746-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:48046871 C>A maps to NM_152782.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:48046776 G>A maps to NM_152782.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:48046904 C>A maps to NM_152782.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:48046905 C>A maps to NM_152782.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:48046871 C>A maps to NM_152782.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr20:31573550 G>A maps to NM_080675.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:31575558 G>A maps to NM_080675.3 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:21821871 T>C maps to NM_007192.3 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:21852071 C>T maps to NM_007192.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:21840047 C>G maps to NM_007192.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:39962249 A>G maps to NM_003169.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:39959769 C>T maps to NM_003169.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:39964972 C>T maps to NM_003169.3 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:39962242 A>G did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr17:27011937 A>T maps to NM_003170.3 K816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:27014203 C>A maps to NM_003170.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr17:27008930 G>A maps to NM_003170.3 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:27011620 C>G maps to NM_003170.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr17:27016440 G>A maps to NM_003170.3 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:27000439 C>T maps to NM_003170.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:27020739 G>T maps to NM_003170.3 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr17:27027367 G>C maps to NM_003170.3 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr17:27003435 T>G maps to NM_003170.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr17:27002068 G>T maps to NM_003170.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr17:27010350 G>T maps to NM_003170.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr17:27013421 A>T maps to NM_003170.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:27880517 C>G maps to NM_014860.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:70951418 A>T maps to NM_003171.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr10:70956823 G>T maps to NM_003171.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:136234179 G>A maps to NM_033161.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:136198958 C>A maps to NM_006753.4 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:136200574 C>T maps to NM_006753.4 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:114919842 C>A maps to NM_022486.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:114875149 T>C did not map to a codon.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr9:114886606 G>A maps to NM_022486.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:24580909 T>G did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr9:95841755 A>T maps to NM_145006.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr9:95846816 A>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:223465925 T>C maps to NM_017982.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:223402655 C>A maps to NM_017982.3 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:223400985 G>T maps to NM_017982.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:223536631 G>A maps to NM_017982.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr3:33249306 C>T maps to NM_015551.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr3:33194356 C>A maps to NM_015551.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:33194434 C>A maps to NM_015551.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:48558964 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:48558669 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:14939284 T>C maps to NM_001193424.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:14939209 C>T maps to NM_001193424.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:67941311 T>A maps to NM_017635.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:67925475 G>A maps to NM_017635.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:67925553 G>A maps to NM_017635.3 N753N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:55858681 C>T maps to NM_032701.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:149881029 A>G maps to NM_014849.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:149877499 G>A maps to NM_014849.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:149885085 G>T maps to NM_014849.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:149878385 C>T maps to NM_014849.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr1:149877571 G>A maps to NM_014849.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr1:149884959 G>A maps to NM_014849.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:149885314 C>A maps to NM_014849.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr1:149884837 C>T maps to NM_014849.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:149882450 G>A maps to NM_014849.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:149882196 G>A maps to NM_014849.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:149884825 C>A maps to NM_014849.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:149882226 G>C maps to NM_014849.3 Y328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr15:91827440 C>G maps to NM_014848.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr15:91769846 C>A maps to NM_014848.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:91835637 T>C maps to NM_014848.4 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr15:91769555 C>T maps to NM_014848.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr15:91769717 G>T maps to NM_014848.4 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:75427938 G>T maps to NM_014979.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr5:75505589 C>A maps to NM_014979.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:75427817 G>T maps to NM_014979.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:75621335 G>C maps to NM_014979.1 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:75490885 T>C maps to NM_014979.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:113208288 C>A maps to ENST00000374463 E1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:113234498 G>T maps to ENST00000374463 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:113169031 C>A maps to ENST00000374463 G2953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:113151816 C>T maps to ENST00000374463 V3294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:113231318 C>A maps to ENST00000374463 G1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113168920 T>G maps to ENST00000374463 R2990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:113312281 G>T maps to ENST00000374463 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:113275212 G>T maps to ENST00000374463 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr9:113259168 T>A maps to ENST00000374463 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr9:113139549 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:113261338 G>A maps to ENST00000374463 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr9:113198697 G>A maps to ENST00000374463 Q1579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:113275338 G>T maps to ENST00000374463 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr9:113173789 C>T maps to ENST00000374463 W2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr9:113265497 C>G did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr9:113148262 A>G maps to ENST00000374463 C3387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr9:113141643 G>T maps to ENST00000374463 S3467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:113139629 T>C maps to ENST00000374463 P3478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:113169172 C>A maps to ENST00000374463 E2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:113217972 A>G maps to ENST00000374463 C1228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:113341694 G>A maps to ENST00000374463 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:29813490 C>A maps to NM_021738.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:29784045 G>A maps to NM_021738.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:29762820 C>T maps to NM_021738.2 E1825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr10:29819538 G>A maps to NM_021738.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr10:29769643 G>A maps to NM_021738.2 G1733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr10:29813478 C>T maps to NM_021738.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:29839886 G>A maps to NM_021738.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:29773637 C>T maps to NM_021738.2 E1634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:29779845 G>A maps to NM_021738.2 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr10:29747232 G>T maps to NM_021738.2 Y2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr10:29822110 T>A maps to NM_021738.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:29819565 C>G maps to NM_021738.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:29820929 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:29815986 T>C did not map to a codon.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr10:29777527 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr10:29784069 G>T maps to NM_021738.2 P1235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:29769595 G>A maps to NM_021738.2 I1749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr12:109306414 G>A maps to NM_018711.2 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr12:109309579 G>C maps to NM_018711.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:109306463 G>T maps to NM_018711.2 C445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:138341201 G>A maps to NM_001139456.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:138305865 C>A maps to NM_001139456.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:138347842 C>A maps to NM_001139456.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:138333798 G>A maps to NM_001139456.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr11:9770692 G>A maps to NM_015055.2 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:16778404 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:16773136 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:16761893 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:16773127 A>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:110592122 C>T maps to NM_001099744.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:110631158 T>C maps to NM_001099744.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:110592164 C>A maps to NM_001099744.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:110587458 G>A maps to NM_001099744.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr10:135368926 C>G maps to NM_001143764.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr10:135372441 G>T maps to NM_001143764.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:135372441 G>A maps to NM_001143764.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135369515 C>T maps to NM_001143764.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:135371399 C>T maps to NM_001143764.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr10:135369107 G>T maps to NM_001143764.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:135369107 G>T maps to NM_001143764.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:13011368 G>A maps to NM_001105578.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr19:13015424 G>A maps to NM_001105578.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:39694849 G>T maps to NM_001080468.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:115487070 G>T maps to NM_003176.2 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:115487076 G>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:115398150 G>T maps to NM_003176.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:58443525 T>A maps to NM_014258.2 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr20:58444870 A>T maps to NM_014258.2 Y1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr20:58450494 C>A maps to NM_014258.2 T1060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr20:58444978 C>A maps to NM_014258.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr20:58490599 T>A maps to NM_014258.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr20:58486869 C>A maps to NM_014258.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr20:58489196 T>A maps to NM_014258.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:58461889 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:10906287 G>C did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr6:10907835 G>A maps to NM_001040274.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:10955440 G>T maps to NM_001040274.2 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr6:10898308 G>A maps to NM_001040274.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:10902979 T>C maps to NM_001040274.2 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:85666081 G>A maps to NM_032184.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:85656029 G>C maps to NM_032184.1 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:85666103 C>T maps to NM_032184.1 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr1:85655929 C>T maps to NM_032184.1 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:85647995 G>A maps to NM_032184.1 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:25551509 G>A maps to NM_015484.4 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:93637066 G>T maps to NM_003177.5 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:93657851 G>A maps to NM_003177.5 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr9:93650065 C>T maps to NM_003177.5 Y539Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:46345508 C>A maps to NM_004819.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr19:46330800 G>A maps to NM_004819.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:46326728 G>C maps to NM_004819.2 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr19:46319249 C>A maps to NM_004819.2 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:46351008 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:47464642 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:47432342 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:47466578 C>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:47435804 C>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:47466575 T>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:47432281 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:47479029 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47436853 T>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:47466568 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:47434533 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:12209920 G>T maps to NM_133625.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr3:12183493 C>T maps to NM_133625.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:12183496 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr3:12046036 C>T maps to NM_133625.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr22:33260910 A>G maps to NM_003490.3 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr22:33260991 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:32934044 C>T maps to NM_003490.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr22:32914052 T>A maps to NM_003490.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr22:32934074 G>A maps to NM_003490.3 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:86349986 C>G maps to NM_006372.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:152599232 G>A maps to NM_182961.2 L6188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:152647560 G>A maps to NM_182961.2 L5055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr6:152751685 T>C maps to NM_182961.2 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:152861100 C>A maps to NM_182961.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:152782764 C>G maps to NM_182961.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:152642999 A>C maps to NM_182961.2 T5313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:152552537 T>A maps to NM_182961.2 L7009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:152673178 G>A maps to NM_182961.2 Q3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr6:152652223 C>T maps to NM_182961.2 V4532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152651068 C>A maps to NM_182961.2 L4917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:152722271 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr6:152725440 A>C maps to NM_182961.2 V2244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:152763329 G>T maps to NM_182961.2 I1296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr6:152792794 C>A maps to NM_182961.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:152443810 C>T maps to NM_182961.2 R8718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:152949439 C>A maps to NM_182961.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr6:152473246 C>G maps to NM_182961.2 L8053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:152558014 G>A maps to NM_182961.2 I6712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:152832220 A>G maps to NM_182961.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152623135 C>T maps to NM_182961.2 K5803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:152658014 C>T maps to NM_182961.2 L4163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr6:152615181 G>C maps to NM_182961.2 S5921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr6:152466646 T>C maps to NM_033071.2 T8269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr6:152671317 T>C maps to NM_182961.2 Q3962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:152497695 C>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr6:152501414 C>G maps to NM_182961.2 R7772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr6:152771824 A>C maps to NM_182961.2 A1110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:152623051 C>A maps to NM_182961.2 L5831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr6:152553321 G>A maps to NM_182961.2 Q6931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:152532663 C>A maps to NM_182961.2 G7518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr6:152652436 T>A maps to NM_182961.2 A4461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr6:152640090 C>T maps to NM_182961.2 R5432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:152804279 G>T maps to NM_182961.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr6:152623098 G>A maps to NM_182961.2 L5816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr6:152510397 G>A maps to NM_182961.2 L7764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr6:152738008 C>A maps to NM_182961.2 E1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:152605205 C>A maps to NM_182961.2 A6038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr6:152469465 T>C maps to NM_182961.2 E8230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr6:152949441 G>T maps to NM_182961.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:152754988 C>A maps to NM_182961.2 E1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:152523045 C>A maps to NM_182961.2 L7686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:152763290 T>A maps to NM_182961.2 R1309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:152777080 T>C maps to NM_182961.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:152501430 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:152652517 C>T maps to NM_182961.2 V4434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:152711482 A>G maps to NM_182961.2 I2703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr6:152599340 C>T maps to NM_182961.2 L6152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr6:152728223 G>T maps to NM_182961.2 C2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:152651956 C>A maps to NM_182961.2 T4621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:152737814 T>C maps to NM_182961.2 L1919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr6:152737744 C>A maps to NM_182961.2 E1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:152671407 T>C maps to NM_182961.2 Q3932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:152558068 C>A maps to NM_182961.2 L6694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr6:152671902 T>A maps to NM_182961.2 S3861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:64635687 A>C maps to NM_182914.2 R5667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:64653252 C>T maps to NM_182914.2 Q5890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:64428340 C>T maps to NM_182914.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:64449498 C>G maps to NM_182914.2 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr14:64469442 C>T maps to NM_182914.2 I1264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:64691222 G>T maps to NM_182914.2 G6809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr14:64428309 C>T maps to NM_182914.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:64557633 G>T maps to NM_182914.2 V3948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr14:64483188 A>G did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr14:64634012 C>G maps to NM_182914.2 L5556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr14:64469511 G>A maps to NM_182914.2 K1287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:64634093 G>T maps to NM_182914.2 L5583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr14:64449506 C>T maps to NM_182914.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:64467392 A>T maps to NM_182914.2 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr14:64522938 C>G maps to NM_182914.2 S3341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:64587669 C>A maps to NM_182914.2 S4350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr14:64447427 T>A maps to NM_182914.2 C542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:64580081 T>G maps to NM_182914.2 A4211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr14:64542736 C>T maps to NM_182914.2 S3647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:64469505 A>T maps to NM_182914.2 V1285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr14:64522938 C>G maps to NM_182914.2 S3341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:33410884 T>A maps to NM_006772.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr6:33408523 G>C maps to NM_006772.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:76167872 C>T maps to NM_004710.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:2042715 G>A maps to NM_004209.5 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr19:48876781 C>T maps to NM_012451.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:48876805 G>A maps to NM_012451.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:34003352 C>G maps to NM_003895.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr21:34072276 G>C maps to NM_003895.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr21:34011220 C>A maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr21:34037309 G>A maps to NM_003895.3 N778N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:158487536 G>T maps to NM_003898.3 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:158487539 C>A maps to NM_003898.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr6:158492669 G>A maps to NM_003898.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:158450010 G>T maps to NM_003898.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:158450043 G>T maps to NM_003898.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr15:99670913 G>A maps to ENST00000336292 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr5:150028559 G>A maps to NM_001166209.1 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:150028935 C>T maps to NM_001166209.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:119951645 G>A maps to NM_133477.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:119951384 A>G maps to NM_133477.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr4:119951018 C>T maps to NM_133477.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:119951000 G>T maps to NM_133477.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr4:119948361 G>T maps to NM_133477.2 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:119944646 C>T maps to NM_133477.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:119978926 C>A maps to NM_133477.2 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr10:75406736 G>A maps to NM_001114133.1 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr10:75406632 G>C maps to NM_001114133.1 S926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:63466558 C>A maps to NM_001130003.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:63542295 C>A maps to NM_001130003.1 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:35945441 C>T maps to NM_007247.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:35902487 C>A maps to NM_007247.4 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:35896110 T>A maps to NM_007247.4 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:35945435 G>T maps to NM_007247.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:49047926 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr23:49048090 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:49048116 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:49050788 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:49047929 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:49054290 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:49054277 A>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:49050733 G>T did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:49047922 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:110022118 G>A maps to NM_001040709.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:110022151 A>T maps to NM_001040709.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:110018285 G>A maps to NM_001040709.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr20:43995535 C>T maps to NM_033542.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr12:79689916 C>A maps to NM_005639.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr12:79689967 C>A maps to NM_005639.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr12:79842859 C>T maps to NM_005639.2 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr12:79837925 C>T maps to NM_005639.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr12:33532834 G>T maps to NM_198992.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:33535419 G>T maps to NM_198992.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr12:33579378 A>T maps to NM_198992.3 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:33592448 G>A maps to NM_198992.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr12:33592375 G>A maps to NM_198992.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:33559972 A>T maps to NM_198992.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:33559807 C>A maps to NM_198992.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:33559882 A>G maps to NM_198992.3 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:33560263 C>T maps to NM_198992.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:33538175 C>A maps to NM_198992.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:33579170 G>A maps to NM_198992.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:155838521 G>C maps to NM_152280.4 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:155851235 G>A maps to NM_152280.4 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:155837813 G>A maps to NM_152280.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr11:66807602 G>T maps to NM_001177880.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr11:66812116 C>A maps to NM_001177880.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:66807361 C>A maps to NM_001177880.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr11:45265821 G>T maps to NM_020826.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:45265683 C>A maps to NM_020826.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr11:45268060 C>T maps to NM_020826.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr11:45274043 G>A maps to NM_020826.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:45307668 A>G maps to NM_020826.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr11:45274073 G>T maps to NM_020826.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:210273727 G>A maps to NM_001146261.1 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:210267766 C>A maps to NM_001146261.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr10:46967662 T>C maps to NM_031912.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:46962008 C>T maps to NM_031912.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr10:46961993 C>A maps to NM_031912.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:46967677 C>T maps to NM_031912.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:62463150 T>G maps to NM_031914.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:62567299 G>T maps to NM_031914.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:62550984 T>A maps to NM_031914.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:62567416 G>T maps to NM_031914.2 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:62547955 A>G maps to NM_031914.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:62463159 G>T maps to NM_031914.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:19195165 C>T maps to NM_016524.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr16:19236032 T>C maps to NM_016524.2 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr16:19194898 C>T maps to NM_016524.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:202574843 G>T maps to NM_177402.4 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr19:51133106 G>A maps to NM_001160329.1 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr19:51135966 G>T maps to NM_001160329.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:51135838 C>G maps to NM_001160329.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:40853934 C>T maps to NM_020783.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr18:40850356 A>T maps to NM_020783.3 C409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:40850491 A>T maps to NM_020783.3 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:40851704 C>A maps to NM_020783.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr18:40854132 C>T maps to NM_020783.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:40851686 G>T maps to NM_020783.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:55686367 C>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:55685986 G>T maps to NM_003180.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr1:114680332 C>A maps to ENST00000369545 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr1:114682355 G>T maps to ENST00000369545 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:114680572 G>C maps to ENST00000369545 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:114682454 A>G maps to ENST00000369545 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:114640499 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:114641765 C>A maps to ENST00000369545 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:114680338 G>T maps to ENST00000369545 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:114682277 G>A maps to ENST00000369545 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr11:61291969 G>C maps to NM_004200.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr11:61291320 G>A maps to NM_004200.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:61295596 G>T maps to NM_004200.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:61295447 C>T maps to NM_004200.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:61323635 G>A maps to NM_004200.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr11:61300517 G>C maps to NM_004200.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr11:61300490 G>A maps to NM_004200.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr11:1858579 C>T maps to NM_138567.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:1858196 G>T maps to NM_138567.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:7441796 C>A maps to NM_175733.3 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr11:7335003 G>T maps to NM_175733.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr11:7324268 G>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:7334682 G>A maps to NM_175733.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:27677308 C>T maps to NM_001193308.1 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:27677380 G>T maps to NM_001193308.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:85459315 T>A maps to NM_001162953.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:85420534 G>A maps to ENST00000359152 G1459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:85438966 T>A maps to ENST00000359152 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:159184494 C>G maps to ENST00000297239 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr6:159184341 C>T maps to ENST00000297239 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr6:159172957 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:99944920 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:99943357 C>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:99956480 C>G did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:99933577 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:99956281 C>A did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:99956501 A>G did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:99942190 T>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:99943409 G>T did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:99955912 C>G did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:99931093 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:99955907 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:99941690 A>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr23:99942237 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:99956256 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:99956568 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:99956569 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:99956240 C>G did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:99956952 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:99956297 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:37984666 T>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:37985882 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:37913576 G>T did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:37985859 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:37965978 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:37985949 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:37969675 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:37984681 T>C did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:37969596 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:37961593 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:37965996 G>T did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:37961678 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:37961679 T>A did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:37935839 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:37969614 G>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr11:64899784 G>A maps to NM_172230.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr6:166571967 C>A maps to NM_003181.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr6:166580163 C>G maps to NM_003181.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132967037 C>A maps to NM_138327.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr6:132966647 G>A maps to NM_138327.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr6:132966950 G>T maps to NM_138327.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:132938807 G>T maps to NM_001033080.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr6:132938903 G>T maps to NM_001033080.1 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr6:132938684 A>G maps to NM_001033080.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:132938666 C>T maps to NM_001033080.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:132909898 G>T maps to NM_003967.2 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:132910325 G>T maps to NM_003967.2 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:132910780 T>A maps to NM_003967.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr6:132910810 G>A maps to NM_003967.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr6:132891804 T>C maps to NM_175067.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr6:132892339 G>T maps to NM_175067.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr6:132891990 G>T maps to NM_175067.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr6:132874343 C>T maps to NM_053278.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr6:132874424 G>T maps to NM_053278.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:132874128 G>T maps to NM_053278.1 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:39817888 G>T maps to NM_006116.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr22:39813816 G>A maps to NM_006116.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr22:39815593 T>C maps to NM_006116.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr22:39817852 C>T maps to NM_006116.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr22:39817936 G>A maps to NM_006116.2 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:149700626 G>T maps to NM_015093.4 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:149700304 C>T maps to NM_015093.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:149700089 C>A maps to NM_015093.4 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:149730711 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:30873049 A>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:30877603 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:30872882 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:30849674 T>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:30873636 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:30864759 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:30873433 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:30873434 T>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:30852175 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:30872240 T>C did not map to a codon.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr7:97363587 G>C maps to NM_003182.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:57409554 G>A maps to NM_013251.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr10:123846989 G>T maps to NM_206862.2 E1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr10:123969978 C>T maps to NM_206862.2 F2013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:123987513 G>T maps to NM_206862.2 A2629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:123844294 T>C maps to NM_206862.2 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr10:123976299 G>C maps to NM_206862.2 L2501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr10:123844948 C>T maps to NM_206862.2 F978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:123842968 G>A maps to NM_206862.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:123842968 G>A maps to NM_206862.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr10:123846925 G>A maps to NM_206862.2 Q1637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:123970197 G>T maps to NM_206862.2 S2086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr10:123845734 C>A maps to NM_206862.2 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr4:1730434 G>T maps to NM_006342.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr4:1730379 G>C maps to NM_006342.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr4:1746480 G>A maps to NM_006342.1 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr4:1729566 A>T maps to NM_006342.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr4:1742644 G>T maps to NM_006342.1 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr2:75276687 G>A maps to NM_001058.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:75280800 T>A maps to NM_001058.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:75276837 G>T maps to NM_001058.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:71164608 G>T maps to NM_001057.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:104577476 C>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:104577452 G>A maps to NM_001059.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:104512717 G>T maps to NM_001059.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:104640571 G>C maps to NM_001059.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr4:104512726 G>A maps to NM_001059.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr4:104640520 G>C maps to NM_001059.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr4:104640634 C>T maps to NM_001059.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:59042389 C>A maps to NM_002353.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:35837014 C>T maps to NM_001166105.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:35825575 G>T maps to NM_001166105.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr17:35830540 G>A maps to NM_001166105.1 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:7056720 A>C maps to NM_152293.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr3:9828901 C>T maps to NM_006354.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:9832952 G>C maps to NM_006354.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:70596934 C>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:70602998 C>G did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:70597537 A>C did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:70683691 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:70627910 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:70614044 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:70598688 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:70608667 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:70598124 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:70586258 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:70626588 A>G did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:70674706 G>C did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:70586170 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:70603919 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:70612818 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:70617291 G>C did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr23:70613944 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:70598760 G>A did not map to a codon.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr23:70598122 A>G did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr23:70618498 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:70601698 T>G did not map to a codon.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:70595135 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:70613231 A>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:70608160 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:70598298 T>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:34144736 C>T maps to NM_139215.1 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:222753118 G>A maps to NM_005681.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:222734834 C>A maps to NM_005681.2 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr1:222736578 C>A maps to NM_005681.2 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:222732097 C>T maps to NM_005681.2 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:84217021 A>T maps to NM_005679.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:84213275 G>T maps to NM_005679.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:84212612 G>T maps to NM_005679.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr16:84215614 C>T maps to NM_005679.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:84212560 G>A maps to NM_005679.2 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:84213088 G>A maps to NM_005679.2 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr9:32633771 G>T maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:32633636 G>C maps to NM_153809.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr9:32635222 C>A maps to NM_153809.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:32633177 C>A maps to NM_153809.2 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:32630209 G>A maps to NM_153809.2 Q1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr9:32633429 T>A maps to NM_153809.2 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr9:32635535 G>A maps to NM_153809.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr9:32635170 G>T maps to NM_153809.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr9:32632529 G>T maps to NM_153809.2 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:32632174 G>A maps to NM_153809.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:32633464 C>A maps to NM_153809.2 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr9:32631109 G>A maps to NM_153809.2 Q1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr9:32632472 C>T maps to NM_153809.2 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr9:32635442 G>A maps to NM_153809.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr9:32635370 C>T maps to NM_153809.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr9:32631683 G>A maps to NM_153809.2 C1298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:32633254 T>A maps to NM_153809.2 K775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:120803608 C>A maps to NM_003184.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:120774806 C>A maps to NM_003184.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr8:120816176 C>T maps to NM_003184.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:120831710 T>C maps to NM_003184.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr8:120758943 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:120810005 A>G maps to NM_003184.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:120807827 C>A maps to NM_003184.3 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:120807871 C>A did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr10:7866335 G>T maps to NM_031923.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr10:8019212 G>T maps to NM_031923.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr10:8007005 G>A maps to NM_031923.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:8006718 G>T maps to NM_031923.2 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr10:8006789 C>T maps to NM_031923.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:8007623 G>A maps to NM_031923.2 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr10:7866285 C>T maps to NM_031923.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr10:8055776 C>T maps to NM_031923.2 D884D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr20:60578832 G>A maps to NM_003185.3 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr20:60575635 C>A maps to NM_003185.3 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:60584200 T>C maps to NM_003185.3 K597K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr18:23861997 C>T maps to ENST00000418698 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:23861979 G>T maps to ENST00000418698 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:105141482 C>G maps to NM_006951.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:229738447 G>A maps to NM_014409.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:229738211 C>T maps to NM_014409.3 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:229738094 A>T maps to NM_014409.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:229750097 G>A maps to NM_014409.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:62550191 C>G maps to NM_006473.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr11:62553844 C>T maps to NM_006473.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr5:140698603 G>A maps to NM_005642.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr5:140698669 G>C maps to NM_005642.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:100530247 C>A did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:100531505 C>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:100537378 A>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:100548012 C>A did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:100547919 C>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:100542517 T>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:100542528 C>T did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:100533108 A>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:100548009 G>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:77394406 G>C did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:77395087 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:77387264 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:77387129 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:77387161 T>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:159457473 G>T maps to NM_054114.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:159457708 G>T maps to NM_054114.3 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr6:159456966 G>T maps to NM_054114.3 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr6:159463124 G>T maps to NM_054114.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:159457614 G>A maps to NM_054114.3 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:159888697 A>G maps to ENST00000368096 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:159890119 C>A maps to ENST00000368096 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:111730691 A>G maps to NM_001008272.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:47685463 G>T maps to ENST00000371883 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:47685805 G>A maps to ENST00000371883 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr1:47685430 A>G maps to ENST00000371883 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:47685792 G>T maps to ENST00000371883 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr1:47685505 G>T maps to ENST00000371883 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:47685772 C>A maps to ENST00000371883 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr9:108424890 G>A maps to NM_005421.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:764306 A>G maps to NM_006755.1 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr11:763397 C>T maps to NM_006755.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:160020026 C>T maps to NM_033394.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:160005758 C>A maps to NM_033394.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:160035566 C>T maps to NM_033394.2 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:160035668 G>A maps to NM_033394.2 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:159922445 G>A maps to NM_033394.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr17:61498458 C>T maps to ENST00000389520 R1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:61391822 G>T maps to ENST00000389520 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr17:61482499 G>T maps to ENST00000389520 G1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:61278169 T>A maps to ENST00000389520 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:162087710 A>G maps to NM_004180.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:27802713 C>A maps to NM_020791.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr17:27809234 T>G maps to NM_020791.2 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:27849413 T>C maps to NM_020791.2 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr16:29998952 G>A maps to NM_016151.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:29994516 C>G maps to NM_016151.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:29997019 C>T maps to NM_016151.2 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:29998976 C>T maps to NM_016151.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr16:29998397 G>C maps to NM_016151.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:118671560 T>C maps to NM_016281.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:118673476 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:118598073 T>C maps to NM_016281.3 E743E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr12:118610378 A>T maps to NM_016281.3 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:32818282 C>A maps to NM_000593.5 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:32820181 G>A maps to NM_000593.5 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr6:32803551 T>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr6:32802972 G>A maps to ENST00000452392 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:33272865 G>A maps to NM_172208.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:6562637 C>A maps to NM_018009.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:234565956 G>A maps to NM_005646.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:234529175 G>A maps to NM_005646.3 Q1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr1:234529404 C>A maps to NM_005646.3 P1474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:234593466 G>A maps to NM_005646.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:234599595 T>C maps to NM_005646.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr1:234541754 T>A maps to NM_005646.3 K1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr7:38305262 T>C maps to ENST00000443402 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:38305108 G>A maps to ENST00000443402 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr5:33457486 A>T maps to ENST00000455217 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr5:33455796 G>T maps to ENST00000455217 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:33455691 G>T maps to ENST00000455217 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr5:33461818 C>T maps to ENST00000455217 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr5:33457372 G>C maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:33458711 T>C maps to ENST00000455217 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:33459939 G>A maps to ENST00000455217 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:33462221 G>A maps to ENST00000455217 K616K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr5:33461005 G>C did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:150477144 C>T maps to NM_025150.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:150464138 G>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr1:150471510 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:102242440 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr15:102197167 C>T maps to NM_152334.2 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:102215835 T>G maps to NM_152334.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:102197239 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:102261471 C>T maps to NM_152334.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:6631142 A>T maps to NM_138697.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:6639556 C>A maps to NM_138697.3 Y813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:6636488 C>A maps to NM_138697.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:19166908 A>T maps to NM_152232.2 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:19166620 G>C maps to NM_152232.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:19166518 C>A maps to NM_152232.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:19175930 C>A maps to NM_152232.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:19167001 G>T maps to NM_152232.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr1:19186124 G>A maps to NM_152232.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:19168238 G>A maps to NM_152232.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:19166998 G>T maps to NM_152232.2 C538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr1:19180710 C>T maps to NM_152232.2 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr1:19184025 C>G maps to NM_152232.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:19175990 G>A maps to NM_152232.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:19166266 G>A maps to NM_152232.2 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:19166383 G>A maps to NM_152232.2 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr1:19166218 G>C maps to NM_152232.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:19166914 G>A maps to NM_152232.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:19181048 G>A maps to NM_152232.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:1267221 G>A maps to NM_152228.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:1268366 G>T maps to NM_152228.1 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:9629952 G>C maps to NM_019599.2 Y64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr5:9629851 C>T maps to NM_019599.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:9629774 T>A maps to NM_019599.2 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr12:10978097 C>A maps to NM_023921.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:11061627 T>A maps to NM_023920.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:11060985 T>C maps to NM_023920.2 *304W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr12:11091223 G>A maps to NM_023922.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:122635592 C>A maps to NM_016945.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:122635133 C>T maps to NM_016945.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr7:122635338 C>T maps to NM_016945.2 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:122635313 C>T maps to NM_016945.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:122634998 G>T maps to NM_016945.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr12:11286553 C>T maps to NM_001097643.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr12:11286267 C>A maps to NM_001097643.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr12:11286837 T>G maps to ENST00000422992 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr12:11286255 C>A maps to NM_001097643.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:11286102 T>A maps to NM_001097643.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr12:11286341 A>G maps to NM_001097643.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:11183829 C>A maps to NM_176885.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr12:11183031 C>A maps to NM_176885.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:11183898 C>A maps to NM_176885.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:141672871 G>A maps to NM_176817.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:141672859 C>G maps to NM_176817.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:142880729 C>A maps to NM_176881.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr7:142880609 C>A maps to NM_176881.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:142880807 C>A maps to NM_176881.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr7:141478323 C>T maps to NM_016944.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:141478656 G>T maps to NM_016944.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:142919809 C>T maps to NM_176882.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr7:142920022 C>T maps to NM_176882.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:143175741 C>T maps to NM_176883.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr7:143175882 G>T maps to NM_176883.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr7:143175789 C>A maps to NM_176883.2 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:143175318 C>A maps to NM_176883.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:143175366 G>T maps to NM_176883.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:143175207 C>A maps to NM_176883.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr7:143175117 G>A maps to NM_176883.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:143175249 C>A maps to NM_176883.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr7:143175139 C>T maps to NM_176883.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr12:11339405 G>A maps to NM_181429.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:11339198 G>T maps to NM_181429.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr12:11214560 G>T maps to NM_176887.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:141490335 C>T maps to NM_018980.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr7:141490166 G>A maps to NM_018980.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:141490553 G>T maps to NM_018980.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:11139351 C>G maps to NM_176890.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr7:143141100 C>A maps to NM_177437.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:143141372 T>C maps to NM_177437.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:143141100 C>A maps to NM_177437.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr7:143141009 C>A maps to NM_177437.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr7:143141420 C>T maps to NM_177437.1 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:143141255 C>G maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:143140673 C>A maps to NM_177437.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:10954611 G>A maps to NM_023919.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr20:13610662 C>A maps to NM_017714.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr20:13463882 T>A maps to NM_017714.2 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:13550199 T>G maps to NM_017714.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:13561608 C>G maps to NM_017714.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:71604707 T>A maps to NM_000353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:125551264 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr8:125534427 A>G maps to NM_032026.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr3:10320618 G>A maps to NM_014760.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr3:10320660 C>A maps to NM_014760.3 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:212977678 C>T maps to NM_001146171.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:212988353 G>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:27827144 G>T maps to ENST00000409980 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr7:27827103 T>A maps to ENST00000409980 L307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:27831773 G>A maps to ENST00000409980 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:27832702 G>T maps to ENST00000409980 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr23:153641822 C>A did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr23:153648423 T>C did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:153649029 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:38037261 G>C maps to NM_015173.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr4:38016287 G>T maps to NM_015173.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr22:30688618 C>T maps to ENST00000403477 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6975-01A-11D-1945-08 chr22:30691007 C>T maps to ENST00000403477 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr16:30380610 C>A maps to NM_015527.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr10:96163323 C>T maps to NM_015188.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr10:96291055 G>T maps to NM_015188.1 G700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr10:96162369 G>A did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr4:7026817 G>T maps to NM_001113361.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:7006647 G>T maps to NM_001113361.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:72316794 G>T maps to NM_022771.4 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr17:77987337 C>A maps to NM_019020.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:50391573 C>T maps to NM_024682.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr19:50385318 C>G maps to NM_024682.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr4:26744201 C>T maps to NM_018317.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr4:26638831 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:26661217 G>T did not map to a codon.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr4:26741525 G>A maps to NM_018317.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr15:74178874 G>T maps to NM_153356.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr15:74179998 G>T maps to NM_153356.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr15:74173741 G>T maps to NM_153356.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:74177203 C>A maps to NM_153356.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr22:47290723 G>A maps to NM_014346.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr6:37250727 G>A maps to NM_017772.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr6:37254841 A>G maps to NM_017772.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:100014010 A>T maps to ENST00000394144 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:100002544 T>A maps to ENST00000394144 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr3:100025387 G>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:99998522 A>C maps to ENST00000394144 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr16:2550420 T>C maps to ENST00000434757 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr16:2549369 G>A maps to ENST00000434757 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:48419158 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48418388 A>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:48399814 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:48399785 C>A did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr23:48419137 G>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:48418001 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:48418712 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:48418902 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:48418903 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:15641673 C>A maps to NM_178571.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:18541987 G>C maps to NM_001039397.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:78310191 T>G maps to NM_144572.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:78290593 C>A maps to NM_144572.1 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:75886872 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr13:75936626 C>A maps to ENST00000431480 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr13:75884153 C>G maps to ENST00000431480 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:75936221 C>A maps to ENST00000431480 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr13:75863084 G>C maps to ENST00000431480 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:17299996 C>A did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:17446184 C>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:17413736 C>A maps to NM_001134381.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr3:17255707 T>C maps to NM_001134381.1 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr6:13306665 C>T maps to NM_016495.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:101655069 G>T maps to NM_001102426.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr2:101646185 T>A maps to NM_001102426.1 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:101644860 T>C maps to NM_001102426.1 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr2:101646203 G>A maps to NM_001102426.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:101670702 G>A maps to NM_001102426.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr2:101644779 G>T maps to NM_001102426.1 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:106061993 A>G did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:106046139 G>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:106093412 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:106109129 C>G did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:106108790 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:106117036 T>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:106109121 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:106066506 A>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:106116956 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:106084039 G>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:106083312 A>G did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:106111666 C>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:106046174 G>A did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr23:106070415 A>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr4:141590958 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:141543528 C>A maps to NM_015130.2 R1207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:141591908 C>A maps to NM_015130.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:141598059 G>T maps to NM_015130.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr4:141578790 G>A maps to NM_015130.2 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr5:179320366 G>A maps to NM_198868.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr5:179290819 C>G maps to NM_198868.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:179320252 C>A maps to NM_198868.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr5:179292298 T>C maps to NM_198868.2 K1009K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr5:179306762 C>A maps to NM_198868.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr5:179306708 C>A maps to NM_198868.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:76987266 C>T maps to NM_004607.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:186272221 T>G maps to NM_001134415.1 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:186281971 G>A maps to NM_001134415.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:186272083 T>A maps to NM_001134415.1 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:80887118 C>T maps to NM_005993.4 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr17:80895218 C>T maps to NM_005993.4 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:235600786 G>T maps to NM_003193.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:235612019 A>C maps to NM_003193.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:235599074 C>T maps to NM_003193.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:235590527 C>G maps to NM_003193.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:120924345 A>T maps to NM_152715.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:120957513 G>T maps to NM_152715.3 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr11:120918292 G>T maps to NM_152715.3 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:120916425 C>T maps to NM_152715.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:120929157 C>T maps to NM_152715.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:107169464 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:107216291 T>C maps to NM_001163436.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr17:45774120 G>C maps to NM_014726.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:45787861 A>T did not map to a codon.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr23:9660218 C>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:9652090 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:9656206 G>T did not map to a codon.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr23:9661223 C>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:9679740 C>T did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:9683027 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:9673086 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:9656163 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:9622316 A>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:176755884 C>A did not map to a codon.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr24:6955406 C>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr24:6954408 C>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr24:6955418 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:72988715 C>G maps to NM_012453.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:72984916 C>A maps to NM_012453.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr7:72985559 G>T maps to NM_012453.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:72988398 C>A maps to NM_012453.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr7:72985577 G>A maps to NM_012453.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr7:72988329 G>A maps to NM_012453.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr16:2025659 C>T maps to NM_006453.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:2024385 G>T maps to NM_006453.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E6-01A-11D-A24D-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr14:55907238 G>T maps to NM_199047.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr14:55881107 T>A maps to NM_199047.2 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr14:55881150 G>T maps to NM_199047.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:162274295 G>T maps to NM_006593.2 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:162279888 C>T maps to NM_006593.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:162273331 C>T maps to NM_006593.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:162273556 C>T maps to NM_006593.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:45145175 G>T maps to ENST00000404564 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:45145228 C>T maps to ENST00000404564 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:45141141 G>A maps to ENST00000404564 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:45145189 T>A maps to ENST00000404564 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr7:45141999 G>T maps to ENST00000404564 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:45142078 C>T maps to ENST00000404564 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr22:19754233 C>T maps to NM_080647.1 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:67400439 C>T maps to NM_005995.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:67402312 G>A maps to NM_005995.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:119441649 C>A did not map to a codon.
Alternatively spliced codon TCGA-17-Z058-01A-01W-0747-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:119469161 G>A maps to ENST00000369429 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:119427377 G>A maps to ENST00000369429 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:119466121 C>A maps to ENST00000369429 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:119474342 G>A maps to ENST00000369429 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:119441666 G>T maps to ENST00000369429 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:119427738 G>T maps to ENST00000369429 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:119466091 C>G maps to ENST00000369429 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:85447029 G>T maps to NM_001080508.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr6:85453976 A>C did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr6:85457658 G>T maps to NM_001080508.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr6:85446453 G>T maps to NM_001080508.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:85446744 G>T maps to NM_001080508.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr6:85447050 G>A maps to NM_001080508.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr6:85446666 A>T maps to NM_001080508.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:168282074 G>T maps to NM_005149.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:168260634 G>T maps to NM_005149.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:59482615 G>T maps to NM_005994.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:59482038 A>T maps to NM_005994.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:35271186 C>T maps to NM_001077653.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr7:35242074 G>A maps to NM_001077653.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:35280502 G>T maps to NM_001077653.2 Y267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr7:35271146 G>T maps to NM_001077653.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr7:35289648 G>T maps to NM_001077653.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:35242293 G>T maps to NM_001077653.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:45821846 G>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:45811197 G>T maps to NM_013351.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:45822140 C>A maps to NM_013351.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:45822275 T>C maps to NM_013351.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:45820521 C>A maps to NM_013351.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:79286473 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:79282219 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:79279573 C>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:79286260 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:79286129 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:79286130 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:79286463 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:79277846 C>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr23:79279581 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:79286508 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:79286265 A>T did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:79278683 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:79286249 G>T did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:79286019 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:79286490 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:79279560 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:79279561 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:79282216 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:79286260 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:79282806 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:79277774 C>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:79286328 G>C did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:79277932 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:79282283 C>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:79278702 A>G did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:79277917 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:79286254 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:79281105 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:79286083 C>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:79283491 G>A did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:79282363 A>G did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:79286413 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:79286259 C>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:115120978 G>A maps to NM_016569.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:115120696 G>T maps to NM_016569.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:115118695 G>A maps to NM_016569.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:115120783 G>C maps to NM_016569.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:115120935 G>T maps to NM_016569.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr12:115120783 G>C maps to NM_016569.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:59560747 G>A maps to ENST00000393853 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:59544957 G>T maps to ENST00000393853 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr17:59560840 A>T maps to ENST00000393853 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:114823366 C>A maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:114793870 G>T maps to NM_000192.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:114793894 G>T maps to NM_000192.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr12:114793576 C>G maps to NM_000192.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr12:114837433 C>A maps to NM_000192.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:114804105 G>T maps to NM_000192.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:114804197 T>A did not map to a codon.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr12:114832596 G>A maps to NM_000192.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:114793429 G>T maps to NM_000192.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr12:114803928 G>T maps to NM_080718.1 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr12:114804147 G>T maps to NM_000192.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr12:114837317 C>T maps to NM_000192.3 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr12:114793837 G>T maps to NM_000192.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:114793471 A>C maps to NM_000192.3 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:114841687 C>A maps to NM_000192.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:114793672 G>T maps to NM_000192.3 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr12:114793759 G>T maps to NM_000192.3 C378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr16:30097620 G>C maps to NM_004608.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:3600593 C>A maps to NM_201636.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr7:139575436 G>A maps to ENST00000422328 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:139657445 C>A maps to NM_001166253.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:92251688 C>A maps to NM_001128596.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr14:92249554 C>T did not map to a codon.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr14:92268647 A>T maps to NM_001128596.1 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:92268676 G>A maps to NM_001128596.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:37821713 C>G maps to NM_003673.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:54896922 C>T maps to NM_006756.2 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:54906315 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:62697831 G>T maps to NM_003195.4 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:62698290 C>T maps to NM_003195.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr23:102885085 G>T did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:101382383 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:101381868 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:101381935 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:101382343 G>A did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr23:101382088 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:101382206 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:102864487 C>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:102864515 C>A did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:102864327 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:102841913 G>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:102841901 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:102529197 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:102528905 C>A did not map to a codon.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr23:102529025 G>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:102529325 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:102529193 G>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:102528945 C>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:102528959 G>A did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr23:102528960 A>T did not map to a codon.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr23:102529222 G>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:102529097 G>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:102528880 G>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:102529379 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:102528918 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:102528905 C>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:101395807 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:101395903 G>T did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:101395955 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:101396141 T>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:101396214 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:102508697 C>G did not map to a codon.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr23:13680666 A>G did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:13680882 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:13681007 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:13681424 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:2821498 G>A maps to NM_207013.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:24077442 G>A maps to NM_003198.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr18:44560666 C>T maps to NM_016427.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr18:44561101 G>T maps to NM_016427.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr18:44561429 A>T maps to NM_016427.2 L69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:44560051 C>A maps to NM_016427.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:44560033 G>T maps to NM_016427.2 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:44560255 T>C maps to NM_016427.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:44554580 G>A maps to NM_145653.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr18:44555055 A>T maps to NM_145653.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:44555238 G>T maps to NM_145653.3 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr18:44555226 G>A maps to NM_145653.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr18:44555157 G>A maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr18:44555157 G>A maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr5:145883475 C>A maps to NM_006706.3 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr5:145838661 G>A maps to NM_006706.3 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr5:145838661 G>A maps to NM_006706.3 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr5:145849209 A>G maps to NM_006706.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr5:145838695 C>T maps to NM_006706.3 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr5:145843189 T>G maps to NM_006706.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr5:145849134 C>T maps to NM_006706.3 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr10:133106582 C>T maps to NM_174937.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:133107514 G>T maps to NM_174937.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr10:133106582 C>A maps to NM_174937.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr10:132965131 C>A maps to NM_174937.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr20:590587 G>A maps to NM_004609.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:31129473 C>T maps to NM_007109.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr6:31129530 C>A maps to NM_007109.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr22:42605701 G>A maps to NM_005650.1 G1870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr22:42610585 G>A maps to NM_005650.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr22:42605677 C>A maps to NM_005650.1 A1878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:42611185 T>A maps to NM_005650.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr22:42575678 G>T maps to NM_005650.1 A1895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr22:42564736 G>A maps to NM_005650.1 P1935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr2:27373193 G>A maps to NM_175769.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:27373005 G>T maps to NM_175769.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:27373133 C>A maps to NM_175769.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:89958628 A>T maps to NM_014972.2 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr16:89967041 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr16:89967050 G>C maps to NM_014972.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:89940101 G>T maps to NM_014972.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr16:89977540 G>A maps to NM_014972.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr16:89977622 G>T maps to NM_014972.2 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:1612272 C>A maps to NM_001136139.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:1623967 C>A maps to NM_003200.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr19:1632116 T>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:52942960 A>T maps to ENST00000398339 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr18:52899792 C>T maps to ENST00000398339 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr18:52896227 C>A maps to ENST00000398339 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr18:52921778 C>G maps to ENST00000398339 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr18:52924592 C>A maps to ENST00000398339 G469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:52937194 C>A did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr2:85531117 A>C maps to NM_031283.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr10:114925375 C>G maps to NM_030756.4 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:114918423 A>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr10:114905796 G>T maps to NM_030756.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr10:114925397 G>T maps to NM_030756.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:61485406 C>T maps to NM_006602.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr20:61492863 C>T maps to NM_006602.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:152080961 A>G maps to NM_007113.2 R1577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:152083861 C>A maps to NM_007113.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:152080151 C>G maps to NM_007113.2 A1847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:152084546 C>T maps to NM_007113.2 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:152084936 C>A maps to NM_007113.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:152082860 C>T maps to NM_007113.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:152081941 G>T maps to NM_007113.2 R1251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:152081863 G>T maps to NM_007113.2 R1277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:152081033 A>T maps to NM_007113.2 R1553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:152080400 C>A maps to NM_007113.2 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:152085431 A>G maps to NM_007113.2 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152081543 C>A maps to NM_007113.2 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr1:152080457 G>A maps to NM_007113.2 R1745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:152082680 C>T maps to NM_007113.2 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:152059799 G>A maps to NM_001008536.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:152057835 G>T maps to NM_001008536.1 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:152058336 C>G maps to NM_001008536.1 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr1:152058210 G>A maps to NM_001008536.1 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr1:152057967 G>T maps to NM_001008536.1 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:152057926 G>T maps to NM_001008536.1 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr1:152060547 G>A maps to NM_001008536.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:152059650 T>A maps to NM_001008536.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:152058086 C>A maps to NM_001008536.1 G691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:152059245 A>T maps to NM_001008536.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:152058228 T>C maps to NM_001008536.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr12:110348912 G>T maps to NM_032300.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr12:110341740 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr11:67818086 G>A maps to NM_006019.3 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:96180318 C>A maps to NM_021966.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr14:96180343 G>T maps to NM_021966.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr14:96178092 C>T maps to NM_021966.2 *115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr14:96152896 C>G maps to NM_004918.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr11:59620775 G>T maps to NM_001062.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:59620691 G>A maps to NM_001062.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:59626663 T>C maps to NM_001062.3 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr11:59630100 C>T maps to NM_001062.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:59622150 G>T maps to NM_001062.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr11:59629096 G>T maps to NM_001062.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:59631428 G>T maps to NM_001062.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr22:31018993 C>G maps to NM_000355.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr22:31008874 G>A maps to NM_000355.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr22:31006972 C>T maps to NM_000355.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:149772987 C>A maps to ENST00000451292 A1255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr5:149754930 G>A maps to ENST00000451292 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr5:149771735 C>T maps to ENST00000451292 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:149749092 G>A maps to ENST00000451292 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr6:167789538 C>A maps to NM_004610.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr21:33949214 C>A maps to NM_144659.5 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:167592551 A>T maps to NM_001145121.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr6:167585685 G>A maps to NM_001145121.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:35090036 G>T maps to NM_001093728.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:35088394 C>T maps to NM_001093728.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:35107831 G>T maps to NM_018679.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr6:35086068 C>A maps to NM_001093728.1 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:35087017 G>A maps to NM_001093728.1 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:33065471 G>A maps to NM_001145541.1 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:44255480 C>A maps to NM_182539.3 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:44250095 G>A maps to NM_182539.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr6:44248036 C>A maps to NM_182539.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:44250143 G>A maps to NM_182539.3 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:196043062 C>A maps to NM_152773.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:111078322 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:124184346 C>T maps to NM_024809.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:124192152 G>T maps to NM_024809.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:124158241 C>A maps to NM_024809.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:124175077 A>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr10:97440279 C>A maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr10:97440279 C>T maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:104379501 G>A maps to NM_003211.4 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr12:104373741 C>T maps to NM_003211.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:104380777 G>T maps to NM_003211.4 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:46620583 G>C did not map to a codon.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr4:156841117 C>A maps to NM_005651.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:156831355 T>A maps to NM_005651.2 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:156841130 G>T maps to NM_005651.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr14:90437533 G>T maps to NM_018319.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr14:90429940 G>T maps to NM_018319.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr14:90446934 C>T maps to NM_018319.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr14:90450919 G>A maps to NM_018319.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr10:115963325 G>A maps to NM_198795.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:115971636 G>A maps to NM_198795.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr10:115970635 C>T maps to NM_198795.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:115963867 C>T maps to NM_198795.1 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr10:115973183 A>T maps to NM_198795.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:154517339 C>G maps to NM_001098475.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:154480954 A>T maps to NM_001098475.1 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:154519883 G>C did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:61057958 G>T maps to NM_001146070.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr13:61102532 G>T maps to NM_001146070.1 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:179631267 G>T maps to ENST00000444136 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:179631372 C>T maps to ENST00000444136 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:179620107 T>A maps to ENST00000444136 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr1:179562701 G>T maps to ENST00000444136 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:179608976 C>T maps to ENST00000444136 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:179561782 G>T maps to ENST00000444136 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:179659918 A>G maps to ENST00000444136 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:179604988 C>A maps to ENST00000444136 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr6:46658780 A>T maps to NM_001010870.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:46663670 G>T maps to NM_001010870.2 E2054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:46657598 G>T maps to NM_001010870.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:46660739 G>C maps to NM_001010870.2 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:46659780 A>T maps to NM_001010870.2 K1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr6:46657739 C>A maps to NM_001010870.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr9:100258035 C>T maps to NM_014290.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr9:100245540 G>C maps to NM_014290.2 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr9:100245168 T>C maps to NM_014290.2 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:100194382 G>C maps to NM_014290.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:100190914 G>A maps to NM_014290.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr14:104470656 T>G maps to NM_153046.2 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr14:104462106 T>A maps to NM_153046.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:104491912 G>T maps to NM_153046.2 G911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr1:151747948 C>A maps to NM_001083965.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr1:151755441 C>A maps to NM_001083965.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr11:12901385 G>A maps to NM_021961.5 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:49858628 G>A maps to NM_003598.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:49854622 C>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:49845838 C>A maps to NM_003598.1 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:35445091 G>T maps to ENST00000357281 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:3129839 G>T maps to NM_003213.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:3149425 G>T did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:3127714 G>A maps to NM_003213.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:48139452 C>A maps to NM_003215.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:48170629 T>A maps to NM_003215.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:48169818 C>T maps to NM_003215.2 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr4:48147133 C>A maps to NM_003215.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr7:97870216 G>T maps to ENST00000379795 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:97852405 C>A maps to ENST00000379795 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:97870246 G>A maps to ENST00000379795 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr7:97862144 C>G maps to ENST00000379795 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:97862898 C>T maps to ENST00000379795 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr7:97857327 G>A maps to ENST00000379795 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr14:102906782 C>T maps to NM_014844.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr14:102901025 G>A maps to NM_014844.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:102910131 G>T maps to NM_014844.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:14674069 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:65146796 G>T maps to NM_001010874.4 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:65275039 C>T maps to NM_001010874.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:65275045 G>T maps to NM_001010874.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:65170926 A>G maps to NM_001010874.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:65188409 G>T maps to NM_001010874.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr4:65146796 G>T maps to NM_001010874.4 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr4:65180481 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr4:65145917 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:65274862 T>G maps to NM_001010874.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr4:65194245 A>G maps to NM_001010874.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:65180436 G>T maps to NM_001010874.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr4:65175609 G>T maps to NM_001010874.4 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr4:65165691 C>A maps to NM_001010874.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr4:65188466 T>A maps to NM_001010874.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:65147200 G>T maps to NM_001010874.4 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr4:65147239 G>T maps to NM_001010874.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr4:65146771 T>A maps to NM_001010874.4 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:120996138 C>T maps to NM_005422.2 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:120998995 G>T maps to NM_005422.2 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:120984387 G>T maps to NM_005422.2 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr11:120983878 C>A maps to NM_005422.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:120998968 A>C maps to NM_005422.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:121028871 C>A maps to NM_005422.2 S1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr11:120989282 G>A maps to NM_005422.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:120998689 G>T maps to NM_005422.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr11:121008502 C>T maps to NM_005422.2 Y1105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:120989333 C>T maps to NM_005422.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr11:121016775 C>T maps to NM_005422.2 C1352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr11:121016436 T>A maps to NM_005422.2 G1239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr11:120983918 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:120996477 G>A maps to NM_005422.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr10:114059273 C>T maps to NM_058222.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:182369332 A>T maps to NM_172000.3 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:41783640 C>T maps to ENST00000417325 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr9:27197412 T>C maps to NM_000459.3 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr9:27202995 G>A maps to NM_000459.3 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr9:27209125 C>A maps to NM_000459.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr9:27169604 C>A maps to NM_000459.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr17:6722662 C>A maps to NM_053285.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:6703488 G>A maps to NM_053285.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:6716244 G>A maps to NM_053285.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr17:15217420 C>A maps to NM_031898.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:15222465 T>A did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr17:15215661 G>A maps to NM_031898.2 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:95537425 C>T maps to NM_144705.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:95540640 C>G maps to NM_144705.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4512-01A-21D-1855-08 chr16:10788535 C>A maps to NM_144674.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:10721631 G>A maps to NM_144674.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:10788223 C>T maps to NM_144674.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:1545619 C>T maps to NM_016111.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:1551497 G>T maps to NM_016111.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr16:1547464 G>T maps to NM_016111.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:53454530 C>T maps to NM_170754.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:20850849 C>A maps to NM_007110.4 E1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr14:20845890 G>A maps to NM_007110.4 L1915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr14:20837664 T>C maps to NM_007110.4 E2498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:20859919 C>T maps to NM_007110.4 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:20876105 C>A maps to NM_007110.4 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:20851721 G>T maps to NM_007110.4 I1264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr14:20854331 C>A maps to NM_007110.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:20849738 C>A maps to NM_007110.4 E1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:20872850 C>T maps to NM_007110.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr14:20837501 C>A did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr14:20845912 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr14:20869740 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:20876538 C>A maps to NM_007110.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:20849470 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr14:20876562 T>A maps to NM_007110.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr14:20857776 T>A maps to NM_007110.4 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20841880 G>C maps to NM_007110.4 S2187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr14:20843946 G>A maps to NM_007110.4 V2110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr14:20859841 C>A maps to NM_007110.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:20856103 C>A maps to NM_007110.4 E882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr14:20864839 C>G maps to NM_007110.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr14:20851368 G>A maps to NM_007110.4 Y1337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:58011779 C>A maps to NM_199046.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:58019393 C>T maps to NM_199046.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:69404451 G>C maps to NM_005652.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr16:75690286 C>T maps to NM_018975.3 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr5:1264700 C>A maps to NM_198253.2 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:1278791 G>A maps to NM_198253.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:1293515 G>A maps to NM_198253.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:1253848 C>T maps to NM_198253.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr5:1280365 G>C maps to NM_198253.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:1293518 G>A maps to NM_198253.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:115892430 C>T maps to NM_015641.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:35606260 A>T maps to NM_006285.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:70332961 C>A maps to NM_030625.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr10:70450633 C>G maps to NM_030625.2 S1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:70332191 G>T maps to NM_030625.2 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr10:70451364 G>T maps to NM_030625.2 E2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr10:70405962 G>T maps to NM_030625.2 R1159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:70333279 A>T maps to NM_030625.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr4:106155396 G>T maps to ENST00000513237 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr4:106196706 G>A maps to ENST00000513237 Q1701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr4:106180774 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr4:106158267 G>T maps to ENST00000513237 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:106155434 G>A maps to ENST00000513237 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:74328906 C>A maps to ENST00000409262 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:74274235 C>T maps to ENST00000409262 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:74274225 C>T maps to ENST00000409262 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:74307666 C>T maps to ENST00000409262 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:74307622 A>G did not map to a codon.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr19:43922332 G>A maps to NM_031451.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:43920615 G>C maps to NM_031451.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:70080746 G>T did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:69849460 C>A did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:69849575 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:69902601 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:69849523 A>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:69898724 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:69828957 T>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr23:69960639 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:69774578 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:69825331 C>A did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:69825285 C>G did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:69890291 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:69890280 G>C did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:69890340 T>A did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:69811631 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:69902566 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:70073098 G>T did not map to a codon.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr23:104463697 C>G did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:104463836 C>A did not map to a codon.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr23:104463662 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:104464211 C>G did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:104463998 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:104463889 G>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:104464180 G>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:104464706 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:104465058 G>C did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:104463938 C>A did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:104464956 G>T did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:104464798 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:104463766 C>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:104463877 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:104463954 A>G did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:104464009 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:104465031 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107224967 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107225335 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:107224960 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:107224573 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:107225112 T>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:107224448 C>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:107224762 G>T did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:107224605 G>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:107225238 G>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:107225221 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr23:107224902 T>A did not map to a codon.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr17:56679775 C>G maps to ENST00000240361 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr17:56638912 C>A maps to ENST00000240361 V1421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr17:56650540 C>G did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:56707799 C>A did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:56676545 G>T maps to ENST00000240361 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:56692696 C>T maps to ENST00000240361 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr17:56679853 G>T maps to ENST00000240361 Y484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:56679299 C>T maps to ENST00000240361 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr17:56676479 G>A maps to ENST00000240361 H748H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr17:56700348 A>T maps to ENST00000240361 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr17:56699147 C>G did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:56688568 G>T maps to ENST00000240361 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr17:56682357 G>A maps to ENST00000240361 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr17:56694957 G>A maps to ENST00000240361 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:30695123 C>T maps to NM_031271.3 S2509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr8:30703089 T>A maps to NM_031271.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr8:30706086 A>T maps to NM_031271.3 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:30705978 G>T maps to NM_031271.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:30695246 T>C maps to NM_031271.3 T2468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr8:30703671 C>T maps to NM_031271.3 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr8:30700550 G>A maps to NM_031271.3 Q1995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:30699764 G>A maps to NM_031271.3 Q2257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:30703266 C>A maps to NM_031271.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:30706074 A>G maps to NM_031271.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:30701124 G>T maps to NM_031271.3 C1803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:30704667 G>T maps to NM_031271.3 Y622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:30701509 C>T maps to NM_031271.3 W1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:30702721 A>T maps to NM_031271.3 L1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr8:30702132 C>A maps to NM_031271.3 A1467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr8:30695426 G>A maps to NM_031271.3 C2408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr8:30704568 T>A maps to NM_031271.3 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:30704583 C>T maps to NM_031271.3 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:30694317 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:30703551 G>T maps to NM_031271.3 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:30706010 C>A maps to NM_031271.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr8:30695123 C>A maps to NM_031271.3 S2509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr8:30694769 C>T maps to NM_031271.3 Q2627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr8:30702132 C>T maps to NM_031271.3 A1467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr17:80320451 C>T maps to NM_207459.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr17:62230408 C>T maps to NM_018469.3 K1019K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:62272301 C>A maps to NM_018469.3 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr17:62291187 C>A maps to NM_018469.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr17:62271033 G>C maps to NM_018469.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:71220882 T>G maps to NM_144582.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:71216144 G>A maps to NM_144582.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr3:51733558 G>T maps to NM_015926.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:51733555 T>C maps to NM_015926.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr15:56681598 G>A did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr3:133473426 C>T maps to NM_001063.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:133467265 G>T maps to NM_001063.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:133485248 C>A maps to NM_001063.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:133495984 A>G maps to NM_001063.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:133483099 C>T maps to NM_001063.3 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:133494433 C>T maps to NM_001063.3 C615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr6:10410283 C>G maps to ENST00000379613 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:10398805 G>A maps to ENST00000379613 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:10404841 G>T maps to ENST00000379613 L223L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-75-7031-01A-11D-1945-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:10410445 T>G maps to ENST00000379613 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:50810879 C>T maps to ENST00000263046 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:50803984 C>T maps to ENST00000263046 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:50791329 C>T maps to ENST00000263046 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr6:50810921 C>T maps to ENST00000263046 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr6:50805756 G>A maps to ENST00000263046 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:55208436 G>T maps to NM_003222.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr20:55209277 G>A maps to NM_003222.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr20:55211798 A>G maps to NM_003222.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:50683241 C>A maps to NM_172238.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:50683292 G>T maps to NM_172238.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr6:50696930 C>A maps to NM_172238.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:50683151 G>T maps to NM_172238.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr6:50712887 G>T maps to NM_172238.3 G318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:50686840 C>A maps to NM_172238.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:50712949 C>A maps to NM_172238.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr6:50683154 C>A maps to NM_172238.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr6:50696701 C>T maps to NM_172238.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:50683175 G>A maps to NM_172238.3 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:50712877 C>A maps to NM_172238.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:50696617 C>A maps to NM_172238.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:50683112 G>T maps to NM_172238.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:4310162 G>A maps to NM_003223.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312330 G>A maps to NM_003223.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:4312569 G>T maps to NM_003223.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:4310142 G>T maps to NM_003223.2 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr16:4308229 G>T maps to NM_003223.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:155635463 T>C maps to NM_016020.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr6:155619653 T>C maps to NM_016020.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:155606412 T>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr1:246707917 A>G maps to NM_022366.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr12:51501051 A>G maps to NM_005653.4 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:122004482 G>A maps to NM_014553.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:121999985 G>T maps to NM_014553.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr13:114288851 G>T maps to NM_007111.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr13:114288330 G>T maps to NM_007111.4 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr13:114287473 A>G maps to NM_007111.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:141682712 T>A maps to NM_001178139.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:141671483 G>A maps to NM_001178139.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:141692892 C>A maps to NM_001178139.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:141682739 C>A maps to NM_001178139.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:141697430 C>A maps to NM_001178139.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:141697399 C>A maps to NM_001178139.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:132352131 G>A did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr23:132351569 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:132351800 G>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:132351955 A>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:132351909 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:132351984 G>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:132351733 T>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:132351528 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:132351378 C>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr23:48891689 G>A did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:48896716 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr23:48896790 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr23:48896747 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:48888918 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr6:41658481 G>A maps to ENST00000343317 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr6:41652555 G>T maps to ENST00000343317 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr6:41658523 C>T maps to ENST00000343317 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:115580862 G>T maps to NM_012252.2 C262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:100463678 C>T maps to NM_001007565.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:100467174 C>T maps to NM_001007565.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:26902739 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:26892177 G>A maps to NM_012143.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr22:26895072 G>A maps to NM_012143.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr7:93519620 C>T maps to NM_006528.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr19:54618076 G>A maps to NM_013342.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:195798335 G>A maps to NM_001128148.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr8:133898771 G>A maps to NM_003235.4 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr8:133953767 C>A maps to NM_003235.4 V1738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr8:133984966 C>T maps to NM_003235.4 F2060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:133906049 G>A maps to NM_003235.4 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:133980046 C>T maps to NM_003235.4 Q1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:134125712 C>A maps to NM_003235.4 Y2540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:133961040 C>T maps to NM_003235.4 L1752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:133906085 C>G maps to NM_003235.4 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:134145719 C>A maps to NM_003235.4 P2668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr8:133925379 G>T maps to NM_003235.4 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:133883767 G>T maps to NM_003235.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:133885382 G>C maps to NM_003235.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:133984077 C>A maps to NM_003235.4 C2005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:133898949 C>T maps to NM_003235.4 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr8:133900352 G>T maps to NM_003235.4 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr8:133900691 G>T maps to NM_003235.4 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:133881997 C>A maps to NM_003235.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:134108550 A>T maps to NM_003235.4 V2502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:134144054 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr8:133984059 G>A maps to NM_003235.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr8:133980141 C>T maps to NM_003235.4 D1930D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr8:134108460 G>C maps to NM_003235.4 V2472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:133920471 C>T maps to NM_003235.4 Q1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:133913596 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:133913769 C>A maps to NM_003235.4 R1202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:95235490 C>G did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:95231009 T>A maps to NM_014305.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:41847786 C>A did not map to a codon.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:41847855 C>T maps to NM_000660.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr19:41847917 G>A maps to NM_000660.4 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:41854259 C>T maps to NM_000660.4 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:31488240 C>A maps to NM_001042454.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:31484843 C>T maps to NM_001042454.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr16:31488201 C>A maps to NM_001042454.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr16:31488303 C>G maps to NM_001042454.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:218578520 G>T maps to NM_001135599.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr14:76437954 G>C maps to NM_003239.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr5:135390480 G>A maps to NM_000358.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr5:135382090 G>T maps to NM_000358.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:101907146 A>G maps to NM_004612.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:101911460 G>T did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:30713589 C>T maps to NM_001024847.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr3:30686266 C>T maps to NM_001024847.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:30733000 C>T maps to NM_001024847.2 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr1:92185500 G>C maps to NM_003243.4 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:92174228 C>A maps to NM_003243.4 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr1:92200335 C>A maps to NM_003243.4 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:92161252 A>G maps to NM_003243.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:92193305 C>T maps to NM_003243.4 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:92185022 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:105885839 G>A maps to NM_004257.4 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:105883920 T>C maps to NM_004257.4 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr2:105924095 G>A maps to NM_004257.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr20:35219608 A>G maps to NM_021809.6 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:89177680 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:89177630 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:89177586 C>A did not map to a codon.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr23:89177554 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:89177644 C>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr23:89177107 G>T did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr23:89177430 G>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr23:89177128 G>T did not map to a codon.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr23:89177153 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:89177191 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:89177193 A>G did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:89177209 A>T did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:89177795 G>T did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:89177402 C>G did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:89177141 C>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:89177267 G>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:89177680 C>A did not map to a codon.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr23:89177699 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:89177311 C>A did not map to a codon.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr23:89177719 C>A did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:89177382 G>T did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:89177187 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:89177225 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:89177275 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:89177529 G>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:89177479 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:89177275 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:89177276 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:89177649 C>G did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:89177443 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr24:3447317 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr24:3447686 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:24728974 G>T maps to NM_000359.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr20:36759568 G>A maps to NM_004613.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr20:36759492 A>T did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr20:2320588 G>T maps to NM_003245.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr20:2293580 T>A maps to NM_003245.3 L193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr20:2290899 G>A maps to NM_003245.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr20:2306539 G>A maps to NM_003245.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr20:2321196 G>A maps to NM_003245.3 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr3:44943062 G>T maps to NM_003241.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr3:44943080 A>C maps to NM_003241.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr3:44945469 C>A maps to NM_003241.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:44951753 C>A maps to NM_003241.3 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:44955192 G>A maps to NM_003241.3 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr15:43526972 C>T maps to NM_201631.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr15:43525418 G>T maps to NM_201631.3 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr15:43552355 C>T maps to NM_201631.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr15:43552772 T>C maps to NM_201631.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr20:2413144 C>G maps to NM_198994.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:2375140 C>G maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:2411673 G>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr20:2411239 C>A maps to NM_198994.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:2398109 G>T maps to NM_198994.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:2411246 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr20:2361621 G>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:2411242 C>A maps to NM_198994.2 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:2384236 G>T maps to NM_198994.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr20:2384051 T>C maps to NM_198994.2 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr15:43577064 C>A maps to NM_052955.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr15:43585710 G>C maps to NM_052955.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr15:43579652 G>A maps to NM_052955.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr15:43572138 C>T maps to NM_052955.2 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr15:43585153 T>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr15:43579514 G>T maps to NM_052955.2 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:85554632 C>T maps to ENST00000409015 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:85554095 A>C maps to ENST00000409015 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr2:85554206 A>G maps to ENST00000409015 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr8:56695310 C>T maps to NM_024831.6 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr8:56699162 G>T maps to NM_024831.6 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:2185531 C>A maps to NM_199292.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:2191094 G>T maps to NM_199292.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:57566479 C>T maps to NM_198976.1 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr20:57568154 G>A maps to NM_198976.1 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:57566099 C>T maps to NM_198976.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr20:57569700 C>T maps to NM_198976.1 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:43735789 T>A maps to ENST00000330266 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:43797576 C>A maps to ENST00000330266 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:43779385 G>A maps to ENST00000330266 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:43783685 C>T maps to ENST00000330266 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr2:43779440 T>C maps to ENST00000330266 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr16:67876780 G>A maps to NM_020457.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr16:67876780 G>A maps to NM_020457.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:242573057 C>A maps to NM_015963.5 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:76442140 G>A maps to NM_144721.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr4:83839863 C>G maps to NM_024672.4 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:83838447 G>A maps to NM_024672.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:83839596 C>G maps to NM_024672.4 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:83825978 A>C maps to NM_024672.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr4:83827745 A>G maps to NM_024672.4 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:39874445 C>T maps to NM_003246.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr15:39883423 G>A maps to NM_003246.2 Q762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr15:39881467 C>T maps to NM_003246.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:169648859 C>A maps to NM_003247.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:169626328 A>T maps to NM_003247.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:169626292 C>A maps to NM_003247.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:169648694 G>T maps to NM_003247.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:169637358 G>A maps to NM_003247.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr6:169648613 G>A maps to NM_003247.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:169637774 G>A maps to NM_003247.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:169620302 G>A maps to NM_003247.2 Y1167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr6:169648751 C>G maps to NM_003247.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr6:169621550 A>G maps to NM_003247.2 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:169648570 G>A maps to NM_003247.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr6:169648564 C>A maps to NM_003247.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr6:169637752 G>T maps to NM_003247.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr6:169639700 G>T maps to NM_003247.2 C374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:155167904 C>A maps to NM_007112.3 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr5:79375017 G>A maps to NM_003248.4 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr5:79366217 C>A maps to NM_003248.4 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr5:79368107 A>G maps to NM_003248.4 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr5:79351686 G>T maps to NM_003248.4 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr5:79355629 C>T maps to NM_003248.4 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr5:79351728 C>G maps to NM_003248.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:362331 G>A maps to NM_016585.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:375943 G>T maps to NM_016585.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr19:375670 A>T maps to NM_016585.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:362421 G>T maps to NM_016585.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:362232 T>C maps to NM_016585.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:151820328 G>T maps to NM_182578.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr1:151820256 G>T maps to NM_182578.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:151820279 G>A maps to NM_182578.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr6:128135073 G>T maps to NM_001164685.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:128134639 G>T maps to NM_001164685.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr5:157158615 G>A maps to NM_017872.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr10:25313015 C>T maps to NM_024838.4 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:25313552 G>A maps to NM_024838.4 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:25313811 A>T maps to NM_024838.4 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr2:88485518 G>T maps to NM_018271.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:88474920 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:122840793 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:122765623 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:122757643 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:122747509 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:122747256 C>A did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:122747257 C>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:122771947 G>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:122769969 G>C did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:122756690 G>A did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr23:122778517 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:122778711 G>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:122760369 A>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:122757066 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:122799683 C>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:122799518 G>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:122802053 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:122755272 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:122765683 T>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:122757775 T>G did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:122765636 T>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:122802160 A>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:122830594 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:122747328 G>T did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:122747260 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:122757748 A>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:122760511 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:122846714 T>C did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:122830693 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:122760478 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:79846181 T>G maps to NM_005782.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:79847109 C>A maps to NM_005782.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr22:29935323 C>A maps to NM_003678.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr22:29908009 C>A maps to NM_003678.4 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:2796158 G>T maps to NM_003249.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:2799685 G>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:2810717 G>T maps to NM_003249.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:2799700 C>T maps to NM_003249.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr3:184090558 G>T maps to NM_000460.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr3:184090621 C>T maps to NM_000460.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:184093301 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:38240227 C>T maps to NM_003250.5 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:38245465 G>C maps to NM_003250.5 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr17:38244646 G>T maps to NM_003250.5 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:38243027 C>T maps to NM_003250.5 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:38244754 T>C did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:36755041 G>T maps to NM_005119.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:36767167 A>G maps to NM_005119.3 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr1:36755326 C>A maps to NM_005119.3 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:36752725 C>T maps to NM_005119.3 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr3:24174821 C>T maps to NM_001128177.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:24231780 G>T maps to NM_001128177.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr3:24174827 T>C maps to NM_001128177.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:24164617 T>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:24231826 T>C did not map to a codon.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr13:52971718 C>A maps to NM_018676.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr13:52951956 A>G maps to NM_018676.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr13:52952346 C>T maps to NM_018676.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr13:52971985 C>T maps to NM_018676.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr13:52972282 T>A maps to NM_018676.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:52971466 C>T maps to NM_018676.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr13:52952469 C>T maps to NM_018676.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr13:52952523 C>T maps to NM_018676.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:11521553 G>T maps to ENST00000423059 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:11871398 G>A maps to ENST00000423059 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr7:11415465 T>A maps to ENST00000423059 R1643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:11441425 A>G maps to ENST00000423059 C1469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:11675886 C>A maps to ENST00000423059 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:11675980 G>T maps to ENST00000423059 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:11630168 C>A maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:11675947 G>T maps to ENST00000423059 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:11485952 T>C did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr7:11450929 C>G maps to ENST00000423059 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr7:11630123 G>A maps to ENST00000423059 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:11485702 T>A maps to ENST00000423059 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr7:11486887 A>G maps to ENST00000423059 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:11521484 G>T maps to ENST00000423059 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr7:11676583 T>C maps to ENST00000423059 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:11676214 G>T maps to ENST00000423059 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:11676039 C>A maps to ENST00000423059 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:11464414 G>C maps to ENST00000423059 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:11630162 G>T maps to ENST00000423059 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr7:11676357 C>A maps to ENST00000423059 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:11581096 C>A maps to ENST00000423059 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:137990655 G>T maps to ENST00000272643 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:138413069 G>A did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:137988704 C>T maps to ENST00000272643 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:138378216 C>A maps to ENST00000272643 C1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:138208559 A>C maps to ENST00000272643 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:137814683 C>G maps to ENST00000272643 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:137872774 G>A maps to ENST00000272643 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:138373848 G>A maps to ENST00000272643 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:138000065 T>A maps to ENST00000272643 C730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:138000025 G>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:138169389 C>A maps to ENST00000272643 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:138169177 G>T did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:137814158 C>G maps to ENST00000272643 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:137988680 C>A maps to ENST00000272643 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:138400070 G>T maps to ENST00000272643 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:138169275 T>A maps to ENST00000272643 Y931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:137814158 C>A maps to ENST00000272643 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:138163243 A>G maps to ENST00000272643 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:137852611 G>T maps to ENST00000272643 G374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr2:138208577 G>T maps to ENST00000272643 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:137814206 C>T maps to ENST00000272643 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:137928359 A>G maps to ENST00000272643 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr14:24026244 T>C maps to NM_024328.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:20748249 T>A maps to ENST00000431224 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr16:20748339 C>T maps to ENST00000431224 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:39993216 C>A maps to NM_025264.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:39964186 A>G maps to NM_025264.4 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:70441500 T>A maps to NM_022173.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:70454898 T>A maps to NM_022173.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:70451748 C>A maps to NM_022173.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr17:27401082 C>T maps to NM_004740.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr10:121335209 G>A maps to NM_001033925.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:32537341 G>A maps to NM_003253.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr21:32639192 G>A maps to NM_003253.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:32617895 C>A maps to NM_003253.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:32617896 C>A maps to NM_003253.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:32617976 C>A did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr21:32638883 G>T maps to NM_003253.2 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr21:32492883 C>T maps to NM_003253.2 E1526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr21:32492775 G>A maps to NM_003253.2 I1562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr21:32537364 C>A maps to NM_003253.2 E969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr21:32624130 C>T maps to NM_003253.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr21:32624241 G>A maps to NM_003253.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr21:32598230 G>T maps to NM_003253.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr21:32595769 C>A maps to NM_003253.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr21:32638637 C>A maps to NM_003253.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:32537368 G>T maps to NM_003253.2 C967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr21:32582527 C>A maps to NM_003253.2 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr21:32598173 C>A maps to NM_003253.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr21:32537280 T>A maps to NM_003253.2 K997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr21:32526653 G>A maps to NM_003253.2 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr21:32492987 G>A maps to NM_003253.2 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr21:32638874 G>A maps to NM_003253.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr21:32526582 C>T maps to NM_003253.2 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr21:32525452 C>A did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr21:32639189 C>A maps to NM_003253.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr21:32598164 G>A maps to NM_003253.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr21:32537380 C>G maps to NM_003253.2 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr21:32638649 C>A maps to NM_003253.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr21:32554780 G>T maps to NM_003253.2 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr6:155465908 C>T maps to ENST00000456144 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:155532365 A>T maps to ENST00000456144 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:155451280 G>T maps to ENST00000456144 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:155498023 T>C maps to ENST00000456144 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:155465913 T>C did not map to a codon.
Sequencing variant TCGA-97-8177-01A-11D-2284-08 chr6:155458654 C>G maps to ENST00000456144 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:43778156 T>A maps to NM_005424.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:43774756 G>A maps to NM_005424.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:43772921 C>T maps to NM_005424.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:43770804 G>T maps to NM_005424.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:43774688 G>T maps to NM_005424.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:43782937 C>G maps to NM_005424.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:43773164 C>A maps to NM_005424.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:43779073 A>G maps to NM_005424.2 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:43787121 G>A maps to NM_005424.2 Q1068Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:43783063 C>A maps to NM_005424.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:43772828 C>T maps to NM_005424.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:43783063 C>A maps to NM_005424.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:43779470 C>A maps to NM_005424.2 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:43788390 T>A maps to NM_005424.2 *1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:43778231 C>A maps to NM_005424.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:43778195 G>A maps to NM_005424.2 Q617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr1:43788392 A>G maps to NM_005424.2 *1139W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr5:134785608 G>T maps to NM_001099221.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:90034802 T>C maps to NM_145715.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:65123347 C>G maps to NM_145719.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:65124211 G>A maps to NM_145719.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:153692093 T>C maps to NM_145720.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:153691100 T>C maps to NM_145720.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:3350040 G>A maps to NM_033208.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr16:3349432 G>A maps to NM_033208.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:3350422 T>A maps to NM_033208.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:114014611 C>A maps to ENST00000481065 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr3:114026902 C>T maps to ENST00000481065 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr3:114014611 C>T maps to ENST00000481065 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:114018504 G>T maps to ENST00000481065 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr5:156381591 T>A maps to NM_138379.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr5:156381702 C>G maps to NM_138379.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr5:156375475 G>A maps to NM_138379.2 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr5:156349188 G>T maps to NM_138379.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr5:156346536 T>A maps to NM_138379.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:156378553 C>T maps to NM_138379.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr5:156376711 C>T maps to NM_138379.2 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:56811917 C>A maps to NM_003920.3 E1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr12:56822746 G>A maps to NM_003920.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:56826269 G>A maps to NM_003920.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr12:56815549 C>A maps to NM_003920.3 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:48754087 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:48754089 G>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:48751399 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:48754134 C>T did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr19:7992607 G>A maps to NM_006351.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:7998445 C>T maps to NM_006351.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr19:8002965 G>A maps to NM_006351.3 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr23:100601581 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:100603637 G>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr14:58877569 T>C maps to NM_012460.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:47444635 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:47445944 G>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:47444659 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:33253255 G>A maps to NM_000362.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr3:12200289 C>T maps to NM_003256.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr3:12195026 G>A maps to NM_003256.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:12195176 C>A maps to NM_003256.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:54185440 G>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:54208148 T>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:54219384 G>T maps to NM_014464.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr6:54212270 T>C maps to NM_014464.3 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr6:54214561 C>A maps to NM_014464.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr6:54208043 T>C maps to NM_014464.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr14:24709002 T>A maps to NM_001099274.1 *452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr14:24709507 G>A maps to NM_001099274.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr3:156396124 C>T maps to NM_015508.4 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr15:66629364 C>T maps to NM_017858.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr11:126162537 C>T maps to NM_148910.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr6:43472821 G>A maps to NM_001146016.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr15:30024943 G>A maps to NM_003257.3 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:30020221 C>T maps to NM_003257.3 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr15:30053373 G>A maps to NM_003257.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr15:30033548 T>C maps to NM_003257.3 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:30000946 C>A maps to NM_003257.3 E1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr15:30026559 G>A maps to NM_003257.3 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr9:71869203 G>T maps to NM_004817.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:71861603 A>C did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:71851088 G>A maps to NM_004817.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:3738614 G>A maps to NM_014428.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:3747814 C>T maps to NM_014428.1 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr19:3736195 C>G maps to NM_014428.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:53275234 C>T maps to ENST00000423516 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:153539355 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:153524337 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:153551619 G>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:153540999 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:153539220 T>C did not map to a codon.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr23:153556304 G>A did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:153541037 C>A did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:153551613 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:153539265 T>G did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr23:153553708 C>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:153551629 C>A did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:153539219 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153524333 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153539222 C>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:153539223 T>A did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:153549136 C>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:153549128 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:153533763 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:164393185 G>T maps to NM_032136.4 Y567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:164394814 C>A maps to NM_032136.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:164393899 C>G maps to NM_032136.4 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr4:164394733 G>C maps to NM_032136.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:164394568 G>A maps to NM_032136.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr4:164393601 C>A maps to NM_032136.4 G429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:164394868 G>T maps to NM_032136.4 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr4:164393094 G>A maps to NM_032136.4 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:84228379 G>A maps to NM_005077.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:84208118 C>A maps to NM_005077.3 G468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:84267184 G>A maps to NM_005077.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:3005720 G>C maps to NM_003260.4 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:70342447 C>T maps to NM_005078.2 E769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr9:82323091 G>T maps to ENST00000376537 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr9:82187719 G>T maps to ENST00000376537 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:82340022 G>T maps to ENST00000376537 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr9:82333885 G>T maps to ENST00000376537 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr9:82333886 G>T did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr9:82333669 G>A maps to ENST00000376537 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr9:82333780 C>T maps to ENST00000376537 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr9:82333635 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:2987938 C>A maps to NM_001143986.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:171867900 G>T maps to ENST00000360843 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:171871452 C>T maps to ENST00000360843 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:171910293 C>A maps to ENST00000360843 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:172016854 C>T maps to ENST00000360843 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:60683535 G>A maps to ENST00000326270 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr17:60601667 A>G maps to ENST00000326270 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:166986902 C>T maps to ENST00000507499 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:166981295 A>T maps to ENST00000507499 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:166795202 T>C maps to ENST00000507499 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr4:166924541 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:166981178 G>T did not map to a codon.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr4:166946522 C>A maps to ENST00000507499 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:166929147 G>T maps to ENST00000507499 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr4:166960582 A>T maps to ENST00000507499 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:166960576 A>G maps to ENST00000507499 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:166999058 G>A maps to ENST00000507499 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:166935712 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:167020571 C>T maps to ENST00000507499 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr4:166999169 C>T maps to ENST00000507499 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr4:166929093 G>T did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr4:166795154 T>C maps to ENST00000507499 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr10:98188476 G>T maps to NM_012465.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr10:98273370 C>A maps to NM_012465.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr10:98129869 G>A maps to NM_012465.3 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:98170136 G>T maps to NM_012465.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:98180729 G>T maps to NM_012465.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr10:98165041 C>T maps to NM_012465.3 W405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:98192669 G>A maps to NM_012465.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr10:98157012 G>A maps to NM_012465.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr10:98157008 G>T maps to NM_012465.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:98155654 C>A maps to NM_012465.3 G503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:98155655 C>A maps to NM_012465.3 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr10:98165088 G>T maps to NM_012465.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr10:98146740 G>A maps to NM_012465.3 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:98138813 G>A maps to NM_012465.3 Q744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:35712915 C>G maps to NM_006289.3 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr9:35699424 G>A maps to NM_006289.3 Q2268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:35700301 G>A maps to NM_006289.3 I2182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:35719610 C>T maps to NM_006289.3 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:35704722 G>A maps to NM_006289.3 P1941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr9:35707124 C>A maps to NM_006289.3 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr9:35712043 C>G maps to NM_006289.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr15:62950010 C>T maps to NM_015059.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr15:62948148 G>A maps to NM_015059.2 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:63055812 C>T maps to NM_015059.2 N1671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:63031647 G>T maps to NM_015059.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr15:63102153 G>T maps to NM_015059.2 E2232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr15:63102158 G>A maps to NM_015059.2 V2233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:63031602 A>T maps to NM_015059.2 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr15:63008573 G>C maps to NM_015059.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:63029074 A>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr15:63030532 G>T did not map to a codon.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr15:63053960 C>T maps to NM_015059.2 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr15:63011989 C>T maps to NM_015059.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:63058584 A>T maps to NM_015059.2 T1720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr15:62995023 G>C maps to NM_015059.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:38799908 C>A maps to NM_003263.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:38798775 C>A maps to NM_003263.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr4:38799405 C>A maps to NM_003263.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:38800293 C>A maps to NM_003263.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:38798661 C>A maps to NM_003263.3 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr4:38776143 G>T maps to NM_030956.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:38776688 T>G maps to NM_030956.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr4:38775674 C>A maps to NM_030956.3 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:38774913 A>T maps to NM_030956.3 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:38775276 A>T maps to NM_030956.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:154624695 C>T maps to NM_003264.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:154626146 C>T maps to NM_003264.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:154626386 A>G maps to NM_003264.3 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:154626395 A>G maps to NM_003264.3 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr4:154625612 A>G maps to NM_003264.3 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr4:154624527 G>T maps to NM_003264.3 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr4:187003652 A>G maps to NM_003265.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:187004711 C>T maps to NM_003265.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:187003532 C>G maps to NM_003265.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:187005191 C>G maps to NM_003265.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr9:120476466 G>A maps to NM_138554.3 W687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:120474736 G>T maps to NM_138554.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:120476442 C>A maps to NM_138554.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:120476379 G>T maps to NM_138554.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:120476797 G>T maps to NM_138554.3 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:120476556 C>T maps to NM_138554.3 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr9:120466836 C>A maps to NM_138554.3 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:120474984 A>C maps to NM_138554.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr9:120470920 C>T maps to NM_138554.3 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr9:120470884 C>G maps to NM_138554.3 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:120476742 C>T maps to NM_138554.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr9:120475596 G>T maps to NM_138554.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr9:120476415 T>A maps to NM_138554.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:120476447 C>A maps to NM_138554.3 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr9:120475272 A>G maps to NM_138554.3 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr9:120474685 G>T maps to NM_138554.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:120476082 C>A maps to NM_138554.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr9:120466806 C>A maps to NM_138554.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr9:120475920 G>A maps to NM_138554.3 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:120470854 T>A maps to NM_138554.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr9:120476553 G>T maps to NM_138554.3 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr9:120476200 C>T maps to NM_138554.3 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr9:120476616 G>T maps to NM_138554.3 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr1:223284788 T>G maps to NM_003268.5 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:223283955 G>A maps to NM_003268.5 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:223285670 C>A maps to NM_003268.5 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:223284335 T>A maps to NM_003268.5 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:38829071 C>A maps to NM_006068.3 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr4:38830296 C>G maps to NM_006068.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:12905271 T>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:12904106 C>T did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:12905245 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:12905188 G>T did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:12904931 T>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:12904698 G>T did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:12904027 T>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:12905855 A>T did not map to a codon.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr23:12905920 C>T did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr23:12905136 A>T did not map to a codon.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr23:12905432 G>A did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:12904781 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:12904320 C>G did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:12905989 C>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:12906276 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:12905117 C>A did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:12904998 C>A did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr23:12904460 C>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:12904259 G>A did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:12905741 C>A did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:12906730 C>G did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:12906089 G>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:12904875 T>G did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:12906749 T>C did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:12938518 C>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:12939283 G>A did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:12937570 C>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:12939283 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:12940113 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:12937851 C>G did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:12938713 C>G did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:12940137 G>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:12940185 G>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:12939364 A>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:12937313 G>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:12937479 C>A did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:12938020 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:12938345 T>C did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:12938503 C>A did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:12938643 C>T did not map to a codon.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr23:12938974 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:12937817 T>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:12940172 C>A did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:12939589 G>C did not map to a codon.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr23:12939942 C>A did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:52257314 A>C maps to ENST00000494383 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr3:52257071 C>A maps to ENST00000494383 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr3:52256012 G>A maps to ENST00000494383 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr3:52257296 G>A maps to ENST00000494383 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:52257046 C>A maps to ENST00000494383 G582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr10:102896654 G>T maps to NM_005521.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr2:74742766 C>G maps to NM_016170.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr5:170736692 A>T maps to NM_021025.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr8:38848891 G>A maps to NM_031940.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:38852974 C>A maps to NM_031940.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:102191955 G>A maps to NM_078474.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr3:149089554 T>C maps to ENST00000383054 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:228228709 G>T maps to NM_024795.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:228228598 G>A maps to NM_024795.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:228235642 G>A maps to NM_024795.3 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:228228679 A>G maps to NM_024795.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr3:149193608 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr3:149216655 G>A maps to NM_004617.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:149205512 T>C maps to NM_004617.2 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr17:4684112 G>T maps to NM_003963.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr15:83791515 T>A maps to NM_023003.3 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:19381870 G>A maps to NM_001001524.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:19378886 C>A maps to NM_001001524.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:19379528 G>A maps to NM_001001524.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:19377419 T>C did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:19378818 G>T maps to NM_001001524.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:64882401 C>T maps to NM_003273.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:27128437 G>A maps to NM_016551.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr8:105360971 C>T maps to NM_030788.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:105360983 G>C maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr8:105360887 C>A maps to NM_030788.2 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr8:105361673 C>T maps to NM_030788.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:105360856 G>A maps to NM_030788.2 W26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr8:105361676 C>T maps to NM_030788.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:105367343 G>A maps to NM_030788.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr8:105361662 C>T maps to NM_030788.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr8:105361634 G>A maps to NM_030788.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:105360929 C>A maps to NM_030788.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:105361228 G>A maps to NM_030788.2 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:105367360 C>G maps to NM_030788.2 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr8:105360983 G>A maps to NM_030788.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:105361748 A>G maps to NM_030788.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr8:105361091 G>A maps to NM_030788.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr8:105361739 C>A maps to NM_030788.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr8:105361082 T>A maps to NM_030788.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr8:105360818 T>C maps to NM_030788.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr13:100153955 G>A maps to NM_004800.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr10:98307730 G>A maps to NM_020123.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr10:98311144 A>G maps to NM_020123.3 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr10:98311155 C>A maps to NM_020123.3 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr10:98325169 T>A maps to NM_020123.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30729321 G>A maps to NM_014742.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:30730904 G>T maps to NM_014742.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr20:30720910 C>T maps to NM_014742.3 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:219146816 C>G maps to NM_022152.4 L16L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-69-7760-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:50152022 C>T maps to NM_001098576.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr12:50155485 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:50153002 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:75387408 G>A maps to NM_138691.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr9:75387390 G>A maps to NM_138691.2 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:2597906 G>A maps to NM_080751.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:2616631 G>T maps to NM_080751.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr20:2552860 C>T maps to NM_080751.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr20:2597951 G>T maps to NM_080751.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr15:81637295 T>A maps to ENST00000454937 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr15:81633756 G>T maps to ENST00000454937 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr15:81627113 A>T maps to ENST00000454937 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:54675652 G>A maps to NM_001145303.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:54673268 C>T maps to NM_001145303.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:54667499 C>T maps to NM_001145303.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:19451965 G>T maps to NM_001105248.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr16:19451966 G>T maps to NM_001105248.1 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:19477480 C>T maps to NM_001105248.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:19475096 G>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:19501761 C>G maps to NM_001105248.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr16:19490848 A>T maps to NM_001105248.1 R756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:19070735 A>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:19020720 G>T maps to NM_024847.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:76135284 C>T maps to NM_152468.4 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:129389290 C>A maps to NM_001017395.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr3:129370422 C>A maps to NM_001017395.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:129370401 C>A maps to NM_001017395.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:205210769 C>A maps to NM_014858.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:205238490 G>T maps to NM_014858.3 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46V-01A-11D-A24D-08 chr1:205238181 G>A maps to NM_014858.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:205238775 C>T maps to NM_014858.3 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr1:205210916 C>T maps to NM_014858.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:205238712 G>A maps to NM_014858.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:205238835 G>T maps to NM_014858.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:205238835 G>A maps to NM_014858.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:205210775 T>C maps to NM_014858.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:94975549 C>A maps to NM_020698.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:94975858 G>T maps to NM_020698.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:94975690 C>T maps to NM_020698.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr12:94975771 G>T maps to NM_020698.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:165697283 T>G maps to NM_019026.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:40713902 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:40713881 C>T maps to NM_001008740.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr13:114150318 C>T maps to NM_017905.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr13:114164725 G>T maps to NM_017905.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:20063934 G>A maps to NM_181719.4 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:20107214 G>A maps to NM_181719.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr15:38229077 C>T maps to NM_152453.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr16:68912102 C>G maps to NM_024562.1 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr16:68941375 G>A maps to NM_024562.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr16:69117398 C>T maps to NM_024562.1 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:10945980 G>A maps to NM_006858.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:10946029 C>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr15:79614469 C>T maps to NM_007364.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:79614394 G>T maps to NM_007364.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:93625729 G>A maps to NM_016040.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr16:69377432 G>A maps to NM_144676.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr5:177019266 C>T maps to NM_017510.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr5:177020658 G>A maps to NM_017510.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr5:177019588 G>C maps to NM_017510.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr9:103310024 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:103338819 G>T maps to NM_001198812.1 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr9:103261149 A>G maps to NM_001198812.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr9:103310115 A>T maps to NM_001198812.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:103275608 G>T maps to NM_001198812.1 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:192863879 A>T maps to NM_016192.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:193059163 T>C maps to NM_016192.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:53798104 C>T maps to NM_001099640.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr17:7340296 C>T maps to NM_178518.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:72832429 C>T maps to NM_017728.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr17:72815929 C>T maps to NM_017728.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:41367824 G>T maps to NM_145041.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr7:12270708 C>T maps to NM_018374.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:48360467 G>A maps to NM_001143842.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:48358150 C>T maps to NM_001143842.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:48361988 G>T maps to NM_001143842.1 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:8079331 G>A maps to NM_032354.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr17:8079141 G>A maps to NM_032354.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:133099997 C>T maps to NM_001136469.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr3:133099202 C>A maps to NM_001136469.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr3:133098752 G>C maps to NM_001136469.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:44605101 C>A maps to NM_032256.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr12:44782163 G>A maps to NM_032256.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:44781885 A>T maps to NM_032256.1 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:44782157 A>G maps to NM_032256.1 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:44782259 A>T maps to NM_032256.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:44338118 G>C maps to NM_032256.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:44781920 G>C maps to NM_032256.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:44537358 C>T maps to NM_032256.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr12:108985619 G>A maps to NM_181724.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:108985844 G>T maps to NM_181724.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr12:108985526 G>T maps to NM_181724.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199629 C>T maps to NM_001080825.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:122199640 C>G maps to NM_001080825.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr12:122190117 C>T maps to NM_001080825.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:122188330 C>T maps to NM_001080825.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr14:105995419 C>T maps to NM_025268.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr11:102272283 A>T maps to NM_052932.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:102323342 G>A maps to NM_052932.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:96919800 G>A maps to NM_017849.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:1719958 C>G maps to NM_001127266.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr7:98449143 G>T maps to NM_001134450.1 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:98446203 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr7:98460873 G>A maps to NM_001134450.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:98392317 C>T maps to NM_015348.1 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:98408867 C>A maps to NM_015348.1 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:98375499 G>A maps to NM_015348.1 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:60699469 G>A maps to NM_017870.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:60695129 C>T maps to NM_017870.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr11:60698116 A>T maps to NM_017870.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr11:60695270 C>T maps to NM_017870.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr11:60702145 G>A maps to NM_017870.3 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:60699544 G>A maps to NM_017870.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr11:60704297 C>T maps to NM_017870.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr11:60694736 C>T maps to NM_017870.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr12:126138199 C>T maps to NM_052907.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:125834058 C>T maps to NM_052907.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126137135 C>G maps to NM_052907.2 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr12:126138764 T>C maps to NM_052907.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:126135489 C>A maps to NM_052907.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:126128650 G>T maps to NM_052907.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:125834676 G>T maps to NM_052907.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:126135289 C>T maps to NM_052907.2 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:126137060 G>T maps to NM_052907.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr12:125834847 C>G maps to NM_052907.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:126135312 T>A maps to NM_052907.2 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr12:126138781 G>A maps to NM_052907.2 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr12:126135285 C>A maps to NM_052907.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:125834187 C>A maps to NM_052907.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:126138379 C>G maps to NM_052907.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr12:125834064 G>T maps to NM_052907.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr12:130185163 G>A maps to NM_133448.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr12:129559340 G>T maps to NM_133448.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr12:130184929 G>T maps to NM_133448.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr12:129559151 C>G maps to NM_133448.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr12:129566483 C>A maps to NM_133448.2 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:129569091 G>T maps to NM_133448.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129558884 G>T maps to NM_133448.2 Y945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:129566495 C>G maps to NM_133448.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:129559373 C>A maps to NM_133448.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr12:129566309 G>T maps to NM_133448.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr12:130184919 G>T maps to NM_133448.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr12:129559172 G>C maps to NM_133448.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr12:130184784 G>T maps to NM_133448.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr12:129563212 C>A maps to NM_133448.2 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr12:129566387 G>A maps to NM_133448.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr12:130184794 G>C maps to NM_133448.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:129822321 C>A maps to NM_133448.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:129559061 G>A maps to NM_133448.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:129566542 C>A maps to NM_133448.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:129822343 G>T maps to NM_133448.2 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr12:129569123 G>T maps to NM_133448.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr12:129563159 G>A maps to NM_133448.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:129559034 G>A maps to NM_133448.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:129566309 G>T maps to NM_133448.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:129566326 C>A maps to NM_133448.2 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr12:129566432 C>A maps to NM_133448.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr12:129566507 C>T maps to NM_133448.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr12:129822295 T>A maps to NM_133448.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr12:129559565 G>T maps to NM_133448.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr12:129558446 G>C maps to NM_133448.2 Y1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:130184740 G>T maps to NM_133448.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr17:32964722 C>A maps to NM_207313.1 C809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:32963123 C>A maps to NM_207313.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:32959727 C>T maps to NM_207313.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:32955605 C>G maps to NM_207313.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961967 C>T maps to NM_207313.1 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr17:32961988 G>A maps to NM_207313.1 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:32964617 G>T maps to NM_207313.1 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr17:32961946 C>T maps to NM_207313.1 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr17:32961819 C>G maps to NM_207313.1 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:32954025 C>A maps to NM_207313.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr17:32962069 G>T maps to NM_207313.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr17:32953545 C>T maps to NM_207313.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:32964837 C>T maps to NM_207313.1 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr17:32961854 G>T maps to NM_207313.1 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr17:32954001 G>T maps to NM_207313.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:32955580 G>C did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr11:100863356 C>A maps to NM_032021.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:86802402 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:86868445 G>T maps to NM_022918.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr11:86868381 G>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:120201130 A>C maps to NM_001198670.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:120198203 G>T maps to NM_001198670.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:120198287 C>T maps to NM_001198670.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:142983813 G>A maps to NM_153345.1 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:142983157 C>A maps to NM_153345.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr7:142983073 G>C maps to NM_153345.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:134849483 C>A maps to NM_018295.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:134849421 C>A maps to NM_018295.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:48863334 C>A maps to NM_018273.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:159174648 A>G maps to NM_018342.4 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr4:159161475 C>T maps to NM_018342.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:159136418 A>G maps to NM_018342.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr4:159158781 G>T maps to NM_018342.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:42827826 G>T maps to ENST00000406159 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:42821920 G>T maps to ENST00000406159 G335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:42824589 G>C did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:42821934 G>T maps to ENST00000406159 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:5778497 C>A maps to NM_152784.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:5746012 C>A maps to NM_152784.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:36038270 G>T maps to NM_032635.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:36230815 G>A maps to NM_024660.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:36231334 G>A maps to NM_024660.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:36230868 G>A maps to NM_024660.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:36231352 G>A maps to NM_024660.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:10755444 A>G maps to NM_030969.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr19:55831930 G>A maps to NM_001085488.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr4:83417292 C>T maps to NM_001080506.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:66061838 C>A maps to NM_153266.3 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr4:122682831 C>A maps to NM_152399.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:122682990 G>T maps to NM_152399.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr4:38995480 C>A maps to NM_024943.1 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:21181906 G>T maps to ENST00000451578 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:87494825 C>T maps to NM_153354.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:87494879 C>A maps to NM_153354.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr5:87502891 T>A maps to NM_153354.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:87492305 C>A did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:87492306 T>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr23:109388103 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:109310585 G>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:56262445 G>T maps to NM_018475.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr5:82360852 G>C maps to NM_174909.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:109635560 C>G maps to NM_020141.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr7:112424367 A>G maps to NM_022484.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:112407371 G>A maps to NM_022484.4 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr7:112407326 C>T maps to NM_022484.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:112415279 C>A maps to NM_022484.4 G408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:216964783 C>A maps to NM_138390.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:216960770 C>T maps to NM_138390.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:216960748 C>T maps to NM_138390.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:216965042 C>A maps to NM_138390.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:75498463 G>T maps to NM_145254.1 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr5:72419373 G>T maps to NM_173490.6 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:72419664 C>T maps to NM_173490.6 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr5:72469216 G>C maps to NM_153217.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:72469360 C>G maps to NM_153217.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr5:72469549 G>T maps to NM_153217.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr5:72469210 G>T maps to NM_153217.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr5:72469540 G>T maps to NM_153217.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr4:949543 C>A maps to NM_032326.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr4:946153 G>A did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:944992 A>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:150498727 C>A maps to NM_018487.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:150500823 C>T maps to NM_018487.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr7:150501928 G>A maps to NM_018487.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr7:150500760 C>T maps to NM_018487.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:150488657 C>A maps to NM_014020.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:150490382 G>A maps to NM_014020.3 L131L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-44-3398-01A-01D-1105-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:150490204 C>A maps to NM_014020.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr2:120439040 C>T maps to NM_030577.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:120439109 G>A maps to NM_030577.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:120438965 G>A maps to NM_030577.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr2:120438941 G>T maps to NM_030577.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:39931219 G>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:39944150 G>T maps to NM_152390.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr11:62554926 C>T maps to NM_199337.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:675548 G>A maps to NM_152834.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:675508 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:675579 C>A maps to NM_152834.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr10:104233399 G>T maps to NM_024789.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr10:104233339 C>A maps to NM_024789.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr6:159028349 C>T maps to NM_020823.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr6:159028286 G>C maps to NM_020823.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:159006334 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:158957858 G>A maps to NM_020823.1 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:158994511 C>G maps to NM_020823.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:159029728 C>T maps to NM_020823.1 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:103414409 C>T maps to NM_144632.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:103414331 T>C maps to NM_144632.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:103431210 C>A maps to NM_144632.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr4:148545211 G>C did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr23:148692994 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:148690312 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:148690400 C>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:148693002 C>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:148690454 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:148690347 C>G did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:148693043 T>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr16:8890051 C>T maps to NM_015421.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:153247609 G>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:153247645 G>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:153247964 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:153247657 C>T did not map to a codon.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr20:48744619 G>A maps to NM_199203.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr12:72091177 C>A maps to NM_018279.3 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr12:72094702 G>T maps to NM_018279.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr4:166033913 C>A maps to NM_001100389.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:166009710 G>A maps to NM_001100389.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr12:57457953 G>A maps to NM_001130963.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:57457865 G>A maps to NM_001130963.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:15433804 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:15470661 T>A maps to NM_001004320.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:15430513 G>T maps to NM_001004320.1 C231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:15599800 C>T maps to NM_001004320.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:15599896 C>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr7:15240918 A>T maps to NM_001004320.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr7:15599800 C>A maps to NM_001004320.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:15584520 G>T maps to NM_001004320.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr7:15405793 C>T maps to NM_001004320.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr7:15405838 C>A maps to NM_001004320.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:19765325 G>A maps to NM_152774.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:220413949 G>T maps to NM_001005209.1 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:220412304 C>T maps to NM_001005209.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr2:220412408 G>A maps to NM_001005209.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:74365094 T>C maps to NM_013390.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr9:74345088 G>A maps to NM_013390.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr9:74365118 C>T maps to NM_013390.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:74305069 C>A maps to NM_013390.2 T1263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr9:74360075 G>A maps to NM_013390.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:130761605 C>A maps to NM_052913.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:130762208 G>T maps to NM_052913.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr6:130762163 C>T maps to NM_052913.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:130762883 G>T maps to NM_052913.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:130761971 T>A maps to NM_052913.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:130762082 G>A maps to NM_052913.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr6:130762770 C>A maps to NM_052913.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr6:130762586 C>T maps to NM_052913.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:130762589 C>A maps to NM_052913.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:130761698 C>A maps to NM_052913.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr6:130762913 C>A maps to NM_052913.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:130761974 C>T maps to NM_052913.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr6:130762061 C>A maps to NM_052913.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr1:29447668 G>T maps to NM_001003682.3 Y224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:9658629 C>T maps to NM_001130924.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr15:72698970 T>C maps to NM_001080462.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr15:72691080 C>T maps to NM_001080462.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr15:72690673 C>T maps to NM_001080462.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr15:72698973 C>A maps to NM_001080462.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1604798 C>A maps to NM_024600.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr16:1604882 C>A maps to NM_024600.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr1:212560332 G>A maps to NM_001198862.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:129813779 C>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr7:129825205 C>G maps to NM_032842.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:129841875 T>A maps to NM_032842.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:27258026 G>T maps to NM_017727.4 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr9:32784339 C>T maps to NM_212558.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:32784570 C>G maps to NM_212558.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:32784315 C>A maps to NM_212558.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:32784513 G>T maps to NM_212558.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr9:32784843 T>C maps to NM_212558.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:32784184 C>A maps to NM_212558.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:136573445 T>C maps to NM_025246.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:136573861 C>G maps to NM_025246.2 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:123754045 G>C maps to NM_001013743.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr11:123755299 G>T maps to NM_001013743.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:123754006 C>T maps to NM_001013743.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr11:123754036 G>T maps to NM_001013743.1 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr11:123753961 A>G maps to NM_001013743.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:67940295 G>A maps to NM_182526.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr14:67940628 G>C maps to NM_182526.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:75574073 T>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:118403764 G>T maps to NM_032780.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:63170400 G>A maps to NM_178505.6 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr10:63212758 C>G maps to NM_178505.6 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr10:63212677 G>A maps to NM_178505.6 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr23:15657826 C>G did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:75969071 G>A maps to NM_018247.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:102968776 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:102968619 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:102968695 C>T did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:102968775 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:102968922 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:16799109 G>A maps to NM_024074.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr19:16798998 C>T maps to NM_024074.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:16797131 C>G maps to NM_024074.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr9:108536210 G>A maps to NM_018112.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr1:32557578 C>A maps to NM_018056.2 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:32568033 C>T maps to NM_018056.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:32557332 C>G maps to NM_018056.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:32542877 C>T maps to NM_018056.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:32542910 C>G maps to NM_018056.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:9305014 G>A maps to NM_015012.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:194313774 C>A maps to ENST00000273580 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:100275602 G>T did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:34657370 A>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:34675042 A>T did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:34648554 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:54266522 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:54262707 C>G maps to NM_018087.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:54266441 G>C maps to NM_018087.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:57915654 G>T did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr12:64202607 G>T maps to NM_014254.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr12:64202607 G>A maps to NM_014254.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:64173796 C>T maps to NM_014254.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:15541736 G>T maps to NM_018022.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:1849836 C>A maps to NM_178545.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:1849479 G>A maps to NM_178545.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:92033632 C>G did not map to a codon.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr8:92008880 C>G did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:92007982 G>A maps to NM_018710.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr8:92052929 G>A maps to NM_018710.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr14:20927363 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:20926798 G>A maps to NM_001100814.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:25785239 C>T maps to NM_018202.4 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:25824923 C>T maps to NM_018202.4 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:18731226 C>T maps to NM_012109.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:18729266 C>T maps to NM_012109.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:18724996 G>T maps to NM_012109.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:18724956 T>C maps to NM_012109.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr1:55457595 T>A maps to NM_182532.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr15:43476675 G>T maps to NM_024956.3 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:226054363 C>A maps to NM_014698.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:44121557 C>T maps to NM_018426.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr6:44119702 C>G maps to NM_018426.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:44116018 G>T maps to NM_018426.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr6:44107278 G>T maps to NM_018426.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:44122118 A>T maps to NM_018426.1 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:44107258 C>T maps to NM_018426.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr6:44102329 C>G maps to NM_018426.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr14:77685838 A>G did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr14:77709293 A>T maps to NM_020431.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:77710723 G>T maps to NM_020431.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr14:77715174 G>C maps to NM_020431.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr8:91643779 C>T maps to NM_001008495.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr8:125343016 T>A maps to NM_194291.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:29924384 A>G maps to NM_016127.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:29924380 C>A maps to NM_016127.4 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:94797463 C>T maps to NM_153704.5 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr8:94767324 G>T maps to NM_153704.5 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr8:94807656 G>T maps to NM_153704.5 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr8:94767312 C>A maps to NM_153704.5 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:94767280 G>T maps to NM_153704.5 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:46159474 G>A maps to NM_016486.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:133726419 G>T maps to ENST00000395406 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:133734361 C>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr8:133740122 T>C maps to ENST00000395406 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:133764149 G>T maps to ENST00000395406 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:133764239 G>A maps to ENST00000395406 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr10:45430218 C>T maps to NM_001123376.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr8:109797064 G>C maps to NM_153015.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:109796729 G>T maps to NM_153015.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr11:702963 A>G maps to ENST00000449452 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr1:205053358 G>A maps to NM_203376.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:16070920 C>A maps to NM_001013641.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:16073380 C>A maps to NM_001013641.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:16070899 G>T maps to NM_001013641.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:18722736 C>T maps to NM_153347.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr11:18723357 A>C maps to NM_153347.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:42529729 C>G maps to ENST00000389834 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:112839075 C>T maps to NM_032824.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr17:7758929 C>A maps to NM_203411.1 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:424343 C>T maps to NM_021259.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr16:424295 G>A maps to NM_021259.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:424376 C>A maps to NM_021259.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr9:35853737 G>T maps to NM_001042590.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:35852852 C>T maps to NM_001042590.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:136384028 G>T maps to NM_001080483.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:136380687 C>T maps to NM_001080483.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr1:201115926 C>A maps to ENST00000421960 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr14:74876054 C>T maps to NM_001105579.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr14:74874384 G>T maps to NM_001105579.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr14:74874276 C>T maps to NM_001105579.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr20:24565622 C>A maps to NM_024893.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr20:24565544 G>A maps to NM_024893.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr20:24524041 G>C maps to NM_024893.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr20:24523999 C>A maps to NM_024893.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr20:24646014 C>T maps to NM_024893.1 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr20:24523732 C>A did not map to a codon.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr17:48355985 C>T maps to NM_153229.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr17:48356302 C>T maps to NM_153229.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr17:31267869 G>T maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr11:8970007 A>G maps to NM_020644.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:69077406 T>A maps to NM_007114.2 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:46751144 G>A maps to NM_147196.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:28656338 G>A maps to NM_206832.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr17:28651903 G>A maps to NM_206832.1 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:28651840 A>T maps to NM_206832.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:4292731 G>T maps to NM_144615.2 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8512-01A-11D-2393-08 chr19:4292688 G>T maps to NM_144615.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr19:4292882 C>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr23:154736667 G>A did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:154736777 C>A did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:154736725 A>G did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:154736680 G>T did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:154743761 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:154736657 T>C did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:154736706 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:154754266 G>C did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:154741369 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:154736620 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr9:100353717 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr9:100326389 G>C maps to NM_003275.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr9:100331256 C>T maps to NM_003275.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:52155204 G>T maps to NM_014547.4 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr15:52192419 G>A maps to NM_014547.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr12:98938260 T>A maps to NM_001032283.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr12:98927618 A>T maps to NM_003276.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:33134916 C>T maps to NM_001039770.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr4:68780440 G>A maps to NM_182606.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr4:68810290 G>A maps to NM_182606.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:68788573 G>T maps to NM_182606.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:68810256 G>A maps to NM_182606.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:69094993 C>T maps to NM_182502.3 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:69097042 T>G maps to NM_182502.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:69097024 C>A maps to NM_182502.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr4:69097069 G>T maps to NM_182502.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr4:69095206 G>C maps to NM_182502.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:69111266 A>C did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr4:69111267 C>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68725317 G>T maps to NM_004262.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr4:68699043 G>T maps to NM_004262.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:68708298 G>T maps to NM_004262.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:68725386 A>T maps to NM_004262.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr4:69342096 C>T maps to NM_014058.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:68964602 A>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:68934400 G>T maps to NM_207407.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:68956359 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr4:68930430 G>T maps to NM_207407.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:68938039 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr4:68964643 C>A maps to NM_207407.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr4:68919626 C>G maps to NM_207407.2 *439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr12:51281253 C>A maps to NM_182559.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr12:51252603 T>C maps to NM_182559.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr11:117787939 C>A maps to ENST00000413475 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6212-01A-11D-1753-08 chr11:117784511 G>A maps to ENST00000413475 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:117779459 C>A maps to ENST00000413475 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr21:19642342 G>T maps to NM_002772.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr21:19704407 C>A maps to NM_002772.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:19732103 C>A maps to NM_002772.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr21:19666684 C>T maps to NM_002772.2 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr21:19775897 G>A maps to NM_002772.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr21:19698821 G>T maps to NM_002772.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr21:19666591 C>A maps to NM_002772.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr21:19725369 C>G did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr21:19744510 A>T maps to NM_002772.2 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr21:19770545 G>A maps to NM_002772.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr21:19687574 T>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:19698806 C>T maps to NM_002772.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr21:19687565 G>A maps to NM_002772.2 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr21:42861482 C>G maps to NM_001135099.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr21:42852431 C>A maps to NM_001135099.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr21:42866465 C>A maps to NM_001135099.1 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:42861482 C>A maps to NM_001135099.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr21:43805593 G>T maps to ENST00000380399 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:117984016 G>T maps to NM_019894.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:117969813 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr11:117979591 G>T maps to NM_019894.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr11:113558997 T>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:113558996 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr11:113568012 C>A maps to NM_030770.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:37494470 G>T maps to ENST00000381792 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr22:37462202 G>A maps to ENST00000381792 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr22:37485703 G>T maps to ENST00000381792 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr22:37482362 G>A maps to ENST00000381792 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:111780675 G>T maps to ENST00000443106 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr3:111785290 C>A maps to ENST00000443106 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:111797685 C>A maps to ENST00000443106 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr3:111766637 G>C maps to ENST00000443106 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:111785272 C>T maps to ENST00000443106 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:111795983 C>T maps to ENST00000443106 H727H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:2410316 C>T maps to NM_182973.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr19:2405396 G>A maps to NM_182973.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:2389902 C>G maps to NM_182973.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr19:2399123 G>T maps to NM_182973.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:2408536 C>A maps to NM_182973.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:85133173 C>G maps to NM_021103.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:29904682 C>T maps to NM_001193451.1 W285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:29670371 G>T maps to NM_001193451.1 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:29669311 G>T maps to NM_001193451.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:29904704 G>T maps to NM_001193451.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:29725151 C>G did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr12:29671460 C>T maps to NM_001193451.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr12:29908640 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:29904702 C>A maps to NM_001193451.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:29664977 T>A maps to NM_001193451.1 K836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr12:29920926 C>A maps to NM_001193451.1 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:29911707 C>A maps to NM_001193451.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr12:29659853 C>G maps to NM_001193451.1 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:29904702 C>A maps to NM_001193451.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:29670431 G>T maps to NM_001193451.1 Y699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr12:83526011 G>T maps to NM_152588.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr12:83250787 G>T did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr12:88589116 T>C maps to NM_181783.3 N812N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr12:88586449 G>T maps to NM_181783.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:88584228 G>C did not map to a codon.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr12:88548079 G>T maps to NM_181783.3 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:88570061 G>A maps to NM_181783.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101287160 G>A maps to NM_032813.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:101321049 T>C did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr13:101278088 C>T maps to NM_032813.2 R548R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-69-7979-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr18:66344376 C>T maps to NM_019022.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr20:7964453 T>C maps to NM_021156.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:117838395 C>T maps to NM_002160.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr9:117838356 C>T maps to NM_002160.2 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr9:117826312 G>T maps to NM_002160.2 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:117800546 G>T maps to NM_002160.2 G1835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:117826977 A>C maps to NM_002160.2 Y1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr9:117852844 G>A maps to NM_002160.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr9:117826312 G>A maps to NM_002160.2 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr9:117800573 C>T maps to NM_002160.2 V1826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr9:117848659 G>A maps to NM_002160.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr17:26666552 G>A maps to NM_021137.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr14:103596403 G>T maps to NM_006291.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BD-01A-11D-A24D-08 chr14:103593768 C>T maps to NM_006291.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr14:103596136 C>T maps to NM_006291.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:138199922 G>T maps to NM_006290.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr6:138199567 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr6:138199844 G>A maps to NM_006290.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr2:152222681 C>A maps to NM_007115.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8087-01A-11D-2238-08 chr8:23049392 G>T maps to NM_003844.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr8:23054711 C>A maps to NM_003844.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr8:22880393 A>G maps to NM_003842.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:22926372 G>T maps to NM_003842.4 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr18:60036548 G>T maps to NM_003839.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:60036185 G>T maps to NM_003839.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr8:119945314 G>C maps to NM_002546.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:119945464 G>C maps to NM_002546.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:3070411 C>A maps to NM_016639.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:16855817 G>A maps to NM_012452.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr17:16875340 G>A maps to NM_012452.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:42321442 G>A maps to NM_052945.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr22:42321412 A>G maps to NM_052945.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr22:42322153 C>A maps to NM_052945.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:2489851 C>T maps to NM_003820.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:12061592 T>A maps to NM_001192.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr13:24200844 G>C did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr13:24243245 C>T maps to NM_018647.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr13:24190103 G>T maps to NM_018647.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr13:24242197 T>C maps to NM_018647.2 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr12:6439175 G>A maps to NM_001065.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:12248920 A>T maps to NM_001066.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:12252976 G>T maps to NM_001066.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:6525226 C>T maps to ENST00000355862 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:6521751 G>C maps to ENST00000355862 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:1148429 G>A maps to NM_003327.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:1149498 C>A maps to NM_003327.3 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:1147361 G>A maps to NM_003327.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:12164496 C>T maps to NM_001243.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:12144555 C>A maps to NM_001243.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:12157230 G>T maps to NM_001243.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr1:12186059 C>T maps to NM_001243.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:12186293 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:12202461 G>T maps to NM_001243.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:12183825 C>A maps to NM_001243.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:12175697 C>A maps to NM_001243.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:7995186 T>A maps to NM_001561.5 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:7993276 G>A maps to NM_001561.5 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:7993220 C>G did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr3:172224320 G>A maps to ENST00000382750 D269D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-67-6215-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr3:172241057 G>A maps to ENST00000382750 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr13:43181006 C>T maps to NM_003701.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr13:43180709 G>T maps to NM_003701.3 G204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:7463671 G>C maps to NM_003808.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr9:117553072 G>A maps to NM_005118.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:173010769 G>A maps to NM_005092.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:173019956 C>T maps to NM_005092.3 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:173155819 C>T maps to NM_003326.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:173155711 C>T maps to NM_003326.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:170858244 C>A maps to NM_015028.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr3:170811639 C>T maps to NM_015028.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:170800135 G>A maps to NM_015028.2 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:170843811 C>T maps to NM_015028.2 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:170857324 T>C maps to NM_015028.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr3:171177824 G>A maps to NM_015028.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr5:150422187 C>T maps to NM_006058.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:150444521 T>C maps to NM_006058.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:2757800 C>G maps to NM_024309.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr4:2757761 G>A maps to NM_024309.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:195593857 C>G maps to NM_001010938.1 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:195594627 C>A maps to NM_001010938.1 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr3:195611829 G>A maps to NM_001010938.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:195594533 C>A maps to NM_001010938.1 E942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:9413470 C>T maps to NM_003747.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:9609135 T>G maps to NM_003747.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:57080340 G>C maps to NM_033396.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:57068045 G>A maps to NM_033396.2 Q1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr11:57068419 G>A maps to NM_033396.2 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr11:57089341 G>A maps to NM_033396.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr11:57070016 G>A maps to NM_033396.2 S1533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr11:57085326 G>A maps to NM_033396.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr11:57080490 A>G maps to NM_033396.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr10:93608226 A>T maps to NM_025235.3 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:93596718 G>T maps to NM_025235.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr10:93608351 A>T maps to NM_025235.3 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:93593608 G>T did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:99854594 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:99849301 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:99852499 G>C did not map to a codon.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr23:99854658 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:175048793 G>C maps to NM_022093.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:175049309 C>T maps to NM_022093.1 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:175066707 C>T maps to NM_022093.1 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:175048829 G>T maps to NM_022093.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:175092569 G>A maps to NM_022093.1 W895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:175046688 C>T maps to NM_022093.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175053003 A>T maps to NM_022093.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:175067699 G>A maps to NM_022093.1 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr1:175092533 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:175046638 G>T maps to NM_022093.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:175097169 G>A maps to NM_022093.1 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr1:175086137 G>A maps to NM_022093.1 W728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175048553 C>T maps to NM_022093.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:175049401 C>A maps to NM_022093.1 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:175067609 G>T maps to NM_022093.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr1:175054539 G>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:175087838 G>A maps to NM_022093.1 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr1:175097241 C>T maps to NM_022093.1 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:175067501 G>A maps to NM_022093.1 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr1:175092698 T>G maps to NM_022093.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr1:175066814 G>A maps to NM_022093.1 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:175067616 G>T maps to NM_022093.1 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:175066574 G>T maps to NM_022093.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:175066704 G>T maps to NM_022093.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:175046646 C>T maps to NM_022093.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr1:175116203 C>T maps to NM_022093.1 F1299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:175046811 C>T maps to NM_022093.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:175067499 C>A maps to NM_022093.1 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:175063277 G>T maps to NM_022093.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:175106084 C>A maps to NM_022093.1 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:175097286 C>A maps to NM_022093.1 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:175105026 G>A maps to NM_022093.1 W1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:175054577 G>A maps to NM_022093.1 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr1:175106086 G>A maps to NM_022093.1 R1186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:175048694 C>A maps to NM_022093.1 C212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr3:52486122 G>A maps to NM_003280.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:1862434 A>T maps to ENST00000381906 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:55666159 C>A maps to ENST00000344887 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:55665550 G>T maps to ENST00000344887 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:55666155 C>A maps to ENST00000344887 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:55665403 G>A maps to ENST00000344887 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:74834795 C>G maps to NM_001112808.2 S572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:74902191 C>T maps to NM_001112808.2 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:74835263 G>A maps to NM_001112808.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr1:74902156 G>T did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:74929196 C>A maps to NM_001112808.2 S796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:55653267 A>T maps to NM_003283.4 L50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:201334413 C>A maps to ENST00000421663 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:201334384 C>A maps to ENST00000421663 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:201334423 C>G maps to ENST00000421663 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:1953716 C>A maps to ENST00000397301 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:1953726 G>T maps to ENST00000397301 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr11:1955807 C>A maps to ENST00000397301 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:217724643 C>T maps to NM_003284.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr5:72201203 A>G maps to NM_002270.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:12816140 G>C maps to NM_001136196.1 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr7:128610228 G>C maps to ENST00000471166 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr7:128630044 C>A maps to ENST00000471166 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr7:128630054 T>A maps to ENST00000471166 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:128612602 C>A maps to ENST00000471166 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:175360439 C>A maps to NM_003285.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:175375583 C>T maps to NM_003285.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:175304847 C>A maps to NM_003285.2 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325527 G>T maps to NM_003285.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:175325589 C>A maps to NM_003285.2 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:175331942 C>A maps to NM_003285.2 G904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:175331943 C>A maps to NM_003285.2 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:175372465 C>T maps to NM_003285.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr1:175362955 G>T maps to NM_003285.2 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:175372525 C>A maps to NM_003285.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:175299341 G>A maps to NM_003285.2 Q1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:175362996 C>T maps to NM_003285.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:175372401 C>A maps to NM_003285.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:175328853 A>G maps to NM_003285.2 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:175372390 G>T maps to NM_003285.2 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr1:175372341 G>A maps to NM_003285.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:175375610 G>T maps to NM_003285.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:175355362 G>A maps to NM_003285.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr1:175362963 C>T maps to NM_003285.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr1:175355327 G>A maps to NM_003285.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:175355186 G>T maps to NM_003285.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:175372483 G>T maps to NM_003285.2 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:175372558 G>A maps to NM_003285.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:175304847 C>A maps to NM_003285.2 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:175375784 C>G maps to NM_003285.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr1:175335275 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:175335274 C>G did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:175304874 G>A maps to NM_003285.2 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr1:175336416 A>T maps to NM_003285.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:175334161 C>A maps to NM_003285.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:175304934 C>T maps to NM_003285.2 Q1181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:175335227 G>T maps to NM_003285.2 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:175328814 G>T maps to NM_003285.2 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:175323590 C>A maps to NM_003285.2 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr1:175365872 C>T maps to NM_003285.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:175365731 G>A maps to NM_003285.2 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:5410698 C>A maps to NM_001080495.2 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr7:5360179 G>A maps to NM_001080495.2 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:5352382 C>T maps to NM_001080495.2 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr7:5410645 T>A maps to NM_001080495.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:5355641 C>A maps to NM_001080495.2 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr7:5427960 G>A maps to NM_001080495.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr16:24834869 C>T maps to NM_014494.2 S1877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr16:24828155 A>G maps to NM_014494.2 P1617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr16:24800802 A>G maps to NM_014494.2 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr22:40661742 A>G maps to ENST00000454349 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr22:40711401 G>T maps to ENST00000454349 L1612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr22:40661418 C>T maps to ENST00000454349 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr22:40696556 G>C maps to ENST00000454349 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr2:218713342 G>A maps to NM_022648.4 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:218700934 C>G did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:218712608 G>A maps to NM_022648.4 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:218713784 T>A maps to NM_022648.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:218686626 T>G maps to NM_022648.4 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:218712410 G>A maps to NM_022648.4 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:218677118 C>A maps to NM_022648.4 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:47440029 C>T maps to NM_022748.11 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:47343037 C>A maps to NM_022748.11 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:47343136 G>T maps to NM_022748.11 P956P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr7:47342883 G>A maps to NM_022748.11 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:47467915 G>C maps to NM_022748.11 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr17:38636950 C>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr17:38643290 C>A maps to NM_032865.5 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr17:38636076 G>A maps to NM_032865.5 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr6:32011607 G>A maps to ENST00000375244 I3816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:32029429 C>A maps to ENST00000375244 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:32023847 A>T maps to ENST00000375244 P2749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:32046819 C>T maps to ENST00000375244 V1455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:32018015 C>T maps to ENST00000375244 L3066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:32020720 C>T maps to ENST00000375244 P2947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:32025990 T>A maps to ENST00000375244 K2557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:32053671 C>A maps to ENST00000375244 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:32035473 G>T maps to ENST00000375244 R2170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr6:32036611 G>A maps to ENST00000375244 V1963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr6:32023711 C>A maps to ENST00000375244 E2795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:32017940 C>A maps to ENST00000375244 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr6:32011570 G>T maps to ENST00000375244 R3829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr6:32036263 G>A maps to ENST00000375244 T2041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:32012930 C>A maps to ENST00000375244 T3593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:32020581 G>A maps to ENST00000375244 Q2994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:32046971 G>A maps to ENST00000375244 Q1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr6:32036218 G>A maps to ENST00000375244 Y2056Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:32021387 G>T maps to ENST00000375244 T2856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr6:32023793 G>A maps to ENST00000375244 T2767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr17:48940955 G>A maps to NM_005749.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr17:48941170 G>A maps to NM_005749.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:45807213 C>T maps to NM_025077.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr11:1316877 T>C maps to ENST00000382211 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:1298460 G>A maps to ENST00000382211 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr22:35719781 C>T maps to ENST00000451197 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr22:35729395 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:52991147 G>T maps to NM_005486.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr17:52990024 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:52990139 A>T maps to NM_005486.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr17:17764828 A>G maps to NM_001082968.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr17:17801987 C>T maps to NM_001082968.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:235277205 T>C maps to NM_014765.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr14:58862761 C>G maps to NM_207377.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr14:58863043 G>A maps to NM_207377.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr20:43585111 C>A maps to NM_006809.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:45404027 C>T maps to NM_006114.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:161198066 G>T maps to NM_032174.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr20:39741459 G>A maps to NM_003286.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr20:39750424 G>A maps to NM_003286.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:144411636 C>T maps to NM_052963.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:144399932 G>C maps to NM_052963.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38545890 C>T maps to ENST00000357601 K1529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr17:38562658 C>A maps to ENST00000357601 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:25665828 G>C maps to ENST00000264331 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr3:25654004 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:25639968 C>G did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr22:22323137 A>G maps to NM_003935.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr3:133342988 G>A maps to NM_007027.3 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:133368262 G>A maps to NM_007027.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:133368280 C>A maps to NM_007027.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr3:133363055 T>C maps to NM_007027.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:132586259 G>A maps to ENST00000437532 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr9:132585012 C>T maps to ENST00000437532 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr9:132576286 C>A maps to ENST00000437532 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:179887218 A>T maps to ENST00000398836 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr1:179887121 C>T maps to ENST00000398836 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:179815259 C>A maps to NM_145034.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr1:179833975 T>C maps to NM_022347.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr9:132571213 G>T maps to NM_014506.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr9:132566478 C>G maps to NM_014506.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:59720702 G>A maps to NM_014729.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:42695415 C>A maps to ENST00000348077 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr20:42694512 C>G maps to ENST00000348077 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr20:42694686 G>T maps to ENST00000348077 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr20:42695473 G>T maps to ENST00000348077 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr20:42679965 G>T maps to ENST00000348077 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr20:42574566 C>A maps to ENST00000348077 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr20:42635365 C>A maps to ENST00000348077 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr20:42694461 G>T maps to ENST00000348077 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:42694746 G>A maps to ENST00000348077 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr20:42635371 C>T maps to ENST00000348077 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr20:42694449 C>A maps to ENST00000348077 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr20:42680028 C>A maps to ENST00000348077 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr20:42680133 C>A maps to ENST00000348077 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:52484374 C>T maps to ENST00000407228 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:21963404 G>A maps to NM_014828.2 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr14:21961227 C>T maps to NM_014828.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:7578554 C>A did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:7578257 C>A maps to NM_001126112.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7577141 C>A maps to NM_001126112.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:7577142 C>T maps to NM_001126112.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr17:7577530 G>A maps to NM_001126112.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr17:7579493 T>A maps to NM_001126112.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr17:7573966 G>A maps to NM_001126112.1 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr17:7577156 T>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:7573981 C>A maps to NM_001126112.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr17:7579527 C>T maps to NM_001126112.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:7578223 T>A maps to NM_001126112.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr17:7578289 C>A did not map to a codon.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:7577084 C>A maps to NM_001126112.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr17:7573990 C>A maps to NM_001126112.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7726-01A-11D-2167-08 chr17:7578506 G>T maps to NM_001126112.1 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr17:7579532 G>A maps to NM_001126112.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr17:7574011 C>A maps to NM_001126112.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr17:7577017 C>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:7578554 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:7573975 T>A maps to NM_001126112.1 K351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr17:7577572 G>T maps to NM_001126112.1 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:7578436 G>A maps to NM_001126112.1 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr17:7577508 C>A maps to NM_001126112.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr17:7579590 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr17:7579309 A>T did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr17:7579524 G>A maps to NM_001126112.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr11:128807550 G>T maps to ENST00000263583 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:43771674 C>T maps to NM_001141980.1 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:43769856 G>A maps to NM_001141980.1 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr15:43738702 C>A maps to NM_001141980.1 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr15:43699768 C>T did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:223990465 C>T maps to NM_001031685.2 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:223985992 C>G maps to NM_001031685.2 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:223990486 C>G maps to NM_001031685.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:44958878 C>A maps to NM_006034.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr20:33298101 C>T maps to NM_021202.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:45315856 T>A maps to NM_033550.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr20:44003714 G>A maps to NM_014477.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:189590691 G>A maps to NM_003722.4 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr3:189526251 A>G maps to NM_003722.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:189612210 C>A maps to NM_003722.4 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr1:3599744 G>A did not map to a codon.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr6:83074866 C>T maps to NM_006670.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr6:83075379 C>T maps to NM_006670.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr6:83075280 G>T maps to NM_006670.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113710466 C>T maps to NM_001143819.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715133 C>T maps to NM_001143819.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113715146 C>T maps to NM_001143819.1 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr12:113717995 C>T maps to NM_001143819.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr12:113716623 G>A maps to NM_001143819.1 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr12:113722425 G>A maps to NM_001143819.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:68846200 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:68846406 C>T maps to NM_139075.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr11:68853219 G>A maps to NM_139075.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:80976711 C>A did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr8:80976820 C>T maps to NM_001025252.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:125541339 G>T did not map to a codon.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:62505073 C>T maps to NM_199360.1 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:62521252 A>T maps to NM_199360.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr20:62505103 C>G maps to NM_199360.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr9:6328729 C>G maps to NM_033516.5 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:6328618 C>G maps to NM_033516.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:6328768 G>T maps to NM_033516.5 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr9:6328607 A>C maps to NM_033516.5 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:18057530 T>G maps to ENST00000341556 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr11:18042605 C>A maps to ENST00000341556 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:18051102 A>G maps to ENST00000341556 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr11:18048161 A>T maps to ENST00000341556 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr12:72372741 C>T maps to ENST00000389376 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:72338117 G>T maps to ENST00000389376 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr12:72338364 G>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr12:72372747 G>T maps to ENST00000389376 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr12:6976726 C>T maps to NM_001159287.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr12:6978852 T>C maps to NM_001159287.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr7:144380018 G>T maps to NM_022445.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr7:144380066 A>T maps to NM_022445.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:144245631 C>A maps to NM_022445.3 G189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr15:63335042 G>A maps to ENST00000357980 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr1:154148673 T>C maps to NM_001043351.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr1:154141851 G>C maps to ENST00000328159 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:154163706 C>T maps to ENST00000271850 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:154142942 T>C maps to NM_001043351.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:16186907 G>T maps to NM_001145160.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:1426847 C>A maps to NM_000547.5 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:1499812 G>T maps to NM_000547.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:1459996 G>T maps to NM_000547.5 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:1426886 C>A maps to NM_000547.5 Y55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:1499823 C>A maps to NM_000547.5 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:1457591 C>A maps to NM_000547.5 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr2:1480943 C>G maps to NM_000547.5 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:1418188 G>A maps to NM_000547.5 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:1546230 G>T maps to NM_000547.5 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:1481039 G>T maps to NM_000547.5 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:1418260 A>G maps to NM_000547.5 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:1440132 C>A maps to NM_000547.5 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:1480949 C>T maps to NM_000547.5 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr2:1488399 C>A maps to NM_000547.5 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr11:6637558 C>A maps to ENST00000453338 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:6637570 C>A maps to ENST00000453338 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr13:103317144 G>T maps to ENST00000376052 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr13:103301781 A>T maps to ENST00000376052 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:103249426 C>T maps to ENST00000376052 H13H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr13:103301760 A>T maps to ENST00000376052 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr13:103249522 G>A maps to ENST00000376052 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr13:103309519 G>T maps to ENST00000376052 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr13:103290629 C>A maps to ENST00000376052 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr13:103292685 A>T maps to ENST00000376052 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr13:103289511 G>T maps to ENST00000376052 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr13:103280274 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr5:678031 G>A maps to NM_007030.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr14:21498832 C>A maps to NM_173846.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr14:21499291 G>T maps to NM_173846.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:186306191 C>A maps to NM_003292.2 E1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:186326649 G>A maps to NM_003292.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr1:186307307 T>A maps to NM_003292.2 R1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:186315293 T>C maps to NM_003292.2 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:186322930 T>G maps to NM_003292.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr1:186329116 A>C maps to NM_003292.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:186344043 C>T maps to NM_003292.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:186310291 C>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:186310225 G>A maps to NM_003292.2 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:186302286 G>T maps to NM_003292.2 R1808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr3:127292396 T>A maps to NM_001136053.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:127294631 G>T maps to NM_001136053.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:189028213 G>T maps to NM_198485.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr16:1308350 C>T maps to NM_012217.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:1306325 G>A maps to NM_012217.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:1306298 C>A maps to NM_012217.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr16:1306673 G>T maps to NM_012217.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr16:1308195 G>T maps to NM_012217.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr16:1308349 C>A maps to NM_012217.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:1306311 C>T maps to NM_012217.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr16:1272751 G>T maps to NM_012467.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:65705739 C>T maps to NM_003596.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr22:26936822 G>A maps to NM_003595.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr22:26936941 C>A maps to NM_003595.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr21:10941906 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:10959796 C>G maps to NM_199261.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr21:10920155 C>A maps to NM_199261.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr21:10934114 T>A maps to NM_199261.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:10952929 T>C maps to NM_199261.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:10970031 G>C maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr21:10934985 C>G maps to NM_199261.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr21:10916475 C>A did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10933879 G>T maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr21:10951374 G>A maps to NM_199261.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr21:10910327 C>G maps to NM_199261.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr21:10969089 G>T maps to NM_199261.2 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:10934070 G>T maps to NM_199261.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr21:10959796 C>G maps to NM_199261.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr21:10944711 G>A maps to NM_199261.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr21:10934046 G>A maps to NM_199261.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr21:10941906 C>G did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr21:10920081 A>G did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr21:10920082 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr21:10908883 T>A maps to NM_199261.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr21:10934070 G>T maps to NM_199261.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr21:10933855 G>T maps to NM_199261.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr21:10959759 C>A maps to NM_199261.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr21:10942711 T>A maps to NM_199261.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr21:10970058 T>A maps to NM_199261.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr21:10921972 A>G maps to NM_199261.2 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:20010404 G>A maps to NM_199254.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr13:20024285 G>C maps to NM_199254.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr20:30370061 C>T maps to ENST00000340513 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:30386190 C>T maps to ENST00000340513 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr20:30345326 C>T maps to ENST00000340513 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:30365314 C>T maps to ENST00000340513 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:30345356 A>T maps to ENST00000340513 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr20:30363694 G>T maps to ENST00000340513 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:67188569 G>A maps to NM_003789.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:67190464 C>A maps to NM_003789.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr9:123675734 C>G maps to NM_001190945.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr9:139793299 C>A maps to ENST00000359662 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr9:139794920 C>T maps to ENST00000359662 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr2:239234518 C>T maps to NM_015650.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:239257489 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:239237913 G>C maps to NM_015650.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7143-01A-11D-2036-08 chr6:111912596 G>C maps to ENST00000340026 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr6:111896951 C>G maps to ENST00000340026 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr1:209955489 C>A maps to NM_025228.2 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:209951492 G>A maps to NM_025228.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:209951495 G>A maps to NM_025228.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:209933635 C>A maps to NM_025228.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:209948948 C>A maps to NM_025228.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr1:211526710 A>T maps to ENST00000427925 K44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:211545755 C>T maps to ENST00000427925 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:211534058 T>C maps to ENST00000427925 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr11:36520068 A>G maps to NM_145803.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr11:36511948 G>A maps to NM_145803.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr11:36511801 G>A maps to NM_145803.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:2225514 G>C maps to NM_032271.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr16:2223982 G>T maps to NM_032271.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr12:112578651 C>T maps to NM_006700.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:49866941 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:49866640 G>A maps to NM_005879.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:42229534 A>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr3:42233087 G>A maps to NM_001042646.1 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:42260986 G>A maps to NM_001042646.1 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:42166915 G>T maps to NM_001042646.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:42133017 C>G maps to NM_001042646.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:202245492 T>A maps to NM_015049.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr8:71496018 C>A maps to NM_014294.5 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr8:71508555 C>A maps to NM_014294.5 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:118006122 C>A maps to NM_152402.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr4:118005684 C>A maps to NM_152402.2 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:118006109 G>C maps to NM_152402.2 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:52400607 G>A maps to NM_012288.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:52368024 G>T maps to NM_012288.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr3:36873405 C>G maps to NM_014831.2 S2512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:36899466 G>C maps to NM_014831.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr3:36896850 G>A maps to NM_014831.2 I1410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:36896946 C>G maps to NM_014831.2 S1378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:36896757 G>A maps to NM_014831.2 F1441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr3:36875410 C>T did not map to a codon.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr16:3725360 G>A maps to NM_016292.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:3740935 G>A maps to NM_016292.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:3724426 C>A maps to NM_016292.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr17:7834427 T>C maps to NM_001166621.1 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr17:7833932 C>A maps to NM_001166621.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr21:45522848 C>T maps to NM_003274.4 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr21:45522662 C>T maps to NM_003274.4 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:36603507 G>A maps to NM_014408.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:36605383 G>A maps to NM_014408.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr11:118889680 G>A did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr11:118889680 G>A did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:7747567 G>T maps to NM_001042461.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:7747564 C>T maps to NM_001042461.1 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:141294040 T>A maps to NM_031466.5 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:141294004 G>A maps to NM_031466.5 I797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:141321446 C>A maps to NM_031466.5 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr8:141370269 C>A maps to NM_031466.5 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr8:141297728 C>A maps to NM_031466.5 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:108572675 C>T maps to NM_016388.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:108572489 C>A maps to NM_016388.2 C109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr10:17204236 C>G did not map to a codon.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:123709669 C>A maps to NM_006073.2 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr6:123539832 T>C maps to NM_006073.2 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:123714766 A>G did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:123591003 G>T maps to NM_006073.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:123573560 T>C maps to NM_006073.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:123673699 G>T maps to NM_006073.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr6:41250403 T>C maps to NM_018643.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr6:41129199 G>A maps to NM_018965.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr6:41121751 G>A maps to NM_178174.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr6:41162311 G>T maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr6:41166017 G>T maps to ENST00000373108 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:41165958 G>T maps to ENST00000373108 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:41162353 G>T maps to ENST00000373108 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:41162308 C>T maps to ENST00000373108 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr6:41204318 G>C maps to NM_198153.2 *201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr6:41197839 C>A maps to NM_198153.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr6:41196630 C>A maps to NM_198153.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42235933 C>A maps to NM_033502.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr6:42236656 C>A maps to NM_033502.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr6:42231108 G>A maps to NM_033502.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr6:42236005 C>A maps to NM_033502.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr23:152710690 C>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:152710800 G>C did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:152710395 G>A did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:152710394 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:152710478 C>G did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr12:73012669 G>T did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr12:72680484 G>T maps to NM_013381.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr12:73012715 C>A maps to NM_013381.2 Y744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr12:73046137 A>T maps to NM_013381.2 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr12:72936069 G>C did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:72667124 G>A maps to NM_013381.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr12:73056952 T>G maps to NM_013381.2 L1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:73015531 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:72771777 C>A maps to NM_013381.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr8:110100052 C>A maps to NM_003301.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:110099839 C>T maps to NM_003301.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr8:110099854 G>T maps to NM_003301.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:110131488 C>T maps to NM_003301.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr8:110131365 C>T maps to NM_003301.4 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:110131275 G>T did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr8:110100364 C>A maps to NM_003301.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:120884160 C>T maps to NM_016399.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126445603 C>T maps to NM_025195.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr8:126448608 G>T maps to NM_025195.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr8:126448347 G>T maps to NM_025195.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:126448526 C>T maps to NM_025195.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:12863555 G>C maps to NM_021643.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:12880877 G>A maps to NM_021643.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr20:368839 G>A maps to ENST00000422053 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr6:30128629 G>T maps to NM_006778.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30122174 C>T maps to NM_006778.3 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:30128458 G>T maps to NM_006778.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:228582507 C>A maps to NM_145214.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr1:228582543 C>A maps to NM_145214.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr1:228582918 A>T maps to NM_145214.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr9:100862211 C>T did not map to a codon.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr6:30131593 C>T maps to NM_033229.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:30131760 C>T maps to NM_033229.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:30139657 G>A maps to NM_033229.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr17:15535028 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:228596423 C>T maps to NM_016102.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr4:154216896 G>T maps to NM_015271.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:154249740 G>A maps to NM_015271.3 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr4:154191515 C>A maps to NM_015271.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr4:154191515 C>A maps to NM_015271.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:154217069 C>T maps to NM_015271.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr4:154216474 C>A maps to NM_015271.3 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr11:4406814 G>C maps to NM_003141.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:4406604 G>A maps to NM_003141.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:5729477 G>T maps to NM_006074.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:5727828 G>T maps to NM_006074.4 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr11:5730865 A>G maps to NM_006074.4 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:64910023 C>T maps to NM_001656.3 L89L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-50-5930-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr7:138189107 G>A maps to NM_015905.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr7:138252365 G>A maps to NM_015905.2 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr17:54969299 C>A maps to NM_005082.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr6:30164346 C>A maps to NM_003449.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr6:28872320 C>A maps to NM_006510.4 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr6:28872208 T>G maps to NM_006510.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr6:28872428 C>G maps to NM_006510.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:59060352 A>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:59059659 G>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:119998087 G>T maps to NM_012101.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:120008553 T>A maps to NM_012101.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr11:119983127 G>T maps to NM_012101.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:120008388 T>A maps to NM_012101.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr11:120008295 G>T maps to NM_012101.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr11:119998220 C>A maps to NM_012101.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr11:6472122 T>A maps to NM_033278.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:6478031 C>T maps to NM_033278.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr11:6477671 C>T maps to NM_033278.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr6:30078326 C>T maps to NM_007028.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:30071354 C>T maps to NM_007028.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:114952806 T>A maps to NM_015906.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr1:114969874 A>G maps to NM_015906.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr1:114940326 A>G maps to NM_015906.3 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr11:5655031 A>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr8:27151800 C>A maps to NM_171982.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:27145297 C>A maps to NM_171982.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr5:114482981 G>A maps to NM_018700.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:114469844 C>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr5:114506853 T>A maps to NM_001017397.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:114499326 C>A maps to NM_018700.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:57128684 G>A maps to NM_015294.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:57157190 C>A maps to NM_015294.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:57165659 T>C maps to NM_015294.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:25966890 A>T maps to NM_006355.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr6:30297201 G>A maps to NM_021253.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr6:30309600 G>A maps to NM_021253.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr6:30297375 C>G maps to NM_021253.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr7:99490034 C>A maps to NM_033017.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:99490315 C>A maps to NM_033017.3 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr6:30113787 G>A maps to ENST00000376724 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr6:30113866 G>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr5:180651800 C>T maps to NM_033549.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr5:180651712 C>T maps to NM_033549.3 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:180659676 C>T maps to NM_033549.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr5:180660417 C>T maps to NM_033549.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:180661720 C>G maps to NM_033549.3 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:140397212 C>A maps to NM_152616.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr3:140407230 C>T maps to NM_152616.4 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr3:140407338 C>A maps to NM_152616.4 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr3:140401879 C>T maps to NM_152616.4 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:140401412 C>A maps to NM_152616.4 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr3:140406603 C>T maps to NM_152616.4 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T6-01A-32D-A25L-08 chr3:140397394 C>G maps to NM_152616.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:96261978 C>A maps to NM_138800.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:96260874 A>G maps to NM_138800.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr1:117660812 C>T maps to NM_025188.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:155154466 G>A maps to NM_025058.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:155148067 C>T maps to NM_025058.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:55036729 G>T maps to ENST00000357530 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:55036789 G>C maps to ENST00000357530 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:55032583 C>T maps to ENST00000357530 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr11:55032417 C>G maps to ENST00000357530 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:55032459 C>G maps to ENST00000357530 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:55036732 G>T maps to ENST00000357530 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:89537463 T>A maps to NM_020358.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:89537464 G>T maps to NM_020358.2 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr11:89537472 G>A maps to NM_020358.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr11:89531773 C>A maps to NM_020358.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr7:72727231 G>A maps to NM_178125.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:72738484 C>A maps to NM_178125.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:72734211 C>T maps to NM_178125.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:72738497 G>C maps to NM_178125.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:72727282 G>A maps to NM_178125.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:27505682 C>T maps to NM_032546.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:27529119 G>T maps to NM_032546.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:67064861 G>A maps to NM_184085.1 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:67064862 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:67047231 A>T maps to NM_184085.1 K117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:100732026 G>C maps to NM_030961.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:100732401 G>T maps to NM_030961.1 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr7:100732821 G>T maps to NM_030961.1 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr7:100732050 C>G maps to NM_030961.1 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5429-01A-01D-1625-08 chr1:248039631 C>G maps to NM_015431.3 Y434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:248039403 G>A maps to NM_015431.3 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr1:248028108 G>T maps to NM_015431.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:248020655 C>T maps to NM_015431.3 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:248031160 C>A maps to NM_015431.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:248028155 G>T maps to NM_015431.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:248031333 T>A maps to NM_015431.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:248028107 G>A maps to NM_015431.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:248039617 G>T maps to NM_015431.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:248028071 C>A maps to NM_015431.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr1:248028077 G>A maps to NM_015431.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:248039226 G>T maps to NM_015431.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:248031145 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:248039451 G>T maps to NM_015431.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr1:248028027 C>T maps to NM_015431.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:248020583 G>A maps to NM_015431.3 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr1:248039385 G>T maps to NM_015431.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:248028072 C>T maps to NM_015431.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:248039253 C>A maps to NM_015431.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:160155918 G>A maps to NM_173084.2 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr11:5631422 G>C maps to NM_001003819.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:5624724 C>T maps to NM_001003819.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:165961466 C>A maps to NM_152620.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:165961706 G>A maps to NM_152620.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr4:165961742 A>G maps to NM_152620.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:165962617 C>G maps to NM_152620.2 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr4:165961673 C>T maps to NM_152620.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:33646643 G>A maps to NM_018207.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:26385005 C>A maps to NM_032588.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:26387752 G>C maps to NM_032588.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:231344798 C>T maps to NM_001004342.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:231349599 G>A maps to NM_001004342.3 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr1:231342395 A>G did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr1:231349584 G>A maps to NM_001004342.3 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:231351141 G>T maps to NM_001004342.3 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr15:45047474 A>G maps to NM_182985.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr3:32860297 G>T maps to NM_001039111.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:32933215 G>A maps to NM_001039111.1 Q840Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr16:31230608 G>T did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:31230797 C>T maps to NM_001008274.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:104414407 A>G did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:51561378 C>T maps to ENST00000338969 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr14:51489621 G>T maps to ENST00000338969 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:51444065 C>G maps to NM_015163.5 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr14:51467559 T>C did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr14:51561237 C>A maps to ENST00000338969 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr14:51561183 G>T maps to ENST00000338969 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:51446128 C>G maps to ENST00000338969 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189068294 G>T maps to NM_178556.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:189068507 A>C maps to NM_178556.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:189068504 C>A maps to NM_178556.3 C462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr4:189060756 C>A maps to NM_178556.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:189060976 G>T maps to NM_178556.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr4:189065201 C>T maps to NM_178556.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr4:189063533 G>A maps to NM_178556.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr4:189063557 C>G maps to NM_178556.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr4:189060807 G>T maps to NM_178556.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr4:189068189 C>A maps to NM_178556.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:189012859 C>G maps to ENST00000326754 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr4:189012796 G>A maps to ENST00000326754 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:189022367 C>A maps to ENST00000326754 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr4:189012757 G>C maps to ENST00000326754 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr5:14482704 C>T maps to NM_007118.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr5:14482689 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr5:14479402 C>T maps to NM_007118.2 Q2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr5:14481374 G>T maps to NM_007118.2 L2123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr5:14280533 C>A maps to NM_007118.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr5:14406720 C>T maps to NM_007118.2 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr5:14508362 G>C maps to NM_007118.2 A3042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr5:14331009 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:14507305 G>T maps to NM_007118.2 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:14280518 C>G maps to NM_007118.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:14378119 G>T did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr5:14291312 G>A maps to NM_007118.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr5:14481383 A>G maps to NM_007118.2 S2126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr5:14359474 C>T maps to NM_007118.2 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr5:14387677 G>A maps to NM_007118.2 R1234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:14291249 G>T maps to NM_007118.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:38130881 G>T maps to NM_001039141.2 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:38155174 G>T maps to NM_001039141.2 R2076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr22:38150966 T>C maps to NM_001039141.2 Y1821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:38111768 G>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr22:38121316 T>A maps to NM_001039141.2 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr22:38165043 G>A maps to NM_001039141.2 V2195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr22:38122312 G>T maps to NM_001039141.2 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr22:38150919 C>T maps to NM_001039141.2 Q1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr22:38151585 C>T maps to NM_001039141.2 A1869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr19:6750570 G>A maps to ENST00000313244 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:6750591 G>A maps to ENST00000313244 E535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:6744950 C>T maps to ENST00000313244 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr14:92480595 T>A maps to NM_004239.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:92471708 G>A maps to NM_004239.3 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230693987 C>T maps to ENST00000389044 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:230723818 A>T maps to ENST00000389044 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:230657799 G>A maps to ENST00000389044 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:230678747 C>A did not map to a codon.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:230724102 G>A maps to ENST00000389044 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:230633331 C>A maps to ENST00000389044 G1976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:230723590 G>A maps to ENST00000389044 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:230633404 G>A maps to ENST00000389044 L1951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:230723834 G>C maps to ENST00000389044 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:230661451 G>C maps to ENST00000389044 S1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr2:230642090 T>C maps to ENST00000389044 S1796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:230662489 G>A maps to ENST00000389044 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:230650529 A>C maps to ENST00000389044 S1652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:230679844 T>A maps to ENST00000389044 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr15:64717778 G>T maps to NM_016213.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:100469166 C>A maps to NM_003302.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:13223572 C>A maps to NM_001136035.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr6:126319436 A>G maps to NM_001031712.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr8:125464155 G>T maps to NM_017956.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:125463924 C>T maps to NM_017956.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:100276996 C>G did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:100291989 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:100278505 C>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:100292980 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:100274346 A>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:100291974 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:100292969 C>A did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:100273983 C>A did not map to a codon.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr23:100276114 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:100274024 C>G did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:100274013 G>A did not map to a codon.
Sequencing variant TCGA-55-6981-01A-11D-1945-08 chr14:61446336 T>C maps to NM_020810.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr14:61447679 C>A did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr14:61446564 C>T maps to NM_020810.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr20:5921731 G>A maps to NM_015939.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr20:5923322 G>C maps to NM_015939.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr20:5921748 C>A maps to NM_015939.3 G418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:29093098 C>A maps to NM_017910.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:3189248 C>T maps to NM_182916.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:54950179 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:54954143 A>G did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:54956380 C>A did not map to a codon.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:54950105 C>G did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:54956056 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:54957722 A>T did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr23:54949380 C>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:54949156 C>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:54956524 C>G did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:54955043 G>A did not map to a codon.
Sequencing variant TCGA-55-8619-01A-11D-2393-08 chr23:54957054 G>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:54949549 C>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:54955190 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:54950926 G>T did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:54949607 G>T did not map to a codon.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr23:54949683 A>G did not map to a codon.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr23:54955212 G>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:54956768 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:54956320 C>A did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr23:54952075 C>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:54954191 A>G did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:54956545 G>T did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:54956217 A>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr23:54956055 G>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:54956659 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:54957024 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:54949855 C>G did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:54956234 T>A did not map to a codon.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr23:54949474 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr23:54951137 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr23:54955035 G>T did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:54956903 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr12:49719371 G>T maps to NM_005480.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr12:49725132 C>T maps to NM_005480.3 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr1:193051690 G>C did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:193046116 G>A maps to NM_004600.5 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr1:193038727 C>T maps to NM_004600.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:193038729 A>G maps to NM_004600.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr8:72984006 A>T maps to NM_007332.2 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:72958753 G>T maps to NM_007332.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr8:72973925 G>T maps to NM_007332.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr8:72945893 G>T maps to NM_007332.2 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr8:72969994 A>T maps to NM_007332.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:72948635 C>A maps to NM_007332.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:72946497 G>T maps to NM_007332.2 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr8:72983984 C>A maps to NM_007332.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr8:72983975 C>A maps to NM_007332.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:72968017 G>A maps to NM_007332.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr8:72973957 C>T maps to NM_007332.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:72967970 G>A maps to NM_007332.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr8:72945998 G>T maps to NM_007332.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr8:72946611 T>C maps to NM_007332.2 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:72975735 G>C maps to NM_007332.2 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr8:72970050 C>A maps to NM_007332.2 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr8:72975066 G>T maps to NM_007332.2 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr8:72975147 G>A maps to NM_007332.2 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr8:72936056 C>T maps to NM_007332.2 Q1047Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr8:72958759 A>T maps to NM_007332.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:72935283 C>A maps to NM_007332.2 E1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr8:72951129 A>G maps to NM_007332.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:72951099 C>G maps to NM_007332.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:72987566 C>G maps to NM_007332.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:72938257 G>T maps to NM_007332.2 R996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr3:142499777 G>T maps to ENST00000476941 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:142511802 A>G maps to ENST00000476941 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:142499757 G>T maps to ENST00000476941 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:142503760 A>T maps to ENST00000476941 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr4:122853869 G>T maps to NM_001130698.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:122853734 G>A maps to NM_001130698.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr4:122835997 C>T maps to NM_001130698.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr13:38266166 G>T maps to NM_003306.1 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr13:38320457 G>T maps to NM_003306.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr13:38320544 G>A maps to NM_003306.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr13:38320577 G>T maps to NM_003306.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr13:38225509 G>A maps to NM_003306.1 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:38211670 G>T maps to NM_003306.1 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr13:38225385 C>G did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr13:38266232 C>T maps to NM_003306.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr13:38229320 A>G maps to NM_003306.1 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr13:38225482 G>A maps to NM_003306.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr13:38266181 A>T maps to NM_003306.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr13:38237653 T>C maps to NM_003306.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr13:38213191 G>T maps to NM_003306.1 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:38211558 C>A maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr13:38248494 C>T maps to NM_003306.1 W415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr13:38266343 G>T maps to NM_003306.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr13:38229404 C>T maps to NM_003306.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr13:38229377 C>G maps to NM_003306.1 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:38237680 T>C maps to NM_003306.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr20:33608994 G>A maps to NM_015638.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr20:33665941 T>C maps to NM_015638.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr20:33609049 G>A maps to NM_015638.2 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr20:33592272 C>T maps to NM_015638.2 Q679Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr23:111020009 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:111025233 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:111195494 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr23:111155893 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:111090470 T>A did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:111024415 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:111155652 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:111155675 C>A did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:111095551 A>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:111090459 G>T did not map to a codon.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr23:111195282 G>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:111097032 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:111155751 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:111195528 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:111155629 C>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:111195539 G>C did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:111155829 G>A did not map to a codon.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr23:111097165 C>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:111195530 C>A did not map to a codon.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr23:111078147 C>T did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:111155944 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:111195568 G>C did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:111025180 G>A did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:111195480 C>A did not map to a codon.
Sequencing variant TCGA-55-8096-01A-11D-2238-08 chr23:111078271 T>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:111155753 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:111155725 G>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:111090522 G>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:111090455 A>G did not map to a codon.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr23:111019955 G>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:111090613 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:111195289 C>G did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:111090518 A>G did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:111019951 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:111155734 C>A did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr23:111025331 G>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:111156018 T>A did not map to a codon.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr23:111195484 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:111155607 G>C did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr11:101375221 G>T maps to NM_004621.5 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr11:101359686 C>T maps to NM_004621.5 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:101374792 C>A maps to NM_004621.5 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:101353722 G>T maps to NM_004621.5 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr11:101375479 C>A maps to NM_004621.5 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:101359748 C>A maps to NM_004621.5 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:101342063 G>T maps to NM_004621.5 Y753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr11:101362388 G>A maps to NM_004621.5 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr11:101375284 A>G maps to NM_004621.5 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr11:101347085 A>G maps to NM_004621.5 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr11:101342866 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr5:135587493 T>C maps to NM_020389.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:135602027 G>T maps to NM_020389.2 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:135567187 C>A maps to NM_020389.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr5:135583316 G>A maps to NM_020389.2 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr5:135692424 C>T maps to NM_020389.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:135651314 G>T maps to NM_020389.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:135583383 G>T maps to NM_020389.2 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:135583166 C>A maps to NM_020389.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:135692703 G>T maps to NM_020389.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:135651403 G>T maps to NM_020389.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:135651404 G>T maps to NM_020389.2 C281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr5:135692643 C>T maps to NM_020389.2 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:135692394 A>G maps to NM_020389.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:135692766 C>T maps to NM_020389.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr5:135587337 G>T maps to NM_020389.2 Y526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:31329912 C>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:31355408 C>A maps to NM_002420.4 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr15:31324993 C>A maps to NM_002420.4 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr15:31342758 C>T maps to NM_002420.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr15:31294303 G>T maps to NM_002420.4 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr15:31353686 G>A maps to NM_002420.4 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr15:31355343 C>T maps to NM_002420.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr15:31341652 C>T maps to NM_002420.4 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr15:31362302 G>A maps to NM_002420.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr15:31324990 C>T maps to NM_002420.4 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:31358375 G>A maps to NM_002420.4 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr15:31362263 G>A maps to NM_002420.4 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:31318411 C>A maps to NM_002420.4 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:31354894 C>A maps to NM_002420.4 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr15:31324972 G>T maps to NM_002420.4 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr15:31339442 C>A maps to NM_002420.4 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr15:31332461 C>A maps to NM_002420.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:45815319 C>A maps to ENST00000397932 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr21:45819255 A>T maps to ENST00000397932 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr21:45837908 C>A maps to ENST00000397932 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr21:45784062 C>G maps to ENST00000397932 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:45774529 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:45811201 G>A maps to ENST00000397932 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr21:45825877 C>A maps to ENST00000397932 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr21:45821602 C>T maps to ENST00000397932 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr21:45845685 G>T maps to ENST00000397932 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr21:45810793 G>T maps to ENST00000397932 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr21:45846541 G>C did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr21:45821587 C>A maps to ENST00000397932 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr21:45799049 G>A maps to ENST00000397932 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr21:45861639 C>G maps to ENST00000397932 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr21:45861696 C>A maps to ENST00000397932 Y1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr21:45811306 G>C maps to ENST00000397932 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr21:45819206 C>T maps to ENST00000397932 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr9:73218373 C>A maps to ENST00000419692 G848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr9:73150955 G>T maps to ENST00000419692 S1645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:73150949 C>T maps to ENST00000419692 P1647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:73213553 C>T maps to ENST00000419692 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr9:73152281 C>T maps to ENST00000419692 E1203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr9:73442799 T>C maps to ENST00000419692 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr9:73477940 G>T maps to ENST00000419692 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:73151528 T>G maps to ENST00000419692 S1454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:73150880 G>A maps to ENST00000419692 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr9:73240190 C>T maps to ENST00000419692 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr9:73736141 G>A maps to NM_001007471.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:49704026 C>T maps to NM_017636.3 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:49674992 T>C maps to NM_017636.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:49671868 C>T maps to NM_017636.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:49671652 G>T maps to NM_017636.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:49693475 A>C maps to NM_017636.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr19:49675354 C>G maps to NM_017636.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:49671847 G>T maps to NM_017636.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr19:49674890 G>T maps to NM_017636.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:2432702 G>A maps to ENST00000452833 Y889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr11:2433483 C>A did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:2437189 C>T maps to ENST00000452833 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr11:2441551 G>A maps to ENST00000452833 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr9:77376930 C>T maps to NM_017662.4 K1552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr9:77377952 G>A maps to NM_017662.4 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77411734 A>T maps to NM_017662.4 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:77442832 G>T maps to NM_017662.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:77436693 G>A maps to NM_017662.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr9:77377883 C>A maps to NM_017662.4 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr9:77386752 T>A did not map to a codon.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr9:77353446 C>A maps to NM_017662.4 R1884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr9:77436628 C>A maps to NM_017662.4 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr9:77376683 G>T maps to NM_017662.4 V1571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr9:77377967 G>A maps to NM_017662.4 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:77377179 C>T maps to NM_017662.4 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:77397634 G>T maps to NM_017662.4 Y1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr9:77347646 C>A maps to NM_017662.4 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr9:77378001 A>G maps to NM_017662.4 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77378051 T>C did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr9:77423090 C>A did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr9:77354344 A>T maps to NM_017662.4 A1836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr9:77415378 G>A maps to NM_017662.4 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:77400858 G>A maps to NM_017662.4 F950F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr9:77354665 C>T maps to NM_017662.4 E1820E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr15:50904912 C>T maps to NM_017672.4 W628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:50886680 A>G maps to NM_017672.4 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr15:50899519 T>C maps to NM_017672.4 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:234835271 G>T maps to NM_024080.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr2:234873363 C>T maps to NM_024080.4 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:234851352 C>A maps to NM_024080.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr2:234916744 A>T maps to NM_024080.4 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:234905056 C>G maps to NM_024080.4 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:234835265 G>A maps to NM_024080.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:234878913 C>A maps to NM_024080.4 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:234879033 G>T maps to NM_024080.4 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:234854513 C>G maps to NM_024080.4 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:116616125 C>G maps to NM_014112.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116430677 C>T maps to NM_014112.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:116631412 C>A maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:116616667 T>A maps to NM_014112.2 K510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr8:116426403 A>G maps to NM_014112.2 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr8:116632276 C>T maps to NM_014112.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr8:116616326 C>T maps to NM_014112.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr8:116426523 T>C maps to NM_014112.2 V1204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:116599317 T>G maps to NM_014112.2 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr8:116616863 G>A maps to NM_014112.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr8:116427155 C>A maps to NM_014112.2 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:116631633 C>A maps to NM_014112.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr8:116632236 C>A maps to NM_014112.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr8:116631943 T>C maps to NM_014112.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr8:116616565 G>A maps to NM_014112.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:116430641 C>G maps to NM_014112.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr8:116631982 C>G maps to NM_014112.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:116426595 C>G maps to NM_014112.2 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:63992968 A>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr11:63992090 G>C maps to NM_001160393.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr17:3474933 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:3493204 G>A maps to ENST00000399756 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:3475519 C>G maps to ENST00000399756 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr17:16323551 G>A maps to NM_016113.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr17:16335350 C>T maps to NM_016113.4 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:16338249 C>T maps to NM_016113.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr17:16321155 C>G maps to NM_016113.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr17:16326792 C>A maps to NM_016113.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:16326144 G>A maps to NM_016113.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:3436154 C>T maps to ENST00000381913 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:3446813 C>T maps to ENST00000381913 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr17:3446795 G>A maps to ENST00000381913 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:3436100 G>A maps to ENST00000381913 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:3432259 C>A maps to ENST00000381913 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr12:110236694 A>G maps to NM_021625.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr12:110222181 C>A maps to NM_021625.4 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:110236508 G>A maps to NM_021625.4 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:110246262 G>A maps to NM_021625.4 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:110231794 G>T maps to NM_021625.4 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr12:110236700 C>T maps to NM_021625.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr12:110230573 T>G maps to NM_021625.4 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:110236655 C>T maps to NM_021625.4 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr7:142627207 C>A maps to NM_019841.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr7:142609718 A>G maps to NM_019841.4 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr7:142627276 T>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr7:142622764 C>A maps to NM_019841.4 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:142612511 T>C maps to NM_019841.4 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:142625229 C>A maps to NM_019841.4 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr7:142605735 A>G maps to NM_019841.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr7:142625302 C>T maps to NM_019841.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:142626153 A>G maps to NM_019841.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:142622829 G>A maps to NM_019841.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:142605940 T>A maps to NM_019841.4 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:142625884 G>T maps to NM_019841.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:142627151 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:142572887 G>A maps to NM_018646.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr7:142569473 C>A maps to NM_018646.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr7:142570162 G>A maps to NM_018646.2 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr7:142573310 G>T maps to NM_018646.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:142574531 G>A maps to NM_018646.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr7:142570161 C>A maps to NM_018646.2 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:142572267 G>T maps to NM_018646.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr7:142583207 C>T maps to NM_018646.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr7:142574901 G>A maps to NM_018646.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:142570225 C>A maps to NM_018646.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:142575446 G>A maps to NM_018646.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:142575694 C>T maps to NM_018646.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr7:98589831 C>A maps to ENST00000359863 R3281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:98574386 G>T maps to ENST00000359863 P2740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr7:98547351 C>T maps to ENST00000359863 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:98557025 G>T maps to ENST00000359863 V2127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr7:98508004 A>C maps to ENST00000359863 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr7:98491470 A>G maps to ENST00000359863 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:98573785 C>T maps to ENST00000359863 L2611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:98608811 G>C maps to ENST00000359863 L3678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:98576478 C>T maps to ENST00000359863 C2855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:98554155 A>T maps to ENST00000359863 A2070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:98527769 G>T maps to ENST00000359863 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:98556986 A>T maps to ENST00000359863 T2114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr7:98582623 G>T maps to ENST00000359863 E3120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr7:98535406 A>G maps to ENST00000359863 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr7:98546277 G>A maps to ENST00000359863 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr7:98506437 C>G maps to ENST00000359863 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:98602014 G>A maps to ENST00000359863 T3490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:98554098 C>T maps to ENST00000359863 S2051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:116698035 G>T maps to NM_139169.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:141952342 C>T maps to NM_001001317.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:141957509 G>A maps to NM_001001317.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:141955443 G>T maps to NM_001001317.2 Y30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:141955398 C>T maps to NM_001001317.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr9:135781380 G>A maps to NM_000368.4 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr9:135786047 T>A maps to NM_000368.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr9:135781323 T>C maps to NM_000368.4 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr9:135781221 G>A maps to NM_000368.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr9:135797348 C>A maps to NM_000368.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:2105463 G>T maps to NM_000548.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr16:2104433 A>G maps to NM_000548.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:2115636 G>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr16:2130193 G>T maps to NM_000548.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:2106211 G>C maps to NM_000548.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:2129039 C>T maps to NM_000548.3 Q992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr16:2129275 G>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr13:45149029 G>C maps to NM_183422.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:150128498 G>T maps to NM_014779.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr3:150127772 G>A maps to NM_014779.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:107018415 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:106959972 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr7:100074924 A>T maps to NM_030935.3 L246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr7:100075445 G>A maps to NM_030935.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:12560661 G>T maps to NM_025265.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:12571269 C>T maps to NM_025265.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:12560565 A>G maps to NM_025265.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:18505560 C>T maps to NM_006292.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:18503191 C>G maps to NM_006292.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:99634667 T>C maps to NM_025244.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr2:99636893 G>A maps to NM_025244.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:99636908 C>A maps to NM_025244.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:99721874 C>A maps to NM_025244.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:99725412 T>C maps to NM_025244.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:130364187 A>G maps to NM_052933.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr7:130356549 G>A maps to NM_052933.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:130353958 T>G maps to NM_052933.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr7:130042487 C>A did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr7:130051033 T>G did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr1:115576634 C>A maps to NM_000549.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:81610057 C>T maps to NM_000369.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr14:81609826 C>A maps to NM_000369.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr14:81554320 T>A maps to NM_000369.2 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:81609868 G>A maps to NM_000369.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:81606049 C>A maps to NM_000369.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:81609451 T>A maps to NM_000369.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr14:81610627 T>A maps to NM_000369.2 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:81609992 C>A maps to NM_000369.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr14:81609889 G>A maps to NM_000369.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7540-01A-11D-2063-08 chr14:81609916 C>T maps to NM_000369.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr14:81610576 C>A maps to NM_000369.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:81562991 C>A maps to NM_000369.2 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:81609460 C>T maps to NM_000369.2 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr18:72998564 C>G maps to NM_005786.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr18:73000430 G>T maps to NM_005786.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr18:72998441 G>T maps to NM_005786.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:73000451 G>A maps to NM_005786.4 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr18:72999518 C>T maps to NM_005786.4 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr18:72999632 G>T maps to NM_005786.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:51870275 G>T maps to NM_173485.5 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:51872732 G>T maps to NM_173485.5 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:51872216 G>C maps to NM_173485.5 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr20:51872756 C>T maps to NM_173485.5 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr20:51871778 G>A maps to NM_173485.5 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:51872435 C>T maps to NM_173485.5 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr20:51871007 A>T maps to NM_173485.5 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr20:51870908 T>A maps to NM_173485.5 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:51870956 T>A maps to NM_173485.5 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr20:51872150 C>A maps to NM_173485.5 C718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr20:51870752 C>A maps to NM_173485.5 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:51872492 C>T maps to NM_173485.5 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr20:51872923 C>A maps to NM_173485.5 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:51872087 C>A maps to NM_173485.5 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr20:51871974 G>T maps to NM_173485.5 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:31769067 C>T maps to NM_020856.2 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:31768901 C>T maps to NM_020856.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:31768571 G>T maps to NM_020856.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31767545 G>A maps to NM_020856.2 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:31769591 C>T maps to NM_020856.2 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr19:31768400 C>T maps to NM_020856.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:31769563 C>A maps to NM_020856.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr19:31769001 G>T maps to NM_020856.2 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr19:31768460 G>A maps to NM_020856.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31769849 G>C maps to NM_020856.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:31769269 C>A maps to NM_020856.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31767929 G>T maps to NM_020856.2 I923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:31768284 G>T maps to NM_020856.2 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:31770503 G>T maps to NM_020856.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:31770029 G>A maps to NM_020856.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:31767677 G>A maps to NM_020856.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr19:31767715 G>A maps to NM_020856.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:31768998 G>T maps to NM_020856.2 S567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr19:31770553 C>A maps to NM_020856.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:31767599 G>C maps to NM_020856.2 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:31767986 C>A maps to NM_020856.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:31769687 T>A maps to NM_020856.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:31769261 C>T maps to NM_020856.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:31768664 G>A maps to NM_020856.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:31769771 G>C maps to NM_020856.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr19:31769414 C>A maps to NM_020856.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:31770397 C>A maps to NM_020856.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:31769600 G>T maps to NM_020856.2 Y366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:31769447 A>G maps to NM_020856.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:31768981 G>A maps to NM_020856.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:31768982 G>T maps to NM_020856.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:31768675 G>T maps to NM_020856.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr19:31768676 C>T maps to NM_020856.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:31769503 G>A maps to NM_020856.2 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr19:31770647 G>A maps to NM_020856.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:31768886 C>T maps to NM_020856.2 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr19:31767852 C>T maps to NM_020856.2 W949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:31769261 C>T maps to NM_020856.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:31769911 G>A maps to NM_020856.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr19:31767551 G>T maps to NM_020856.2 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:31768460 G>T maps to NM_020856.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr19:31769252 G>A maps to NM_020856.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr19:50245222 C>T maps to NM_021733.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:50249743 G>C maps to NM_021733.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:50251356 G>T maps to NM_021733.1 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:50266471 C>T maps to NM_021733.1 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:50249940 C>A maps to NM_021733.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:50245186 C>G maps to NM_021733.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:50245189 G>T maps to NM_021733.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:50266450 G>T maps to NM_021733.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:76507337 G>A maps to NM_015516.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr5:110407674 C>A maps to NM_033035.4 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:110407740 G>C maps to NM_033035.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr8:143396365 T>A maps to ENST00000445818 K358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr8:143381846 C>T maps to ENST00000445818 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:143381909 C>T maps to ENST00000445818 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:231700527 G>A maps to NM_005999.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5939-01A-11D-1625-08 chr1:231700635 A>G maps to NM_005999.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:231700428 G>C maps to NM_005999.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr1:231672959 A>G maps to NM_005999.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:231672974 T>G maps to NM_005999.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:231700290 G>A maps to NM_005999.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:67861259 C>A maps to ENST00000339830 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr16:67860155 C>T maps to ENST00000339830 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr16:67860419 C>G maps to ENST00000339830 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr16:67860158 C>A maps to ENST00000339830 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:67860681 G>T maps to ENST00000339830 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:67860940 C>T maps to ENST00000339830 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:67861172 C>T maps to ENST00000339830 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr16:67861178 C>G maps to ENST00000339830 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:67854846 C>A maps to ENST00000339830 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr16:67861862 T>A maps to ENST00000339830 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr17:79612190 C>T maps to NM_031945.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr17:79612589 C>T maps to NM_031945.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:79612331 C>T maps to NM_031945.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:31135491 C>A maps to NM_001080509.2 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr12:31144810 C>A maps to NM_001080509.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:16816731 G>T maps to NM_014399.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr7:16793609 C>T maps to NM_014399.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr10:71265914 C>A maps to NM_012339.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:11408888 C>T maps to NM_012466.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr19:11417395 C>T maps to NM_012466.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:176078789 G>T maps to NM_012171.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:115596059 G>T maps to NM_005725.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr15:77348492 C>A maps to NM_005724.5 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:77348187 G>A maps to NM_005724.5 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr12:58140826 C>A maps to NM_005981.3 C157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:2337895 C>A maps to NM_139022.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr11:2325382 C>T maps to NM_139022.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:2337813 C>T maps to NM_139022.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:128801518 G>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:99890232 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:38420812 G>C did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:38530628 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr12:71533574 C>T maps to NM_004616.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr12:3387627 C>A maps to ENST00000407263 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr6:41011323 C>T maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:53111966 G>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:53114988 T>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:53115107 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:53114876 G>A did not map to a codon.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr23:53114869 A>C did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:53114036 G>T did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr23:53111999 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:53114001 C>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:53113783 C>T did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:53114926 G>C did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:53117089 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:53112193 G>C did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:53114909 A>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:116574052 G>A maps to ENST00000368611 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr6:116574352 T>C maps to ENST00000368611 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:98289595 C>T maps to NM_033512.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr2:54482784 G>T maps to NM_001003937.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:54482310 A>C maps to NM_001003937.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:54466892 G>T did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:54469900 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:54467178 G>C did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:3341794 G>A maps to ENST00000398659 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr2:3197937 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:3200659 C>A maps to ENST00000398659 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:3193149 C>A maps to ENST00000398659 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr5:112769534 T>C maps to NM_032028.3 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:112770509 T>A maps to NM_032028.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:112769885 G>A maps to NM_032028.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:32829694 C>T maps to NM_052841.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:24676507 T>A maps to NM_001184739.1 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr14:24676330 C>A maps to NM_001184739.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr22:37407366 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr8:144698278 G>A maps to NM_003313.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr8:144695113 C>T maps to NM_003313.3 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr8:144696378 C>A maps to NM_003313.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr9:100388079 G>C maps to NM_139246.4 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:100380095 G>A maps to NM_139246.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr6:43250826 G>T maps to NM_032538.1 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:43226904 G>C maps to NM_032538.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43220496 G>T maps to NM_032538.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr6:43251484 C>A maps to NM_032538.1 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr6:43214424 G>A maps to NM_032538.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:43251403 C>T maps to NM_032538.1 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr6:43230704 G>T maps to NM_032538.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:43251597 C>A maps to NM_032538.1 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr6:43251426 C>T maps to NM_032538.1 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:43038397 G>A maps to ENST00000263802 R1515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr15:43086858 C>T maps to ENST00000263802 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr15:43044863 G>A maps to ENST00000263802 D1265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr5:159492029 G>A maps to NM_003314.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr11:113222826 G>T maps to NM_017868.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:113234602 G>T maps to NM_017868.3 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr11:113196367 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:113212615 C>A maps to NM_017868.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:231097013 C>A maps to NM_024525.4 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:231064839 C>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:231042691 G>A maps to NM_024525.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr3:180322026 A>G maps to NM_133462.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr3:180320180 C>T maps to NM_133462.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:3391924 G>A maps to NM_016030.5 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:3391919 G>T maps to NM_016030.5 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:3392185 C>T maps to NM_016030.5 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:3405631 G>T maps to NM_016030.5 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr9:130479637 G>T maps to NM_144965.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr9:130478435 G>C maps to NM_144965.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr11:43436153 G>A maps to NM_018259.5 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr11:43413035 A>T maps to NM_018259.5 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr11:43515320 A>G did not map to a codon.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr10:75082845 C>A maps to NM_145170.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:75059367 G>A maps to NM_145170.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:75107923 G>C maps to NM_145170.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:75072313 T>A maps to NM_145170.3 K404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:75029451 C>A maps to NM_145170.3 E1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr10:75037042 G>T maps to NM_145170.3 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:75072268 C>A maps to NM_145170.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr3:39162657 G>A maps to ENST00000301819 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr3:39167771 C>A maps to ENST00000301819 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:39161448 G>T maps to ENST00000301819 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:166737204 C>A maps to NM_024753.3 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:166786228 C>A maps to NM_024753.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:166747499 T>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:166773862 G>A maps to NM_024753.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:166771853 T>C maps to NM_024753.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:166781138 G>C maps to NM_024753.3 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:166799851 C>G did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:166737188 C>A maps to NM_024753.3 G1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:166788266 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:166799737 C>G maps to NM_024753.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr2:166767948 C>T maps to NM_024753.3 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:166771849 G>A maps to NM_024753.3 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:55253464 C>A maps to NM_001114108.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:99678232 G>A maps to NM_022905.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr5:34880304 C>T maps to NM_144725.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr5:34850396 C>T maps to NM_144725.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr5:34845694 A>T maps to NM_144725.3 K58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:156555589 G>T maps to NM_001105669.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:156555559 C>T maps to NM_001105669.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr1:156555577 G>A maps to NM_001105669.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr17:40093097 C>G maps to ENST00000377543 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr17:40095230 C>T maps to ENST00000377543 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:138849885 C>T maps to NM_024926.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:33003037 A>G maps to NM_017735.4 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:33037581 C>A maps to NM_017735.4 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:32875248 G>T maps to NM_017735.4 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:147796050 C>A maps to ENST00000513335 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr4:147861026 C>A maps to ENST00000513335 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:147796033 C>T maps to ENST00000513335 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr4:147860968 T>A maps to ENST00000513335 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:147861017 T>C maps to ENST00000513335 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr21:38537962 A>T maps to NM_003316.3 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr21:38525504 C>T maps to NM_003316.3 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr21:38459592 G>T maps to NM_003316.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:178482619 A>T maps to NM_152275.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:178417115 C>A maps to NM_152517.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr2:178416999 G>C maps to NM_152517.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:178416759 G>A maps to NM_152517.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:74718474 A>T maps to NM_022492.4 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr2:74710527 C>T maps to NM_022492.4 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr5:94834210 T>C maps to NM_014639.3 K1142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:94872821 T>A maps to NM_014639.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr5:94860189 C>T maps to NM_014639.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:94818287 T>C maps to NM_014639.3 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:94858951 C>A maps to NM_014639.3 G571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr5:94820549 C>T did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr22:46684476 C>T maps to NM_017931.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr22:46671250 C>T maps to NM_017931.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr22:46681154 G>C maps to NM_017931.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr22:46682989 C>T maps to NM_017931.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:51778491 C>A maps to ENST00000447632 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr1:51755687 G>A maps to ENST00000447632 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr9:15189719 T>G maps to NM_001168340.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:15225919 G>A maps to NM_152574.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr9:15192620 C>A maps to NM_152574.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:21711844 G>C did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr14:20767520 G>A maps to NM_138376.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr14:20763565 G>T maps to NM_138376.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr14:20757804 G>T maps to NM_138376.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr14:20767577 C>A maps to NM_138376.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:47287968 G>T maps to ENST00000394850 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr2:47221536 G>A maps to ENST00000394850 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:47300959 C>A maps to ENST00000394850 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:47177658 G>A maps to ENST00000394850 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr2:47206040 G>A maps to ENST00000394850 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr2:47184001 C>T maps to ENST00000394850 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr14:91155921 G>T maps to NM_001010854.1 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr14:91007747 G>T maps to NM_001010854.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:91007789 C>T maps to NM_001010854.1 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr14:91146851 T>C maps to NM_001010854.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr14:91007858 C>A maps to NM_001010854.1 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:91252634 C>A maps to NM_001010854.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr14:89307379 G>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:40724123 G>T maps to NM_152479.5 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:40723264 G>A maps to NM_152479.5 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr19:40722102 C>T maps to NM_152479.5 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62502893 G>T maps to NM_173810.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr11:62496496 C>T maps to NM_173810.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr9:135278198 C>A maps to NM_007344.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr9:135277137 G>A maps to NM_007344.2 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr9:135277989 A>G maps to NM_007344.2 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:135267594 T>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:117626661 T>C maps to NM_003594.3 H642H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:117626716 G>T maps to NM_003594.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:117633164 C>T maps to NM_003594.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:117618899 C>A maps to NM_003594.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:117619350 A>G maps to NM_003594.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:80744815 A>T maps to NM_003318.4 K577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr6:80749411 G>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr6:80741182 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr6:80720636 G>A maps to NM_003318.4 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr6:80749947 C>G maps to NM_003318.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:80720674 G>T did not map to a codon.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr6:80715586 A>G maps to NM_003318.4 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr6:80715699 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr6:80747682 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:113286317 A>T maps to NM_153712.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:113243498 G>T maps to NM_153712.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr22:43435880 C>T maps to NM_012263.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr9:124751500 C>G maps to NM_001139442.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr9:124751413 G>A maps to NM_194252.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr22:43576789 C>T maps to NM_015140.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr15:90799469 C>A maps to ENST00000438251 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr6:167753912 C>A maps to NM_031949.4 Y175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr6:167754800 G>A maps to NM_031949.4 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:167753645 G>T maps to NM_031949.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr6:167753612 G>A maps to NM_031949.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:167754836 A>T maps to NM_031949.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr6:167752173 T>C maps to NM_031949.4 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:9854721 A>T maps to NM_001025930.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr3:9867507 C>A maps to NM_001025930.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:9862309 G>T maps to NM_001025930.3 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr2:219603496 C>T maps to NM_014640.4 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr2:219602947 C>G maps to NM_014640.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:219617845 C>T maps to NM_014640.4 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:219619111 A>G maps to NM_014640.4 *1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr14:76211924 G>T did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr14:76259371 C>T maps to NM_015072.4 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:46847393 C>T maps to NM_001130918.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr17:46868949 G>A maps to NM_001130918.1 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:46867420 C>T maps to NM_001130918.1 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr1:84373138 C>A maps to NM_024686.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:84417624 T>A maps to NM_024686.4 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:84372017 T>A maps to NM_024686.4 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr22:50485614 T>A maps to NM_001080447.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:50468871 C>A maps to NM_001080447.1 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr22:50488603 C>A maps to NM_001080447.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:30521612 C>T maps to NM_001008409.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:30512839 G>A maps to NM_001008409.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr20:30525285 C>A maps to NM_001008409.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:30507692 C>T maps to NM_001008409.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr20:30507719 C>T maps to NM_001008409.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr2:179610733 G>T maps to ENST00000375038 R5467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179403315 C>T maps to NM_133378.4 G30512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179435495 G>T maps to NM_133378.4 I22553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179477886 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179479055 A>T maps to NM_133378.4 A13788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179590275 G>T maps to NM_133378.4 V5641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:179633571 G>T maps to NM_133378.4 I2997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr2:179459154 C>A maps to NM_133378.4 E16788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179427122 G>T maps to NM_133378.4 T25344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179431316 A>G maps to NM_133378.4 D23946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:179441839 G>A maps to NM_133378.4 S20506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179438510 A>G maps to NM_133378.4 N21548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:179641550 G>T maps to NM_133378.4 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:179441914 G>A maps to NM_133378.4 I20481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179431856 C>T maps to NM_133378.4 W23766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179473145 T>A maps to NM_133378.4 L14920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:179602946 T>A maps to NM_133378.4 K3501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:179477550 C>A maps to NM_133378.4 E14065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:179482721 C>A maps to NM_133378.4 G13218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr2:179648940 G>T maps to NM_133378.4 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr2:179421983 A>T maps to NM_133378.4 A26767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:179411925 G>T maps to NM_133378.4 G28874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr2:179437058 G>A maps to NM_133378.4 G22032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:179554015 C>A did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179432975 G>A maps to NM_133378.4 Y23393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179616644 A>C maps to ENST00000375038 S3496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179650682 G>A maps to NM_133378.4 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr2:179659834 G>A maps to NM_133378.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:179397930 G>A maps to NM_133378.4 R31903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:179454470 G>A maps to NM_133378.4 L18093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr2:179465806 G>A maps to NM_133378.4 G16040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr2:179593262 C>A maps to NM_133378.4 G5220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr2:179486301 C>T maps to NM_133378.4 R12515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr2:179604300 A>T maps to NM_133437.3 T4382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr2:179442617 A>T maps to NM_133378.4 P20277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:179632584 A>T maps to NM_133378.4 A3124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr2:179590741 T>A maps to NM_133378.4 I5525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179400234 G>T maps to NM_133378.4 R31135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179437529 G>A maps to NM_133378.4 C21875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179438785 C>A maps to NM_133378.4 E21457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:179611123 C>A maps to ENST00000375038 E5337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr2:179470390 G>A maps to NM_133378.4 S15309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr2:179443596 G>A maps to NM_133378.4 A20152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179443954 G>C maps to NM_133378.4 S20033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179472329 C>T maps to NM_133378.4 V15127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179473549 A>G maps to NM_133378.4 D14828D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179537182 T>A maps to NM_133378.4 P10326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179583274 G>A maps to NM_133378.4 S6942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:179611073 T>A maps to ENST00000375038 P5353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr2:179581897 G>A maps to NM_133378.4 G7277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr2:179414450 G>T maps to NM_133378.4 A28098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr2:179434376 G>A maps to NM_133378.4 D22926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:179616665 T>C maps to ENST00000375038 R3489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179605005 A>G maps to NM_133437.3 S4147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr2:179613695 A>T maps to ENST00000375038 P4479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:179414360 T>A maps to NM_133378.4 A28128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr2:179575542 C>T maps to NM_133378.4 K8183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179417149 G>T maps to NM_133378.4 P27591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:179616021 A>T maps to ENST00000375038 L3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:179595298 C>T maps to NM_133378.4 G4743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr2:179453979 A>T maps to NM_133378.4 A18256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4627-01A-01D-1553-08 chr2:179440814 G>A maps to NM_133378.4 A20780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr2:179592018 T>A maps to NM_133378.4 I5447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:179594233 C>A maps to NM_133378.4 E4973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr2:179434298 T>A maps to NM_133378.4 I22952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr2:179592522 C>T maps to NM_133378.4 K5350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr2:179413469 T>C maps to NM_133378.4 K28393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr2:179479391 G>T maps to NM_133378.4 T13715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440901 G>A maps to NM_133378.4 I20751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr2:179440973 G>A maps to NM_133378.4 A20727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179444016 T>C maps to NM_133378.4 P20012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179451448 A>G maps to NM_133378.4 D18825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179588867 G>T maps to NM_133378.4 R5796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179606385 C>A maps to NM_133437.3 V3687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179611184 A>T maps to ENST00000375038 V5316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:179616286 C>A maps to ENST00000375038 E3616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:179560073 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr2:179423170 C>G maps to NM_133378.4 L26437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr2:179477674 C>T maps to NM_133378.4 L14023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:179599524 C>T maps to NM_133378.4 T3798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:179647563 G>C maps to NM_133378.4 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:179654842 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:179574575 G>A maps to NM_133378.4 L8246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:179396044 A>T maps to NM_133378.4 S32531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr2:179595832 T>A maps to NM_133378.4 T4609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:179442793 G>A maps to NM_133378.4 F20248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:179638772 C>T maps to NM_133378.4 Q2374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr2:179425994 A>T maps to NM_133378.4 I25720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:179610710 A>G maps to ENST00000375038 D5474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179438297 G>C maps to NM_133378.4 L21619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179455350 C>A maps to NM_133378.4 R17799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr2:179466607 C>G did not map to a codon.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179579142 A>C maps to NM_133378.4 S7542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr2:179604933 T>C maps to NM_133437.3 K4171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr2:179395804 G>C maps to NM_133378.4 T32611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr2:179644902 G>A maps to NM_133378.4 Q1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:179455491 G>T maps to NM_133378.4 V17752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:179553412 G>T maps to NM_133378.4 R9486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:179632584 A>G maps to NM_133378.4 A3124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr2:179553412 G>T maps to NM_133378.4 R9486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:179614244 A>G maps to ENST00000375038 F4296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:179477577 G>T maps to NM_133378.4 R14056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr2:179580394 T>C maps to NM_133378.4 L7338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179399494 G>C maps to NM_133378.4 T31381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179447085 C>A maps to NM_133378.4 E19465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:179459374 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr2:179449531 A>C maps to NM_133378.4 A19044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr2:179447907 A>C maps to NM_133378.4 T19306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:179582298 A>G maps to NM_133378.4 A7190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:179592462 A>T maps to NM_133378.4 L5370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr2:179592876 T>A maps to NM_133378.4 V5314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr2:179596137 G>A maps to NM_133378.4 A4541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr2:179667045 G>A maps to NM_133378.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr2:179468735 C>T maps to NM_133378.4 L15658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:179398447 G>A maps to NM_133378.4 I31730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:179616069 C>T maps to ENST00000375038 W3688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:179429006 G>A maps to NM_133378.4 V24716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr2:179455241 G>A maps to NM_133378.4 L17836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:179422609 G>C maps to NM_133378.4 L26589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:179432828 C>T maps to NM_133378.4 Q23442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:179436944 C>T maps to NM_133378.4 E22070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:179615828 A>T maps to ENST00000375038 A3768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:179638601 G>T maps to NM_133378.4 A2431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr2:179496013 A>T maps to NM_133378.4 Y12019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179408636 G>C maps to NM_133378.4 Y29510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179416710 C>A maps to NM_133378.4 G27738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179438816 T>G maps to NM_133378.4 P21446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179444912 G>A maps to NM_133378.4 S19799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179448469 C>T maps to NM_133378.4 Q19245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179595715 T>C maps to NM_133378.4 E4648E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:179596305 G>A maps to NM_133378.4 P4485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:179463630 G>T maps to NM_133378.4 R16368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:179434275 A>T maps to NM_133378.4 L22960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:179499897 G>T maps to NM_133378.4 P11438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:179631171 G>A maps to NM_133378.4 S3213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr2:179474534 C>T maps to NM_133378.4 L14637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:179616221 C>T maps to ENST00000375038 L3637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr2:179597693 G>C maps to NM_133378.4 Y4159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:179629512 C>T maps to NM_133378.4 Q3243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr2:179477611 G>A maps to NM_133378.4 L14044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr2:179664562 G>T maps to NM_133378.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:179598223 G>A maps to NM_133378.4 R4022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr2:179542861 T>C maps to NM_133378.4 P10084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:179437412 G>T maps to NM_133378.4 T21914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:179595265 C>T maps to NM_133378.4 G4754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr2:179632793 A>C maps to NM_133378.4 P3084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr2:179535022 C>G did not map to a codon.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr2:179422792 A>C maps to NM_133378.4 T26528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr2:179599241 T>G maps to NM_133378.4 P3859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr2:179604573 A>T maps to NM_133437.3 V4291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr2:179579019 G>A maps to NM_133378.4 L7583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179443725 G>T maps to NM_133378.4 T20109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr2:179622488 C>A maps to NM_133432.3 A3440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:179451992 G>T maps to NM_133378.4 T18747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:179458736 C>A maps to NM_133378.4 V16893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr2:179641604 G>A maps to NM_133378.4 I1662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:179569684 C>T maps to NM_133378.4 E8627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:179434806 C>T maps to NM_133378.4 W22783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr2:179437739 G>T maps to NM_133378.4 V21805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr2:179590143 G>T maps to NM_133378.4 I5685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:179501218 G>T maps to NM_133378.4 I11177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr2:179593274 C>A maps to NM_133378.4 E5216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:179575398 C>A maps to NM_133378.4 V8231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179395552 G>T maps to NM_133378.4 A32695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr2:179565845 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr2:179614226 T>C maps to ENST00000375038 V4302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7025-01A-12D-1945-08 chr2:179399026 A>G maps to NM_133378.4 V31537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr2:179425862 A>G maps to NM_133378.4 A25764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:179613053 A>G maps to ENST00000375038 S4693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:179614487 G>A maps to ENST00000375038 S4215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:179664218 C>A maps to NM_133378.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:179440742 A>G maps to NM_133378.4 P20804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:179463658 G>T maps to NM_133378.4 T16358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:179590618 T>A maps to NM_133378.4 A5566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:179592014 C>A maps to NM_133378.4 G5449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:179464428 G>C maps to NM_133378.4 L16165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:179553413 C>T maps to NM_133378.4 T9485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:179437832 G>T maps to NM_133378.4 I21774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:179437913 G>T maps to NM_133378.4 Y21747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:179407506 G>A maps to NM_133378.4 H29790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:179481477 C>T maps to NM_133378.4 G13478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:179583948 C>G maps to NM_133378.4 T6812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:179599130 T>A maps to NM_133378.4 A3896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr2:179485574 G>T maps to NM_133378.4 I12686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr2:179455752 G>T maps to NM_133378.4 I17665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr2:179458064 G>A maps to NM_133378.4 R17056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:179612966 A>G maps to ENST00000375038 S4722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:179393494 G>T maps to NM_133378.4 T33093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:179451843 C>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:179478920 G>C maps to NM_133378.4 L13833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:179643650 T>C maps to NM_133378.4 P1386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:179592312 T>A maps to NM_133378.4 T5420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179391981 G>C maps to NM_133378.4 G33343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:179467006 A>G did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:179568919 G>T maps to NM_133378.4 T8815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr2:179593684 C>A maps to NM_133378.4 G5116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:179403901 C>T maps to NM_133378.4 R30352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:179437769 G>T maps to NM_133378.4 A21795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:179485224 C>G maps to NM_133378.4 V12773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:179582400 C>T maps to NM_133378.4 L7156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:179592852 G>T maps to NM_133378.4 G5322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:179642503 T>C maps to NM_133378.4 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr2:179594051 G>A maps to NM_133378.4 G5033G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr2:179542909 G>A maps to NM_133378.4 I10068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179436919 G>A maps to NM_133378.4 R22079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179439521 G>C maps to NM_133378.4 T21211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179499927 T>C maps to NM_133378.4 Q11428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179501526 C>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:179516248 T>A maps to NM_133378.4 K10726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:179436923 G>T maps to NM_133378.4 G22077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:179640215 G>A maps to NM_133378.4 Y2125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:179407395 G>A maps to NM_133378.4 I29827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:179397733 G>A maps to NM_133378.4 L31968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:179436377 A>T maps to NM_133378.4 T22259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr2:179642231 G>T maps to NM_133378.4 A1520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:179611787 T>A maps to ENST00000375038 A5115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr2:179397280 A>T maps to NM_133378.4 L32119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr2:179456034 C>T maps to NM_133378.4 K17571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr2:179436857 G>T maps to NM_133378.4 A22099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:179446891 G>T maps to NM_133378.4 T19500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:179431646 G>A maps to NM_133378.4 T23836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr2:179451887 G>T maps to NM_133378.4 V18782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr2:179581882 G>T maps to NM_133378.4 Y7282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:179664292 G>T maps to NM_133378.4 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AE-01A-21D-A24D-08 chr2:179498610 C>T maps to NM_133378.4 L11637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:179567268 T>G maps to NM_133378.4 T8871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:179586700 G>A maps to NM_133378.4 I6319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:179592840 C>G maps to NM_133378.4 V5326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr2:179447685 G>T maps to NM_133378.4 T19380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr2:179598557 G>T maps to NM_133378.4 T3942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:179582922 C>A maps to NM_133378.4 L7026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr2:179636115 T>C maps to NM_133378.4 P2646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:179466614 A>G maps to NM_133378.4 D15864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:179478578 A>G maps to NM_133378.4 D13909D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr2:179641391 C>A maps to NM_133378.4 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr8:63985590 T>C maps to NM_000370.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr18:29175155 G>T maps to ENST00000432547 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr18:29178619 C>A maps to ENST00000432547 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:54930318 G>C maps to ENST00000391739 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:54946838 C>T maps to ENST00000391739 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr19:54930399 C>T maps to ENST00000391739 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:54932504 C>G maps to ENST00000391739 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:72248389 T>A maps to NM_032646.5 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr17:72256329 G>A maps to NM_032646.5 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr17:72233551 G>T maps to NM_032646.5 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr17:72246115 C>A maps to NM_032646.5 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:72233615 A>T maps to NM_032646.5 K200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:72246133 G>T maps to NM_032646.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:72249297 G>A maps to NM_032646.5 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr7:2696096 C>T maps to NM_025250.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr7:2696039 G>A maps to NM_025250.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr7:2696150 C>T maps to NM_025250.2 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:8122428 G>A maps to NM_003320.4 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:8123160 G>T maps to NM_003320.4 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr11:8123114 G>A maps to NM_003320.4 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:8060506 C>A maps to NM_003320.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:49521754 C>A maps to NM_006082.2 G448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr12:49521848 G>A maps to NM_006082.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:49521983 T>C maps to NM_006082.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:49666755 G>T maps to NM_032704.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr12:49663441 G>T maps to NM_032704.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr13:19752451 G>T maps to NM_006001.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr13:19751381 G>A maps to NM_006001.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:19752463 C>T maps to NM_006001.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr13:19753649 G>T maps to NM_006001.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr13:19748131 G>A maps to NM_006001.1 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr13:19748236 C>A maps to NM_006001.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr13:19748131 G>T maps to NM_006001.1 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:132240384 C>G maps to NM_080386.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:132235909 C>A maps to NM_080386.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:132238108 C>A maps to NM_080386.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr2:132238048 G>A maps to NM_080386.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:132238276 C>A maps to NM_080386.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr2:132237754 G>A maps to NM_080386.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:132237811 G>A maps to NM_080386.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:132237910 C>A maps to NM_080386.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:130953905 G>T maps to NM_207312.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:130953815 G>A maps to NM_207312.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:130949493 G>T maps to NM_207312.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:130951517 G>T maps to NM_207312.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr2:130951589 G>A maps to NM_207312.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:130951769 G>T maps to NM_207312.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:130951937 C>A maps to NM_207312.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr10:5436253 T>A maps to NM_024803.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr10:5435579 C>T maps to NM_024803.2 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A472-01A-11D-A24D-08 chr10:5435745 T>A maps to NM_024803.2 K359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr10:5435836 C>T maps to NM_024803.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr10:5437433 C>A maps to NM_024803.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr20:57599324 C>A maps to NM_030773.3 Y281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr20:57599126 G>A maps to NM_030773.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr9:140137953 C>A maps to NM_006088.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:90001146 G>C maps to ENST00000304984 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:90001392 G>T maps to ENST00000304984 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr16:90001794 G>T maps to ENST00000304984 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr16:90001773 G>T maps to ENST00000304984 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr19:6495935 G>A maps to NM_006087.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:6495432 G>A maps to NM_006087.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr19:6496230 G>A maps to NM_006087.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr19:6496095 C>A maps to NM_006087.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:6495335 T>A maps to NM_006087.2 K392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:6495351 C>G maps to NM_006087.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr18:12325516 G>A maps to NM_032525.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:94594 C>A maps to NM_177987.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr10:93407 G>T maps to NM_177987.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr10:93572 C>G maps to NM_177987.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr10:93392 C>A maps to NM_177987.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr10:93212 G>A maps to NM_177987.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr10:93578 C>A maps to NM_177987.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr10:93917 G>T maps to NM_177987.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr10:94013 G>T maps to NM_177987.2 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:93865 G>T maps to NM_177987.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr10:93862 C>A maps to NM_177987.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:57958409 C>A maps to NM_016261.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:57958296 T>G maps to NM_016261.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr17:57958310 G>A maps to NM_016261.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:112397165 C>A maps to NM_016262.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:40767057 G>A maps to NM_001070.4 *452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:40818441 C>T maps to NM_016437.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:40818412 C>T maps to NM_016437.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:135106115 T>G maps to NM_006659.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:135103474 T>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr10:135106638 G>A maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr10:135116331 C>A maps to NM_006659.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr10:135101713 C>G maps to NM_006659.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:135106004 G>A maps to NM_006659.2 Y404Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr10:135113086 C>T maps to NM_006659.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:113174305 A>T maps to NM_006322.4 L592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr13:113176787 G>A maps to NM_006322.4 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr15:22868966 G>C did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr15:22866790 C>A maps to NM_052903.4 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr15:22840266 G>C maps to NM_052903.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr15:22853732 G>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:22864306 G>T maps to NM_052903.4 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr15:22873223 C>G maps to NM_052903.4 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr15:22861876 G>T maps to NM_052903.4 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr15:22863039 G>T maps to NM_052903.4 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr22:50659382 C>A maps to NM_020461.3 G1135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr22:50659280 G>A maps to NM_020461.3 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr22:50657616 G>A maps to NM_020461.3 A1502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr22:50660930 C>T maps to NM_020461.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr22:50667892 C>G maps to NM_020461.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:28856775 C>T maps to NM_003321.4 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr1:151535161 G>A maps to NM_020127.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:35477039 A>T maps to NM_003322.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr6:35478739 C>A maps to NM_003322.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr6:35480628 G>A maps to NM_003322.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:49387022 G>C maps to NM_003323.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:3018725 C>T maps to NM_001160408.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr12:3040231 C>T maps to NM_001160408.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr6:158924615 G>A maps to NM_020245.3 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr6:158924187 C>T maps to NM_020245.3 R1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:158919844 G>A did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr8:15605884 A>T maps to NM_006765.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:1183627 C>A maps to NM_172367.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62346148 G>A maps to NM_022830.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62348607 G>A maps to NM_022830.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:62356643 T>C maps to NM_022830.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:44196109 T>A maps to NM_002822.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr7:19156410 C>A maps to NM_000474.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr7:19156386 G>A maps to NM_000474.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:19748384 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr18:9396446 G>A maps to NM_020648.5 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr18:9396491 G>A maps to NM_020648.5 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr18:9396395 G>A maps to NM_020648.5 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr4:48106929 T>C maps to NM_003328.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:48115326 C>G did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:48082039 A>G maps to NM_003328.2 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:32650178 G>T maps to NM_175852.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:139564123 C>A maps to ENST00000358430 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr6:139569030 C>A maps to ENST00000358430 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr6:139564043 G>T maps to ENST00000358430 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:139564103 G>C maps to ENST00000358430 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr6:139609687 C>A maps to ENST00000358430 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:16855791 G>C did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:16850762 C>G did not map to a codon.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr23:16859726 T>A did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr23:16855747 C>G did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr16:11782157 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:52486660 G>A maps to NM_015913.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:134223520 G>C maps to NM_024715.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr14:52936817 T>A maps to NM_020784.2 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr14:52907280 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr14:52937398 C>T did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr14:52906027 C>T maps to NM_020784.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:52923869 T>A maps to NM_020784.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr14:52978010 A>G maps to NM_020784.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr14:52957648 A>T maps to NM_020784.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr18:9887621 C>A maps to NM_001098529.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr18:9887582 C>T maps to NM_001098529.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr18:9888080 T>C maps to NM_001098529.1 D535D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr18:9887045 G>A maps to NM_001098529.1 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr7:37889880 A>T maps to NM_016616.4 K5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr7:37890306 G>T maps to NM_016616.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr7:37934116 G>T maps to NM_016616.4 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr3:138023809 G>T maps to ENST00000333911 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr1:145440087 T>C maps to NM_006472.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:145438882 G>T maps to NM_006472.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr1:145439849 G>T maps to NM_006472.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:145440509 T>C maps to NM_006472.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr18:54305659 C>T maps to NM_004786.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr18:54291578 G>T maps to NM_004786.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr22:19864758 T>A did not map to a codon.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr22:19865698 C>G maps to NM_006440.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr22:19883050 C>A maps to NM_006440.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:10478841 C>A maps to NM_003331.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5147-01A-01D-1625-08 chr19:10478969 C>A did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr18:670781 C>A maps to NM_001071.2 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr18:669135 C>T maps to NM_001071.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr18:670728 C>G maps to NM_001071.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:670797 C>T maps to NM_001071.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr11:88924416 C>A maps to NM_000372.4 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr11:88924512 C>A maps to NM_000372.4 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr11:88911126 C>A maps to NM_000372.4 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr11:89028370 C>G maps to NM_000372.4 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr11:88911909 C>A maps to NM_000372.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr11:88911129 G>A maps to NM_000372.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:88911384 C>G maps to NM_000372.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr11:88911920 C>G maps to NM_000372.4 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr11:89028404 C>A maps to NM_000372.4 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr11:88924524 C>A maps to NM_000372.4 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr15:41870230 T>C maps to NM_006293.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:41864677 C>T maps to NM_006293.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:41865601 G>T maps to NM_006293.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr19:36398369 A>T maps to NM_003332.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr7:72267536 C>A maps to NM_001145440.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr7:72081773 A>G maps to NM_001145440.1 H556H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr7:72159742 G>A maps to NM_001145440.1 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr7:72193900 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:72159679 G>C maps to NM_001145440.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:75204453 G>A maps to NM_138467.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr21:44524451 C>A maps to NM_001025203.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr19:36233705 T>A did not map to a codon.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:36234744 G>T maps to ENST00000412391 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr19:56180085 C>G maps to NM_007279.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:56179918 C>T maps to NM_007279.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:56180847 G>T maps to NM_007279.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:70980139 A>G maps to NM_018003.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:70952513 C>A maps to NM_018003.2 R1385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr15:70991942 C>A maps to NM_018003.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr15:70979952 C>T maps to NM_018003.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr15:70975134 C>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr1:162557434 A>T maps to ENST00000367925 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr23:47062564 G>T did not map to a codon.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr23:47060986 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:47062971 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47065666 T>C did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:47061800 G>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:47062072 G>T did not map to a codon.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr23:47071825 A>G did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:34951383 G>T maps to NM_005499.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:34957911 C>G maps to NM_005499.2 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr3:69127008 T>A maps to NM_003968.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr3:69124580 C>T maps to NM_003968.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr4:68490852 T>A maps to NM_018227.5 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr4:68506907 G>A maps to NM_018227.5 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr4:68539438 G>A maps to NM_018227.5 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:68566806 G>A maps to NM_018227.5 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr4:68543400 T>A maps to NM_018227.5 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:68506892 G>A maps to NM_018227.5 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:49848048 C>A maps to NM_003335.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:49845455 G>A maps to NM_003335.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:49847795 C>A maps to NM_003335.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr9:138837784 C>A maps to NM_016172.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr13:99992717 G>T maps to NM_001144072.1 G236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr9:34249795 C>G maps to NM_001171201.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr9:34249886 G>A maps to NM_001171201.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr9:33927813 G>A maps to NM_018449.2 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:33973195 G>C maps to NM_018449.2 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr9:33988989 G>C maps to NM_018449.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr9:33923273 G>A maps to NM_018449.2 Q972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:154223999 C>G maps to NM_014847.3 S512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:154226439 C>T maps to NM_014847.3 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:154229657 C>G maps to NM_014847.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:154231457 A>G maps to NM_014847.3 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr21:43857595 A>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr21:43833559 G>T maps to NM_018961.2 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr21:43838703 G>T maps to NM_018961.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr21:43863427 G>T maps to NM_018961.2 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr21:43857643 C>T maps to NM_018961.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:122650347 G>A maps to NM_032873.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:122650362 G>A maps to NM_032873.4 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:122647788 C>T maps to NM_032873.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr11:122647770 C>T maps to NM_032873.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr11:122669677 T>A maps to NM_032873.4 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr11:122653758 A>T did not map to a codon.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr17:16285700 G>T maps to NM_018955.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:16285718 T>C maps to NM_018955.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr17:16285379 C>A maps to NM_018955.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr12:125398152 G>A maps to NM_021009.5 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr12:125397468 G>A maps to NM_021009.5 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr12:125397414 G>A maps to NM_021009.5 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:125397453 G>A maps to NM_021009.5 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr12:125397359 C>A maps to NM_021009.5 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr6:29527450 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:118717128 A>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:118717178 T>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:118708873 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:118708879 C>T did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:118717137 G>T did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:118708872 G>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:118709338 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:118708683 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr20:44444382 A>G maps to NM_007019.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr20:44444349 G>A maps to NM_007019.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733733 C>A maps to NM_198920.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr6:83733740 A>T maps to NM_198920.1 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr6:83775391 C>A maps to NM_198920.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr10:60124574 T>C maps to NM_003338.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr10:60123427 T>C maps to NM_003338.3 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:60124612 C>G maps to NM_003338.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:138994492 C>A maps to NM_003339.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr4:103723774 G>A maps to NM_181890.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr17:4186204 C>T maps to NM_003342.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr21:46191315 G>A maps to NM_003343.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr6:90039405 C>A maps to NM_016021.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:90039586 C>A maps to NM_016021.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr6:90052102 G>A maps to NM_016021.2 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:90039432 G>A maps to NM_016021.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:1192479 C>A maps to NM_194315.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:1190768 G>A maps to NM_194315.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:1190705 G>C maps to NM_194315.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr11:57319947 C>T maps to NM_004223.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:142967317 T>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:142967313 G>T did not map to a codon.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr23:142967529 C>G did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:142967582 G>T did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:142967420 G>A did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:142967513 A>T did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:142967514 G>C did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr23:142967262 C>T did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:142967629 C>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr23:142967544 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:142967329 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr17:74392593 G>C maps to NM_022066.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:74387491 C>A maps to NM_022066.3 R1137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr1:154530852 G>A maps to NM_017582.6 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr15:76168548 C>T maps to NM_173469.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr15:76168612 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:202304772 C>A did not map to a codon.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:202304861 C>G maps to NM_014176.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:64671319 A>G did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr15:25616899 C>A maps to NM_000462.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr15:25601840 G>A maps to NM_000462.2 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:109921433 G>A maps to NM_183415.1 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr12:109935709 C>G maps to NM_183415.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr11:118243383 G>T maps to NM_004788.2 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr11:118263479 G>T maps to NM_004788.2 E989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr11:118244397 C>T maps to NM_004788.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:10197140 A>G maps to NM_001105562.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:10209283 A>T maps to NM_001105562.2 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr1:10238754 A>T maps to NM_001105562.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:10155608 C>G maps to NM_001105562.2 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:10207065 G>T maps to NM_001105562.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:10166581 A>G maps to NM_001105562.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:11345710 C>T maps to NM_013319.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46U-01A-11D-A24D-08 chr1:11345743 C>G maps to NM_013319.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:11345794 G>T maps to NM_013319.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr13:30341774 A>C maps to NM_007106.3 L94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:110655546 G>T maps to NM_203412.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:9939266 G>A did not map to a codon.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr16:4920916 A>G maps to NM_016936.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:4910737 C>T maps to NM_016936.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:4924687 C>T maps to NM_016936.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr16:4924402 C>T maps to NM_016936.3 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:4911084 C>T maps to NM_016936.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:138921843 G>T did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr20:3102774 C>A maps to NM_014948.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr20:3102753 G>T maps to NM_014948.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr3:33442468 T>C maps to NM_001128161.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:86284186 G>A maps to NM_013438.4 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr9:86293364 T>A maps to NM_013438.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr9:86278911 C>A maps to NM_013438.4 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:56591132 A>C did not map to a codon.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:56591353 A>G did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:56591073 C>G did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:56591818 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:56591010 C>A did not map to a codon.
Sequencing variant TCGA-49-4490-01A-21D-1855-08 chr23:56591553 T>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:56590788 G>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:56591286 G>T did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:56591546 C>G did not map to a codon.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr23:56591110 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:56590573 C>A did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr23:56591881 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:56591626 G>T did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr23:56591150 C>T did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr11:5530284 C>A maps to NM_017481.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr11:5530071 C>A maps to NM_017481.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:5529626 G>A maps to NM_017481.2 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr1:156020952 C>A maps to NM_020131.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:156021555 C>T maps to NM_020131.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr1:156013885 G>A maps to NM_020131.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:156012594 C>A maps to NM_020131.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr11:5537473 C>T maps to NM_145053.4 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:5536687 T>C maps to NM_145053.4 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:5537023 A>T maps to NM_145053.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr11:5537380 G>C maps to NM_145053.4 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:5536897 C>A maps to NM_145053.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:43313526 G>C maps to NM_174916.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:43270091 G>A maps to NM_174916.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr15:43281044 G>A maps to NM_174916.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr15:43328727 G>A maps to NM_174916.2 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr6:42627404 C>G maps to NM_015255.2 S1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:42600600 G>T maps to NM_015255.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:42600414 C>T maps to NM_015255.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr6:42600432 G>A maps to NM_015255.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr6:42615857 G>A maps to NM_015255.2 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:42541584 G>T maps to NM_015255.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr6:42619759 G>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr6:42561936 A>T maps to NM_015255.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:42644555 G>T maps to NM_015255.2 E1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:170863538 G>T maps to ENST00000442603 E1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:19478260 C>A maps to ENST00000375267 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr1:19518752 G>A maps to ENST00000375267 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:19437262 C>T maps to ENST00000375267 L3955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:19511664 C>A maps to ENST00000375267 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr1:19499492 G>C maps to ENST00000375267 S1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:19511673 G>A maps to ENST00000375267 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:19525395 G>A maps to ENST00000375267 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:19513692 G>A maps to ENST00000375267 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:19491399 G>C maps to ENST00000375267 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:19497253 A>T did not map to a codon.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr1:19423144 C>G did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:19440471 G>T maps to ENST00000375267 C3765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:19467999 C>A maps to ENST00000375267 E2777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:19468000 C>A maps to ENST00000375267 L2776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:19513100 G>A maps to ENST00000375267 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr8:103317409 T>C maps to NM_015902.4 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:103359294 C>A maps to NM_015902.4 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:103287961 C>A maps to NM_015902.4 E2202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr8:103311752 C>A maps to NM_015902.4 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:103273472 A>G maps to NM_015902.4 P2619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:103297391 G>A maps to NM_015902.4 R1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr14:93686678 C>T maps to NM_175748.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P8-01A-11D-A24P-08 chr14:93685005 G>A maps to NM_175748.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr5:171639031 G>T maps to NM_152277.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:42286811 G>A maps to NM_014233.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:42293285 G>C maps to NM_014233.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr17:42288498 G>A maps to NM_014233.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:62444317 C>A maps to NM_015853.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:20517068 C>T maps to NM_152376.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:20517386 C>G maps to NM_152376.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:26624542 G>A maps to NM_183008.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:24205880 G>T maps to NM_181713.3 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr8:59329440 G>A maps to NM_001077619.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:136528275 C>T maps to NM_014607.3 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr2:136505933 C>G maps to NM_014607.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr2:136537772 C>T maps to NM_014607.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr2:136519470 C>T maps to NM_014607.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8278-01A-11D-2284-08 chr2:136527344 A>G maps to NM_014607.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:196134244 T>G maps to NM_015562.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:196089297 C>G maps to NM_015562.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr8:30623910 G>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:41262813 G>T maps to NM_004181.4 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr4:41266138 G>A maps to NM_004181.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr1:192998664 T>A maps to ENST00000367450 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:165876981 G>T maps to NM_012474.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:165865546 G>T maps to NM_012474.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:165865505 C>A maps to NM_012474.4 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:165865516 C>T maps to NM_012474.4 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:62571608 T>A maps to NM_017859.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr4:141483348 C>T maps to NM_021833.4 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr4:141484330 G>A maps to NM_021833.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr11:73686561 C>T maps to NM_003355.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr11:18568598 T>C did not map to a codon.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr11:18587906 T>A maps to NM_001040697.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr1:161123882 G>A maps to NM_016406.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr22:19455526 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr4:186339796 G>T maps to NM_018359.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr4:186329174 C>A maps to NM_018359.3 G346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr4:39515800 C>A maps to NM_003359.3 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:128873836 A>G did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:128870687 C>T maps to NM_020120.3 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:128941254 A>G maps to NM_020120.3 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr2:128936143 G>T did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:128861573 C>A maps to NM_020120.3 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:128861574 A>T maps to NM_020120.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr13:96505870 C>A maps to NM_020121.3 G1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:96508410 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr13:96553180 C>T maps to NM_020121.3 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr13:96638603 G>A maps to NM_020121.3 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr13:96601612 G>A maps to NM_020121.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr13:96705545 C>G maps to NM_020121.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr13:96506723 C>T maps to NM_020121.3 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr2:234681012 C>G maps to ENST00000373460 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr2:234669196 G>T maps to NM_000463.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:234680958 G>A maps to ENST00000373460 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:234545479 T>C maps to NM_019075.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:234638104 C>T maps to NM_019093.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:234627525 C>T maps to NM_007120.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr2:234627777 A>G maps to NM_007120.2 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:234628318 A>T maps to NM_007120.2 K285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:234622110 G>T maps to NM_019078.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr2:234622443 C>A maps to NM_019078.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr2:234590804 G>A maps to NM_019077.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr2:234590852 C>T maps to NM_019077.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:234526901 C>T maps to NM_019076.4 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr2:234526614 C>A maps to NM_019076.4 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:234581232 T>G maps to NM_021027.2 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr2:234580711 G>T maps to ENST00000373460 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr2:234581344 G>A maps to NM_021027.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:234581325 C>G maps to NM_021027.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:70513223 C>A maps to ENST00000514019 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70460880 A>G maps to ENST00000514019 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:70460322 G>T maps to ENST00000514019 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:70465026 T>C maps to ENST00000514019 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr4:70455182 G>T maps to ENST00000514019 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr4:70513316 C>A maps to ENST00000514019 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr4:70505335 G>T did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr4:70505157 A>G maps to ENST00000514019 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr4:70505118 A>G maps to ENST00000514019 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:70504986 T>C maps to ENST00000514019 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr4:70504926 C>T maps to ENST00000514019 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr4:69817244 A>G maps to NM_024743.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:69817193 C>T maps to NM_024743.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr4:69796262 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr4:69682205 G>T maps to NM_001075.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr4:69692147 G>T maps to NM_001075.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:69696437 A>T maps to NM_001075.4 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr4:69692183 G>C maps to NM_001075.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr4:70079861 G>T maps to NM_001073.1 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr4:70074115 C>A maps to NM_001073.1 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr4:70066307 G>T maps to NM_001073.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr4:70070362 A>G maps to NM_001073.1 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr4:70071279 C>A maps to NM_001073.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr4:70078377 G>T maps to NM_001073.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr4:70080012 G>T maps to NM_001073.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr4:69533795 C>A maps to NM_001076.2 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr4:69403561 C>A maps to NM_001076.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr4:69535946 A>G maps to NM_001076.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69416468 G>T maps to NM_001076.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:69416513 C>A maps to NM_001076.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:69416546 A>G maps to NM_001076.2 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:69536126 A>T maps to NM_001076.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:69433870 G>C maps to NM_001076.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr4:69519924 G>T maps to NM_001076.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:69416612 A>T maps to NM_001076.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:69519972 A>T maps to NM_001076.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:70160484 C>T maps to NM_053039.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr4:70155468 A>G maps to NM_053039.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:70160246 G>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:70156322 C>G maps to NM_053039.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr4:70146307 C>A maps to NM_053039.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr4:70156379 G>T maps to NM_053039.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr4:70361225 T>A maps to NM_021139.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346426 C>A maps to NM_021139.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr4:70346555 G>T maps to NM_021139.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70346366 C>T maps to NM_021139.2 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr4:70361151 G>T maps to NM_021139.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:70359505 G>T maps to NM_021139.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:70361498 C>A maps to NM_021139.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr4:70352325 C>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr4:70359448 C>A maps to NM_021139.2 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr4:70351104 G>T maps to NM_021139.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr4:70351083 G>T maps to NM_021139.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7030-01A-11D-1945-08 chr4:70355192 A>G maps to NM_021139.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:70361288 C>T maps to NM_021139.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr4:70352324 A>T did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr4:70361159 T>C maps to NM_021139.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr4:70361501 C>A maps to NM_021139.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr4:69962327 A>T maps to NM_001074.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr4:69962774 T>A maps to NM_001074.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr4:69978249 C>T maps to NM_001074.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:69978312 C>T maps to NM_001074.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:69973926 A>G maps to NM_001074.2 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr5:35965802 C>A maps to NM_152404.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr5:35957470 C>A maps to NM_152404.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr5:35988626 G>T maps to NM_152404.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr5:35965590 C>T maps to NM_152404.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:35968220 C>A maps to NM_152404.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr5:36049052 G>A maps to NM_174914.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr5:36035964 C>A maps to NM_174914.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr5:36035967 C>T maps to NM_174914.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr5:36036072 G>C maps to NM_174914.3 Y433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr5:36049272 G>A maps to NM_174914.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr4:115585281 A>G maps to NM_003360.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr4:115544482 T>C maps to NM_003360.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:162473554 T>C maps to NM_175866.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:162470835 T>G maps to NM_175866.4 L232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:162470700 A>T did not map to a codon.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr19:4911001 G>C maps to ENST00000398240 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:34802577 C>A maps to NM_017754.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr6:34789480 G>A maps to NM_017754.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr6:34826854 C>T maps to NM_017754.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr6:34802532 C>T maps to NM_017754.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr12:100451510 C>A maps to NM_015054.1 E1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:100453137 T>A maps to NM_015054.1 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:100453665 C>A maps to NM_015054.1 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr12:100478281 T>C maps to NM_015054.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr12:100452830 G>A maps to NM_015054.1 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr12:100491163 G>A maps to NM_015054.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr12:100453821 C>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:6433942 C>T maps to NM_152896.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr9:6499926 A>G maps to NM_152896.1 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr5:176338367 C>T maps to ENST00000377219 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr5:176338361 C>T maps to ENST00000377219 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr12:132400694 C>T maps to NM_003565.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr12:132394478 C>G maps to NM_003565.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr12:132380369 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr12:132396623 G>T maps to NM_003565.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr17:19679691 C>A maps to NM_014683.3 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:19680989 C>A maps to NM_014683.3 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:19705182 C>A maps to NM_014683.3 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr17:19699553 G>C maps to NM_014683.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr17:19687054 G>A maps to NM_014683.3 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr15:75131079 G>A maps to NM_001099436.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr3:41504622 G>A maps to NM_017886.2 H1116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:41746638 C>A maps to NM_017886.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:41759237 C>A maps to NM_017886.2 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr3:41497017 C>T maps to NM_017886.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr3:41996203 A>T maps to NM_017886.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:41977432 C>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:41291038 C>T maps to NM_017886.2 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr3:41973471 C>G maps to NM_017886.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:20362002 G>A maps to ENST00000424589 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:20352543 C>T maps to ENST00000424589 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:20357558 G>T maps to ENST00000424589 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr16:20348728 C>A maps to ENST00000424589 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr16:20348642 G>C maps to ENST00000424589 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:20357477 G>T maps to ENST00000424589 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr16:20352615 C>T maps to ENST00000424589 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr16:20347977 G>T maps to ENST00000424589 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr16:20360469 G>T maps to ENST00000424589 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:20344650 G>C maps to ENST00000424589 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:20359764 G>T maps to ENST00000424589 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:20352474 G>A maps to ENST00000424589 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr16:20355377 G>A maps to ENST00000424589 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:20355494 C>T did not map to a codon.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr16:20359824 G>T maps to ENST00000424589 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr16:20352528 C>A maps to ENST00000424589 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr21:43529798 G>C maps to NM_173568.3 R549R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-44-2656-01A-02D-0969-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr21:43557547 G>T did not map to a codon.
Multiple mappings detected for codon TCGA-55-8619-01A-11D-2393-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr21:43531671 C>A maps to NM_173568.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:124453974 A>T maps to NM_000373.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr3:124449467 G>A maps to NM_000373.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr12:121154530 A>T maps to NM_001080533.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:17785515 C>G maps to ENST00000428389 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z048-01A-01W-0746-08 chr19:17743622 G>A maps to ENST00000428389 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:17758110 G>A maps to ENST00000428389 D757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:17752260 C>T maps to ENST00000428389 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:17766705 G>T maps to ENST00000428389 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:17753677 A>G maps to ENST00000428389 H904H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:17741495 C>A maps to ENST00000428389 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr19:17756534 C>G maps to ENST00000428389 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:17780380 C>A maps to ENST00000428389 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr9:35403185 G>T maps to ENST00000396787 V1451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr9:35310541 T>C maps to ENST00000396787 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr9:35389883 G>T maps to ENST00000396787 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:54817796 T>C maps to ENST00000260323 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr15:54825192 A>T maps to ENST00000260323 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr15:54916083 G>A maps to ENST00000260323 K2097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr15:54793049 G>A maps to ENST00000260323 E1725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr15:54707188 A>G maps to ENST00000260323 Q1619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr15:54307610 T>A maps to ENST00000260323 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:54586107 C>A maps to ENST00000260323 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr15:54542457 G>T maps to ENST00000260323 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr15:54306849 C>A maps to ENST00000260323 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr15:54527296 C>T maps to ENST00000260323 V1047V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr15:54630677 A>T maps to ENST00000260323 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr15:54307910 C>G maps to ENST00000260323 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr15:54914576 T>G maps to ENST00000260323 T2053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr17:73830749 C>A maps to ENST00000412096 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:73836586 C>T did not map to a codon.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr17:73831962 G>A maps to ENST00000412096 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr15:91496491 C>T maps to NM_018671.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:91491054 G>T maps to NM_018671.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr15:91479204 A>T maps to NM_018671.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr15:91490083 G>T maps to NM_018671.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:91489889 C>T maps to NM_018671.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr15:91479539 C>G maps to NM_018671.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr15:91482980 G>A maps to NM_018671.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr17:33475290 G>A maps to NM_173167.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:33513322 C>A maps to NM_173167.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr17:33504148 G>T maps to NM_173167.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr17:33510507 G>T maps to NM_173167.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr17:33504106 C>A maps to NM_173167.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:33501389 T>C did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:33491041 G>T maps to NM_173167.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr17:33481606 C>A maps to NM_173167.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr17:33497246 C>G maps to NM_173167.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:33475422 G>T maps to NM_173167.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr17:33501352 C>A maps to NM_173167.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:33510498 G>T maps to NM_173167.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr17:33501325 G>T maps to NM_173167.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr17:33497162 G>T maps to NM_173167.2 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr17:33513458 G>T maps to NM_173167.2 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr17:33504149 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr17:33503016 G>A maps to NM_173167.2 K665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:99226377 G>A maps to ENST00000409347 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr2:99232732 T>A maps to ENST00000409347 Y172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:176306802 C>T maps to NM_133369.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr5:176306760 C>A maps to NM_133369.2 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr5:176304926 C>A maps to NM_133369.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:176295215 C>A maps to NM_133369.2 C126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr5:176305064 C>A maps to NM_133369.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr5:176297416 G>T maps to NM_133369.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr5:176301047 C>A maps to NM_133369.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr5:176295795 C>A maps to NM_133369.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:176289767 C>T maps to NM_133369.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr5:176289623 G>C did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr10:73050705 G>T maps to NM_170744.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr10:73055623 G>T maps to NM_170744.3 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr10:73048445 G>T maps to NM_170744.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr10:73048712 A>T did not map to a codon.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:73047491 C>T maps to NM_170744.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr10:73048322 A>T did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr10:73053227 G>A maps to NM_170744.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:73044573 C>T maps to NM_170744.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr10:73051291 C>T maps to NM_170744.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:73039800 C>T maps to NM_170744.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:96222766 C>T maps to NM_003728.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr4:96091426 G>T maps to NM_003728.3 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr4:96124010 C>A maps to NM_003728.3 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr4:96137360 T>A maps to NM_003728.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr4:96091390 G>T maps to NM_003728.3 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr4:96123950 G>A maps to NM_003728.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr4:96166191 G>T maps to NM_003728.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr4:96469939 G>T maps to NM_003728.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr4:96140246 G>T maps to NM_003728.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr4:96469927 G>T maps to NM_003728.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr4:96106323 C>T maps to NM_003728.3 Q720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr4:96123959 G>A maps to NM_003728.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr4:96106275 G>T maps to NM_003728.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:35608281 C>A maps to ENST00000416672 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:35583677 C>T maps to ENST00000416672 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr8:35648014 C>T maps to ENST00000416672 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr8:35606140 G>A maps to ENST00000416672 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr8:35608191 T>A maps to ENST00000416672 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr8:35606110 C>T maps to ENST00000416672 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr8:35542148 C>A maps to ENST00000416672 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:35541201 C>A maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:35624418 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:35624419 G>T maps to ENST00000416672 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:35608158 G>C maps to ENST00000416672 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:35624505 C>A maps to ENST00000416672 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr8:35544126 G>T maps to ENST00000416672 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:35583847 A>T maps to ENST00000416672 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:167711433 G>A maps to NM_018974.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr6:167719509 C>A maps to NM_018974.3 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr6:167728938 G>A maps to NM_018974.3 *458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr6:167721398 G>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr6:167719495 A>T maps to NM_018974.3 K312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:1273219 C>T maps to NM_001080461.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr7:1275634 G>A maps to NM_001080461.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr7:1273286 G>T maps to NM_001080461.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:109539804 G>T did not map to a codon.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr12:109536196 G>T maps to NM_003362.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr17:73813471 C>T maps to NM_001080419.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr17:73780813 C>T maps to NM_001080419.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr16:1453188 C>A maps to ENST00000508903 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr22:24896176 C>A maps to NM_016327.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr22:24898152 C>T maps to NM_016327.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:18968169 G>C maps to ENST00000418384 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:18967009 G>A maps to ENST00000418384 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:18967078 G>A maps to ENST00000418384 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:18965952 G>T maps to ENST00000418384 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr10:12043819 T>A maps to NM_015542.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:12071171 T>A maps to NM_015542.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:118979169 T>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:118975154 C>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:118968898 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:118972012 G>T did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:118975148 T>A did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr23:118979177 A>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:118972439 T>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:118974608 A>G did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:36159434 C>A maps to NM_007000.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:36164162 C>A maps to NM_007000.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:36168763 C>A maps to NM_007000.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr3:118905626 C>A maps to NM_006952.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr3:118909141 C>T maps to NM_006952.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:118913202 G>T maps to NM_006952.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7284-01B-11D-2238-08 chr11:118828882 C>T maps to NM_006760.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr22:45689185 C>A maps to NM_006953.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr22:45683164 G>C maps to NM_006953.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:158974391 C>A maps to NM_001135098.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:158971767 C>A maps to NM_001135098.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:158974355 C>A maps to NM_001135098.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:74513311 C>A did not map to a codon.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr23:74494130 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:74494433 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr23:74519630 G>T did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:74494379 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:74519686 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:97245422 G>A maps to NM_006294.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr8:97244135 C>A maps to NM_006294.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr3:48637543 C>T maps to NM_003365.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr3:48637933 G>A maps to NM_003365.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr3:48646609 A>G maps to NM_003365.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:48643286 C>T maps to NM_003365.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr16:21969920 G>C did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr16:21973828 G>T maps to NM_003366.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:29698966 C>A maps to NM_006003.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:229783447 C>T maps to NM_014777.2 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:229781637 G>A maps to NM_014777.2 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:229779277 A>G did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr1:229771835 G>T maps to NM_014777.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr1:229773857 A>C maps to NM_014777.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr1:229770665 C>T maps to NM_014777.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:229773572 C>T maps to NM_014777.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:229772384 A>G maps to NM_014777.2 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr1:229773395 C>G maps to NM_014777.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr1:229783306 C>T maps to NM_014777.2 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:43921535 C>A maps to NM_001077663.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr7:43917545 G>A maps to NM_001077663.1 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr7:43917297 C>A maps to NM_001077663.1 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr7:43918524 C>A maps to NM_001077663.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr7:43916859 T>C maps to NM_001077663.1 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr3:126220155 C>A did not map to a codon.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr3:126226901 C>A maps to NM_001165974.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr3:126219610 G>A maps to NM_001165974.1 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:126202311 C>T did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr3:126211341 T>G maps to NM_001165974.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr3:126220754 C>T maps to NM_001165974.1 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr10:127503660 G>A maps to NM_000375.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:17330078 C>T maps to NM_018467.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:161011630 C>A maps to NM_007122.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:161012386 G>A maps to NM_007122.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:35769859 G>T maps to NM_003367.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr11:17517198 C>A maps to NM_153676.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr11:17522676 G>T maps to NM_153676.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr11:17517184 C>A maps to NM_153676.3 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr11:17527436 A>T maps to NM_153676.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr11:17531181 C>A maps to NM_153676.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr11:17542493 C>T maps to NM_153676.3 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:17522655 G>T maps to NM_153676.3 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr11:17531109 G>T maps to NM_153676.3 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr11:17519756 G>T maps to NM_153676.3 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:17538962 C>T maps to NM_005709.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:72919126 C>A maps to NM_173477.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:72915757 C>A maps to NM_173477.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:72915568 C>A maps to NM_173477.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:215847653 T>C maps to ENST00000366943 S4533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:216262469 C>T maps to ENST00000366943 V1590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:215802230 G>A maps to ENST00000366943 L5172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:216062334 G>T maps to ENST00000366943 T2552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr1:216373151 G>A maps to ENST00000366943 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:216040370 G>A maps to ENST00000366943 I2941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr1:216373188 G>T maps to ENST00000366943 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:216371751 A>T maps to ENST00000366943 L1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:216372966 A>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:216019166 C>A maps to ENST00000366943 G3018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:216166437 G>A maps to ENST00000366943 G2243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4433-01A-22D-1855-08 chr1:215823978 A>G maps to ENST00000366943 S4766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:216373436 G>A maps to ENST00000366943 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr1:215847452 C>T maps to ENST00000366943 K4600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr1:216246297 T>A maps to ENST00000366943 R1930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:216052419 G>T maps to ENST00000366943 L2748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:215987216 G>T maps to ENST00000366943 P3200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:215901464 G>T maps to ENST00000366943 P3991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:216270502 T>G maps to ENST00000366943 A1560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr1:216243584 G>C maps to ENST00000366943 Y1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr1:216373194 A>T maps to ENST00000366943 C1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:216260105 G>A maps to ENST00000366943 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:216256821 G>A maps to ENST00000366943 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr1:215820888 C>T maps to ENST00000366943 W4922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:216051128 C>T maps to ENST00000366943 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215901707 T>C maps to ENST00000366943 E3910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:215972390 C>A maps to ENST00000366943 P3272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr1:216498838 C>A maps to ENST00000366943 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:216251554 C>G maps to ENST00000366943 V1816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr1:216074236 G>T maps to ENST00000366943 G2437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr1:216348675 C>T maps to ENST00000366943 T1515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:216172294 T>A maps to ENST00000366943 T2197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr1:215847617 A>T maps to ENST00000366943 P4545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:216380660 G>T maps to ENST00000366943 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr1:215802170 G>T maps to ENST00000366943 G5192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr1:216051136 C>A maps to ENST00000366943 G2882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr1:216017806 G>A maps to ENST00000366943 V3029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr1:216262460 A>G maps to ENST00000366943 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr1:215963478 C>T maps to ENST00000366943 Q3368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216370053 G>A maps to ENST00000366943 F1364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:216420068 C>T maps to ENST00000366943 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:216138677 C>A maps to ENST00000366943 G2367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr1:215956215 C>T maps to ENST00000366943 G3483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr1:216348700 G>T maps to ENST00000366943 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:215813951 G>T maps to ENST00000366943 R4972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr1:216420206 G>T maps to ENST00000366943 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:215821946 T>C maps to ENST00000366943 P4835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:216243461 G>T maps to ENST00000366943 V2010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:216595373 G>T maps to ENST00000366943 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:216595578 G>T maps to ENST00000366943 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:216371663 T>A maps to ENST00000366943 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:216420314 G>C maps to ENST00000366943 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr1:216262381 G>A maps to ENST00000366943 Q1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:216373185 G>T maps to ENST00000366943 Y1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr1:216243536 C>T maps to ENST00000366943 E1985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr1:216256928 C>G did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:215802296 G>T maps to ENST00000366943 I5150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:215853718 C>T did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:216420143 T>A maps to ENST00000366943 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr1:216348686 G>A maps to ENST00000366943 L1512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:215813996 C>T maps to ENST00000366943 L4957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr1:216062176 G>T maps to ENST00000366943 S2605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:216062280 T>C maps to ENST00000366943 L2570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr1:216496886 G>A maps to ENST00000366943 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:215972261 G>T maps to ENST00000366943 Y3315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:215956146 C>T maps to ENST00000366943 T3506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr1:216419956 G>A maps to ENST00000366943 Q927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr1:216500976 T>A maps to ENST00000366943 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:216138683 G>A maps to ENST00000366943 F2365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:215847951 G>T maps to ENST00000366943 S4434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:216348732 G>C maps to ENST00000366943 P1496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr1:215901716 A>T maps to ENST00000366943 A3907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr1:215960024 C>A maps to ENST00000366943 T3458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:216380684 G>C maps to ENST00000366943 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:216405432 G>T maps to ENST00000366943 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr1:216062171 C>A maps to ENST00000366943 G2607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:215802353 G>T maps to ENST00000366943 P5131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:216498789 G>T maps to ENST00000366943 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:216373398 G>C maps to ENST00000366943 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr1:216172258 T>C maps to ENST00000366943 L2209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr1:215963534 T>A maps to ENST00000366943 K3350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:216380726 A>C maps to ENST00000366943 S1068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr1:216380773 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:215847983 G>T maps to ENST00000366943 A4423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:215848154 G>T maps to ENST00000366943 A4366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:215848205 G>T maps to ENST00000366943 I4349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:216246499 G>A maps to ENST00000366943 S1905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr1:216258141 C>A maps to ENST00000366943 E1689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr1:216172400 C>A did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr1:216420065 G>T maps to ENST00000366943 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr1:215956230 G>T maps to ENST00000366943 A3478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr1:216369928 G>T maps to ENST00000366943 S1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:215931935 C>A did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:216258220 T>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr1:215901644 G>C maps to ENST00000366943 T3931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr1:215931991 T>A maps to ENST00000366943 P3778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr1:216595491 G>T maps to ENST00000366943 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr1:216262361 T>A maps to ENST00000366943 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr1:216051188 T>C maps to ENST00000366943 P2864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:216373050 G>A maps to ENST00000366943 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:216462735 C>A maps to ENST00000366943 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:215953365 G>T maps to ENST00000366943 T3586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr1:216420086 C>T maps to ENST00000366943 E883E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:215847764 A>G maps to ENST00000366943 D4496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:216062172 T>C maps to ENST00000366943 K2606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr4:76703977 A>G maps to NM_003715.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr1:62908991 T>C did not map to a codon.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr1:62910725 C>G maps to NM_003368.4 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr1:62916039 G>A maps to NM_003368.4 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr16:84778660 G>T maps to NM_005153.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:47103905 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:47107227 G>A did not map to a codon.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr23:47106709 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:47092492 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:47092493 G>T did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr23:47104819 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:47104810 G>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:47107247 G>C did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:47104482 G>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:47107327 G>C did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:47104296 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:47101480 G>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:179483593 G>T maps to NM_003940.2 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:179439296 G>T maps to NM_003940.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr3:179437821 G>T maps to NM_003940.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr3:179499558 G>T maps to NM_003940.2 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:179478936 C>G maps to NM_003940.2 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:179460064 G>T maps to NM_003940.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:179501841 G>T maps to NM_003940.2 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:179472616 C>A maps to NM_003940.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr3:179439296 G>T maps to NM_003940.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:179439257 G>T maps to NM_003940.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr12:62783401 A>T maps to ENST00000280377 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr12:62784974 C>T maps to ENST00000280377 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr12:62783683 C>A maps to ENST00000280377 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:62778049 A>G maps to ENST00000280377 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr21:30400248 G>A maps to NM_006447.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr8:11994733 G>T maps to NM_201402.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr8:11995030 G>T maps to NM_201402.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr3:49151717 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:49153912 C>T maps to ENST00000434032 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr3:49152705 C>A maps to ENST00000434032 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:119228470 C>A maps to NM_004205.4 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr11:119230295 G>A maps to NM_004205.4 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4425-01A-01D-1753-08 chr9:132637633 C>T maps to NM_001008563.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:132637848 C>T maps to NM_001008563.3 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:132630678 G>T maps to NM_001008563.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr9:132637911 G>T maps to NM_001008563.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr9:132620783 C>T maps to NM_001008563.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr9:132630288 C>T maps to NM_001008563.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:132637027 G>A maps to NM_001008563.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr9:132620768 G>T maps to NM_001008563.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:161130615 G>T maps to NM_012475.4 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:161134864 C>T maps to NM_012475.4 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr1:55598340 G>A maps to NM_015306.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:55604670 A>T maps to NM_015306.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:55589207 T>C maps to NM_015306.2 Q1396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:55562680 G>A maps to NM_015306.2 I1960I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:55619929 C>T maps to NM_015306.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr1:55562207 G>A maps to NM_015306.2 C2008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr21:17214815 C>G maps to ENST00000285681 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr21:17202920 G>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr21:17196426 G>T maps to ENST00000285681 G384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:132162133 C>A did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr23:132161730 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:132159957 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:132160952 G>T did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:132161440 G>C did not map to a codon.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr23:132161640 T>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:132159637 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:132160098 G>T did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:132160482 G>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:132160156 G>A did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:132160972 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:132161321 C>T did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:132161024 T>A did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:132160978 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:132161213 T>G did not map to a codon.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr23:132160639 G>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:132160638 T>A did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:132161951 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:132160221 G>T did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:132160222 G>T did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr23:132159787 C>T did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:132160164 T>C did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:132161910 C>A did not map to a codon.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr23:132159645 G>C did not map to a codon.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr23:132159517 G>T did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:113711321 G>A maps to NM_020886.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:113679904 G>A maps to NM_020886.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr11:113699990 A>T maps to NM_020886.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr11:113675627 C>A maps to NM_020886.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr11:113675621 C>T maps to NM_020886.2 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:113705002 G>A maps to NM_020886.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr11:113688418 G>T maps to NM_020886.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:113673936 C>A maps to NM_020886.2 G935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:57641419 C>T maps to NM_020903.2 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:57640186 A>T maps to NM_020903.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:57640927 C>A maps to NM_020903.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:57640594 G>T maps to NM_020903.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57642508 C>A maps to NM_020903.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:57640798 T>C maps to NM_020903.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:57642760 G>T maps to NM_020903.2 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:57640628 A>T maps to NM_020903.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:57641308 C>A maps to NM_020903.2 C422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:57642181 T>C maps to NM_020903.2 N713N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:57640598 G>T maps to NM_020903.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr16:23099056 C>A maps to NM_020718.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23080338 G>C maps to NM_020718.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:23085136 C>G maps to NM_020718.3 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:23079777 C>T maps to NM_020718.3 K1216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr16:23085046 C>A maps to NM_020718.3 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr16:23080835 T>A maps to NM_020718.3 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:23080431 T>A maps to NM_020718.3 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:23101979 C>T maps to NM_020718.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:23096294 A>G maps to NM_020718.3 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr16:23085049 C>A maps to NM_020718.3 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr16:23119381 G>T maps to NM_020718.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:58332589 C>T maps to NM_032582.3 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr17:58313587 G>A maps to NM_032582.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr17:58258863 C>A maps to NM_032582.3 E1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr17:58303469 C>T maps to NM_032582.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr17:58299795 C>A maps to NM_032582.3 G575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:78193989 G>A maps to NM_015017.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr1:78187555 T>C maps to NM_015017.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr1:78189128 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:78193977 A>G did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr2:61577740 G>A maps to NM_014709.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr2:61516013 T>G did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:61571045 C>A maps to NM_014709.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:61508293 A>C maps to NM_014709.3 S1694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr2:61473587 G>T maps to NM_014709.3 S2140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr2:61448648 C>T maps to NM_014709.3 Q2629Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr11:77907353 G>T maps to NM_020798.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr11:77921492 C>T maps to NM_020798.2 Y864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:77909054 C>T maps to NM_020798.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr11:77911201 C>T maps to NM_020798.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr11:77907332 G>T maps to NM_020798.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr11:77918629 C>T maps to NM_020798.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr17:76831479 G>A maps to NM_025090.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:76831488 C>A maps to NM_025090.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr17:76810547 G>A maps to NM_025090.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr17:76823388 C>A maps to NM_025090.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr4:144135081 C>G maps to NM_032557.5 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:144124647 T>C maps to NM_032557.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr4:144141530 C>T maps to NM_032557.5 N1017N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr4:144109081 A>G maps to NM_032557.5 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:144106690 G>T maps to NM_032557.5 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr2:85875929 G>C maps to NM_006590.2 *566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr3:49337974 C>T maps to NM_003363.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr3:49338024 C>A maps to NM_003363.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:49322305 A>G maps to NM_003363.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr3:49362160 T>G maps to NM_003363.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr3:49362338 T>C maps to NM_003363.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr3:49335337 A>T maps to NM_003363.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr2:234436079 T>C maps to NM_018218.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr2:234460096 C>T maps to NM_018218.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr2:234394526 C>T maps to NM_018218.2 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:234421212 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:234463171 C>A maps to NM_018218.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:6189872 A>G maps to ENST00000404835 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:9604946 G>T maps to NM_153210.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:9604538 C>T maps to NM_153210.3 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr17:9613390 G>T maps to NM_153210.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr17:9613324 G>C maps to NM_153210.3 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr12:95927531 T>C maps to NM_032147.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr12:95922616 T>C maps to NM_032147.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:95927966 G>C maps to NM_032147.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:53492220 C>A maps to NM_022832.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr1:22033295 G>A maps to NM_032236.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:22078011 C>A maps to NM_032236.5 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:22030037 G>A maps to NM_032236.5 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr1:22078008 T>C maps to NM_032236.5 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:22079056 G>A maps to NM_032236.5 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:6965283 G>T maps to NM_001098536.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr12:6965957 C>T maps to NM_001098536.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr12:6970679 G>T maps to NM_001098536.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:55514857 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:55513991 G>T did not map to a codon.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr23:55513781 C>G did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:55514883 C>A did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:55513305 G>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:55514651 T>A did not map to a codon.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr23:55513496 C>A did not map to a codon.
Sequencing variant TCGA-50-6591-01A-11D-1753-08 chr23:55513805 C>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:55515249 C>A did not map to a codon.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr23:55513510 A>G did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:55515107 G>C did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:55514937 C>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:55513740 T>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:55513961 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:55514456 C>A did not map to a codon.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr23:55513729 G>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:55513960 C>A did not map to a codon.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr23:55514403 C>G did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:55513781 C>A did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:55514839 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:55515097 T>C did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:120170027 G>C maps to NM_019050.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:120170028 G>T maps to NM_019050.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:120188591 C>T maps to NM_019050.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr4:120188599 C>T maps to NM_019050.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr10:75290090 C>T maps to NM_152586.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr10:75296159 G>A maps to NM_152586.3 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:75277237 C>T maps to NM_152586.3 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr17:5042784 T>A maps to NM_004505.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr17:5071267 G>A maps to NM_004505.2 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr17:5064885 C>T maps to NM_004505.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:5039176 C>T maps to NM_004505.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr17:5050376 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr10:11531200 C>A maps to NM_001080491.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:11504481 C>T maps to NM_001080491.2 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr10:11504624 G>A maps to NM_001080491.2 Q785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr10:11505387 G>T maps to NM_001080491.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:11505372 G>T maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr10:11505454 G>T maps to NM_001080491.2 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr16:8988971 C>T maps to NM_003470.2 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:9004655 T>A maps to NM_003470.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:9009137 G>A maps to NM_003470.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr16:8995983 C>A maps to NM_003470.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr15:50774205 A>T maps to NM_005154.3 K583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:50789392 G>A maps to NM_005154.3 W1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr15:50769638 T>G maps to NM_005154.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr15:50791224 A>T maps to NM_005154.3 S1099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:41025462 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:41075816 G>A did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:41012323 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:41057841 G>T did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:41075523 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:41055568 G>T did not map to a codon.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr23:41075706 G>C did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr23:41025387 G>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:41043660 C>T did not map to a codon.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr23:41073862 T>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:41029761 C>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:41082624 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:41088906 C>T did not map to a codon.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr23:41000346 A>G did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:41089774 C>A did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:41069769 G>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:41000657 G>C did not map to a codon.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr23:41077679 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:40994007 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:41043332 C>A did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:41055511 G>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:41029418 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:41075555 T>C did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:41088851 G>T did not map to a codon.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr23:40999907 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:41091775 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:41056748 G>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr23:41010267 G>C did not map to a codon.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr24:14890149 A>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr24:14851539 G>T did not map to a codon.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr24:14838714 C>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr24:14903475 G>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr13:31233060 C>T maps to NM_005800.4 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr13:31231662 G>A maps to NM_005800.4 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:149208152 A>T maps to NM_005715.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:149340273 G>A did not map to a codon.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr1:38483402 A>T maps to NM_016037.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:129054694 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:129055434 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:129059012 C>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:129053161 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:129063310 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:129054700 G>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr23:129058937 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:129063439 G>A did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:129055265 G>A did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr23:129058862 G>C did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr23:129059057 C>T did not map to a codon.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr23:129063424 C>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:129060312 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:129053161 C>G did not map to a codon.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr23:129055496 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:129055512 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:129059172 T>A did not map to a codon.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr13:52603876 A>T maps to NM_021645.5 K313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr13:52603227 A>T maps to NM_021645.5 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr5:72875738 T>A maps to NM_032175.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr5:72875895 G>T maps to NM_032175.2 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:72865489 C>G maps to NM_032175.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr12:101689352 C>A maps to NM_014503.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr12:101702084 G>A maps to NM_014503.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr12:101761654 G>A maps to NM_014503.2 L2095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr12:101777043 C>A maps to NM_014503.2 R2628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr12:101732711 T>C maps to NM_014503.2 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr12:101723227 G>A did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr12:101706033 G>A maps to NM_014503.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr12:101779469 G>A maps to NM_014503.2 E2722E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:117783871 G>T maps to NM_032334.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr17:30207727 C>A maps to NM_018428.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:30216302 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr17:30228588 C>A maps to NM_018428.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:144758882 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr6:145069548 C>T maps to NM_007124.2 L2703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr6:145021221 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:144806606 C>T maps to NM_007124.2 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr6:145124170 G>T did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:144769761 G>T maps to NM_007124.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:144878441 A>G maps to NM_007124.2 K2428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:145157478 C>T maps to NM_007124.2 L3289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr6:144794969 G>A did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr6:144806565 G>T maps to NM_007124.2 E1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr1:7912985 G>A maps to NM_006786.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:7907834 G>T maps to NM_006786.3 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr1:7912997 A>T maps to NM_006786.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:190993091 C>A maps to NM_198152.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr3:190993122 T>C maps to NM_198152.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:80333309 C>A maps to NM_018949.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr24:15467249 C>G did not map to a codon.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr24:15372252 G>A did not map to a codon.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr24:15508853 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:75727940 C>G maps to NM_003369.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr11:75852455 G>T maps to NM_003369.3 *700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:75562950 C>T maps to NM_003369.3 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr2:106761739 G>A maps to ENST00000283148 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr2:106761802 C>A maps to ENST00000283148 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:47516657 C>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:47517011 C>A did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47518286 C>A did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr16:70796855 C>A maps to NM_018052.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr16:70726815 G>A maps to NM_018052.3 Y698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:171675513 C>A maps to NM_003762.4 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:155119182 T>A did not map to a codon.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr23:155169365 C>G did not map to a codon.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr23:155127855 G>A did not map to a codon.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr23:155171641 G>C did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:155119157 G>T did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:155171560 C>T did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:155119209 G>A did not map to a codon.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr23:155125333 C>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:155171605 G>T did not map to a codon.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr23:155171606 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr2:85808748 G>A maps to NM_003761.4 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr1:116202291 C>G maps to NM_001172412.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:116206454 C>T maps to NM_001172412.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr1:116206391 G>T maps to NM_001172412.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:160389246 G>T maps to NM_020335.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr1:160395113 G>T maps to NM_020335.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:160385650 G>T maps to NM_020335.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr1:160385935 C>A maps to NM_020335.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr1:160388875 A>T maps to NM_020335.2 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:160389321 G>A maps to NM_020335.2 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr1:160390875 G>T maps to NM_020335.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:160385650 G>T maps to NM_020335.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:160389255 C>T maps to NM_020335.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr18:9936981 G>T did not map to a codon.
Sequencing variant TCGA-38-A44F-01A-11D-A24D-08 chr18:9950495 A>G maps to NM_003574.5 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr20:56993312 G>A maps to NM_004738.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr20:57016112 C>T maps to NM_004738.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr6:31749538 C>A did not map to a codon.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr6:31751988 A>G did not map to a codon.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr6:31752073 C>A maps to NM_006295.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr6:31747921 G>A maps to NM_006295.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:31749677 C>A maps to NM_006295.2 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr6:30882660 G>A maps to NM_001167734.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr6:30893360 C>T maps to NM_001167734.1 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr14:77242348 C>T maps to NM_014909.4 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:213146047 C>T maps to NM_001136474.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr1:213146092 G>T maps to NM_001136474.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr16:4431768 C>T maps to NM_138440.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr16:4432788 A>C maps to NM_138440.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:46021239 C>T maps to NM_003370.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:41170196 G>A maps to NM_006373.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr16:77850896 G>T maps to NM_020927.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr16:77918563 G>C maps to NM_020927.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:77896772 G>T maps to NM_020927.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:6772929 C>A maps to NM_005428.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr19:6854070 G>T maps to NM_005428.2 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:6848050 G>T maps to NM_005428.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr19:6828652 C>T maps to NM_005428.2 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:6821691 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:136649541 T>G did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr1:108507485 C>T maps to NM_006113.4 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:108303495 A>T maps to NM_006113.4 C309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:108152587 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:108313275 A>G maps to NM_006113.4 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:108247586 G>A maps to NM_006113.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr1:108138840 G>T maps to NM_006113.4 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:108303502 T>A did not map to a codon.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr1:108185291 G>C maps to NM_006113.4 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr1:108247658 T>A maps to NM_006113.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr1:108307696 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:108138930 G>T maps to NM_006113.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:108116722 C>T maps to NM_006113.4 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr1:108298047 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:108160254 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:118897450 G>T maps to NM_001112704.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:71148363 G>T maps to NM_012476.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:71148412 C>T maps to NM_012476.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr2:71160153 G>A maps to NM_012476.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:71160316 A>T maps to NM_012476.2 K286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:154448518 G>A did not map to a codon.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr23:154456754 G>A did not map to a codon.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr23:154464553 G>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:154456757 G>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr1:101185436 G>T maps to NM_001078.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr1:101196961 C>A maps to NM_001078.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:101188708 C>G maps to NM_001078.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr1:101186080 G>A maps to NM_001078.3 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:101200238 C>A maps to NM_001078.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr1:101194696 C>T maps to NM_001078.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z007-01A-01W-0746-08 chr5:82849189 G>A maps to NM_004385.4 E3167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr5:82833290 C>A maps to NM_004385.4 S1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr5:82837227 C>A maps to NM_004385.4 S2802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr5:82785998 T>A maps to NM_004385.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr5:82815783 A>T maps to NM_004385.4 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr5:82837720 G>T maps to NM_004385.4 E2967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:82849219 A>G maps to NM_004385.4 Q3177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr5:82789452 C>A maps to NM_004385.4 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr5:82833738 A>T maps to NM_004385.4 T1639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr5:82815768 T>C maps to NM_004385.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr5:82833849 A>T maps to NM_004385.4 I1676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr5:82836721 G>T maps to NM_004385.4 E2634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr5:82834299 T>C maps to NM_004385.4 R1826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr5:82835844 A>T maps to NM_004385.4 A2341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:82779403 A>T maps to NM_004385.4 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr5:82786058 G>T maps to NM_004385.4 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr5:82808159 G>A maps to NM_004385.4 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr5:82833253 G>T maps to NM_004385.4 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr5:82875805 C>T maps to NM_004385.4 C3296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr5:82816595 C>G maps to NM_004385.4 S824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:82841368 C>A maps to NM_004385.4 C3093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:82817221 G>T maps to NM_004385.4 E1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr5:82835667 A>G maps to NM_004385.4 T2282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr10:75843122 G>T did not map to a codon.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr10:75849104 C>T maps to NM_014000.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr9:35061053 G>A maps to NM_007126.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr9:35062998 C>A maps to NM_007126.3 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:35060351 C>T maps to NM_007126.3 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:67579088 C>A maps to NM_025054.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:7811751 C>A did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:7811732 C>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:7811670 C>T did not map to a codon.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr23:7811658 G>T did not map to a codon.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr23:7811744 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:7811723 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:8433567 C>A did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:8434330 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr10:76989400 G>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:42259419 C>T maps to ENST00000417062 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr8:42262389 A>G maps to ENST00000417062 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr12:48238660 G>A maps to NM_001017535.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr12:48238558 C>A maps to NM_001017535.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:48240118 T>A maps to NM_001017535.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr12:48251337 G>A maps to NM_001017535.1 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:177648930 C>A did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr4:177649042 C>T maps to NM_005429.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr4:177608434 G>A maps to NM_005429.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr4:177608441 G>A maps to NM_005429.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr4:177650750 G>T maps to NM_005429.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr4:177648973 C>A maps to NM_005429.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr10:135053497 G>A maps to NM_014468.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr10:135053794 G>A maps to NM_014468.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:135051580 C>A maps to NM_014468.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr3:157131777 T>A maps to NM_001167912.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:156979108 C>T maps to NM_001167912.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr17:56060313 T>C maps to NM_007146.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:95645843 A>G maps to NM_017599.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:95694209 C>T maps to NM_017599.3 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr7:100807694 C>A maps to NM_003378.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:100806507 C>T maps to NM_003378.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:135631058 A>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:135618241 G>A did not map to a codon.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:135631166 T>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:135631063 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:135630894 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:135630859 C>A did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:135630860 A>T did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:135618284 G>T did not map to a codon.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr23:135630899 G>T did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:135618293 A>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:135618367 G>T did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:135630822 A>C did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:135618271 C>A did not map to a codon.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr6:117589563 G>T maps to NM_182645.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:117589583 G>A maps to NM_182645.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr3:87017812 G>A maps to NM_016206.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr3:87027792 C>A maps to NM_016206.2 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:87018165 G>A maps to NM_016206.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr3:87017926 A>T maps to NM_016206.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr3:10183845 G>T maps to NM_000551.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:10188228 A>C maps to NM_000551.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr1:156268935 C>A maps to NM_001004319.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:156268965 C>A maps to NM_001004319.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:219297605 C>A maps to NM_007127.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:219294031 C>T maps to NM_007127.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr2:219301980 C>T maps to NM_007127.2 H702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr2:219301246 G>A maps to NM_007127.2 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr2:219296824 C>T maps to NM_007127.2 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr3:38043984 G>T maps to NM_015873.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr10:17275633 G>T maps to NM_003380.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr10:17271972 C>T maps to NM_003380.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr10:17276748 C>T maps to NM_003380.3 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr6:153076458 C>T maps to NM_003381.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr6:153077289 T>A maps to NM_003381.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:42560739 C>G maps to NM_004624.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr3:42569524 C>T maps to NM_004624.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr7:158824739 C>G maps to ENST00000402066 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:37028518 T>A maps to NM_053276.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr2:37041395 C>T maps to NM_053276.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr2:37000952 C>T maps to NM_053276.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:37032693 G>T maps to NM_053276.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr2:37035874 G>T maps to NM_053276.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr2:37036015 G>A maps to NM_053276.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:37036037 A>T maps to NM_053276.3 K605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:37032713 G>T maps to NM_053276.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:36970273 C>A maps to NM_053276.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr2:37035871 C>A maps to NM_053276.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr16:31105879 G>T maps to ENST00000319788 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr9:2635510 G>A maps to NM_003383.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr9:2643479 C>T maps to NM_003383.3 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr23:150573481 G>A did not map to a codon.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr23:150572113 C>T did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:150573508 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:150572141 G>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:150572113 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:4688710 G>A maps to NM_182566.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:57967674 G>T maps to NM_020633.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:57967671 C>A maps to NM_020633.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53762539 C>A maps to NM_173856.2 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:53762488 C>T maps to NM_173856.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:53762620 C>A maps to NM_173856.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:53762773 C>A maps to NM_173856.2 C382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:53762293 G>A maps to NM_173856.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr19:53762758 C>A maps to NM_173856.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:53770624 G>T maps to NM_173857.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr6:133004456 G>T maps to NM_004666.2 S455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr6:133035009 C>A maps to NM_004666.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr6:133073611 G>A maps to NM_004665.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr6:133073885 G>C maps to NM_004665.2 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr6:133072640 T>A maps to NM_004665.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr7:55540619 C>A maps to NM_030796.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr3:51457539 C>A maps to ENST00000273612 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr3:51477788 G>T maps to ENST00000273612 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:51457357 T>C maps to ENST00000273612 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:51458158 C>A maps to ENST00000273612 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:118939978 G>T maps to NM_021729.4 *87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr11:118948670 C>T maps to NM_021729.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:118948941 C>T maps to NM_021729.4 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr11:118944507 A>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr11:118952212 T>C maps to NM_021729.4 F901F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr9:79929508 A>G maps to ENST00000376646 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr9:79980488 G>A maps to ENST00000376646 K2776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:79890421 G>T maps to ENST00000376646 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr9:79908411 A>G maps to ENST00000376646 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr9:79862172 A>C did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:79929504 C>A maps to ENST00000376646 S1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:79936429 A>C maps to ENST00000376646 G1866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr9:79966230 A>T did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr9:79974309 A>G maps to ENST00000376646 S2700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr9:79898508 C>T maps to ENST00000376646 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr9:79816283 C>T maps to ENST00000376646 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr8:100454672 G>T maps to NM_017890.3 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:100832295 G>A maps to NM_017890.3 E3005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:100883034 T>G maps to NM_017890.3 L3830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr8:100182371 C>T maps to NM_017890.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr8:100832256 C>A maps to NM_017890.3 I2992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr8:100866416 C>T maps to NM_017890.3 F3625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr8:100168775 G>A did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:100865783 C>T maps to NM_017890.3 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr8:100831069 C>T maps to NM_017890.3 Q2884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr8:100871592 G>T maps to NM_017890.3 G3668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr8:100733167 A>T maps to NM_017890.3 R2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr8:100108600 C>G maps to NM_017890.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:100568675 A>G did not map to a codon.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr8:100866350 C>T maps to NM_017890.3 L3603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr8:100514084 A>G maps to NM_017890.3 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr8:100829871 G>A maps to NM_017890.3 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8075-01A-11D-2238-08 chr8:100654691 G>A maps to NM_017890.3 V1983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr8:100479816 C>G maps to NM_017890.3 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:100844811 A>G maps to NM_017890.3 R3207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr8:100493867 C>A maps to NM_017890.3 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr8:100732571 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr8:100883804 C>T maps to NM_017890.3 V3900V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-NJ-A4YF-01A-12D-A25L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr8:100523678 C>T maps to NM_017890.3 V1549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr15:62239392 A>G maps to NM_020821.2 H1625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr15:62320619 C>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr15:62276212 T>C did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr15:62221814 C>T maps to NM_020821.2 L2057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr15:62302682 C>A maps to NM_020821.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr15:62292764 C>A maps to NM_020821.2 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr15:62146657 A>C maps to NM_020821.2 *3754E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr15:62304304 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr15:62202475 G>C maps to NM_020821.2 S2915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr15:62176407 C>T maps to NM_020821.2 Q3134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr15:62208142 C>A maps to NM_020821.2 E2712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr15:62302672 G>A maps to NM_020821.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr1:12322046 C>T maps to NM_015378.2 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:12414216 G>T maps to NM_015378.2 T3206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:12475196 C>T maps to NM_015378.2 L4030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr1:12566972 G>A maps to NM_015378.2 L4287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:12304474 C>T maps to NM_015378.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr1:12439541 A>G maps to NM_015378.2 R3694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr1:12342994 C>T maps to NM_015378.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr1:12336515 G>C maps to NM_015378.2 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8090-01A-11D-2238-08 chr1:12342796 A>G maps to NM_015378.2 L1546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:12414216 G>A maps to NM_015378.2 T3206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr1:12408887 A>T maps to NM_015378.2 S3026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:12403043 C>T maps to NM_015378.2 R2941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:12567032 C>T maps to NM_015378.2 L4307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:12381925 C>T maps to NM_015378.2 Q2537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:12382621 C>T maps to NM_015378.2 L2578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:12368512 C>T maps to NM_015378.2 C2155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:12374348 C>A maps to NM_015378.2 T2371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:2846895 C>A maps to NM_022575.2 Y770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr20:2846896 G>T maps to NM_022575.2 E771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr20:2847153 G>T maps to NM_022575.2 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr20:2845909 T>G maps to NM_022575.2 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:2846071 G>T maps to NM_022575.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr15:41188134 G>T did not map to a codon.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr15:41193185 G>T maps to NM_020857.2 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr11:134095108 C>T maps to NM_052875.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr11:134109947 A>C maps to NM_052875.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:145651591 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr8:145650099 C>G did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr12:122726941 G>A maps to NM_022916.4 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr12:122750937 G>A maps to NM_022916.4 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:122723132 C>A did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:53008926 C>A did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr13:53010451 G>C maps to NM_016075.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr8:17132388 A>T maps to NM_152415.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr11:60901508 C>A maps to NM_017966.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:60901537 C>A maps to NM_017966.4 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:73085403 C>T maps to NM_001077621.1 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:42454304 C>T maps to ENST00000348544 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:38785204 C>T maps to NM_014396.3 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:38805188 T>C maps to NM_014396.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:38835163 C>A maps to NM_014396.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr16:69353392 C>T maps to NM_013245.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr18:61077679 C>G did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:33237775 C>T maps to NM_022553.4 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr2:64147083 T>A maps to NM_016516.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr2:64169643 G>C maps to NM_016516.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr2:64208812 T>C maps to NM_016516.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr2:64139748 C>A maps to NM_016516.2 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr1:151158032 G>A maps to ENST00000354473 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:184711793 A>G maps to ENST00000437079 K1203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr3:184654066 G>T maps to ENST00000437079 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr14:97304097 G>T did not map to a codon.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr14:97321559 G>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr2:58276043 C>A maps to NM_001130480.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:58315575 C>A maps to NM_001130480.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:58276091 G>A maps to NM_001130480.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:58311221 A>T did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr2:58366862 C>T maps to NM_001130480.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:50496115 C>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:107320446 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:107315960 C>A did not map to a codon.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr23:107320543 C>T did not map to a codon.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr23:107310330 C>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:107315990 G>C did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:107319356 G>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:107315989 G>T did not map to a codon.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr23:107310217 G>A did not map to a codon.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr23:107310292 A>G did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr12:118504444 C>A maps to NM_019086.5 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:118520235 T>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr11:124618383 C>A maps to NM_014312.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr11:124617481 C>T maps to NM_014312.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr23:65252504 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:65253607 G>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:65259824 C>A did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:65242212 T>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:65242193 C>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:65253490 C>T did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:65242163 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:65247910 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr1:159832287 G>A maps to NM_001013661.1 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:17830708 C>A maps to NM_003385.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:54561569 C>G maps to NM_198481.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:54545591 G>A maps to NM_198481.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:54617552 C>A maps to ENST00000404951 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:54617720 C>G maps to ENST00000404951 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr20:25059380 A>T maps to NM_199425.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr20:25059449 A>G maps to NM_199425.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr20:25059521 A>G maps to NM_014588.4 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr14:74726375 G>T maps to NM_182894.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr14:74726387 C>A maps to NM_182894.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr14:74726369 C>A maps to NM_182894.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr6:142491481 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:142539635 G>A maps to NM_016485.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr10:114298042 G>A maps to NM_145206.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr17:26697215 G>T maps to NM_000638.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:26695910 G>T maps to NM_000638.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr17:26696372 G>T maps to NM_000638.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr17:26694404 A>C maps to NM_000638.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr1:1372745 C>A maps to NM_022834.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr10:116038541 C>T maps to NM_198496.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr10:116032544 A>T maps to NM_198496.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr16:22152984 G>C maps to NM_173615.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr16:22144267 C>A maps to NM_173615.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:22128451 A>C maps to NM_173615.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr16:22149823 G>T maps to NM_173615.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr2:98887339 G>A maps to NM_144992.4 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:98732113 G>T did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:98709642 G>T maps to NM_144992.4 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr2:98736073 C>T maps to NM_144992.4 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr2:98887264 A>T maps to NM_144992.4 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr11:124007381 G>C did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr11:123994448 G>T maps to NM_014622.4 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr11:123988582 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr7:49842350 G>C maps to NM_198570.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr7:49815691 C>A maps to NM_198570.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:49842402 G>T maps to NM_198570.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:49842401 C>A maps to NM_198570.3 Y264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:215279061 C>A maps to NM_001080500.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:215278950 C>T maps to NM_001080500.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr11:61026769 G>A maps to NM_152718.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr11:61039227 G>A maps to NM_152718.2 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr11:61053873 G>T maps to NM_152718.2 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr11:61026548 A>G maps to NM_152718.2 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:6125811 G>A maps to NM_000552.3 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085305 G>A maps to NM_000552.3 Q2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr12:6085324 G>A maps to NM_000552.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr12:6167108 C>T maps to NM_000552.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:6143931 C>G maps to NM_000552.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr12:6182845 G>T maps to NM_000552.3 C312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr12:6121270 C>T maps to NM_000552.3 E1882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr12:6161857 G>T maps to NM_000552.3 C679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr12:6143943 G>A maps to NM_000552.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr12:6182794 G>T maps to NM_000552.3 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr12:6127900 G>T maps to NM_000552.3 I1561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr12:6121285 C>T maps to NM_000552.3 R1877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr12:6058255 G>A maps to NM_000552.3 T2789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr12:6128066 G>T maps to NM_000552.3 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr12:6125933 G>C maps to NM_000552.3 S1719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr12:6134817 G>T maps to NM_000552.3 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr12:6103685 T>G maps to NM_000552.3 R2051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:6132860 A>G maps to NM_000552.3 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr12:6145657 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr12:6181545 C>A maps to NM_000552.3 G354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr12:6143898 C>A maps to NM_000552.3 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:6080791 C>A maps to NM_000552.3 R2507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr12:6058233 C>A maps to NM_000552.3 E2797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr12:6103064 G>A maps to NM_000552.3 N2187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr10:28905205 C>G maps to NM_016628.3 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr10:28905205 C>G maps to NM_016628.3 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6146-01A-11D-1753-08 chr10:28900788 C>T maps to NM_016628.3 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr10:88220931 C>G did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr10:88203070 G>T maps to ENST00000342368 Y1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr14:100820130 C>G maps to NM_173701.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr14:100801256 C>T maps to NM_173701.1 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr1:119575581 T>C maps to NM_015836.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:119575562 C>A maps to NM_015836.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr1:119575682 C>A maps to NM_015836.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr1:119575956 T>A maps to NM_015836.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr23:48549499 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:48547173 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:48547292 C>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:48546835 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:48546813 G>A did not map to a codon.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr23:48547149 G>C did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:48543996 C>A did not map to a codon.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr23:48547387 G>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:48545177 G>T did not map to a codon.
Sequencing variant TCGA-73-7499-01A-11D-2184-08 chr23:48545337 G>T did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr6:110434598 G>T maps to NM_003931.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr13:27256783 G>T maps to NM_006646.5 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr13:27259894 G>T maps to NM_006646.5 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr13:27259980 G>T maps to NM_006646.5 *503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr13:27257050 G>T maps to NM_006646.5 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:123334767 C>A did not map to a codon.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr7:123349178 T>C maps to NM_003941.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:123334895 C>T maps to NM_003941.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:123388755 C>A maps to NM_003941.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:123332589 C>T maps to NM_003941.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr2:74687009 G>C maps to ENST00000393972 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr12:14947585 A>G maps to NM_016312.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr17:73851354 C>T maps to NM_012478.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:102612684 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:102612792 C>A did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:102612909 T>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr23:102612716 A>G did not map to a codon.
Sequencing variant TCGA-97-A4M6-01A-11D-A24P-08 chr23:102612726 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:71135037 C>T maps to NM_022479.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr7:70853322 C>A maps to NM_022479.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:71036293 G>T maps to NM_022479.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr7:71134994 A>G maps to NM_022479.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:70881040 C>A maps to NM_022479.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:71036375 C>T maps to NM_022479.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr7:71134962 G>T maps to NM_022479.1 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr7:70880935 G>T maps to NM_022479.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:70853322 C>A maps to NM_022479.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:71134976 T>A maps to NM_022479.1 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:70853280 G>A maps to NM_022479.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr7:73249146 G>A maps to NM_152559.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:73254794 G>A maps to NM_152559.2 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr7:73255477 G>A maps to NM_152559.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:73280070 G>T maps to NM_182504.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr13:52325502 C>T maps to NM_052950.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr13:52293448 A>T maps to NM_052950.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr4:85724620 C>A did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr4:85678285 C>A maps to NM_014991.4 G1739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr4:85642648 T>C maps to NM_014991.4 Q2506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:85771118 G>A maps to NM_014991.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr4:85752721 C>A maps to NM_014991.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr4:85623504 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:85687017 T>G maps to NM_014991.4 G1711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr4:85738543 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr4:85656258 C>T maps to NM_014991.4 W2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr4:85626627 G>A maps to NM_014991.4 L2752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr4:85687161 C>T maps to NM_014991.4 V1663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr4:85781563 C>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr4:85600129 G>A maps to NM_014991.4 P3363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-8520-01A-11D-2393-08 chr4:85658403 G>A maps to NM_014991.4 H2230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr4:85707200 C>A maps to NM_014991.4 V1331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:85687122 C>T maps to NM_014991.4 E1676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:85660261 C>A maps to NM_014991.4 G2159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr4:85731344 T>C maps to NM_014991.4 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr4:85672767 C>A maps to NM_014991.4 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr4:85654534 C>A maps to NM_014991.4 A2407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr4:85634325 C>G maps to NM_014991.4 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:55493427 C>A did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr14:55462531 C>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr14:55455826 G>C maps to NM_007086.3 S482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr14:55411172 G>A maps to NM_007086.3 F1022F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:10099382 G>A maps to NM_017491.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr4:10090302 G>A maps to NM_017491.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr4:10100689 G>A maps to NM_017491.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr4:10083004 G>A maps to NM_017491.3 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr4:10079460 C>A maps to NM_017491.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr10:122630691 A>T maps to NM_018117.11 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr10:122648615 C>T maps to NM_018117.11 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr10:122668119 C>T maps to NM_018117.11 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr10:122648678 G>A maps to NM_018117.11 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr2:203764279 G>A maps to NM_018256.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr2:203776156 A>G did not map to a codon.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr23:48458940 G>T did not map to a codon.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr23:48457295 A>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:48458016 T>G did not map to a codon.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr23:48460280 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:48457260 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:48460173 G>T did not map to a codon.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr23:48457769 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:48460214 C>A did not map to a codon.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr23:48460277 A>G did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:9538751 C>T maps to NM_145054.4 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr17:9532102 C>T maps to NM_145054.4 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr17:9511435 G>T maps to NM_145054.4 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr4:177058692 G>T maps to NM_170710.4 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr4:177041038 G>A maps to NM_170710.4 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr4:177077245 C>A maps to NM_170710.4 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr4:177069484 T>C maps to NM_170710.4 Y656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:992087 G>T maps to NM_024100.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr4:39233831 C>T maps to NM_025132.3 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr4:39279779 G>T maps to NM_025132.3 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr4:39245930 C>A maps to NM_025132.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr4:39217614 A>T maps to NM_025132.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr14:100934398 C>T maps to NM_001161476.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr14:100847836 C>T maps to NM_001161476.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr14:100996230 G>T maps to NM_001161476.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr1:224605975 G>A maps to NM_025160.6 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr6:170068146 C>A maps to NM_182552.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr6:170068176 C>G maps to NM_182552.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr1:118477139 C>T maps to NM_006784.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:118495149 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr1:118479396 A>T maps to NM_006784.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:116085308 C>A maps to NM_001012361.2 G151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr2:128477084 C>A maps to NM_018383.4 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr2:128476970 G>A maps to NM_018383.4 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr2:128481959 C>A maps to NM_018383.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:128479466 T>C maps to NM_018383.4 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8395-01A-11D-2323-08 chr2:128477060 C>T maps to NM_018383.4 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:128471545 C>T maps to NM_018383.4 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr2:128525864 C>A maps to NM_018383.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:128522331 C>A maps to NM_001006622.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr2:128467293 T>G maps to NM_018383.4 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:128522373 T>A maps to NM_001006622.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr9:131403137 C>T maps to NM_052844.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr9:131398629 C>T maps to NM_052844.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:20145668 C>A maps to NM_001006657.1 G586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110440496 A>T maps to NM_139281.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:110446485 G>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:110428060 C>G maps to NM_139281.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr5:110428090 G>A maps to NM_139281.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr10:1118121 G>T maps to ENST00000416775 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr9:127618015 G>A maps to NM_001045476.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr21:44272434 C>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:117577636 G>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:117570672 T>C did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:117540865 A>C did not map to a codon.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr23:117532433 G>C did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:117566801 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:117530972 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:117543509 A>T did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:117570725 G>C did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:117528038 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:117538406 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:117526693 A>C did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr23:117526803 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:117527113 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:117540950 C>G did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr23:48933219 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:48933403 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:48933082 C>A did not map to a codon.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr23:48933332 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:48933295 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:48934358 C>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr6:33255143 G>C maps to NM_005452.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:109554148 T>C maps to NM_001142550.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr3:167240119 T>C maps to NM_178824.3 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr3:167272541 C>A maps to NM_178824.3 G232G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-69-7979-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr3:167245609 G>A maps to NM_178824.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:167254656 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr3:167218055 C>G maps to NM_178824.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:137007122 C>G maps to NM_052821.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr9:137007536 C>G maps to NM_052821.3 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr9:137005058 G>T maps to NM_052821.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr3:113084978 C>A maps to NM_001164496.1 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr3:113120583 T>A maps to NM_001164496.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr3:113120481 G>A maps to NM_001164496.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr3:113082351 C>A maps to NM_001164496.1 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr3:113152504 C>A maps to NM_001164496.1 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:113115475 T>C maps to NM_001164496.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:113128134 A>G maps to NM_001164496.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr3:113119470 G>T maps to NM_001164496.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr3:196288031 C>A maps to NM_182627.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:74652752 T>C maps to NM_032118.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:140048959 C>G maps to NM_017706.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr5:140044601 C>T maps to NM_017706.4 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:74976634 C>T did not map to a codon.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr16:74951892 A>G maps to NM_030581.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr16:74920198 G>A maps to NM_030581.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:74972088 C>A maps to NM_030581.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr16:74982428 G>A maps to NM_030581.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:74927608 C>A maps to NM_030581.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr16:74927675 G>C maps to NM_030581.3 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr16:74957889 G>A maps to NM_030581.3 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:74943459 C>T maps to NM_030581.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:74908271 G>A maps to NM_030581.3 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr3:49049968 A>C maps to NM_018031.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr3:49051254 C>G maps to NM_018031.3 S793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr3:49050634 G>T maps to NM_018031.3 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:49049782 C>T maps to NM_018031.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr3:49052719 G>A maps to NM_018031.3 *1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr7:158715069 C>T maps to NM_018051.4 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:36590380 G>T maps to NM_001083961.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:36564348 C>T maps to NM_001083961.1 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:36558727 A>T did not map to a codon.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:85547061 A>T maps to NM_145172.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:85592308 G>A maps to NM_145172.3 W743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:85550362 G>A maps to NM_145172.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:85561703 G>C did not map to a codon.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr1:85546999 G>T maps to NM_145172.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr1:85559236 C>G maps to NM_145172.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr1:85561660 G>A maps to NM_145172.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr1:241958534 C>T maps to NM_144625.4 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:241907700 G>T maps to NM_144625.4 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:241943304 G>C did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr1:241886719 C>A maps to NM_144625.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr1:43649514 C>A maps to NM_001195831.1 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr1:43650888 T>C maps to NM_001195831.1 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr12:122399997 G>T maps to NM_144668.4 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:122361784 G>A maps to NM_144668.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr12:122396982 C>T maps to NM_144668.4 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr12:122392024 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr12:122396298 C>T maps to NM_144668.4 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:122396298 C>T maps to NM_144668.4 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr12:122380854 G>T maps to NM_144668.4 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr8:124132399 C>T maps to NM_145647.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:124105845 T>C maps to NM_145647.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr2:228758627 T>G maps to NM_178821.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr2:228767797 G>A maps to NM_178821.1 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6986-01A-11D-1945-08 chr2:228762933 T>C maps to NM_178821.1 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:228771915 A>T maps to NM_178821.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr2:228786186 C>T maps to NM_178821.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr18:54398737 G>A maps to NM_015285.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr18:54446672 T>C maps to NM_015285.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr18:54361911 G>C maps to NM_015285.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr18:54694275 G>T maps to NM_015285.2 S1437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr18:54398638 G>T maps to NM_015285.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr18:54358457 C>T maps to NM_015285.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr18:54629723 A>T maps to NM_015285.2 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr18:54339865 C>T maps to NM_015285.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr18:54694329 G>T maps to NM_015285.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr18:54448786 G>T maps to NM_015285.2 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr18:54339880 C>T maps to NM_015285.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:37381787 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr5:37396475 G>T did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr5:37725120 G>A maps to NM_018034.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:37379591 G>A maps to NM_018034.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr5:37516682 C>G maps to NM_018034.2 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr5:37443460 C>T maps to NM_018034.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:54015096 C>T maps to NM_182758.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:53889378 G>T maps to NM_182758.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr15:53809910 G>A maps to NM_182758.2 P1098P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr15:53997422 T>A maps to NM_182758.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr15:54025289 G>A maps to NM_182758.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr15:53907848 C>A maps to NM_182758.2 G852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr15:53998259 A>T maps to NM_182758.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr15:53908227 C>G maps to NM_182758.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr11:62606599 G>A maps to NM_018093.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr2:190315684 C>T maps to NM_032168.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:190334800 G>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:190334124 G>A maps to NM_032168.1 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr15:44158514 C>T maps to NM_024908.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:111985354 C>G maps to NM_024102.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:67303404 T>A maps to NM_024763.4 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr1:67288076 C>G maps to NM_024763.4 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr1:67299718 C>A maps to NM_024763.4 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr1:67370901 G>A maps to NM_024763.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr1:67288200 C>G did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:3548039 C>T maps to NM_017818.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr17:1640948 A>T maps to NM_001163809.1 S1932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:1640810 C>T maps to NM_001163809.1 T1886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:1637106 C>A maps to NM_001163809.1 G1592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr19:12780996 C>T maps to NM_032332.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:151097184 C>A did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr7:151093185 C>A maps to ENST00000426624 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8206-01A-11D-2238-08 chr19:33639805 C>T maps to NM_173479.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr19:33639781 C>T maps to NM_173479.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr14:64066554 G>A maps to NM_080666.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr16:705381 C>T maps to NM_145294.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr16:706347 C>T maps to NM_145294.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr16:716792 G>T did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:715996 G>A maps to NM_145294.4 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr16:706404 G>T maps to NM_145294.4 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr16:705354 C>T maps to NM_145294.4 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:700151 C>G maps to NM_145294.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr16:711451 C>T maps to NM_145294.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:716960 G>T maps to NM_145294.4 G1687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:134879796 T>A maps to NM_014149.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:134881056 T>A maps to NM_014149.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:134878403 C>A maps to NM_014149.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:134889089 G>C maps to NM_014149.3 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr2:68358577 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr15:90255261 T>C maps to NM_020212.1 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr2:160104949 T>G maps to NM_001128212.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:27620599 C>T maps to ENST00000319394 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr1:27624464 G>A maps to ENST00000319394 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr8:124440235 T>G maps to NM_018024.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr8:124449545 G>T maps to NM_018024.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr8:124449566 G>A maps to NM_018024.1 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr11:9598728 G>T maps to NM_003390.3 G354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr7:141424062 G>A maps to NM_001105558.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:141423009 C>A maps to NM_001105558.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr7:141429402 G>A maps to NM_001105558.1 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr7:141408875 C>A maps to NM_001105558.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:141418963 C>A maps to NM_001105558.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:141420839 G>A maps to NM_001105558.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr16:84353037 A>T maps to NM_021197.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr20:44313525 T>C maps to NM_172131.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5932-01A-11D-1753-08 chr20:43752487 C>A maps to NM_080869.1 *112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:43753034 C>A maps to NM_080869.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr20:43739333 G>T maps to ENST00000307971 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:48917074 C>A maps to NM_175575.5 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:48918081 C>A maps to NM_175575.5 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr17:48918349 C>T maps to NM_175575.5 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr17:48916966 C>A maps to NM_175575.5 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr17:48917893 C>T maps to NM_175575.5 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr17:48917104 C>A maps to NM_175575.5 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr4:6304140 C>T maps to NM_006005.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr4:6303291 G>A maps to NM_006005.3 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr4:6303876 C>T maps to NM_006005.3 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:1952803 G>T maps to NM_133335.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr4:1962799 C>T maps to NM_133335.3 D1098D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr4:1918694 A>G maps to NM_133335.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:1955222 C>T maps to NM_133335.3 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr4:1952851 C>T maps to NM_133335.3 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr4:1957769 G>A maps to NM_133335.3 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr8:38162186 G>A maps to NM_023034.1 Y843Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr8:38146169 C>A maps to NM_023034.1 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr8:38172975 C>T maps to NM_023034.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:38189014 A>G maps to NM_023034.1 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr8:38189080 C>T maps to NM_023034.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:38146988 C>T maps to NM_023034.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr4:2010530 C>T maps to NM_005663.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8457-01A-11D-2323-08 chr4:1993409 G>A maps to NM_005663.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr4:1989723 G>A maps to NM_005663.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr12:56297211 C>A maps to NM_032345.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr12:65462664 T>A maps to NM_007191.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr12:65445188 C>T maps to NM_007191.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:175440099 C>A maps to NM_003387.4 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:175436452 C>A maps to NM_003387.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:175437060 T>G maps to NM_003387.4 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:175437139 C>A maps to NM_003387.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr2:175436602 C>G maps to NM_003387.4 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr2:175437100 T>A maps to NM_003387.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:175450271 C>G maps to NM_003387.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:175436471 G>C maps to NM_003387.4 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3919-01A-02D-1458-08 chr17:38430161 C>G maps to NM_133264.4 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:29915474 G>A maps to NM_001080529.1 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr7:5256249 G>A maps to NM_015610.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:5239289 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:5266858 C>T maps to NM_015610.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:5265456 C>T maps to NM_015610.3 C248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr8:134225225 G>T maps to NM_003882.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr8:134232986 G>T maps to NM_003882.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr8:134225386 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr20:43355731 C>A maps to NM_003881.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr20:43355749 C>G maps to NM_003881.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr6:112382435 G>T maps to NM_198239.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr6:112386140 C>A maps to NM_198239.1 S195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr6:112390714 C>A maps to NM_198239.1 C337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:68611686 G>A maps to NM_024911.6 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:994340 A>C maps to NM_001184985.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr12:991214 A>T maps to NM_001184985.1 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr12:980451 C>T maps to NM_001184985.1 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr12:1005334 G>A maps to NM_001184985.1 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr12:994562 G>A maps to NM_001184985.1 K1791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:994775 C>T maps to NM_001184985.1 P1862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr12:977997 G>T maps to NM_001184985.1 E1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr12:989169 A>G maps to NM_018979.3 P935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr12:970231 C>A maps to NM_001184985.1 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr12:977029 A>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:980428 A>T did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr9:96061493 G>T maps to ENST00000297954 S2059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr9:96051764 G>T maps to ENST00000297954 E1614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr9:96054671 C>T maps to ENST00000297954 V1710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr9:96055149 G>T maps to ENST00000297954 V1838V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr9:95947795 C>G maps to ENST00000297954 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr9:95992120 G>T maps to ENST00000297954 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr9:96062414 C>A maps to ENST00000297954 P2103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:54337610 T>C did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:54337550 C>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:54334455 C>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:54321230 G>T did not map to a codon.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr23:54337557 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:54335696 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:54319352 G>T did not map to a codon.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr23:54264887 T>C did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr23:54359976 T>C did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:54328225 T>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:54334507 A>G did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:54337692 C>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:54224970 G>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:54224971 G>T did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:54259270 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:54337651 G>T did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:54319418 C>A did not map to a codon.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr23:54359890 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:54275592 G>C did not map to a codon.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr23:54285746 C>G did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:54275343 G>A did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:54319406 C>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:54263728 C>T did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:54319699 G>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:54275170 G>A did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:54275770 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:54280509 T>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:54282274 A>G did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr23:54228561 C>G did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:54275484 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:54275517 T>G did not map to a codon.
Sequencing variant TCGA-97-A4M1-01A-11D-A24P-08 chr23:54282207 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:54275958 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr17:40939378 G>A maps to NM_032387.4 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr17:40932967 C>T maps to NM_032387.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr17:40940343 G>T maps to NM_032387.4 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:40948568 G>C maps to NM_032387.4 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr2:219754757 C>T maps to NM_025216.2 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr2:219754781 G>T maps to NM_025216.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:219755015 G>T maps to NM_025216.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:219754830 G>T maps to NM_025216.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr12:49359952 A>G maps to NM_003394.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr12:49361935 G>T maps to NM_003394.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:49360084 G>A maps to NM_003394.3 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr12:49360249 T>A maps to NM_003394.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr12:49361888 G>C maps to NM_003394.3 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:120969704 C>A maps to NM_057168.1 C60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr7:120969619 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr7:120971840 C>A maps to NM_057168.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr7:120965498 C>A maps to ENST00000414945 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr7:116937674 G>T maps to NM_003391.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr7:116937843 G>C maps to NM_003391.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr7:116960807 G>A maps to NM_003391.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr7:116963034 G>A maps to NM_003391.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr1:113033703 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr17:44851199 G>T maps to NM_030753.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:228210454 C>A maps to ENST00000366753 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:228210415 C>T maps to ENST00000366753 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr1:228246784 C>A maps to ENST00000366753 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr1:228238392 C>A maps to ENST00000366753 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr1:228246922 C>T maps to ENST00000366753 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr1:228210487 C>A maps to ENST00000366753 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:22456244 C>T maps to NM_030761.4 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr1:22456295 C>G maps to NM_030761.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr3:55504431 C>A maps to NM_003392.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr12:1741937 C>A maps to NM_032642.2 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:219736486 A>T maps to NM_006522.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr2:219736267 G>T maps to NM_006522.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:13860914 C>T maps to NM_004625.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr3:13896088 C>T maps to NM_004625.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr3:13860823 C>A maps to NM_004625.3 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr3:13916468 G>C maps to NM_004625.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr5:137419792 T>C maps to NM_058244.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:102242449 C>A maps to NM_003393.3 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:102242110 G>A maps to NM_003393.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr1:228109635 C>A maps to NM_003395.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:228109638 C>T maps to NM_003395.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr1:228109548 G>A maps to NM_003395.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr1:228109377 G>A maps to NM_003395.2 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr17:44950056 C>G maps to NM_003396.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr17:44952704 C>T maps to NM_003396.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z036-01A-01W-0746-08 chr17:7606725 A>T maps to NM_018081.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr17:7606310 G>C maps to NM_018081.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr17:7593015 A>G maps to NM_018081.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:7606071 C>G maps to NM_018081.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr17:7606340 G>T maps to NM_018081.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:30954340 G>T maps to NM_000553.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr8:30924679 T>C maps to NM_000553.4 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr8:30958371 G>T maps to NM_000553.4 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr8:30973962 A>T maps to NM_000553.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr8:30938526 A>T maps to NM_000553.4 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr17:25631887 G>T maps to NM_015626.8 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr17:25628922 T>C maps to NM_015626.8 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr17:25630660 G>T maps to NM_015626.8 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:25630600 C>T maps to NM_015626.8 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr17:6021386 T>A maps to NM_015253.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr17:6014169 G>A maps to NM_015253.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr17:6023849 C>A maps to NM_015253.1 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr17:5993694 G>T maps to NM_015253.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr17:5991403 C>T maps to NM_015253.1 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr17:5998420 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr17:5998515 G>T maps to NM_015253.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr12:108604017 G>C maps to ENST00000261400 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:108641766 G>C did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:108589636 C>A maps to ENST00000261400 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr12:108589971 G>C maps to ENST00000261400 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr12:108604066 G>T maps to ENST00000261400 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr12:108603896 G>T did not map to a codon.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr12:108589824 G>T maps to ENST00000261400 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr12:108589746 G>T maps to ENST00000261400 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr12:108618564 C>T maps to ENST00000261400 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:108600147 C>A maps to ENST00000261400 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr12:108603896 G>T did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr12:108642077 G>C maps to ENST00000261400 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr12:108642020 G>T maps to ENST00000261400 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr12:108604048 C>A maps to ENST00000261400 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr12:108604023 C>A maps to ENST00000261400 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr12:108600105 G>A maps to ENST00000261400 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr11:32413610 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:32414251 A>G maps to NM_024426.4 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:32456444 C>A maps to NM_024426.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr11:32413516 C>T did not map to a codon.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr11:32456381 G>C maps to NM_024426.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:32410624 G>T maps to NM_024426.4 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr6:160176509 C>G maps to NM_004906.3 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:34983972 C>T maps to ENST00000270288 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:167850741 G>T maps to NM_001161661.1 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr5:167855768 G>A maps to NM_001161661.1 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr5:167850750 C>G maps to NM_001161661.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr5:167881063 G>T maps to NM_001161661.1 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:167891838 G>T maps to NM_001161661.1 E1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr5:167826494 C>T maps to NM_001161661.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr5:167798480 G>T maps to NM_001161661.1 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr4:184233491 A>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr4:184205470 G>T maps to ENST00000448232 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr4:184205515 A>T maps to ENST00000448232 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:184210673 G>A maps to ENST00000448232 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:10085244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:10109475 G>C did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:10066579 G>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:10085241 C>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:10078059 G>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr23:10096091 C>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:10093090 C>A did not map to a codon.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr23:10092350 G>C did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:10096669 G>C did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:10106946 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:10093087 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:10093088 C>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:10094300 G>T did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr23:10062250 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:10085252 C>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:10094315 A>G did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:10096647 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:10096092 C>T did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr23:10062260 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:10035346 C>T did not map to a codon.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr23:10107494 G>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:10106816 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr23:10047838 G>C did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:10058825 G>T did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr16:78458909 C>G maps to NM_016373.1 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:87424097 A>G maps to NM_007013.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:69970319 C>T maps to NM_007014.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:69942662 G>T did not map to a codon.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr16:69965410 G>A did not map to a codon.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:149374754 G>A maps to NM_001168278.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:7687538 C>A maps to NM_020196.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr19:7684527 G>T maps to NM_020196.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr19:7685329 C>T maps to NM_020196.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:7692715 G>A maps to NM_020196.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr19:7692211 G>T maps to NM_020196.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8552-01A-11D-2393-08 chr19:7688088 G>C maps to NM_020196.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:52893843 C>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:52896081 A>T did not map to a codon.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr23:52893882 A>C did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:52896111 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:52842244 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:52844148 C>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:52842249 G>T did not map to a codon.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr23:52844155 A>G did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr22:29191698 G>A maps to ENST00000403532 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168549358 G>A maps to NM_002995.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr1:168550403 C>A maps to NM_002995.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr1:168511286 C>T maps to NM_003175.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:46062815 G>T maps to NM_005283.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr3:46063106 G>A maps to NM_005283.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr3:46063307 G>T maps to NM_005283.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:31588954 C>T maps to NM_000379.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr2:31595227 C>A maps to NM_000379.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr2:31573032 C>T maps to NM_000379.3 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr2:31598367 G>A maps to NM_000379.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr2:31621490 C>A maps to NM_000379.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr2:31602825 G>A maps to NM_000379.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:31587068 C>A maps to NM_000379.3 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr2:31571172 C>A maps to NM_000379.3 G1036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JP-01A-11D-A24P-08 chr2:31595110 C>T maps to NM_000379.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr2:31621553 G>T maps to NM_000379.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr23:2712624 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:2712643 G>T did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:2688629 C>A did not map to a codon.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr23:2729459 C>G did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:2712604 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:123020297 G>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:123040875 G>T did not map to a codon.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:123020084 C>A did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:123019557 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:123019763 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:123019992 T>A did not map to a codon.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr23:123040863 C>G did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:123019760 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:123041010 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:39226646 G>T maps to NM_194293.2 A1430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr3:39230225 C>G maps to NM_194293.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39227078 G>T maps to NM_194293.2 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:39228032 C>T maps to NM_194293.2 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:39227261 G>T maps to NM_194293.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr3:39229100 T>A maps to NM_194293.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr3:39228103 G>T maps to NM_194293.2 R945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr3:39227570 C>T maps to NM_194293.2 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:39227603 G>T maps to NM_194293.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr3:39229550 C>G maps to NM_194293.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr3:39227927 A>T maps to NM_194293.2 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr2:168101336 A>T maps to NM_152381.5 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:168107426 C>A maps to NM_152381.5 P3175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr2:168107679 G>T maps to NM_152381.5 E3260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168067242 A>T did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr2:168101658 G>T maps to NM_152381.5 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr2:168102743 C>A maps to NM_152381.5 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:168102030 G>T maps to NM_152381.5 E1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:168100622 G>T maps to NM_152381.5 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168102687 C>T maps to NM_152381.5 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:168107270 T>C maps to NM_152381.5 F3123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr2:168106379 A>C maps to NM_152381.5 S2826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr2:168102023 C>A maps to NM_152381.5 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:167760381 A>T maps to NM_152381.5 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr2:168104771 A>C maps to NM_152381.5 P2290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr2:168107682 G>T maps to NM_152381.5 E3261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:168114370 G>T maps to ENST00000420519 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr2:167992447 G>T maps to NM_152381.5 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr2:168107879 G>A maps to NM_152381.5 V3326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr2:168108350 G>T maps to NM_152381.5 T3483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:168105191 C>A maps to NM_152381.5 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:168102044 G>A maps to NM_152381.5 K1381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr2:168104900 G>A maps to NM_152381.5 K2333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr2:168114687 G>A maps to ENST00000420519 E577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168099599 G>A maps to NM_152381.5 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr2:168106953 C>T maps to NM_152381.5 Q3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:168106648 C>G maps to NM_152381.5 S2916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr2:167760138 G>A maps to NM_152381.5 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:167760006 G>A maps to NM_152381.5 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr2:168103166 G>A maps to NM_152381.5 L1755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr2:168101739 G>T maps to NM_152381.5 E1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:168105800 G>T maps to NM_152381.5 S2633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr2:168107039 C>A maps to NM_152381.5 P3046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:168102002 T>A maps to NM_152381.5 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr2:168114603 T>A maps to ENST00000420519 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168103075 C>A maps to NM_152381.5 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:168104597 C>T maps to NM_152381.5 H2232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr2:168104681 C>A maps to NM_152381.5 S2260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:168098401 C>A maps to NM_152381.5 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:168108196 C>A maps to NM_152381.5 S3432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr2:168104327 G>A maps to NM_152381.5 K2142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr2:168074800 A>G maps to NM_152381.5 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr2:168105644 A>G maps to NM_152381.5 T2581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:168100532 T>C maps to NM_152381.5 H877H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr2:168100847 C>T maps to NM_152381.5 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr2:168115059 T>C maps to ENST00000420519 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:168105197 T>C maps to NM_152381.5 H2432H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:168114826 G>T maps to ENST00000420519 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr2:168106784 G>T maps to NM_152381.5 V2961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:168101942 G>A maps to NM_152381.5 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr2:168104333 T>A maps to NM_152381.5 P2144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:168107312 T>A maps to NM_152381.5 T3137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr2:168107642 T>C maps to NM_152381.5 A3247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:168100535 A>T maps to NM_152381.5 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:168105068 T>C maps to NM_152381.5 S2389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:168099386 G>A maps to NM_152381.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr2:168102029 A>G maps to NM_152381.5 Q1376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:168104537 T>C maps to NM_152381.5 L2212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr2:168105671 A>G maps to NM_152381.5 Q2590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr2:168107381 G>C maps to NM_152381.5 S3160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr2:168100899 C>T maps to NM_152381.5 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr2:168104561 C>A maps to NM_152381.5 S2220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:167760209 C>A maps to NM_152381.5 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:168100392 G>T maps to NM_152381.5 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr2:168104711 C>G maps to NM_152381.5 S2270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr2:168104093 C>T maps to NM_152381.5 V2064V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr2:168103979 A>G maps to NM_152381.5 V2026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr2:168100031 G>T maps to NM_152381.5 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:37587591 C>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:37545434 T>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:37545269 C>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:37587551 G>T did not map to a codon.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr23:37587653 G>T did not map to a codon.
Sequencing variant TCGA-78-7163-01A-12D-2063-08 chr23:37553662 C>A did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:37587350 G>C did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr22:17264940 G>C maps to NM_175878.3 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:17280688 G>A maps to NM_175878.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr8:56436338 C>A maps to NM_052898.1 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr8:56015095 C>T maps to NM_052898.1 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr8:10755668 C>T maps to NM_173683.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr8:11058764 G>A maps to NM_173683.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr8:10755776 C>A maps to NM_173683.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:10756121 T>A maps to NM_173683.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:10756149 C>T maps to NM_173683.3 W413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:30584557 G>A maps to NM_001011718.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr20:30584764 C>T maps to NM_001011718.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:30585070 G>C maps to NM_001011718.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr20:30584329 C>G maps to NM_001011718.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr20:30556124 G>C maps to NM_001011718.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr20:30584710 G>A maps to NM_001011718.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:30584608 C>A maps to NM_001011718.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr20:30584929 G>C maps to NM_001011718.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr20:30585238 G>T maps to NM_001011718.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:30585220 G>T maps to NM_001011718.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:71619240 G>T maps to NM_001011720.1 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:100182990 A>G did not map to a codon.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr23:100169468 T>C did not map to a codon.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:100178003 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:100183083 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:100178006 C>G did not map to a codon.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr23:100169410 A>G did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:14193876 C>A maps to NM_004628.4 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr3:14207052 G>A maps to NM_004628.4 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:111633123 C>T did not map to a codon.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr10:111667571 G>A maps to NM_020383.3 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr10:111639975 G>T maps to NM_020383.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr10:111646060 T>A maps to NM_020383.3 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:128901652 G>A did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:128886269 C>G did not map to a codon.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr23:128896678 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:128901639 T>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:128890484 C>A did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr23:128881583 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:128880264 T>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:128876112 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:128901595 G>T did not map to a codon.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr23:128877984 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:128890489 C>G did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:128884514 G>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:128880266 G>A did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:128902343 G>A did not map to a codon.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr23:128887221 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:128876095 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:128894497 C>T did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:128890528 C>T did not map to a codon.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr23:128873206 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:128901598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:41318432 C>T maps to NM_022098.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr22:41282318 G>T maps to NM_022098.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr2:61721087 C>A maps to NM_003400.3 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr2:61753557 C>A maps to NM_003400.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr2:61726957 G>A maps to NM_003400.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr13:21476837 G>A maps to NM_022459.4 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr13:21442841 T>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:43499296 G>C maps to NM_020750.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr6:43496604 T>C maps to NM_020750.2 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr16:28133054 G>A maps to NM_015171.2 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr16:28112853 T>C maps to NM_015171.2 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr16:28128692 G>A maps to NM_015171.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr16:28124238 G>A maps to NM_015171.2 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:28112946 G>A maps to NM_015171.2 H1036H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr16:28128749 G>A maps to NM_015171.2 Y631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr16:28164032 G>A maps to NM_015171.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr16:28157506 G>A maps to NM_015171.2 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr16:28167756 G>A maps to NM_015171.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr8:21860755 C>T maps to ENST00000434536 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:21835335 T>A maps to ENST00000434536 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:21833877 G>A maps to ENST00000434536 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr8:21840308 G>T maps to ENST00000434536 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr8:21843106 A>G maps to ENST00000434536 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:21859695 T>A maps to ENST00000434536 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr12:64828638 C>T maps to NM_007235.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr12:64833061 G>T maps to NM_007235.3 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr12:64814178 G>T maps to NM_007235.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:180832880 G>T maps to NM_004736.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:180775251 G>T maps to NM_004736.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr1:180804095 G>T maps to NM_004736.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:44058903 G>C maps to NM_006297.2 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:44047544 C>T maps to NM_006297.2 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:44051122 G>C maps to NM_006297.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr19:44079130 G>C maps to NM_006297.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr2:217012885 C>G maps to NM_021141.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:217012853 C>T maps to NM_021141.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7953-01A-11D-2184-08 chr2:216990663 C>G maps to NM_021141.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr2:217057440 G>A maps to NM_021141.3 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr22:42032774 G>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr12:58350589 G>T maps to NM_033276.2 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr12:58335606 C>T maps to NM_033276.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr3:142123762 T>C maps to NM_019001.3 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr3:142090171 T>A did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:142051223 C>T maps to NM_019001.3 K1404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr3:142133084 G>A maps to NM_019001.3 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7760-01A-11D-2167-08 chr3:142116273 G>A maps to NM_019001.3 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr3:142145684 T>A did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr3:38420766 C>T maps to NM_005108.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:38415992 G>T maps to NM_005108.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr3:38407196 C>T maps to NM_005108.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr3:38411652 A>G maps to NM_005108.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:17221696 T>A maps to NM_022166.3 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr16:17353088 G>T maps to NM_022166.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:17202797 G>T maps to NM_022166.3 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:17292208 G>T maps to NM_022166.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr16:17294469 C>A maps to NM_022166.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr16:17211811 C>A maps to NM_022166.3 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:17202755 C>A maps to NM_022166.3 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr16:17353220 A>T maps to NM_022166.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr16:17202590 C>T maps to NM_022166.3 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr16:17353049 C>A maps to NM_022166.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr16:17221525 G>A maps to NM_022166.3 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr16:17292085 C>T maps to NM_022166.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:17202826 C>A maps to NM_022166.3 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:17228340 C>T maps to NM_022166.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr16:17232210 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:17202620 G>A maps to NM_022166.3 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:17353100 G>T maps to NM_022166.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:17353196 A>G maps to NM_022166.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr16:17211517 G>A maps to NM_022166.3 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr16:17202848 C>A maps to NM_022166.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:17211545 G>A maps to NM_022166.3 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr16:17232304 G>C maps to NM_022166.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr16:17228582 G>T maps to NM_022166.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:48433492 C>A maps to NM_022167.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr17:48435698 C>T maps to NM_022167.2 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr11:102033252 A>T maps to NM_001130145.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr11:102100562 G>A maps to NM_001130145.2 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr1:33272109 C>T maps to NM_003680.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr1:33276517 C>T maps to NM_003680.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:33245124 C>G did not map to a codon.
Sequencing variant TCGA-55-6980-01A-11D-1945-08 chr17:7192944 G>A maps to NM_015982.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr17:7193722 T>A maps to NM_015982.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:183446630 G>T maps to NM_018023.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr3:183446631 G>T maps to NM_018023.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:183432967 A>T maps to NM_018023.4 R6R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-49-4486-01A-01D-1265-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr3:183490250 G>T maps to NM_018023.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr3:183472055 A>T maps to NM_018023.4 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr3:183471912 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr3:183474376 C>T maps to NM_018023.4 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr3:183446515 C>G maps to NM_018023.4 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr18:756704 T>C maps to NM_005433.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr18:743352 G>A maps to NM_005433.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr18:743035 T>C maps to NM_005433.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr18:732912 C>A maps to NM_005433.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr11:66052151 G>A maps to ENST00000376904 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr1:54344343 G>A maps to NM_018982.4 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr1:54332052 T>A maps to NM_018982.4 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr6:43480051 C>T maps to ENST00000506469 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr2:32530694 A>T maps to NM_032312.3 *245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr5:143539984 G>A maps to NM_030799.7 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:67733216 C>A did not map to a codon.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr23:67731777 T>C did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr4:44638038 C>A maps to NM_182592.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr4:44638038 C>T maps to NM_182592.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr14:75248654 G>T maps to NM_019589.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr14:75276210 A>T maps to NM_019589.2 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr14:75266343 C>G maps to NM_019589.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr14:75230866 G>A maps to NM_019589.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:75283737 C>T maps to NM_019589.2 I1930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:75230536 C>G maps to NM_019589.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr14:75230732 C>T maps to NM_019589.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr14:75265291 C>T maps to NM_019589.2 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr14:75248809 G>T maps to NM_019589.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr14:75248678 C>T maps to NM_019589.2 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr10:27437843 G>C maps to NM_139312.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr10:27425219 C>A maps to NM_139312.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr10:27436424 A>G did not map to a codon.
Sequencing variant TCGA-80-5607-01A-31D-1945-08 chr10:27437884 G>A maps to NM_139312.1 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TE-01A-22D-A25L-08 chr10:27423039 G>T maps to NM_139312.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr2:135744395 G>A maps to NM_025052.3 N682N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr2:135738893 G>A maps to NM_025052.3 F1139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr2:135744470 A>T maps to NM_025052.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr2:135744056 G>A maps to NM_025052.3 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:135779283 C>A did not map to a codon.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr2:135756461 G>T maps to NM_025052.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:135744682 A>G maps to NM_025052.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:135738404 G>A maps to NM_025052.3 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr2:135744716 C>T maps to NM_025052.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr4:69203447 G>A maps to NM_001031732.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr4:69195781 C>A maps to NM_001031732.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr4:69197846 C>A maps to NM_001031732.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr4:69195742 G>C maps to NM_001031732.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr5:112878168 C>G maps to NM_022828.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr5:112903394 C>T maps to NM_022828.3 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr5:112849744 C>T maps to NM_022828.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr5:112917374 G>T maps to NM_022828.3 E1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr5:112927871 G>T maps to NM_022828.3 G1403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr5:112915283 G>T maps to NM_022828.3 V1082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:64098704 G>C did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr20:43530260 G>A maps to NM_139323.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr7:75988082 C>A maps to NM_012479.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:32352123 A>C did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr8:101936181 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr1:155629621 T>G maps to ENST00000368339 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr1:155638450 G>A maps to ENST00000368339 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr1:155629945 G>A maps to ENST00000368339 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr1:155638423 G>A maps to ENST00000368339 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr23:21874863 G>T did not map to a codon.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr23:21875588 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:21874908 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:21875263 C>T did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:21875214 G>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:21874982 G>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:21875275 C>A did not map to a codon.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr23:21875363 C>G did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:21875378 C>G did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:21875590 C>G did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:21875098 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr17:74077484 T>A did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr17:74078567 C>G maps to NM_180990.3 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr2:174131330 T>C maps to NM_016653.2 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr2:174086029 G>A maps to NM_133646.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:100364780 C>T maps to ENST00000349350 N1587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:100373108 A>T maps to ENST00000349350 K1980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:100344278 G>C maps to ENST00000349350 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:100361491 G>T maps to ENST00000349350 S1350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:100389699 A>G maps to ENST00000349350 V2547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100344251 G>A maps to ENST00000349350 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr7:100388667 C>T maps to ENST00000349350 P2487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:100350424 C>A maps to ENST00000349350 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr7:100388610 G>T maps to ENST00000349350 A2468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:100350634 C>A maps to ENST00000349350 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr7:100348467 C>A maps to ENST00000349350 Y490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr7:100348416 G>C maps to ENST00000349350 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr7:100350046 C>T maps to ENST00000349350 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:100363023 C>A maps to ENST00000349350 C1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:100334226 G>T maps to ENST00000349350 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr7:100350646 G>A maps to ENST00000349350 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr7:100386860 G>A maps to ENST00000349350 P2416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:100373326 C>A maps to ENST00000349350 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr7:100349611 C>A maps to ENST00000349350 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr7:100364792 G>T maps to ENST00000349350 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr7:100345263 G>A maps to ENST00000349350 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr7:100391520 C>T maps to ENST00000349350 P2622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr7:100349485 C>A maps to ENST00000349350 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:98349796 G>T maps to NM_001079.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-6178-01A-11D-1753-08 chr2:98354269 C>A maps to NM_001079.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:98351823 C>A maps to NM_001079.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:98354341 C>T maps to NM_001079.3 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr3:167086303 C>A maps to ENST00000307529 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:167090620 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr3:167051691 C>A maps to ENST00000307529 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:167068219 T>G maps to ENST00000307529 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr3:167023706 G>A maps to ENST00000307529 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr3:167000058 C>A maps to ENST00000307529 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:167016241 A>T maps to ENST00000307529 L577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr3:167033536 C>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr3:167016161 C>A maps to ENST00000307529 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr3:167045852 G>A maps to ENST00000307529 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr23:2407350 G>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:2407569 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:2407022 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:2406875 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:2406876 C>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:2407790 G>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:2407786 G>C did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:2408366 C>A did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:2407796 A>C did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:2406919 G>A did not map to a codon.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr23:2406933 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr23:2408324 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:111312892 G>T maps to NM_024508.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr3:111312501 C>A maps to NM_024508.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr22:50280789 G>A maps to NM_014838.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr22:50278347 G>T maps to NM_014838.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr22:50277564 G>A maps to NM_014838.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr22:50280621 G>A maps to NM_014838.2 W1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr22:50279733 C>T maps to NM_014838.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:50278845 G>A maps to NM_014838.2 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr22:50279145 G>A maps to NM_014838.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr20:56191345 A>T maps to NM_030776.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr20:56186834 G>T maps to NM_030776.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr20:56186807 G>T maps to NM_030776.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:56188231 G>A maps to NM_030776.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr8:81412048 C>T maps to NM_001105539.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr6:31868935 G>A maps to NM_181842.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr6:31869004 G>A maps to NM_181842.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr11:114121117 G>T maps to NM_001018011.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr11:113935029 G>C maps to NM_001018011.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:113934618 C>A maps to NM_001018011.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr11:113934378 G>A maps to NM_001018011.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:113934448 G>T maps to NM_001018011.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:16269619 G>A maps to ENST00000375733 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:16272688 G>A maps to ENST00000375733 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:114069646 T>C maps to NM_001164342.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr3:114069769 G>A maps to NM_001164342.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr3:114070510 G>A maps to NM_001164342.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr3:114070029 C>A maps to NM_001164342.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr3:114070630 G>A maps to NM_001164342.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr3:114070242 C>A maps to NM_001164342.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr3:114070126 C>A maps to NM_001164342.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr6:33282995 C>A maps to NM_001145338.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:33284435 G>C maps to NM_001145338.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr6:33284168 G>A maps to NM_001145338.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr6:109802712 C>A maps to NM_014797.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr6:109798035 G>T maps to NM_014797.2 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr6:109787214 G>A maps to NM_014797.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr14:64954636 G>A maps to NM_006977.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr14:64954029 G>A maps to NM_006977.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr9:125682048 G>A maps to NM_020924.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr9:125681460 G>A maps to NM_020924.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr9:125680983 C>A maps to NM_020924.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr9:125681087 G>A maps to NM_020924.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr11:62519824 G>T maps to NM_024784.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr11:62520803 G>A maps to NM_024784.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr11:62519744 G>A maps to NM_024784.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr11:62519813 G>A maps to NM_024784.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:36205629 C>A maps to NM_014383.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:36207479 C>T maps to NM_014383.1 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:36205666 C>T maps to NM_014383.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr23:119387449 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:119388308 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:119387930 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:119389208 C>T did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:119388141 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:119388003 C>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:119388872 G>T did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr23:119387406 A>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:119388095 C>T did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:141163053 A>T maps to NM_001080412.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr3:141163938 C>T maps to NM_001080412.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr12:57398383 A>G maps to NM_014830.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr12:57396733 C>A maps to NM_014830.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr12:57396913 C>T maps to NM_014830.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr17:7366180 C>T maps to NM_020899.3 W707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr17:7369061 C>T maps to NM_020899.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr1:22837824 G>T maps to NM_014870.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:22817989 A>G maps to NM_014870.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr1:22837736 C>A maps to NM_014870.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:22850840 C>T maps to NM_014870.3 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7149-01A-11D-2036-08 chr1:22817949 C>G maps to NM_014870.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr1:197169210 T>A maps to NM_194314.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr1:197168773 G>C maps to NM_194314.2 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:197128670 G>A maps to NM_194314.2 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr1:197160927 T>A maps to NM_194314.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr11:130131093 G>C maps to ENST00000397753 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr19:59028203 A>C maps to NM_032792.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr20:62421330 A>T maps to NM_025224.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr20:62407079 G>A maps to NM_025224.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr20:62421978 C>T maps to NM_025224.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:42701284 C>T maps to NM_145166.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:6641241 G>A maps to NM_005341.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr1:6640756 C>T maps to NM_005341.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr4:4323003 G>T maps to NM_145291.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr9:37442081 G>C maps to NM_014872.2 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:4055176 G>A maps to NM_015898.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr1:154987711 G>T maps to ENST00000417934 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:154988887 C>G maps to ENST00000417934 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:154988869 C>T maps to ENST00000417934 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr18:45566353 C>A maps to NM_001039360.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:45555912 C>A maps to NM_001039360.2 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr6:33424181 A>T maps to NM_152735.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8505-01A-11D-2393-08 chr12:56514720 T>C maps to NM_032786.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr1:203819697 A>G maps to NM_014827.4 K665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr1:203802970 A>G maps to NM_014827.4 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr1:203798747 A>G maps to NM_014827.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr1:37941168 C>T maps to NM_025079.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr1:37948854 C>T maps to NM_025079.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:64722024 G>C did not map to a codon.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:64722394 C>T did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr23:64722831 A>G did not map to a codon.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr23:64722401 C>T did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:64719039 C>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:64722957 C>G did not map to a codon.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr23:64718907 G>A did not map to a codon.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr23:64722998 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:64709137 G>A did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:64722396 G>A did not map to a codon.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr23:64721748 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:64722498 A>T did not map to a codon.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr23:64718893 G>A did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:64709218 C>A did not map to a codon.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr23:64722913 T>C did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:64721935 T>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:64722882 G>T did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:64709192 G>A did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:64708992 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:64722526 G>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr11:110023680 A>T maps to NM_033390.1 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr11:110036056 C>T maps to NM_033390.1 D749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr11:110035865 A>C maps to NM_033390.1 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr13:46559777 C>G maps to ENST00000242848 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr13:46559767 T>A maps to ENST00000242848 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr13:46543897 C>G maps to ENST00000242848 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr13:46544031 C>A maps to ENST00000242848 E883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr13:46559509 T>A maps to ENST00000242848 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr13:46549545 C>T maps to ENST00000242848 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr13:46549881 C>A maps to ENST00000242848 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr13:46543168 C>A maps to ENST00000242848 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr13:46544073 G>A maps to ENST00000242848 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr14:89061132 G>A maps to NM_207662.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr14:89061322 G>T maps to NM_207662.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr14:89039333 G>T maps to NM_024824.4 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr14:89061355 G>T maps to NM_207662.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr14:89038456 G>T maps to NM_024824.4 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr2:187366000 T>G maps to NM_018471.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr2:187371498 A>G maps to NM_018471.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr16:88694394 C>G maps to ENST00000452588 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:88644073 G>A maps to ENST00000452588 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:144621344 G>A maps to NM_015117.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr8:144590043 A>G maps to NM_015117.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr8:144557622 G>C maps to NM_015117.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:144522322 C>T maps to NM_015117.2 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr8:144557622 G>A maps to NM_015117.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr8:144620696 C>A maps to NM_015117.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr8:144620207 G>A maps to NM_015117.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:144620309 T>G maps to NM_015117.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:47570647 G>A maps to NM_015168.1 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:47569696 C>A maps to NM_015168.1 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:47585438 A>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:47589763 G>T maps to NM_015168.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:47584879 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:113088699 A>G maps to NM_198581.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:11855294 G>A maps to NM_014153.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:11855763 A>G did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr16:11873189 A>G maps to NM_014153.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr22:41742175 G>T maps to ENST00000351589 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr22:41737149 G>A maps to ENST00000351589 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr7:138764581 G>A maps to ENST00000464606 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr23:64141710 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:64140030 C>A did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr23:64139002 A>T did not map to a codon.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr23:64138938 G>T did not map to a codon.
Sequencing variant TCGA-50-5044-01A-21D-1855-08 chr23:64141840 G>C did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:64137683 C>T did not map to a codon.
Sequencing variant TCGA-91-6840-01A-11D-1945-08 chr23:64139009 G>T did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:64140088 C>A did not map to a codon.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:52901104 G>A maps to NM_001009881.2 Q1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr1:52926895 C>A did not map to a codon.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr1:52911671 A>G maps to NM_001009881.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr1:52981708 C>A maps to NM_001009881.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr1:52902466 T>C maps to NM_001009881.2 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr1:52991904 C>T maps to NM_001009881.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr23:117960044 G>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:117960104 A>G did not map to a codon.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr23:117959386 C>A did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:117959225 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr23:117960319 G>T did not map to a codon.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr23:117960177 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:117959241 G>A did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:117959423 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:117960377 G>T did not map to a codon.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr23:117960348 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:117959821 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:117959579 G>T did not map to a codon.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr23:117960016 C>G did not map to a codon.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr23:117960151 G>T did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:117959830 C>T did not map to a codon.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:117960200 C>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:117960035 G>A did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:117960205 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:117959871 G>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:117959310 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:117960380 C>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:73524208 T>C did not map to a codon.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr23:73524476 G>T did not map to a codon.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr23:73524137 G>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:73524365 C>A did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:73524387 G>T did not map to a codon.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr16:87446013 A>G maps to NM_015144.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr16:87445371 G>A maps to NM_015144.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:111698881 A>C did not map to a codon.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr23:111698883 C>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:111698311 G>C did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:111698291 C>A did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:111698576 C>G did not map to a codon.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr23:111698304 G>T did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:111698204 A>T did not map to a codon.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr23:111698839 C>A did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:111698532 C>T did not map to a codon.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr23:111698856 C>A did not map to a codon.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr23:111698618 C>G did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr23:111698526 C>A did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:111698206 C>G did not map to a codon.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr23:111698858 G>A did not map to a codon.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr23:111698579 G>C did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:111698591 C>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:111698401 A>T did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr23:111698802 T>C did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:111698694 C>A did not map to a codon.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr23:111698015 A>G did not map to a codon.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr23:111698466 C>T did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:103359389 C>A did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:60241758 A>G maps to NM_017742.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr18:60242088 C>G maps to NM_017742.4 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr20:279018 G>T maps to NM_033089.6 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr4:25351146 G>T maps to NM_024936.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:77912724 G>T did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:77912692 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:77913148 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:77913591 G>A did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr23:77912914 C>A did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr23:77913899 T>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:77913598 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:77912644 C>T did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr23:77912648 C>T did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:77913900 G>T did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:77912682 G>T did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:77913581 T>C did not map to a codon.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr23:77912811 A>G did not map to a codon.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr23:77912977 C>G did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:77912565 G>T did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:77912566 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:77912558 A>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:77912668 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:77913875 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:77913661 G>C did not map to a codon.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr23:77912773 G>A did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:77912660 G>T did not map to a codon.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr23:77912981 G>T did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr23:77912814 G>T did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:77912627 G>T did not map to a codon.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr23:77913137 A>G did not map to a codon.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr23:77913734 G>T did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr23:77913897 G>T did not map to a codon.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr23:77912926 G>A did not map to a codon.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr23:77913592 G>T did not map to a codon.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr23:77913553 C>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr23:77912742 A>G did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:77912750 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:77913725 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:77913592 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr23:77913324 T>C did not map to a codon.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr23:77912896 T>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:88938431 C>A maps to NM_024617.3 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr9:88953755 T>C maps to NM_024617.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr9:37126664 A>T maps to NM_032226.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr12:122958139 C>T maps to NM_017612.2 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr12:122973979 T>A maps to NM_017612.2 K152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr5:80608438 G>T maps to NM_032280.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr5:80604807 G>A maps to NM_032280.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr12:42707553 C>A maps to NM_033114.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr7:100002652 C>A maps to NM_017984.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr3:28454783 A>G maps to NM_001040432.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:207174981 A>C maps to NM_020923.1 S1910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:207169695 C>A maps to NM_020923.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr2:207172244 C>G maps to NM_020923.1 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr2:207174291 G>T maps to NM_020923.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr2:207174787 C>T maps to NM_020923.1 L1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr2:207175446 C>A maps to NM_020923.1 P2065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:207171009 T>C maps to NM_020923.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:207175065 G>A maps to NM_020923.1 Q1938Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr2:207174291 G>T maps to NM_020923.1 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr16:67428916 C>A maps to NM_013304.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr5:843742 C>A maps to NM_024786.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr5:850512 T>A maps to NM_024786.2 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr5:825341 C>T maps to NM_024786.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:840718 C>A maps to NM_024786.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr5:850633 G>A maps to NM_024786.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr5:837563 G>T maps to NM_024786.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr5:840640 C>A maps to NM_024786.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr11:19177404 C>T maps to NM_019028.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr6:157963721 C>T maps to NM_024630.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:158053869 A>T maps to NM_024630.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr6:158053870 C>T maps to NM_024630.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr23:74742810 G>A did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:74670724 A>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr23:74742845 C>A did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:74644524 T>G did not map to a codon.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr23:74742845 C>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:74698764 C>G did not map to a codon.
Sequencing variant TCGA-67-6216-01A-11D-1753-08 chr23:74644505 G>C did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:74648924 G>C did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:74644563 G>T did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:74670758 T>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:74742844 C>A did not map to a codon.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr12:77209681 C>T maps to NM_015336.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr1:27176876 C>G maps to NM_032283.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr1:27159093 G>A maps to NM_032283.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr3:195936324 G>T maps to NM_001039617.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:195935335 C>A maps to NM_001039617.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:17063253 A>G maps to NM_016353.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr3:113672952 A>T maps to NM_173570.3 K190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr11:66307260 G>A maps to NM_207340.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:114192138 A>T maps to NM_022494.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr10:114200366 T>A maps to NM_022494.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr16:85010787 G>A maps to NM_001145548.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr23:128946791 G>C did not map to a codon.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr23:128975898 T>A did not map to a codon.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr23:128975780 C>A did not map to a codon.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr23:128962955 C>A did not map to a codon.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr23:128975777 T>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:128945379 A>C did not map to a codon.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr23:128945478 C>A did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr23:128946762 G>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:128957771 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:128963062 C>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr10:31749999 A>G maps to NM_001174096.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:31810710 C>T maps to NM_001174096.1 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr10:31813003 G>A maps to NM_001174096.1 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:31815706 A>T maps to NM_001174096.1 K965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:31810746 G>C maps to NM_001174096.1 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr10:31799727 C>T maps to NM_001174096.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:31750086 C>T maps to NM_001174096.1 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr10:31799618 C>G maps to NM_001174096.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr10:31809606 C>A maps to NM_001174096.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr10:31812882 C>A maps to NM_001174096.1 S876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr2:145156854 G>T maps to NM_014795.3 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr2:145161554 G>C maps to NM_014795.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr2:145156751 C>A maps to NM_014795.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:145156128 C>A maps to NM_014795.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr2:145157511 G>A maps to NM_014795.3 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6673-01A-11D-1945-08 chr2:145147071 C>T maps to NM_014795.3 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr2:145158816 T>A maps to NM_014795.3 K289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr2:145147525 G>T maps to NM_014795.3 S1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:145157606 C>A maps to NM_014795.3 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr2:145156185 T>A maps to NM_014795.3 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr2:145274896 C>A maps to NM_014795.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr2:145156846 A>T maps to NM_014795.3 L636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr2:145274905 C>A maps to NM_014795.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:145156878 G>T maps to NM_014795.3 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:145157186 T>A maps to NM_014795.3 K523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:145161656 C>A maps to NM_014795.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:145157595 G>C maps to NM_014795.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr2:145155884 G>T maps to NM_014795.3 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr2:145157658 G>A maps to NM_014795.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr2:145147079 C>A maps to NM_014795.3 E1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr9:131502331 G>A maps to NM_006336.2 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr9:131495702 A>T did not map to a codon.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr9:131504096 C>T maps to NM_006336.2 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr8:82615027 T>A maps to NM_024699.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr8:82626215 T>A maps to NM_024699.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr7:1195211 G>A maps to ENST00000401903 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr2:220072626 G>T maps to NM_138802.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:38084405 G>A maps to NM_021943.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr15:80415142 G>A did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr8:135524845 T>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:135614377 C>T maps to NM_020863.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr8:135533235 T>A maps to NM_020863.3 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:135613822 G>A maps to NM_020863.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:135614083 C>A maps to NM_020863.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr12:72057189 G>A maps to NM_144982.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z052-01A-01W-0747-08 chr12:72056937 G>A maps to NM_144982.4 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr12:72056982 C>A maps to NM_144982.4 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr12:72008718 C>T did not map to a codon.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr12:72026207 C>A maps to NM_144982.4 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr12:72022763 T>G maps to NM_144982.4 R1294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr12:72004835 A>C did not map to a codon.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr12:72057060 G>A maps to NM_144982.4 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr12:72017963 G>A maps to NM_144982.4 Q1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr12:72017242 A>G maps to NM_144982.4 N1547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr12:72025988 T>C maps to NM_144982.4 R1041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr16:72984793 C>G maps to NM_006885.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr16:72991599 C>A maps to NM_006885.3 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr16:72992424 G>C maps to NM_006885.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr16:72821647 G>A maps to NM_006885.3 G3509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr16:72991662 C>T maps to NM_006885.3 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A471-01A-12D-A24D-08 chr16:72831615 C>G maps to NM_006885.3 V1655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr16:72832260 A>T maps to NM_006885.3 T1440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr8:77763195 G>T maps to NM_024721.4 E1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr8:77618057 C>A maps to NM_024721.4 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77763344 G>A maps to NM_024721.4 K1396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr8:77776173 C>A maps to NM_024721.4 C3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr8:77765001 G>T maps to NM_024721.4 G1949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77690535 G>C maps to NM_024721.4 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr8:77767646 C>A maps to NM_024721.4 S2830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr8:77767550 C>A maps to NM_024721.4 T2798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr8:77616703 A>T maps to NM_024721.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77761890 G>T maps to NM_024721.4 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr8:77768369 A>G maps to NM_024721.4 S3071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:77776275 C>A maps to NM_024721.4 V3442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr8:77766143 G>T maps to NM_024721.4 T2329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr8:77618300 G>T maps to NM_024721.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr8:77766326 C>A maps to NM_024721.4 P2390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr8:77768312 G>T maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr8:77690475 C>A maps to NM_024721.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr8:77618315 G>T maps to NM_024721.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr8:77765474 T>G maps to NM_024721.4 S2106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:77618173 G>A maps to NM_024721.4 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr8:77761809 C>T maps to NM_024721.4 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr8:77763962 C>A maps to NM_024721.4 Y1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:77690523 C>A maps to NM_024721.4 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:77768312 G>A maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:77768453 C>A maps to NM_024721.4 P3099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:77775756 G>T maps to NM_024721.4 G3269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:77776467 G>A maps to NM_024721.4 Q3506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr8:77767111 G>A maps to NM_024721.4 W2652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr8:77768282 G>A maps to NM_024721.4 Q3042Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr8:77764046 T>A maps to NM_024721.4 G1630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr8:77764394 G>T maps to NM_024721.4 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:77767958 G>T maps to NM_024721.4 T2934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr8:77618690 A>T maps to NM_024721.4 K790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr8:77775894 G>C maps to NM_024721.4 L3315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7573-01A-11D-2036-08 chr8:77617546 G>C maps to NM_024721.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr8:77763200 G>A maps to NM_024721.4 Q1348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7914-01A-11D-2167-08 chr8:77768312 G>C maps to NM_024721.4 P3052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr8:77620234 C>T maps to NM_024721.4 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr8:77776617 A>G maps to NM_024721.4 S3556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr8:77766752 C>A maps to NM_024721.4 P2532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:77618581 C>T maps to NM_024721.4 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:77766143 G>A maps to NM_024721.4 T2329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr8:77767634 C>A maps to NM_024721.4 T2826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:77690595 C>A maps to NM_024721.4 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr8:77618386 G>T maps to NM_024721.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:77762549 C>A maps to NM_024721.4 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:77766326 C>T maps to NM_024721.4 P2390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr8:77766176 T>C maps to NM_024721.4 D2340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr8:77616521 G>T maps to NM_024721.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr8:77619867 C>G maps to NM_024721.4 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr8:77765792 C>T maps to NM_024721.4 P2212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr8:77768252 T>A maps to NM_024721.4 I3032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:77617294 G>T maps to NM_024721.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr8:77618440 C>A maps to NM_024721.4 Y706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr8:77768222 C>T maps to NM_024721.4 I3022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr8:77766815 C>A maps to NM_024721.4 G2553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr8:77619979 C>A maps to NM_024721.4 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr8:77616868 T>A maps to NM_024721.4 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr8:77619808 G>T maps to NM_024721.4 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr8:77775796 C>T maps to NM_024721.4 Q3283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr8:77764904 T>C maps to NM_024721.4 F1916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr8:77763229 C>A maps to NM_024721.4 S1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:77618830 G>T maps to NM_024721.4 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:77765033 T>C maps to NM_024721.4 L1959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr8:77766812 G>T maps to NM_024721.4 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr8:77616572 G>T maps to NM_024721.4 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr8:77767728 G>T maps to NM_024721.4 E2858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr8:77616572 G>T maps to NM_024721.4 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr8:77766875 G>T maps to NM_024721.4 T2573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr8:77766840 C>T maps to NM_024721.4 Q2562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr8:77690581 C>A maps to NM_024721.4 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6849-01A-11D-1945-08 chr8:77767691 G>T maps to NM_024721.4 L2845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr8:77765001 G>T maps to NM_024721.4 G1949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:77764982 C>T maps to NM_024721.4 N1942N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr8:77767910 C>A maps to NM_024721.4 P2918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr8:77766125 G>A maps to NM_024721.4 R2323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:77616857 C>T maps to NM_024721.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr8:77618492 C>T maps to NM_024721.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr8:77690658 C>A maps to NM_024721.4 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr8:77763746 G>A maps to NM_024721.4 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr15:42729558 T>G maps to NM_022473.1 P1516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr15:42742933 G>C maps to NM_022473.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr15:42742656 G>A maps to NM_022473.1 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr19:44847408 G>A maps to ENST00000412927 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:44833073 T>A maps to ENST00000412927 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:44832118 G>A maps to ENST00000412927 Q748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:44833055 G>A maps to ENST00000412927 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:44833573 G>A maps to ENST00000412927 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:44844695 T>C did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:44844682 T>A maps to ENST00000412927 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:36831323 G>A maps to NM_020917.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr19:36832175 G>A maps to NM_020917.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr18:5291981 G>A maps to NM_003409.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr18:5291653 G>A maps to NM_003409.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr18:5291200 C>A maps to NM_003409.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr18:5291624 C>G maps to NM_003409.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr5:178358865 A>G maps to NM_030613.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr19:57066565 G>A maps to NM_020828.1 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:38126700 A>G maps to NM_014898.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:38134226 T>A maps to NM_014898.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr19:38135585 C>A maps to NM_014898.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr19:38134172 C>T maps to NM_014898.2 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:39898873 G>A maps to NM_003407.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:39898381 G>T did not map to a codon.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr19:39899161 G>C maps to NM_003407.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr19:39898885 C>G maps to NM_003407.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:39899333 G>T maps to NM_003407.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr14:69256989 C>A maps to NM_004926.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr14:69256984 C>T maps to NM_004926.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr14:69256564 G>T maps to NM_004926.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr14:69256497 C>A maps to NM_004926.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5935-01A-11D-1753-08 chr14:69259640 G>C maps to NM_004926.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr14:69256497 C>A maps to NM_004926.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr2:43452606 C>T maps to NM_006887.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr9:115818902 C>T maps to NM_003408.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr8:144332048 G>A maps to NM_173832.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr4:188924515 G>C maps to NM_174900.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr4:188924348 G>T maps to NM_174900.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr4:188924129 G>T maps to NM_174900.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr4:188924140 T>A maps to NM_174900.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr6:29640786 C>T maps to NM_001109809.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:29643737 C>T maps to NM_001109809.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr6:29640953 G>A maps to NM_001109809.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr6:29640987 G>T maps to NM_001109809.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr20:50769143 C>T maps to NM_018197.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr20:50701361 G>A maps to NM_199427.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr20:50769915 G>T maps to NM_018197.2 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr20:50769535 T>A maps to NM_018197.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr20:50768963 C>G maps to NM_018197.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:36884791 A>G maps to NM_133466.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:36884637 C>A maps to NM_133466.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr19:36884571 T>A maps to NM_133466.2 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr19:36884553 C>A maps to NM_133466.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:68598219 A>T maps to NM_133458.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr16:68598295 C>A maps to NM_133458.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr16:68597523 G>T maps to NM_133458.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr11:58385170 G>T maps to NM_053023.4 G569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr8:106801084 G>C maps to NM_012082.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr8:106813842 T>C maps to NM_012082.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr8:106456505 A>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr8:106431375 G>T maps to NM_012082.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr8:106813564 G>T maps to NM_012082.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr8:106815564 T>A maps to NM_012082.3 A1085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr8:106815426 A>T maps to NM_012082.3 R1039R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:106456568 G>T maps to NM_012082.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr8:106814833 C>A maps to NM_012082.3 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr8:106815546 C>T maps to NM_012082.3 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr8:106814835 G>T maps to NM_012082.3 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr8:106813428 G>A maps to NM_012082.3 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr8:106815141 C>A maps to NM_012082.3 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:106801078 C>G maps to NM_012082.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr8:106814406 C>T maps to NM_012082.3 H699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr8:106815465 G>A maps to NM_012082.3 E1052E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:106815240 A>T maps to NM_012082.3 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7348-01A-21D-2036-08 chr8:106814551 G>T maps to NM_012082.3 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr8:106813863 T>A maps to NM_012082.3 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr8:106813663 C>T maps to NM_012082.3 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr8:106815036 C>G maps to NM_012082.3 Y909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr8:106815340 G>T maps to NM_012082.3 E1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr5:32355982 C>G maps to NM_016107.3 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr5:32417828 T>C maps to NM_016107.3 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr5:32415137 C>A maps to NM_016107.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:3831426 T>A maps to NM_015174.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:3822090 C>G maps to NM_015174.1 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:3822105 C>T maps to NM_015174.1 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:24228808 C>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:24228511 G>A did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:24229382 C>G did not map to a codon.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr23:24197627 G>T did not map to a codon.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr23:24228776 A>T did not map to a codon.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr23:24228470 A>G did not map to a codon.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr24:2847525 A>C did not map to a codon.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr24:2829331 C>A did not map to a codon.
Sequencing variant TCGA-91-7771-01A-11D-2167-08 chr24:2829422 A>T did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr14:73448513 G>A maps to NM_021260.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr14:73440836 G>A maps to NM_021260.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47B-01A-11D-A24D-08 chr14:73444900 T>C maps to NM_021260.2 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr14:73464727 G>C maps to NM_021260.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr5:79746334 G>A maps to NM_014733.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr5:79733150 C>G maps to NM_014733.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:15116212 G>A maps to NM_022340.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr3:15123930 C>T maps to NM_022340.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr3:15124017 G>A maps to NM_022340.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr3:15115624 T>A maps to NM_022340.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr14:68222715 T>C maps to NM_015346.3 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr14:68282536 C>T maps to NM_015346.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr14:68234552 T>A maps to NM_015346.3 L1886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr14:68219063 G>A maps to NM_015346.3 P2456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr14:68222663 C>A did not map to a codon.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr14:68272203 G>A maps to NM_015346.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr14:68217814 T>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr4:2307055 G>T maps to NM_020972.2 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr4:2306275 G>T maps to NM_020972.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr4:2321998 C>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr4:2306940 C>A maps to NM_020972.2 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:52769569 C>T maps to NM_004799.2 I1137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:52800420 C>G maps to NM_004799.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7145-01A-11D-2036-08 chr1:52800414 C>T maps to NM_004799.2 Y1215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6562-01A-11D-1753-08 chr1:52703521 G>T maps to NM_004799.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr1:52704946 A>T maps to NM_004799.2 K620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:2881898 C>T maps to NM_145252.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:2880468 C>T maps to NM_145252.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:2880330 T>A did not map to a codon.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr16:2880253 G>T maps to NM_145252.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr16:2880740 C>T maps to NM_145252.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:10415841 C>A maps to NM_001103167.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr20:62366087 C>A maps to NM_032527.4 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr20:62364616 C>T maps to NM_032527.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:62364704 G>T did not map to a codon.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr20:62340054 G>A maps to NM_032527.4 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8074-01A-11D-2238-08 chr20:62340075 G>A maps to NM_032527.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr20:62340198 G>T maps to NM_032527.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SU-01A-11D-A24P-08 chr8:124266182 T>A maps to NM_007222.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr8:124265954 C>A maps to NM_007222.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr8:123966128 C>T maps to NM_014943.3 Y793Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr8:123964311 A>T maps to NM_014943.3 K188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr8:123965336 C>T maps to NM_014943.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832385 G>A maps to NM_015035.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr20:39832733 G>A maps to NM_015035.3 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr20:39833103 C>T maps to NM_015035.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr20:39832587 G>A maps to NM_015035.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr20:39832029 C>G maps to NM_015035.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr20:39832860 G>A maps to NM_015035.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr3:147130437 G>T maps to NM_003412.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr3:147131310 T>A maps to NM_003412.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8460-01A-11D-2323-08 chr3:147128441 G>T maps to NM_003412.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:147128528 C>T maps to NM_003412.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr3:147128846 C>G maps to NM_003412.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr3:147128660 G>T maps to NM_003412.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:147131138 A>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr3:147128438 G>A maps to NM_003412.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr3:147128525 C>A maps to NM_003412.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:136652124 G>T did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr23:136652165 A>C did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:136649479 C>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:136648930 G>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:136649220 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:136648857 T>A did not map to a codon.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr23:136649337 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:136649657 C>A did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:136649746 G>T did not map to a codon.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr23:136649370 C>T did not map to a codon.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr23:136651059 G>A did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:136649432 C>T did not map to a codon.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr23:136649857 G>C did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr23:136649680 G>A did not map to a codon.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr23:136649619 A>G did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr23:136649309 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:136649402 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:136649404 C>A did not map to a codon.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr23:136649817 C>T did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:136649485 C>A did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:136649890 C>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:136649357 G>C did not map to a codon.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr3:147113996 G>C maps to NM_001168379.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:147120536 G>T maps to NM_001168379.1 Y54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr3:147108740 C>G maps to NM_001168379.1 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr3:147114032 G>T maps to NM_001168379.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr3:147108803 G>T maps to NM_001168379.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr3:147113969 G>C maps to NM_001168379.1 Y157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:147114059 C>A maps to NM_001168379.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr3:147108854 C>A maps to NM_001168379.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr3:147108893 C>A maps to NM_001168379.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr3:147113924 C>A maps to NM_001168379.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr3:147114089 C>A maps to NM_001168379.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr3:147120599 C>A did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr13:100622426 G>C maps to NM_033132.3 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr13:100617834 G>A maps to NM_033132.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:58101521 C>T maps to NM_001010879.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr19:58101736 G>T maps to NM_001010879.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:57286127 G>A maps to NM_001146326.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:57647095 T>C maps to NM_052882.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:57646287 A>G maps to NM_052882.1 *473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:57647011 G>T maps to NM_052882.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr19:57646336 G>A maps to NM_052882.1 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:57646644 C>A maps to NM_052882.1 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:57646669 G>T maps to NM_052882.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:57647047 C>T maps to NM_052882.1 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:57646870 G>T maps to NM_052882.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr7:99621375 C>T maps to NM_003439.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7030-01A-11D-1945-08 chr16:25258178 T>C maps to NM_001012981.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr16:25251952 C>T maps to NM_001012981.4 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr16:25268334 C>G maps to NM_001012981.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr16:25258711 C>T did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:28331555 G>T maps to NM_024493.2 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr6:28219569 C>T maps to NM_019110.3 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr7:99129088 T>A maps to NM_014569.3 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr7:99128746 T>C maps to NM_014569.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:99104017 T>C maps to NM_014569.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr23:101152921 C>T did not map to a codon.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr23:101138620 A>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:101139126 T>G did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr23:101138770 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:101152934 C>A did not map to a codon.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr23:101153122 T>A did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:101138655 T>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:101139698 T>A did not map to a codon.
Sequencing variant TCGA-95-8039-01A-11D-2238-08 chr23:101138517 C>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:101153126 C>A did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr8:40532225 T>A maps to NM_024645.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr22:30127237 C>T maps to NM_019103.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:81065335 G>T maps to NM_020338.3 G801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr10:81065349 C>T maps to NM_020338.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:81058293 G>T maps to NM_020338.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:81050909 C>T maps to NM_020338.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr10:81053409 G>A maps to NM_020338.3 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5645-01A-01D-1625-08 chr7:44806174 G>A maps to NM_031449.3 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:44796637 A>G maps to NM_031449.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:44802526 G>T maps to NM_031449.3 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr7:44807179 G>A maps to NM_031449.3 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr1:40758301 A>G maps to NM_005857.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr1:40734154 G>A maps to NM_005857.3 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr1:35561418 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr1:35561463 G>T maps to NM_024772.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr23:70462879 T>A did not map to a codon.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr23:70467343 G>T did not map to a codon.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr23:70464285 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:70466305 G>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:70470375 G>A did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:70465221 G>C did not map to a codon.
Sequencing variant TCGA-55-7911-01A-11D-2167-08 chr23:70470503 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:70467598 C>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:70468354 C>A did not map to a codon.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr23:70473063 G>T did not map to a codon.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr23:70464208 C>A did not map to a codon.
Sequencing variant TCGA-62-A46R-01A-11D-A24D-08 chr23:70470311 G>T did not map to a codon.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr23:70463770 C>A did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:70461188 C>T did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr23:70465568 C>A did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:70465189 C>G did not map to a codon.
Sequencing variant TCGA-97-A4M0-01A-11D-A24P-08 chr23:70472695 G>T did not map to a codon.
Sequencing variant TCGA-J2-A4AG-01A-11D-A24D-08 chr23:70466526 G>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:70465659 C>G did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:35847280 G>T maps to NM_005095.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:35881307 A>T maps to NM_005095.2 S1434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr1:35863112 G>T maps to NM_005095.2 E1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr1:35854604 A>G maps to NM_005095.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr1:35884119 T>C maps to NM_005095.2 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5643-01A-01D-1625-08 chr13:20411848 T>A maps to NM_001142684.1 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6775-01A-11D-1855-08 chr13:20411810 A>G maps to NM_001142684.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr13:20425887 C>A maps to NM_001142684.1 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr13:20411924 T>C maps to NM_001142684.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr1:35477542 G>C maps to NM_007167.3 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:35485053 C>A maps to NM_007167.3 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:35485165 T>C maps to NM_007167.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr1:35476083 G>A maps to NM_007167.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47F-01A-11D-A24D-08 chr3:50382590 G>A maps to NM_015896.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr3:50379320 G>T maps to NM_015896.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr10:255921 A>T maps to NM_006624.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr10:294439 G>A maps to NM_006624.4 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:42898959 C>G did not map to a codon.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr1:42898846 G>A maps to NM_032257.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4403-01A-01D-1265-08 chr17:4648195 G>A maps to NM_001136046.1 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr17:4648622 C>T maps to NM_001136046.1 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7537-01A-11D-2063-08 chr9:140476995 C>A maps to NM_138462.2 *228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr20:45905073 G>A maps to ENST00000471951 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr20:45912380 G>A maps to ENST00000471951 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr20:45853098 T>A maps to ENST00000471951 K1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr12:133732503 C>T maps to NM_015394.4 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr12:133732743 G>T maps to NM_015394.4 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:21909901 T>C maps to NM_173531.3 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:21910504 T>C maps to NM_173531.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:21910333 G>A maps to NM_173531.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:19790268 A>C maps to NM_033204.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr19:19790025 G>T maps to NM_033204.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z013-01A-01W-0746-08 chr7:64168662 G>T maps to NM_016220.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr7:64167567 G>T maps to NM_016220.3 G296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr7:64168334 C>A maps to NM_016220.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6144-01A-11D-1753-08 chr7:64168598 A>T maps to NM_016220.3 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr7:64168706 A>T maps to NM_016220.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr7:64167093 G>T maps to NM_016220.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr7:64167290 T>C maps to NM_016220.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:64166699 A>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr19:48790035 G>A maps to NM_153608.1 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8097-01A-11D-2238-08 chr19:48789255 T>C maps to NM_153608.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8359-01A-11D-2323-08 chr19:48789045 C>T maps to NM_153608.1 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr7:64438540 C>A maps to NM_015852.3 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr7:6731810 C>T maps to ENST00000330442 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr7:6737390 G>A maps to ENST00000330442 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:9677031 C>A maps to NM_001008727.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9677451 C>A maps to NM_001008727.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr1:247320308 G>T maps to NM_003431.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:247319987 A>G maps to NM_003431.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:247320032 T>C maps to NM_003431.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr1:247319924 A>G maps to NM_003431.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr5:43161515 G>T maps to ENST00000509156 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7903-01A-11D-2167-08 chr5:43175088 G>T maps to ENST00000509156 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7764-01A-11D-2167-08 chr5:43174700 A>T maps to ENST00000509156 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:18296739 T>C maps to ENST00000401790 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr20:18296997 A>C maps to ENST00000401790 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr20:18297070 G>T maps to ENST00000401790 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr20:18296556 C>T maps to ENST00000401790 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr19:58132405 G>T maps to NM_003435.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:58131685 G>T maps to NM_003435.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:58574841 C>A maps to NM_007134.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:58579318 A>G maps to NM_007134.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58572989 G>T maps to NM_007134.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:58579297 C>A maps to NM_007134.1 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:58578994 C>T maps to NM_007134.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr19:58578971 C>T maps to NM_007134.1 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:58578565 A>G maps to NM_007134.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:58573027 G>T maps to NM_007134.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:58572945 A>T did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr19:12298426 A>T maps to NM_003437.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr19:19823804 T>C maps to NM_021030.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr4:337569 G>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr2:219508190 C>T maps to NM_001105537.1 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr2:219513426 G>A maps to NM_001105537.1 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr2:219508687 G>A maps to NM_001105537.1 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr2:219521074 C>T maps to NM_001105537.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr11:9534019 G>T maps to NM_003442.5 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr3:124953170 C>A maps to NM_021964.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr3:124953149 C>A maps to NM_021964.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:58216287 A>T maps to NM_001085384.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr19:58214094 G>T maps to NM_001085384.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5420-01A-01D-1625-08 chr19:44495758 G>A maps to NM_003445.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr23:47272882 G>T did not map to a codon.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:47272469 G>T did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr23:47271876 A>G did not map to a codon.
Sequencing variant TCGA-17-Z037-01A-01W-0746-08 chr23:47272630 G>A did not map to a codon.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr23:47269684 C>T did not map to a codon.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr23:47272548 G>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:47269736 C>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:47272597 C>A did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:47271816 C>G did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:47272964 G>A did not map to a codon.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr8:146156369 G>A maps to NM_006958.2 Y601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr8:146156798 T>C maps to NM_006958.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr19:53572310 T>C maps to NM_001102603.1 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:53573326 C>A maps to NM_001102603.1 G154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr6:28056533 G>C maps to NM_003447.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr6:28053588 G>T maps to NM_003447.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr6:28053455 A>T maps to NM_003447.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:28056878 G>A maps to NM_003447.3 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr6:28053503 C>T maps to NM_003447.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr6:28053314 T>A maps to NM_003447.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr6:28053272 A>T maps to NM_003447.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr3:44611963 C>G maps to NM_018651.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr3:44598650 C>T maps to NM_018651.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:97062214 A>T maps to NM_194320.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr9:97054748 G>T maps to NM_194320.2 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:57931585 A>T maps to NM_006959.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:57931867 G>A maps to NM_006959.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:52090621 G>A maps to NM_007147.2 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr19:52090282 C>T maps to NM_007147.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr19:52090720 C>T maps to NM_007147.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7553-01A-21D-2036-08 chr19:52090626 C>A maps to NM_007147.2 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr19:52091500 A>G maps to NM_007147.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:9491792 G>A maps to NM_001172651.1 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:9491820 C>T maps to NM_001172651.1 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr17:11895945 G>A maps to NM_144680.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr17:11895930 T>C maps to NM_144680.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr17:11881680 T>A maps to NM_144680.2 K415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:44980969 C>A maps to NM_013256.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr19:35232519 A>T maps to ENST00000392232 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:47835971 T>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:47835778 G>T did not map to a codon.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr23:47836372 C>A did not map to a codon.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr23:47836868 T>C did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:47836119 T>A did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:47836530 C>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:47836556 C>A did not map to a codon.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr6:27419945 G>A maps to NM_007149.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr6:27425158 C>A maps to NM_007149.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr6:27420577 C>A maps to NM_007149.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr6:27420616 G>A maps to NM_007149.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr6:27419485 C>A maps to NM_007149.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:152083040 T>G did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:152083305 G>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:152083699 G>T did not map to a codon.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr23:152087525 G>C did not map to a codon.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr23:152086638 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:152101460 C>T did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:152088939 C>A did not map to a codon.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr9:104170865 A>G maps to NM_003452.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr6:28116256 C>T maps to NM_006298.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr6:28121476 G>C maps to NM_006298.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr6:28116463 G>T maps to NM_006298.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr6:28116493 A>G maps to NM_006298.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr11:3381327 C>A maps to NM_001130520.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr11:3380815 G>A maps to NM_001130520.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:3392921 C>T maps to NM_001130520.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr11:3392867 G>A maps to NM_001130520.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr3:44684350 C>T maps to NM_006991.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8253-01A-11D-2284-08 chr3:44683587 G>A maps to NM_006991.3 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr3:44670828 C>T maps to NM_006991.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:95847559 G>T maps to ENST00000453539 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr2:95843286 G>T maps to ENST00000453539 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:95847463 G>A maps to ENST00000453539 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:12243511 C>A maps to NM_021143.2 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7552-01A-11D-2036-08 chr16:3274334 T>G maps to NM_198088.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr11:123598270 G>A maps to NM_003455.2 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr11:123601245 T>A maps to NM_003455.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr11:123597076 T>A maps to NM_003455.2 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr11:123597328 G>A maps to NM_003455.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TH-01A-31D-A25L-08 chr11:123598271 G>A maps to NM_003455.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr11:123601239 C>T maps to NM_003455.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr16:3170214 C>T maps to NM_001042428.1 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr17:30696360 G>T maps to ENST00000394679 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:22155564 G>T maps to NM_007153.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:22155158 C>A maps to NM_007153.3 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22156941 C>G maps to NM_007153.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr19:22154762 C>A maps to NM_007153.3 G1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:22157391 G>T maps to NM_007153.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:22154535 A>T maps to NM_007153.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:22156887 T>C maps to NM_007153.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:22170038 C>A maps to NM_007153.3 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:22154079 G>T maps to NM_007153.3 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:22154112 A>T maps to NM_007153.3 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:22156742 C>A maps to NM_007153.3 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:22155263 C>A maps to NM_007153.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-71-6725-01A-11D-1855-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr19:22171639 C>T maps to NM_007153.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:22155951 C>T maps to NM_007153.3 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:22156553 C>A maps to NM_007153.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr19:22155387 C>T maps to NM_007153.3 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:22154426 C>A maps to NM_007153.3 G1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr19:58152630 C>T maps to NM_006385.3 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:58145429 G>C did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:58146121 G>T maps to NM_006385.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6978-01A-11D-1945-08 chr7:148947287 C>G maps to NM_012256.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:148947614 G>T maps to NM_012256.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr16:3190699 C>G maps to NM_001134655.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr11:7022735 C>A maps to NM_013249.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr11:7021683 T>C maps to NM_013249.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr11:7022214 C>T maps to NM_013249.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr11:7021683 T>C maps to NM_013249.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr11:6953865 C>T maps to NM_013250.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr11:6977309 C>T maps to NM_013250.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6953713 G>T maps to NM_013250.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr11:6962864 C>G maps to NM_013250.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr11:6953823 G>A maps to NM_013250.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:52193385 G>C maps to NM_006526.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr20:52192872 A>G maps to NM_006526.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr20:52193349 C>A maps to NM_006526.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6983-01A-11D-1945-08 chr20:52198291 C>T maps to NM_006526.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr20:52198699 G>T maps to NM_006526.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr20:52193559 A>G maps to NM_006526.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr20:52198207 G>T maps to NM_006526.2 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr20:52192803 G>A maps to NM_006526.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr14:21560930 C>T maps to NM_001102454.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr10:45499095 C>T maps to NM_006963.4 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:44471324 G>T maps to NM_013359.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:44470667 C>T maps to NM_013359.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:44470959 C>T maps to NM_013359.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:44536245 C>G maps to NM_001129996.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:44536510 T>A maps to NM_001129996.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr19:44570524 G>T maps to NM_013361.4 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:44570266 G>T maps to NM_013361.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:44570391 A>G maps to NM_013361.4 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:44570524 G>T maps to NM_013361.4 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:44570322 T>C maps to NM_013361.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr19:44605072 C>T maps to NM_013398.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:44604976 G>T maps to NM_013398.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-6217-01A-11D-1753-08 chr19:44635940 C>T maps to NM_013362.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr19:44636269 C>A maps to NM_013362.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr19:44635500 C>G maps to NM_013362.2 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:44636249 C>T maps to NM_013362.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:44681151 G>T maps to NM_001032372.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:44681619 C>T maps to NM_001032372.1 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:44679173 G>C maps to NM_001146220.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr19:44933334 C>A maps to NM_014518.2 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:44933602 G>A maps to NM_014518.2 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:44933221 C>G maps to NM_014518.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:44932852 G>T maps to NM_014518.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr19:44932735 G>T maps to NM_014518.2 Y740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6205-01A-11D-1753-08 chr19:44933923 C>G maps to NM_014518.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:44932549 C>T maps to NM_014518.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr16:71482162 T>A maps to NM_145911.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr16:71482342 C>A maps to NM_145911.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr16:71483108 G>A maps to NM_145911.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:44515429 C>G maps to NM_006300.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:44515276 A>G maps to NM_006300.3 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr17:5012904 C>A maps to NM_014519.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr17:5009655 C>T maps to NM_014519.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:44778387 C>T maps to NM_181756.1 A525A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-97-7938-01A-11D-2167-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr19:44652982 G>T maps to NM_006630.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:44660543 C>A maps to NM_006630.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:44661635 C>A maps to NM_006630.2 C489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:44661342 G>T maps to NM_006630.2 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr19:44792867 A>G maps to NM_004234.4 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:44792340 G>C maps to NM_004234.4 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:44793055 T>A maps to NM_004234.4 K178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:44791836 G>C maps to NM_004234.4 S584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr18:74583759 C>T maps to NM_007345.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr18:74622667 A>G maps to NM_007345.3 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr18:74620297 C>T maps to NM_007345.3 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr18:74672731 C>G maps to NM_007345.3 Y1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr18:74680238 G>T maps to NM_007345.3 E1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr18:74587598 C>T maps to NM_007345.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr18:74610972 A>G did not map to a codon.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr18:74639994 A>G maps to NM_007345.3 A1507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr18:74607113 C>T maps to NM_007345.3 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr18:74649172 G>C maps to NM_007345.3 S1550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr18:74617119 A>T maps to NM_007345.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:74649226 G>T maps to NM_007345.3 T1568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr18:74639026 G>T maps to NM_007345.3 G1352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr18:74671704 A>G maps to NM_007345.3 K1723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6835-01A-11D-1855-08 chr18:74587575 C>T maps to NM_007345.3 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr18:74637299 C>T maps to NM_007345.3 Q1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr1:244217637 G>T maps to NM_205768.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr1:244218617 G>A maps to NM_205768.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr1:244218389 G>A maps to NM_205768.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr10:44052833 C>A maps to NM_001099284.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:32917600 G>A maps to NM_006965.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr10:38120852 G>C maps to NM_021045.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr10:38121208 C>G maps to NM_021045.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:38127038 C>A maps to NM_021045.1 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr10:38126614 C>T maps to NM_021045.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5125-01A-01D-1753-08 chr10:38121741 C>A maps to NM_021045.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr10:38121805 G>A maps to NM_021045.1 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4510-01A-01D-1265-08 chr10:38241750 T>C maps to NM_145011.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr10:38246346 C>A did not map to a codon.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr10:38245972 T>C maps to NM_145011.2 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr8:146107493 C>T maps to NM_021061.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr8:145947274 C>A maps to NM_138367.1 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr8:145947735 C>A maps to NM_138367.1 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20003498 A>C maps to NM_021047.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:20002571 C>T maps to ENST00000427401 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:20002724 C>T maps to NM_021047.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr19:24309884 G>A maps to NM_203282.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:24309420 G>T maps to NM_203282.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:24310355 C>G maps to NM_203282.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z059-01A-01W-0747-08 chr19:58452653 G>A maps to NM_005773.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:58452489 G>A maps to NM_005773.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:58455328 C>A maps to NM_005773.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:22270888 T>C maps to NM_033468.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr19:22271584 C>T maps to NM_033468.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:22271619 T>G maps to NM_033468.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:22272169 G>T maps to NM_033468.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr19:22270959 T>A maps to NM_033468.2 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:22271928 C>A maps to NM_033468.2 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:22271346 C>A maps to NM_033468.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr19:22271698 C>A maps to NM_033468.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:22255609 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr11:116654244 C>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37005528 C>T maps to NM_001166038.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr19:37005407 C>A maps to NM_001166038.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:37005825 G>A maps to NM_001166038.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr16:3339735 C>T maps to NM_005741.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr16:3340374 A>G maps to NM_005741.4 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8076-01A-31D-2238-08 chr16:3340302 A>G maps to NM_005741.4 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr19:57723653 A>T maps to NM_003417.4 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4505-01A-01D-1931-08 chr16:31926643 C>G maps to NM_003414.4 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr16:31927348 G>T maps to NM_003414.4 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr16:31885290 G>A did not map to a codon.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr16:31895887 C>T maps to NM_003414.4 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr12:133768557 G>T maps to NM_001165881.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr12:133764455 A>T did not map to a codon.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr12:133768116 G>T maps to NM_001165881.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:58724290 C>T maps to NM_133502.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:58722996 G>A maps to NM_133502.1 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:58724055 G>T maps to NM_133502.1 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T7-01A-11D-A24P-08 chr19:58724154 G>T maps to NM_133502.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr23:152613061 G>C did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:152612744 G>T did not map to a codon.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr23:152613092 G>A did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:152612487 G>T did not map to a codon.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr23:152612493 C>G did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr23:152612392 G>C did not map to a codon.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr23:152612792 C>T did not map to a codon.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr16:89789077 G>T maps to NM_001113525.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr7:111846827 G>C maps to NM_021994.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:111926926 G>C did not map to a codon.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr22:22868937 G>T maps to NM_080740.3 C339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr22:22869460 G>C maps to NM_080740.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr22:22869398 C>A maps to NM_080740.3 G186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr22:22869780 G>A maps to NM_080740.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr22:22868751 G>T maps to NM_080740.3 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr22:22842727 C>T maps to NM_080764.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr22:22842826 C>A maps to NM_080764.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr22:22842892 C>T maps to NM_080764.2 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr22:22842567 G>A maps to NM_080764.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr22:22842748 C>A maps to NM_080764.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:129354379 C>A did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:129349243 G>C did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:129354418 T>G did not map to a codon.
Sequencing variant TCGA-55-8621-01A-11D-2393-08 chr23:129377556 C>A did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:129363012 T>A did not map to a codon.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr23:129364678 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:129349168 C>T did not map to a codon.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr23:129360820 T>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:129343686 G>T did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr23:129361675 C>T did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr15:56993397 C>A maps to NM_017661.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:44351433 A>G maps to NM_181845.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr19:44352228 C>T maps to NM_181845.1 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr19:44352475 G>T maps to NM_181845.1 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:44590803 G>T maps to NM_001037813.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:44590659 C>G maps to NM_001037813.2 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:44591016 G>A maps to NM_001037813.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:44590984 G>T maps to NM_001037813.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr19:44891466 T>A maps to NM_152354.3 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr19:44891283 C>A maps to NM_152354.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr19:44891532 C>A maps to NM_152354.3 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr19:44891617 G>A maps to NM_152354.3 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:44892225 T>A maps to NM_152354.3 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:44891050 C>A maps to NM_152354.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr17:15619790 C>G maps to NM_020652.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr17:18566443 T>G maps to NM_001145045.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr17:18565819 C>A maps to NM_001145045.1 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8280-01A-11D-2284-08 chr17:18565408 A>G maps to NM_001145045.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr17:16456321 C>T maps to NM_020653.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr17:16469844 C>A maps to NM_020653.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr6:87968812 A>G maps to NM_015021.1 K1822K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr6:87968146 C>T maps to NM_015021.1 T1600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr6:87966691 T>C maps to NM_015021.1 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr6:87970159 G>T maps to NM_015021.1 S2271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr6:87967552 A>G maps to NM_015021.1 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr6:87967282 G>T maps to NM_015021.1 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr21:43411969 C>T maps to NM_020727.4 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr21:43413862 C>G maps to NM_020727.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr21:43411293 C>A maps to NM_020727.4 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr21:43412358 C>A maps to NM_020727.4 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr21:43411534 T>A maps to NM_020727.4 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:45575761 G>A maps to NM_145288.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr19:45579058 G>A maps to NM_145288.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr7:99669592 C>A maps to NM_032924.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr7:99669593 G>A maps to NM_032924.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr7:99669712 G>A maps to NM_032924.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr19:35422793 G>T maps to NM_001099438.1 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:35175845 C>T maps to ENST00000221282 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:35174078 A>G maps to ENST00000221282 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:57867854 C>T maps to ENST00000391705 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr19:57867552 G>T maps to ENST00000391705 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:57868145 A>T maps to ENST00000391705 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:57868709 G>T maps to ENST00000391705 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr19:57868710 C>T maps to ENST00000391705 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:57867767 A>G maps to ENST00000391705 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:57863062 C>T maps to ENST00000391705 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr6:28963356 C>T maps to NM_001010877.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:9271827 G>T maps to NM_020933.4 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:9270788 G>A did not map to a codon.
Sequencing variant TCGA-55-8508-01A-11D-2393-08 chr19:9271172 A>G maps to NM_020933.4 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:9271754 C>T maps to NM_020933.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr19:9271250 G>A maps to NM_020933.4 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr6:43323077 G>C maps to NM_014345.2 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr6:43308231 C>A maps to NM_014345.2 V1168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr6:43307715 C>T maps to NM_014345.2 V1340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr6:43305981 C>T maps to NM_014345.2 E1918E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr6:43306101 G>C maps to NM_014345.2 L1878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr6:43308096 T>C maps to NM_014345.2 K1213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr6:43306478 C>A maps to NM_014345.2 E1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:43323187 G>A maps to NM_014345.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr6:43323346 T>A maps to NM_014345.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr16:58031335 G>A maps to NM_020807.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr10:44139647 C>T maps to NM_006973.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr6:28295181 G>A maps to NM_030899.4 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:28294029 G>C maps to NM_030899.4 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:58983206 G>T maps to NM_014347.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:58965139 C>T maps to NM_207395.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:90484243 G>T maps to NM_182976.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr1:90478796 G>T did not map to a codon.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:58640000 T>C maps to NM_024620.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr4:142152623 A>G maps to NM_014487.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:54080156 G>T maps to NM_001079907.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:54080095 C>T maps to NM_001079907.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:54072639 G>T did not map to a codon.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:14815882 G>T maps to NM_032433.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:14830004 G>A maps to NM_032433.2 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:14829434 G>T maps to NM_032433.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:14810032 C>T maps to NM_032433.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:45130107 C>A maps to NM_018102.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:44588901 G>C maps to NM_022095.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4395-01A-01D-1265-08 chr20:44578471 C>T maps to NM_022095.3 Q1212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:44592117 C>A maps to NM_022095.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:44598228 G>A maps to NM_022095.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7944-01A-11D-2184-08 chr20:44592629 C>T did not map to a codon.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr20:44590775 C>A maps to NM_022095.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr20:25656822 C>T maps to NM_015655.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr20:25656841 G>T maps to NM_015655.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr20:25656524 G>A maps to NM_015655.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr20:25667035 G>T maps to NM_015655.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr20:25655783 C>A maps to NM_015655.2 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr10:38305839 G>T maps to NM_006954.1 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr10:38344698 G>A maps to NM_006954.1 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:38305894 C>T maps to NM_006954.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr10:38343660 T>C maps to NM_006954.1 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr8:145999820 G>A maps to NM_030580.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr8:145999667 T>C maps to NM_030580.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr20:32332940 A>T maps to ENST00000375200 K59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr20:32357949 G>T maps to ENST00000375200 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr20:32357915 T>A maps to ENST00000375200 C480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr20:2464418 G>A maps to NM_024325.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr20:2463959 G>T maps to NM_024325.4 Y549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr20:2464826 C>A maps to NM_024325.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr20:2464391 C>A maps to NM_024325.4 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr20:2463908 G>A maps to NM_024325.4 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:2473447 C>A maps to NM_024325.4 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr20:2473392 G>A maps to NM_024325.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8175-01A-11D-2284-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:37368304 G>T maps to NM_003419.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr19:37368459 C>A maps to NM_003419.3 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:53645327 C>T maps to NM_001172674.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr19:53644587 G>C maps to NM_001172674.1 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:53645321 T>C maps to NM_001172674.1 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:53644970 C>T maps to NM_001172674.1 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr3:44701144 C>T maps to NM_003420.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr3:44700296 C>T maps to NM_003420.3 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:52468934 T>A maps to NM_021632.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:52472343 C>T maps to NM_021632.3 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr5:178139060 C>T maps to NM_005649.2 *606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr5:178140562 C>A maps to NM_005649.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr5:178293995 A>T maps to NM_058230.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr5:178310766 T>A maps to NM_058230.2 Y438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr5:178310481 A>G maps to NM_058230.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr5:178505711 A>G maps to NM_014594.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr5:178506335 A>T maps to NM_014594.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr5:178505817 G>T maps to NM_014594.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr5:178506303 C>T maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr19:7585564 C>A maps to NM_018083.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:7585781 G>T maps to NM_018083.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr1:33760818 C>T maps to NM_152493.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr10:64158503 A>T maps to NM_014951.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr10:64429972 T>A maps to NM_199451.2 L434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr10:64159472 G>T maps to NM_014951.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr10:64136479 T>C maps to NM_199451.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr10:64136181 C>G maps to NM_199451.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756117 G>A maps to NM_152625.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr5:71756207 G>A maps to NM_152625.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4626-01A-01D-1553-08 chr5:71756813 C>A maps to NM_152625.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr5:71740094 G>A maps to NM_152625.1 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr9:99157135 G>T maps to NM_153695.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr9:99160597 T>G did not map to a codon.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr10:38403680 A>G did not map to a codon.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr10:38403762 G>A maps to NM_003421.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr10:38404183 A>T maps to NM_003421.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5072-01A-21D-1855-08 chr19:37117731 C>T maps to NM_032825.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:37117542 C>A maps to NM_032825.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:37118439 G>T maps to NM_032825.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:37117629 C>G maps to NM_032825.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr19:37117245 A>T maps to NM_032825.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37734244 G>A maps to NM_152604.1 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr19:37733741 G>T maps to NM_152604.1 E202*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-53-7626-01A-12D-2063-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr12:54767847 G>C maps to NM_001130967.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr12:54765455 C>T maps to NM_001130967.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr2:180308036 C>G maps to NM_152520.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:21606119 G>A maps to NM_024697.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:21478513 C>A maps to NM_024697.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:21466981 A>T did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr3:21552500 G>T maps to NM_024697.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr3:21478545 C>A maps to NM_024697.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr3:21706376 C>A did not map to a codon.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr3:21467010 G>A maps to NM_024697.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr3:21706479 A>T maps to NM_024697.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:21478696 T>A did not map to a codon.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr3:21706451 G>A maps to NM_024697.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr3:21552488 G>T maps to NM_024697.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TC-01A-11D-A24P-08 chr3:21706488 G>A maps to NM_024697.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr6:27368460 A>T maps to NM_001076781.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr6:27368222 C>G maps to NM_001076781.1 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr6:27368574 T>C maps to NM_001076781.1 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr7:99097647 C>G maps to NM_032164.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:99097647 C>A maps to NM_032164.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr8:28209071 C>G maps to NM_018660.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8091-01A-11D-2238-08 chr8:28210812 G>A maps to NM_018660.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr8:28206277 C>G maps to NM_018660.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr18:32949446 C>T maps to NM_145756.2 W247*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-62-8402-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr18:32833590 A>T maps to NM_001166012.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr7:148876131 C>T maps to NM_170686.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr7:148876883 A>G maps to NM_170686.2 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:148876112 G>T maps to NM_170686.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr18:72353079 T>C did not map to a codon.
Sequencing variant TCGA-17-Z004-01A-01W-0746-08 chr18:72344028 A>T maps to NM_017757.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:72345692 G>T maps to NM_017757.2 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr18:72346332 A>T maps to NM_017757.2 K1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2665-01A-01D-1040-01 chr18:72344696 A>G maps to NM_017757.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr18:72344060 T>G maps to NM_017757.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr18:72344864 G>T maps to NM_017757.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr18:72345909 G>T maps to NM_017757.2 G979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6987-01A-11D-1945-08 chr18:72343952 G>T maps to NM_017757.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:72346695 G>T maps to NM_017757.2 G1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr18:72345995 C>T maps to NM_017757.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2661-01A-01D-1105-08 chr11:46726803 C>T maps to NM_024741.2 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr11:46726782 G>T maps to NM_024741.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr11:46724531 A>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr11:46726464 G>T maps to NM_024741.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr23:47306909 C>A did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr23:47308565 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:47308860 C>A did not map to a codon.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr23:47315754 C>T did not map to a codon.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr23:47306909 C>G did not map to a codon.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr23:47306960 C>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr23:47308729 G>C did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:47307810 T>A did not map to a codon.
Sequencing variant TCGA-86-8585-01A-11D-2393-08 chr23:47308384 G>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr23:47307414 C>A did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:47308149 G>C did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr14:74360538 G>T maps to NM_021188.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr19:8577376 C>G did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:53612706 G>A maps to NM_001164309.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:53612163 G>A maps to NM_001164309.1 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:53625930 C>G did not map to a codon.
Sequencing variant TCGA-05-5423-01A-01D-1625-08 chr19:58083956 C>A maps to NM_017879.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58084848 C>T maps to NM_017879.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr19:58420127 C>G maps to NM_152475.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr19:58420460 G>T maps to NM_152475.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:58437915 T>A maps to NM_133460.1 K545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:58439200 C>T maps to NM_133460.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37618138 A>G maps to NM_144689.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37619575 T>C maps to NM_144689.3 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr16:49670419 C>A maps to NM_015069.2 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:49823451 C>A maps to NM_015069.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr16:49672666 C>A maps to NM_015069.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6761-01A-31D-1945-08 chr16:49671868 C>A maps to NM_015069.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr16:49671242 G>T maps to NM_015069.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr16:49557648 G>T maps to NM_015069.2 V1237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr16:49670341 C>A maps to NM_015069.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr16:49672369 G>A maps to NM_015069.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr16:49672435 G>C maps to NM_015069.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7815-01A-11D-2167-08 chr16:49672129 G>T maps to NM_015069.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr16:49672048 G>T maps to NM_015069.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr16:49670950 C>A maps to NM_015069.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr16:49559352 C>A maps to NM_015069.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1681-01A-11D-2063-08 chr16:49669987 G>T maps to NM_015069.2 C1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr16:49672435 G>C maps to NM_015069.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr16:49672681 G>A maps to NM_015069.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:49669912 T>A maps to NM_015069.2 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr16:49670203 C>A maps to NM_015069.2 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr16:49670253 G>T maps to NM_015069.2 R937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr16:49670230 C>A maps to NM_015069.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7941-01A-11D-2184-08 chr16:49669966 C>A maps to NM_015069.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr16:49525206 C>T maps to NM_015069.2 T1278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr16:49671517 A>G maps to NM_015069.2 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z027-01A-01W-0746-08 chr7:148801966 A>G maps to NM_001001661.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z049-01A-01W-0746-08 chr7:148801675 C>T maps to NM_001001661.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:148801756 G>A maps to NM_001001661.2 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1677-01A-01W-0928-08 chr7:148801600 C>T maps to NM_001001661.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z009-01A-01W-0746-08 chr19:9639592 G>A maps to NM_024106.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:9646884 A>G maps to NM_024106.1 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr19:21720465 C>A maps to NM_001001415.2 Y537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:21719512 A>T maps to NM_001001415.2 K220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr19:21720246 G>T maps to NM_001001415.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:22000711 A>G maps to NM_003423.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr19:21991182 G>T maps to NM_003423.2 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr19:21992460 C>T maps to NM_003423.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:21992412 C>T maps to NM_003423.2 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr19:21992267 G>A maps to NM_003423.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3773-01A-01D-1040-01 chr19:21991490 C>A maps to NM_003423.2 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:22002011 T>C maps to NM_003423.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:22000688 C>A did not map to a codon.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:21240397 C>G maps to NM_025189.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:21216306 G>T maps to NM_025189.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr19:21240088 T>C maps to NM_025189.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8669-01A-11D-2393-08 chr19:21240745 A>G maps to NM_025189.3 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:21240397 C>G maps to NM_025189.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T2-01A-11D-A24P-08 chr19:21350416 A>G maps to NM_133473.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:52538202 G>T maps to NM_014650.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52538394 G>A maps to NM_014650.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:52537512 A>G maps to NM_014650.2 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SW-01A-21D-A24P-08 chr19:52537029 G>A maps to NM_014650.2 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-7271-01A-11D-2036-08 chr19:12127012 C>T maps to NM_001080411.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr16:3434810 G>C maps to ENST00000396852 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr1:23693625 G>A maps to NM_001077195.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr1:23688593 G>A maps to NM_001077195.1 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr10:31134131 C>A maps to NM_182755.2 G749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr10:31138373 T>A maps to NM_182755.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr10:31134021 C>A maps to NM_182755.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr10:31138001 T>A maps to NM_182755.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8299-01A-11D-2284-08 chr10:31134353 C>A maps to NM_182755.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr10:31137625 C>A maps to NM_182755.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6593-01A-11D-1753-08 chr19:11978561 C>T maps to NM_152262.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8671-01A-11D-2393-08 chr19:12383623 C>T maps to NM_001164276.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SY-01A-21D-A24P-08 chr19:12384376 A>G maps to NM_001164276.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr19:11943216 C>G maps to NM_152357.2 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z002-01A-01W-0746-08 chr19:12461609 T>C maps to NM_030824.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:12460636 G>T maps to NM_030824.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:12461744 A>G maps to NM_030824.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6828-01A-11D-1855-08 chr19:12461716 C>A maps to NM_030824.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4415-01A-22D-1855-08 chr19:12542604 C>T maps to NM_005815.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:12541845 C>T maps to NM_005815.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:12542628 A>G maps to NM_005815.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:58991891 C>T maps to NM_017908.2 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr23:134494330 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr23:134481223 C>T did not map to a codon.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr23:134494261 G>T did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:134481310 G>T did not map to a codon.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr23:134483123 C>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:134481131 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:134494749 A>C did not map to a codon.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr23:134494567 G>T did not map to a codon.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr23:134494218 G>C did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:134494410 C>A did not map to a codon.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr19:44419175 A>G maps to NM_003425.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:44418200 G>A maps to NM_003425.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr6:56999641 C>T maps to NM_001031623.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr6:57012580 A>G maps to NM_001031623.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr6:56989633 G>T maps to NM_001031623.2 E97*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-50-5930-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr5:178392949 G>A maps to NM_182594.2 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr5:178392678 C>G maps to NM_182594.2 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr5:178392832 C>A maps to NM_182594.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:57802136 C>T maps to NM_006635.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:57803157 G>T maps to NM_006635.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:37129905 C>T maps to NM_153257.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37129922 C>A maps to NM_153257.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:37129868 G>A maps to NM_153257.2 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:37130288 G>A maps to NM_153257.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr9:109692039 G>A maps to NM_021224.4 R1949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z010-01A-01W-0746-08 chr9:109691364 G>T maps to NM_021224.4 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr9:109690044 C>T maps to NM_021224.4 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr9:109690338 G>A maps to NM_021224.4 W1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr9:109692894 G>T maps to NM_021224.4 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr9:109701362 G>T maps to NM_021224.4 P2134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr9:109689687 C>T maps to NM_021224.4 G1165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr9:109746690 G>T did not map to a codon.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:149467541 C>A maps to NM_207336.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr7:149462852 G>A maps to NM_207336.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr19:53344721 C>T maps to NM_001008801.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:53344275 G>C maps to NM_001008801.1 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:53344658 C>T maps to NM_001008801.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr19:57089396 G>T maps to NM_001001668.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr19:57037190 C>T maps to NM_020813.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:50549718 C>T maps to NM_015428.1 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr19:50548182 C>T maps to NM_015428.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr19:50548236 A>T maps to NM_015428.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:50542425 G>C maps to NM_015428.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr7:57188722 A>T maps to NM_033273.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57188665 G>T maps to NM_033273.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr7:57188766 C>A maps to NM_033273.1 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr7:57187792 G>T maps to NM_033273.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:57188188 G>T maps to NM_033273.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr7:57187551 C>A maps to NM_033273.1 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr7:57188672 G>C maps to NM_033273.1 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr7:57193791 G>T maps to NM_033273.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:57193791 G>T maps to NM_033273.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr7:57188854 C>G maps to NM_033273.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr7:57188632 G>T maps to NM_033273.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:57187737 C>A maps to NM_033273.1 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7633-01A-11D-2063-08 chr7:57200006 C>A maps to NM_033273.1 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:57187653 C>A maps to NM_033273.1 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr7:57193820 C>A did not map to a codon.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr7:57194335 A>G maps to NM_033273.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr7:57200006 C>A maps to NM_033273.1 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:57187720 A>G maps to NM_033273.1 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr19:52824859 A>G maps to NM_144684.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:52826032 T>G maps to NM_144684.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr19:52817531 G>T maps to NM_144684.2 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:52825579 A>G maps to NM_144684.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:114289740 G>T maps to NM_133464.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6597-01A-11D-1855-08 chr9:114293153 G>A did not map to a codon.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr9:114304222 G>A maps to NM_133464.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr9:95609374 G>C maps to NM_031486.1 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr9:95610477 T>A maps to NM_031486.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr9:95609411 C>A maps to NM_031486.1 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:20308559 G>A maps to ENST00000428290 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr19:20307981 C>T maps to NM_052852.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr10:48371204 C>T maps to NM_153034.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr10:48371147 C>T maps to NM_153034.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr10:48371095 C>T maps to NM_153034.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr10:48370924 C>A maps to NM_153034.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr10:48371218 C>T maps to NM_153034.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:12691672 G>A maps to NM_020714.2 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr19:12692408 C>A maps to NM_020714.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JO-01A-21D-A24P-08 chr19:11917082 T>C maps to NM_152356.3 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T8-01A-11D-A24P-08 chr19:11917622 A>T maps to NM_152356.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr19:22847719 G>T maps to NM_020855.2 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22847836 A>T maps to NM_020855.2 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:22847455 A>T maps to NM_020855.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8204-01A-11D-2238-08 chr19:21606409 G>T maps to NM_001076678.2 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:21606114 C>T maps to NM_001076678.2 A218A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-95-7567-01A-11D-2063-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:21588563 T>C maps to NM_001076678.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr19:21607375 A>T maps to NM_001076678.2 K639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z020-01A-01W-0746-08 chr1:247464456 C>T maps to NM_032752.1 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:247492104 C>A maps to NM_032752.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:247464315 C>A maps to NM_032752.1 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7283-01A-11D-2036-08 chr1:247492646 C>T maps to NM_032752.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8207-01A-11D-2238-08 chr1:247492784 C>T maps to NM_032752.1 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr1:247464564 C>A maps to NM_032752.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:247463919 G>A maps to NM_032752.1 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:247492574 C>T maps to NM_032752.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:58868092 G>A maps to NM_198458.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr19:58867549 G>A maps to NM_198458.1 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:58868266 C>A maps to NM_198458.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:99226889 G>A maps to NM_145115.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr7:99217441 G>A maps to NM_145115.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr7:99219099 G>T maps to NM_145115.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr7:99227454 G>T maps to NM_145115.2 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr16:4812312 C>A maps to NM_021646.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr16:4815784 C>G maps to NM_021646.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr16:4815624 C>A maps to NM_021646.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr16:4815850 G>A maps to NM_021646.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr3:44776033 C>T maps to NM_145044.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr3:44776080 A>T maps to NM_145044.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7158-01A-11D-2036-08 chr3:44775978 A>G maps to NM_145044.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr3:44762980 A>T maps to NM_033210.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YG-01A-22D-A25L-08 chr3:44763241 G>T maps to NM_033210.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4514-01A-21D-1855-08 chr10:77158902 G>A maps to NM_032772.4 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr10:77158971 C>A maps to NM_032772.4 P492P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-64-1677-01A-01W-0928-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr10:77159439 C>G maps to NM_032772.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr9:99521620 A>G maps to NM_014930.1 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr10:135122931 G>T maps to NM_145806.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr2:27839192 T>C did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr2:27840350 G>T maps to NM_032434.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7031-01A-11D-1945-08 chr20:62594446 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:62595879 C>T maps to NM_020713.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr2:27600624 G>A maps to NM_144631.4 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr2:27600738 A>G maps to NM_144631.4 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:27600828 C>T maps to NM_144631.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:27601658 C>A maps to NM_144631.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr2:27601841 C>T maps to NM_144631.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr2:95815559 G>T maps to NM_032788.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr2:95815740 T>C maps to NM_032788.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr18:74154221 C>A maps to ENST00000443185 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr18:74091114 T>A maps to ENST00000443185 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr18:74074513 T>A did not map to a codon.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr18:74091693 G>A maps to ENST00000443185 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr18:74154839 C>A maps to ENST00000443185 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr18:74091246 C>A maps to ENST00000443185 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr8:146032615 G>A maps to NM_213605.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z047-01A-01W-0747-08 chr10:97916894 C>G maps to NM_014803.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr10:97917555 G>T maps to NM_014803.3 G493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr10:97918310 G>C maps to NM_014803.3 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr10:97920260 C>T maps to NM_014803.3 T1394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr4:10447451 G>A maps to NM_053042.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr4:10445099 C>A maps to NM_053042.2 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr4:10447118 T>C maps to NM_053042.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr4:10446035 C>A maps to NM_053042.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr18:14106160 C>T maps to NM_145287.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr18:14105256 C>A maps to NM_145287.3 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr18:22807007 C>A maps to NM_015461.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr18:22805577 C>T maps to NM_015461.2 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:22805772 G>A maps to NM_015461.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6779-01A-11D-1855-08 chr18:22804461 G>A maps to NM_015461.2 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr18:22901975 C>A maps to NM_015461.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr18:22806285 A>G maps to NM_015461.2 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr18:22804791 G>A maps to NM_015461.2 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr18:22806903 G>T maps to NM_015461.2 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-8459-01A-11D-2323-08 chr18:22806020 G>A maps to NM_015461.2 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr18:22804497 C>T maps to NM_015461.2 E1128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7724-01A-11D-2167-08 chr18:22805025 G>A maps to NM_015461.2 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr18:22805673 G>T maps to NM_015461.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr18:22806392 G>A maps to NM_015461.2 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5774-01A-01D-1625-08 chr18:22804515 C>T maps to NM_015461.2 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr18:22807566 G>A maps to NM_015461.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr18:22805481 G>A maps to NM_015461.2 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr18:22804889 G>A maps to NM_015461.2 Q998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr18:22805127 G>T maps to NM_015461.2 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr18:22807049 G>A maps to NM_015461.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr18:22806581 C>A maps to NM_015461.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr18:22806051 C>T maps to NM_015461.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr18:22804641 C>G maps to NM_015461.2 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr18:22805796 G>A maps to NM_015461.2 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8172-01A-11D-2284-08 chr18:22806822 G>T maps to NM_015461.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr18:22807070 C>A maps to NM_015461.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr18:22805949 T>A maps to NM_015461.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr18:22805487 C>T maps to NM_015461.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46Y-01A-11D-A24D-08 chr19:56114230 C>T maps to NM_153219.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:56114113 G>T maps to NM_153219.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr19:42730534 C>A maps to NM_133444.1 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr19:42728857 G>T maps to NM_133444.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:37879496 G>A maps to NM_032453.1 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52918882 C>T maps to NM_032423.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:52909813 G>A maps to NM_032423.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:58118032 G>A maps to NM_020880.3 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:58118527 G>A maps to NM_020880.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A5C7-01A-11D-A25L-08 chr19:58117186 A>C maps to NM_020880.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z050-01A-01W-0747-08 chr18:56646351 G>A maps to NM_018181.4 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr18:56586481 C>T maps to NM_018181.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr18:56586784 G>T maps to NM_018181.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr18:56648816 G>T maps to NM_018181.4 E1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr18:56586016 G>T maps to NM_018181.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr18:56586013 G>T maps to NM_018181.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr18:56646327 C>T maps to NM_018181.4 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr18:56646333 G>A maps to NM_018181.4 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr18:56585794 G>T maps to NM_018181.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4T9-01A-11D-A24P-08 chr18:56585911 G>T maps to NM_018181.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:52942159 C>T maps to NM_001143939.1 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:52937329 C>T maps to NM_001143939.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:52941034 C>T maps to NM_001143939.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:52941258 G>A maps to NM_001143939.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:30935347 C>T maps to NM_014717.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:30935447 G>T maps to NM_014717.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30935921 A>T maps to NM_014717.1 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:30936281 C>A maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr19:30935935 G>T maps to NM_014717.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:30936292 G>A maps to NM_014717.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr19:30934717 C>A maps to NM_014717.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:30934585 C>A maps to NM_014717.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4422-01A-01D-1265-08 chr19:30936283 G>C maps to NM_014717.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:30934627 G>T maps to NM_014717.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:31039048 C>A maps to NM_014717.1 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:30935618 G>T maps to NM_014717.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935353 C>T maps to NM_014717.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30935950 C>T maps to NM_014717.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:30936550 C>G maps to NM_014717.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr19:31038848 G>A did not map to a codon.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:31040158 C>T maps to NM_014717.1 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:30934597 C>T maps to NM_014717.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3918-01A-01D-1105-08 chr19:30934951 G>T maps to NM_014717.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:30934696 C>A maps to NM_014717.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr19:31040380 C>T maps to NM_014717.1 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:31025802 G>T maps to NM_014717.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:31040290 C>A maps to NM_014717.1 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:30936636 C>G maps to NM_014717.1 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6985-01A-11D-1945-08 chr19:31040320 G>T maps to NM_014717.1 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr19:31048064 T>A maps to NM_014717.1 G1299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:30935539 G>A maps to NM_014717.1 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:30936019 C>T maps to NM_014717.1 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:31039220 G>T maps to NM_014717.1 E899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr19:31040251 G>A maps to NM_014717.1 Q1242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:30935749 C>A maps to NM_014717.1 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:31038920 G>T maps to NM_014717.1 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:30935305 C>A maps to NM_014717.1 C279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:30934681 C>A maps to NM_014717.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:30936449 G>T maps to NM_014717.1 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:31039147 G>C maps to NM_014717.1 T874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5815-01A-01D-1625-08 chr19:30936247 C>T maps to NM_014717.1 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr19:30936031 C>A maps to NM_014717.1 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:30935899 C>A maps to NM_014717.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:31040176 C>A maps to NM_014717.1 P1217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:30934661 G>T maps to NM_014717.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7167-01A-11D-2063-08 chr19:31025820 G>T maps to NM_014717.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:31025764 G>T maps to NM_014717.1 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:30935590 C>T maps to NM_014717.1 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:31039822 C>T maps to NM_014717.1 H1099H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:30936376 C>A maps to NM_014717.1 C636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:31039648 C>A maps to NM_014717.1 C1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:30936547 C>T maps to NM_014717.1 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:31039534 C>T maps to NM_014717.1 C1003C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr19:30935819 C>T maps to NM_014717.1 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:30934612 C>G maps to NM_014717.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr19:31039466 C>A maps to NM_014717.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:30935047 C>A maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:30935668 G>T maps to NM_014717.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:31040323 G>T maps to NM_014717.1 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr19:30934861 G>T maps to NM_014717.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55R-01A-11D-A25L-08 chr19:31038848 G>A did not map to a codon.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:38102960 A>T maps to NM_152606.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8174-01A-11D-2284-08 chr19:38102698 C>G maps to NM_152606.3 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr19:57839444 G>C maps to NM_213598.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:57839240 A>T maps to NM_213598.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8655-01A-11D-2393-08 chr19:57840272 C>T maps to NM_213598.3 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:57839520 G>T maps to NM_213598.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:58772808 C>T maps to NM_014480.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:58773457 C>T maps to NM_014480.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A47A-01A-21D-A24D-08 chr19:40520369 C>G maps to NM_178544.3 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr19:57883172 G>T maps to NM_173631.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr19:57888722 G>T maps to NM_173631.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:57888710 C>T maps to NM_173631.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:57909964 G>T maps to NM_001172773.1 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:57910962 C>T maps to NM_001172773.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:57910782 C>G maps to NM_001172773.1 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8254-01A-11D-2284-08 chr19:57911094 C>T maps to NM_001172773.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4P7-01A-11D-A24P-08 chr19:57909875 C>G maps to NM_001172773.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:58048904 C>G maps to ENST00000376233 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr19:58058873 G>C maps to NM_001039654.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:58196641 G>T maps to ENST00000356715 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:58199620 C>T maps to ENST00000356715 R660*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-67-6217-01A-11D-1753-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr19:58198440 T>G maps to ENST00000356715 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:2832299 G>A did not map to a codon.
Sequencing variant TCGA-38-4630-01A-01D-1265-08 chr19:2877778 C>T maps to NM_024967.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:7083169 C>T maps to NM_024341.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:9452606 A>T maps to NM_032497.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr19:9578910 T>A maps to NM_152476.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:9582049 C>T maps to NM_152476.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:9577764 G>T maps to NM_152476.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr19:9581104 A>G maps to NM_152476.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr19:9578632 A>T maps to NM_152476.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:9721687 C>A maps to NM_152289.2 G217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:12637859 T>C maps to NM_144976.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:36674504 G>A maps to ENST00000355114 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:36963906 C>A maps to NM_001145343.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:36940214 C>A maps to NM_001145343.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:36940319 T>C maps to NM_001145343.1 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr19:36967452 G>A maps to NM_001145343.1 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr19:36967453 A>G maps to NM_001145343.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr19:37210633 G>T maps to ENST00000423498 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr19:37210597 C>G maps to ENST00000423498 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:37210541 G>T maps to ENST00000423498 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:37428073 G>T maps to NM_198539.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:37441969 G>T maps to NM_198539.2 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:37441572 A>T maps to NM_198539.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:37904466 G>A maps to NM_152484.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:37917229 C>T maps to NM_152484.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7669-01A-21D-2063-08 chr19:37904007 C>A maps to NM_152484.2 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YI-01A-11D-A25L-08 chr19:2916086 C>T maps to NM_173480.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:37975291 C>T maps to NM_144694.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:37975730 C>T maps to NM_144694.1 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8668-01A-11D-2393-08 chr19:37975907 C>T maps to NM_144694.1 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr19:37975235 A>T maps to NM_144694.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:37975988 C>T maps to NM_144694.1 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:38055972 C>A maps to NM_016536.3 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr19:38056961 G>C maps to NM_016536.3 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr8:125989913 C>A maps to NM_152412.2 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr8:125988733 G>A maps to NM_152412.2 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr8:125989175 G>T maps to NM_152412.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:38229542 C>A maps to NM_001172690.1 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:42584947 G>T maps to ENST00000222339 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-8067-01A-11D-2284-08 chr19:42584269 C>T maps to ENST00000222339 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:52376332 C>A maps to NM_032679.2 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr19:52381732 G>A maps to NM_032679.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:52376750 C>G maps to NM_032679.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:52376807 G>C maps to NM_032679.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:52376687 G>T maps to NM_032679.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr19:53013860 C>A maps to NM_001099694.1 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr19:53007906 G>T did not map to a codon.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr19:53014458 A>T maps to NM_001099694.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr19:53008023 G>T maps to NM_001099694.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr19:53014174 G>T maps to NM_001099694.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:53015319 C>T maps to NM_001099694.1 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr19:56090051 G>A maps to NM_152600.2 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr19:56156063 C>T maps to NM_016535.3 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:56156246 C>T maps to NM_016535.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:56934257 A>T did not map to a codon.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:56935704 C>T maps to NM_001159861.1 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:58928346 G>T maps to NM_173548.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:37643140 C>A maps to ENST00000356958 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4501-01A-01D-1265-08 chr19:37642865 G>A maps to ENST00000356958 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:37643909 T>A maps to ENST00000356958 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr19:37646812 C>T maps to ENST00000356958 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr19:37643189 G>A maps to ENST00000356958 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:37644494 C>T maps to ENST00000356958 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr19:37677751 G>C maps to NM_152279.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:37677514 A>T maps to NM_152279.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr19:37677112 G>A maps to NM_152279.3 H442H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr19:37676229 G>A maps to NM_152279.3 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:37677688 C>T maps to NM_152279.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr19:58290167 G>A maps to NM_017652.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:58290975 G>T maps to NM_017652.2 G341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58370796 C>T maps to NM_032828.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr15:85326374 G>T maps to NM_014630.2 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr15:85327612 G>A maps to NM_014630.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7574-01A-11D-2036-08 chr15:85345224 G>A maps to NM_014630.2 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr15:85328122 G>A maps to NM_014630.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr15:85327621 C>T maps to NM_014630.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr15:85326840 C>G maps to NM_014630.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr15:85326888 C>A maps to NM_014630.2 S328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8547-01A-11D-2393-08 chr15:85326987 C>A maps to NM_014630.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55O-01A-11D-A25L-08 chr15:85341198 C>T maps to NM_014630.2 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr17:5085736 G>A maps to NM_032530.1 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr17:5085606 C>A maps to NM_032530.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr17:5086081 G>A maps to NM_032530.1 C490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr4:59390 C>A maps to NM_182524.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr4:60023 T>C maps to NM_182524.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr4:59438 G>T maps to NM_182524.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr4:59418 T>C maps to NM_182524.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr4:60017 G>A maps to NM_182524.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7536-01A-11D-2063-08 chr4:59438 G>T maps to NM_182524.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-7109-01A-11D-2036-08 chr16:2050049 G>A maps to ENST00000431526 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Y-01A-11D-A24D-08 chr16:2052213 C>T maps to ENST00000431526 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:35258314 C>T maps to NM_001007248.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:35250447 C>A maps to NM_001007248.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8615-01A-11D-2393-08 chr19:35250892 C>T maps to NM_001007248.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr19:35251147 T>C maps to NM_001007248.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:53268920 A>G maps to NM_198457.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr19:53270801 G>A maps to NM_198457.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr12:133502296 C>A maps to NM_001164715.1 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58490389 G>C maps to NM_025027.3 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr19:58499574 C>A maps to NM_025027.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:58491350 G>A maps to NM_025027.3 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8281-01A-11D-2284-08 chr19:58499671 T>G did not map to a codon.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr19:58511175 C>T maps to NM_025027.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:38190115 C>A maps to NM_032689.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:38189612 T>A maps to NM_032689.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:38190239 G>C maps to NM_032689.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7948-01A-11D-2184-08 chr19:38198842 C>T maps to NM_032689.4 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr5:123980213 G>A maps to NM_020747.2 P1282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr5:123980333 C>T maps to NM_020747.2 W1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4420-01A-01D-1265-08 chr15:64966540 C>T maps to NM_015042.1 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr15:64915054 G>T maps to NM_015042.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4658-01A-01D-1753-08 chr15:64967176 C>A maps to NM_015042.1 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr15:64792229 G>A maps to NM_015042.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:52856948 C>T maps to NM_001161425.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr19:52856957 G>T maps to NM_001161425.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:52868948 A>T did not map to a codon.
Sequencing variant TCGA-44-8119-01A-11D-2238-08 chr19:53208786 C>T maps to NM_001161500.1 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:53208704 C>A maps to NM_001161500.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:52448660 G>T maps to NM_001031721.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr19:52443466 A>T maps to NM_001031721.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr19:52519584 T>A maps to NM_025040.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4675-01A-01D-1265-08 chr19:52519938 A>C maps to NM_025040.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr19:52496470 C>A maps to ENST00000354939 G631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:52618738 G>A maps to NM_178523.3 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:52619864 C>G maps to NM_178523.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr9:116811438 C>T maps to ENST00000374126 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr9:116750741 G>A maps to ENST00000374126 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr9:116811996 C>T maps to ENST00000374126 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr9:116812419 C>T maps to ENST00000374126 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr3:40528958 G>T maps to NM_001145082.2 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7146-01A-11D-2036-08 chr3:40528669 G>A maps to NM_001145082.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr5:16458719 G>A maps to NM_033414.2 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr5:16463792 G>A maps to NM_033414.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr5:16465191 C>A maps to NM_033414.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr5:16451878 G>A maps to NM_033414.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr8:144733133 G>A maps to NM_014789.3 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr17:16527815 C>T maps to NM_020787.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:16527374 G>A maps to NM_020787.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:12256519 A>G maps to ENST00000439556 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr19:20829184 G>T maps to NM_001076675.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:55993189 C>T maps to NM_033113.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z058-01A-01W-0747-08 chr16:30793473 G>A maps to NM_001080417.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr16:30793053 T>A maps to NM_001080417.1 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr16:30794328 G>T maps to NM_001080417.1 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:47919180 G>T did not map to a codon.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr23:47918086 C>A did not map to a codon.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr23:47918713 T>G did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr23:47919083 G>A did not map to a codon.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr23:47918443 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:47919878 C>A did not map to a codon.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr23:47919879 C>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:47920237 C>G did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:47917868 C>G did not map to a codon.
Sequencing variant TCGA-17-Z051-01A-01W-0747-08 chr2:71591197 A>T maps to NM_014497.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr2:71590291 T>C maps to NM_014497.3 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr2:71590315 G>A maps to NM_014497.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr2:71591218 G>C maps to NM_014497.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr2:71654171 C>T maps to NM_014497.3 Q1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr2:71591191 A>T maps to NM_014497.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6979-01A-11D-1945-08 chr2:71653630 G>T maps to NM_014497.3 V1544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr2:71576135 C>T maps to NM_014497.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JQ-01A-11D-A24P-08 chr2:71650869 C>G maps to NM_014497.3 S1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-A4AD-01A-11D-A24D-08 chr2:71653741 G>A maps to NM_014497.3 K1581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A479-01A-31D-A24D-08 chr12:48741849 C>G maps to NM_152320.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr1:40961688 T>C maps to NM_198494.2 H513H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr1:91403084 C>A maps to NM_201269.1 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:91405404 C>A maps to NM_201269.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr1:91406761 G>C maps to NM_201269.1 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6971-01A-11D-1945-08 chr1:91404019 G>T maps to NM_201269.1 S964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr1:91382453 C>A maps to NM_201269.1 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:91405101 C>T maps to NM_201269.1 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr23:22291636 C>A did not map to a codon.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr23:22291374 A>T did not map to a codon.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr23:22292141 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:22291499 A>T did not map to a codon.
Sequencing variant TCGA-55-7995-01A-11D-2184-08 chr23:22291877 C>A did not map to a codon.
Sequencing variant TCGA-55-A494-01A-11D-A24P-08 chr23:22291910 C>A did not map to a codon.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr23:22292160 T>A did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:22291575 T>C did not map to a codon.
Sequencing variant TCGA-83-5908-01A-21D-2284-08 chr23:22292348 C>A did not map to a codon.
Sequencing variant TCGA-J2-8192-01A-11D-2238-08 chr23:22291955 C>T did not map to a codon.
Sequencing variant TCGA-05-4249-01A-01D-1105-08 chr16:31092790 C>T maps to NM_014699.3 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7980-01A-11D-2184-08 chr16:31090320 G>C maps to NM_014699.3 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr16:31087947 C>T maps to NM_014699.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr16:31089216 C>T maps to NM_014699.3 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6830-01A-11D-1945-08 chr16:31090471 C>T maps to NM_014699.3 Q943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr1:182026920 G>T maps to NM_001009992.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr1:182026293 G>T maps to NM_001009992.1 C284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr1:182026680 T>G maps to NM_001009992.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:182026998 A>G maps to NM_001009992.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4659-01A-01D-1265-08 chr1:182026434 C>G maps to NM_001009992.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:182026578 C>A maps to NM_001009992.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:52394292 T>A maps to NM_023074.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr19:52394113 C>A maps to NM_023074.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7701-01A-11D-2167-08 chr19:52394418 C>A maps to NM_023074.3 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5051-01A-21D-1855-08 chr19:11598551 C>A maps to NM_138783.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:11598614 C>T maps to NM_138783.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr3:88189287 C>T maps to NM_018293.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:99169919 G>T maps to NM_001083956.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr9:40773111 T>C maps to NM_033160.5 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr9:40774878 T>A maps to NM_033160.5 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr9:40772607 C>T maps to NM_033160.5 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr9:40773143 C>A maps to NM_033160.5 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8510-01A-11D-2393-08 chr9:40773135 G>T maps to NM_033160.5 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6206-01A-11D-1753-08 chr9:40772844 C>T maps to NM_033160.5 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr9:40772741 G>A maps to NM_033160.5 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr3:42956150 G>T maps to NM_001134656.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr12:124497155 C>T maps to NM_152437.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr12:124497350 C>G maps to NM_152437.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:53668344 G>C maps to NM_024733.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:53667756 G>C maps to NM_024733.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:56973726 G>T maps to ENST00000342634 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48Z-01A-12D-A24P-08 chr19:56953247 G>T maps to ENST00000342634 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:56972075 G>T maps to ENST00000342634 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8497-01A-11D-2393-08 chr19:56953136 T>C maps to ENST00000342634 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr16:31072694 G>A maps to NM_001172669.1 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr16:31072580 C>A maps to NM_001172669.1 R579R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-93-7347-01A-11D-2184-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr16:31072427 C>A maps to NM_001172669.1 L630L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MP-A4SW-01A-21D-A24P-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr1:247265289 T>C maps to NM_024804.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:247264068 A>G maps to NM_024804.2 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z003-01A-01W-0746-08 chr1:247200849 C>T maps to NM_033213.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5146-01A-01D-1625-08 chr1:247201595 C>A maps to NM_033213.3 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr1:247202724 G>A maps to NM_033213.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr23:46322196 C>G did not map to a codon.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr23:46332309 A>T did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:46322200 G>C did not map to a codon.
Sequencing variant TCGA-78-7153-01A-11D-2036-08 chr23:46322631 G>T did not map to a codon.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:46387868 C>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr23:46360579 T>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:46359633 T>A did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:46359635 T>A did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:46360722 C>A did not map to a codon.
Sequencing variant TCGA-97-A4M3-01A-11D-A24P-08 chr23:46360506 C>T did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:46388276 G>A did not map to a codon.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:23836620 C>A maps to NM_138330.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:23836134 T>A maps to NM_138330.2 K534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:23836221 C>A maps to NM_138330.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:23845834 C>A maps to NM_138330.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:22363269 C>A maps to NM_001001411.2 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22363350 C>A maps to NM_001001411.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6777-01A-11D-1855-08 chr19:22363098 C>A maps to NM_001001411.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5933-01A-11D-1753-08 chr19:22363426 G>T maps to NM_001001411.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:22363213 G>A maps to NM_001001411.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:22362814 T>C maps to NM_001001411.2 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:22362843 T>A maps to NM_001001411.2 K559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:22362993 C>A maps to NM_001001411.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:22363717 G>T maps to NM_001001411.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:22363597 T>C maps to NM_001001411.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:22363717 G>T maps to NM_001001411.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8171-01A-11D-2284-08 chr19:22375855 C>T maps to NM_001001411.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr19:22363873 A>G maps to NM_001001411.2 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:22362820 A>T maps to NM_001001411.2 C566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8032-01A-11D-2238-08 chr19:22375857 G>T maps to NM_001001411.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6969-01A-11D-1945-08 chr19:53747080 G>A maps to NM_182609.2 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7728-01A-11D-2184-08 chr19:53740555 C>T maps to NM_182609.2 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:53741798 C>A maps to NM_182609.2 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr1:227843216 C>T maps to NM_178549.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6776-01A-11D-1855-08 chr1:227843490 G>T maps to NM_178549.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr1:227842106 A>T maps to NM_178549.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7725-01A-11D-2167-08 chr1:227842502 T>C maps to NM_178549.3 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8085-01A-11D-2238-08 chr1:227842532 A>T maps to NM_178549.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr1:227843427 G>T maps to NM_178549.3 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr1:227843035 C>G maps to NM_178549.3 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4426-01A-01D-1265-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr7:63726940 C>T maps to NM_153363.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:63726979 C>G maps to NM_153363.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr7:63726646 C>A maps to NM_153363.2 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6642-01A-11D-1855-08 chr7:63720640 G>T maps to NM_153363.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7535-01A-11D-2063-08 chr7:63721248 G>A maps to NM_153363.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:63981859 A>G maps to NM_178558.4 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6848-01A-11D-1945-08 chr7:63982756 A>G maps to NM_178558.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr7:64004735 C>A maps to NM_178558.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:63982110 T>A maps to NM_178558.4 K341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr19:23927876 C>A maps to NM_138286.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:23938260 C>A maps to NM_138286.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr19:23927472 C>T maps to NM_138286.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr19:23927742 A>G maps to NM_138286.2 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr19:20117281 A>G maps to NM_033196.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:26689560 T>A maps to ENST00000436292 K367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr1:26688393 C>T maps to ENST00000436292 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:41012465 C>T maps to NM_152373.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:41012294 G>A maps to NM_152373.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4122-01A-01D-1105-08 chr1:151262665 T>C maps to NM_020832.1 H1011H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1595-01A-01D-0969-08 chr1:151261158 C>T maps to NM_020832.1 H757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr1:151260062 C>T maps to NM_020832.1 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8055-01A-11D-2238-08 chr1:151259297 G>T maps to NM_020832.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr1:151261666 C>T maps to NM_020832.1 C797C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr16:30582409 C>T maps to NM_145271.3 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6211-01A-11D-1753-08 chr16:30581632 G>A maps to NM_145271.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr16:30621284 C>A maps to NM_138447.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr1:249149985 G>A maps to NM_001136036.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:249144509 C>A maps to NM_001136036.2 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr1:249152471 G>T maps to NM_001136036.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr1:247163259 C>G maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr1:247163259 C>T maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr1:247150364 T>A maps to NM_020394.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr1:247162721 C>A maps to NM_020394.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr1:247151519 C>T maps to NM_020394.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr1:247151521 C>A maps to NM_020394.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DG-01A-11D-A24D-08 chr1:247150744 C>A maps to NM_020394.3 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr1:247162680 G>A maps to NM_020394.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr1:120165528 C>T maps to NM_001080470.1 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:9408096 T>C maps to NM_198535.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr8:146066789 C>T maps to ENST00000446747 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr22:24087218 G>A maps to NM_021916.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:12059661 G>T maps to NM_144566.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:12059765 A>G maps to NM_144566.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr19:12060270 G>T maps to NM_144566.1 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:53086275 G>T maps to NM_001172655.1 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr8:81582793 C>G maps to NM_001033723.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr12:8329899 C>A maps to NM_001004328.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr8:144776063 G>T maps to NM_173831.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:21476570 T>C maps to NM_021269.2 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5066-01A-01D-1625-08 chr19:12575151 C>A maps to ENST00000428311 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:12575364 G>A maps to ENST00000428311 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr19:12575933 G>A maps to ENST00000428311 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57133590 G>T maps to NM_021216.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:57133425 C>T maps to NM_021216.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr19:57133758 G>C maps to NM_021216.4 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8120-01A-11D-2238-08 chr15:90611028 A>T maps to NM_198526.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8614-01A-11D-2393-08 chr15:90610770 G>T maps to NM_198526.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4244-01A-01D-1105-08 chr23:84510680 A>T did not map to a codon.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr23:84526808 G>T did not map to a codon.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr23:84525119 G>C did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:84526773 C>A did not map to a codon.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr23:84526751 G>T did not map to a codon.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr23:84526696 T>A did not map to a codon.
Sequencing variant TCGA-50-5045-01A-01D-1625-08 chr23:84520223 G>T did not map to a codon.
Sequencing variant TCGA-50-5942-01A-21D-1753-08 chr23:84526180 C>A did not map to a codon.
Sequencing variant TCGA-50-6594-01A-11D-1753-08 chr23:84525803 G>T did not map to a codon.
Sequencing variant TCGA-55-6970-01A-11D-1945-08 chr23:84526493 G>T did not map to a codon.
Sequencing variant TCGA-55-7910-01A-11D-2167-08 chr23:84520159 G>A did not map to a codon.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr23:84510460 G>T did not map to a codon.
Sequencing variant TCGA-78-7160-01A-11D-2036-08 chr23:84510317 G>C did not map to a codon.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr23:84525149 C>T did not map to a codon.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr23:84520161 G>T did not map to a codon.
Sequencing variant TCGA-86-A456-01A-11D-A24D-08 chr23:84525962 A>T did not map to a codon.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr23:84520184 T>A did not map to a codon.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr23:84510739 T>A did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:84526119 G>T did not map to a codon.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr23:84526405 A>C did not map to a codon.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr23:84526328 A>G did not map to a codon.
Sequencing variant TCGA-97-7937-01A-11D-2167-08 chr23:84523326 A>G did not map to a codon.
Sequencing variant TCGA-L4-A4E5-01A-11D-A24P-08 chr23:84525057 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4T4-01A-11D-A25L-08 chr23:84510734 G>A did not map to a codon.
Sequencing variant TCGA-MP-A4TF-01A-11D-A25L-08 chr23:84510302 C>G did not map to a codon.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr23:84526149 G>T did not map to a codon.
Alternatively spliced codon TCGA-55-8302-01A-11D-2323-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr7:55990970 A>C maps to NM_182633.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:55990946 G>C maps to NM_182633.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr7:57529432 C>A maps to NM_001159279.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:57522833 C>A maps to NM_001159279.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr7:57522777 G>A did not map to a codon.
Sequencing variant TCGA-17-Z014-01A-01W-0746-08 chr7:57528448 C>A maps to NM_001159279.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-8117-01A-11D-2238-08 chr7:57528436 T>A maps to NM_001159279.1 C90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr7:57529214 A>T maps to NM_001159279.1 K350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr7:57510014 C>T maps to NM_001159279.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:57529060 T>C maps to NM_001159279.1 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr7:57522284 C>A maps to NM_001159279.1 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr7:57528739 C>T maps to NM_001159279.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7156-01A-11D-2036-08 chr7:57522863 C>A maps to NM_001159279.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5608-01A-31D-1945-08 chr7:57529324 C>G maps to NM_001159279.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:57522809 C>A maps to NM_001159279.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr7:57528527 G>T maps to NM_001159279.1 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr7:57529240 G>T maps to NM_001159279.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z044-01A-01W-0746-08 chr4:436824 T>C maps to NM_133474.2 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6742-01A-11D-1855-08 chr4:437397 A>G maps to NM_133474.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A4DF-01A-11D-A24D-08 chr4:437795 G>A maps to NM_133474.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr4:265784 A>T maps to ENST00000419098 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr4:289821 G>A maps to ENST00000419098 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z045-01A-01W-0746-08 chr7:63796755 C>G maps to NM_001170905.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:20736524 C>A maps to NM_001159293.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr19:20727616 C>A maps to NM_001159293.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr19:20727931 G>A maps to NM_001159293.1 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr22:20759682 G>T maps to NM_003426.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr22:20760156 C>T maps to NM_003426.2 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr7:149174082 G>A maps to NM_001163474.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z001-01A-01W-0746-08 chr7:149191293 C>T did not map to a codon.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr7:149174739 G>C maps to NM_001163474.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:149174025 T>A maps to NM_001163474.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7281-01A-11D-2036-08 chr7:149191309 C>T maps to NM_001163474.1 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7546-01A-11D-2036-08 chr7:149174136 A>C maps to NM_001163474.1 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TK-01A-11D-A24P-08 chr19:57953308 C>T maps to NM_001023561.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:57953344 G>A maps to NM_001023561.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr17:80789946 C>T maps to NM_024702.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr17:80790149 G>A maps to NM_024702.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr17:80789580 G>A maps to NM_024702.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr17:80789900 C>A maps to NM_024702.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr16:3367622 A>G maps to NM_153028.2 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr16:3367344 G>T maps to NM_153028.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:3363158 G>A maps to NM_153028.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr23:134425433 C>A did not map to a codon.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr23:134426360 C>A did not map to a codon.
Sequencing variant TCGA-17-Z015-01A-01W-0746-08 chr23:134421667 G>T did not map to a codon.
Sequencing variant TCGA-17-Z056-01A-01W-0747-08 chr23:134421076 G>A did not map to a codon.
Sequencing variant TCGA-50-5931-01A-11D-1753-08 chr23:134427709 C>A did not map to a codon.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr23:134421118 G>T did not map to a codon.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr23:134421547 T>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:134427932 G>C did not map to a codon.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr23:134421211 G>T did not map to a codon.
Sequencing variant TCGA-86-8674-01A-21D-2393-08 chr23:134427877 C>T did not map to a codon.
Sequencing variant TCGA-O1-A52J-01A-11D-A25L-08 chr23:134425456 C>A did not map to a codon.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr6:35261525 A>T did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr19:53952871 T>C maps to NM_001008401.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:53958198 G>A maps to NM_001008401.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:53950520 G>C did not map to a codon.
Sequencing variant TCGA-44-3396-01A-01D-1553-08 chr19:12087894 G>T maps to NM_001012753.1 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr16:30569376 A>G maps to NM_033410.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-8494-01A-11D-2323-08 chr16:30567105 G>A maps to NM_033410.3 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:53911496 T>A maps to NM_001040185.1 L230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr19:52793793 G>A maps to NM_001010851.2 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5941-01A-11D-1753-08 chr16:30536016 C>A maps to NM_024671.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A443-01A-12D-A24D-08 chr16:30536893 G>T maps to NM_024671.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr19:2934602 G>C maps to NM_021217.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr19:2939381 C>A maps to NM_021217.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr19:2934106 G>A maps to NM_021217.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M7-01A-11D-A24P-08 chr19:2933765 C>T maps to NM_021217.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4434-01A-01D-1265-08 chr15:35274486 T>C maps to NM_014106.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr15:35275469 C>A maps to NM_014106.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr15:35273922 G>A maps to NM_014106.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr15:35274006 G>A maps to NM_014106.3 N543N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6207-01A-11D-1753-08 chr15:35274618 G>T maps to NM_014106.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8054-01A-11D-2238-08 chr15:35273927 C>A maps to NM_014106.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A470-01A-11D-A24D-08 chr16:30429201 C>T maps to NM_001142305.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z030-01A-01W-0746-08 chr19:57985205 G>A maps to NM_001024596.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6744-01A-11D-1855-08 chr19:57985661 G>T maps to NM_001024596.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5781-01A-01D-1625-08 chr19:58018005 G>A maps to NM_198542.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr19:58018248 C>T maps to NM_198542.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr15:90903721 C>G maps to NM_001004309.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr15:90903396 G>T maps to NM_001004309.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5930-01A-11D-1753-08 chr15:90904513 A>T maps to NM_001004309.2 *484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr15:90903470 G>A maps to NM_001004309.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:150093919 C>T maps to NM_173680.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr7:150094600 C>T maps to NM_173680.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:58265431 C>A maps to NM_173632.3 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr19:58265101 C>T maps to NM_173632.3 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7661-01A-11D-2063-08 chr7:149129310 G>A maps to ENST00000440594 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46S-01A-11D-A24D-08 chr7:149152396 G>A maps to ENST00000440594 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-A4JN-01A-11D-A24P-08 chr7:149133779 C>A maps to ENST00000440594 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:149152288 G>C maps to ENST00000440594 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr16:89293776 G>T maps to NM_182531.2 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr16:89294045 G>T maps to NM_182531.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2657-01A-01D-1105-08 chr19:40580835 C>A maps to NM_001142577.1 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:40587774 C>T maps to NM_001142577.1 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:40541580 C>G maps to NM_001005851.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:38160761 C>T maps to NM_152605.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4389-01A-01D-1265-08 chr9:99581986 G>A maps to NM_001001662.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr9:99580860 C>A maps to NM_001001662.1 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr7:148768939 C>A maps to NM_152411.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr7:148767931 G>A maps to NM_152411.3 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:56599580 C>G maps to NM_001002836.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6147-01A-11D-1753-08 chr9:130198190 T>G maps to NM_007135.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr9:130207407 G>T maps to NM_007135.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6592-01A-11D-1753-08 chr19:37314610 T>A maps to NM_206894.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:37314598 A>G maps to NM_206894.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr19:12735465 G>T maps to NM_153358.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:12739911 C>G maps to NM_153358.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:35451811 G>A maps to NM_175872.4 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:35449725 T>A maps to NM_175872.4 K345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:35451184 A>G maps to NM_175872.4 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr19:38028150 C>T maps to NM_001013659.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr19:38024288 G>T maps to NM_001013659.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4629-01A-02D-1265-08 chr19:12502032 G>A maps to NM_001080821.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr19:12502557 C>A maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:12501875 C>A maps to NM_001080821.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:58806301 A>G maps to NM_021089.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr3:113955273 G>A maps to NM_007136.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr3:113955153 G>A maps to NM_007136.3 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr7:127014854 T>A maps to NM_176814.3 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6774-01A-21D-1855-08 chr7:127014764 C>A maps to NM_176814.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr7:127014752 C>A maps to NM_176814.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr7:127013706 T>A maps to NM_176814.3 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7547-01A-11D-2036-08 chr7:127015089 T>A did not map to a codon.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr7:127014755 G>A maps to NM_176814.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr7:127014561 T>A maps to NM_176814.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr2:185802718 G>T maps to NM_194250.1 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr2:185803624 C>T maps to NM_194250.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr2:185803677 A>T maps to NM_194250.1 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-3398-01A-01D-1105-08 chr2:185802746 T>G maps to NM_194250.1 L875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:185800518 A>T maps to NM_194250.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7671-01A-11D-2063-08 chr2:185801005 G>T maps to NM_194250.1 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4506-01A-01D-1265-08 chr2:185731220 T>A maps to NM_194250.1 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr2:185803191 C>A maps to NM_194250.1 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr2:185801376 C>A maps to NM_194250.1 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr2:185802876 C>T maps to NM_194250.1 V918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7727-01A-11D-2167-08 chr2:185803548 A>T maps to NM_194250.1 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8507-01A-11D-2393-08 chr2:185800855 G>T maps to NM_194250.1 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr2:185801280 C>A maps to NM_194250.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr2:185802574 A>T maps to NM_194250.1 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4662-01A-01D-1265-08 chr2:185798421 C>A maps to NM_194250.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr2:185802438 T>C maps to NM_194250.1 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5126-01A-01D-1753-08 chr2:185801019 C>A maps to NM_194250.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr2:185802297 G>A maps to NM_194250.1 W725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr2:185802585 C>A maps to NM_194250.1 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:185798437 G>T maps to NM_194250.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7542-01A-21D-2063-08 chr2:185801662 G>T maps to NM_194250.1 G514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr2:185801991 G>A maps to NM_194250.1 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr2:185803635 C>A maps to NM_194250.1 I1171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr2:185803230 C>T maps to NM_194250.1 I1036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr2:185802004 G>T maps to NM_194250.1 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:185802450 A>T maps to NM_194250.1 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8672-01A-21D-2393-08 chr2:185802558 G>T maps to NM_194250.1 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:185731143 A>T maps to NM_194250.1 K54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:185801565 A>G maps to NM_194250.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr2:185801338 G>T maps to NM_194250.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8176-01A-11D-2393-08 chr2:185801587 C>T maps to NM_194250.1 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr2:185800717 C>T maps to NM_194250.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr2:185800740 G>T maps to NM_194250.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4384-01A-01D-1753-08 chr7:88964341 C>A maps to NM_181646.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr7:88966075 C>T maps to NM_181646.2 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z016-01A-01W-0746-08 chr7:88965764 A>T maps to NM_181646.2 K1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr7:88966204 C>A maps to NM_181646.2 A1303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7672-01A-11D-2063-08 chr7:88964764 G>A maps to NM_181646.2 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-A4SS-01A-11D-A24P-08 chr7:88962751 C>A maps to NM_181646.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr7:88962751 C>A maps to NM_181646.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr7:88964047 C>T maps to NM_181646.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr7:88847494 A>T maps to NM_181646.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr7:88847581 T>A maps to NM_181646.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:88847531 G>T maps to NM_181646.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr7:88964852 A>C maps to NM_181646.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:88965692 G>T maps to NM_181646.2 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7711-01A-11D-2063-08 chr7:88389325 C>G maps to NM_181646.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr7:88965208 C>A maps to NM_181646.2 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr7:88966330 C>G maps to NM_181646.2 S1345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr7:88963429 C>A maps to NM_181646.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr7:88963523 A>C maps to NM_181646.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4LX-01A-11D-A24P-08 chr7:88965916 C>A maps to NM_181646.2 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr19:57765063 G>T maps to NM_001023563.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z023-01A-01W-0746-08 chr19:53050823 G>C maps to NM_001039886.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:53057984 C>T maps to NM_001039886.3 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:53056600 C>T maps to NM_001039886.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:53057782 T>C maps to NM_001039886.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4430-01A-02D-1265-08 chr23:47774731 G>C did not map to a codon.
Sequencing variant TCGA-38-4632-01A-01D-1753-08 chr23:47775134 G>T did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr23:47755297 C>A did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:47775275 G>T did not map to a codon.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr23:47775276 A>G did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:47775470 G>T did not map to a codon.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr23:47775471 G>T did not map to a codon.
Sequencing variant TCGA-64-5775-01A-01D-1625-08 chr23:47775356 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:47774710 G>T did not map to a codon.
Sequencing variant TCGA-73-7498-01A-12D-2184-08 chr23:47774811 G>C did not map to a codon.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr23:47775255 A>T did not map to a codon.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr19:53994625 G>A maps to NM_001004301.3 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5068-01A-01D-1625-08 chr19:53994016 C>T maps to NM_001004301.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:53993750 G>T maps to NM_001004301.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8394-01A-11D-2323-08 chr19:53994553 G>A maps to NM_001004301.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr19:58384402 G>A maps to NM_001144989.1 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr19:58385659 G>A maps to NM_001144989.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7713-01A-11D-2063-08 chr19:53459278 C>A did not map to a codon.
Sequencing variant TCGA-53-7813-01A-11D-2167-08 chr16:71913843 G>A maps to ENST00000425432 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5428-01A-01D-1625-08 chr19:11833306 G>A maps to NM_001080493.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr19:11833010 A>G maps to NM_001080493.2 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:11833619 C>G maps to NM_001080493.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr4:146806893 C>A maps to ENST00000508784 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6595-01A-12D-1855-08 chr4:146791526 G>A maps to ENST00000508784 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8094-01A-11D-2238-08 chr4:146686249 T>A maps to ENST00000508784 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr4:146807067 C>A maps to ENST00000508784 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr4:146770557 C>A maps to ENST00000508784 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7955-01A-11D-2184-08 chr4:146813418 C>T maps to ENST00000508784 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7761-01A-11D-2167-08 chr19:53116800 G>A maps to NM_018300.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z026-01A-01W-0746-08 chr17:33288890 G>A maps to NM_052857.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4625-01A-01D-1553-08 chr17:33289355 T>C maps to NM_052857.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr20:57769380 C>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr20:57768836 C>T maps to NM_178457.1 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr20:57769382 G>T maps to NM_178457.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:57769598 C>A maps to NM_178457.1 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4628-01A-01D-1265-08 chr20:57768041 G>T maps to NM_178457.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7227-01A-11D-2036-08 chr20:57766578 G>T maps to NM_178457.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr20:57769445 G>T maps to NM_178457.1 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr20:57767498 G>A maps to NM_178457.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8511-01A-11D-2393-08 chr20:57769370 C>A maps to NM_178457.1 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:57766652 G>T maps to NM_178457.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:57768475 G>A maps to NM_178457.1 W801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr20:57769377 G>T maps to NM_178457.1 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A491-01A-11D-A24D-08 chr20:57768128 C>A maps to NM_178457.1 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A493-01A-11D-A24D-08 chr20:57766302 C>T maps to NM_178457.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr20:57768207 G>T maps to NM_178457.1 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-7027-01A-11D-1945-08 chr20:57768320 C>A maps to NM_178457.1 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr20:57767549 C>G maps to NM_178457.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:57768317 G>T maps to NM_178457.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr20:57828093 G>A maps to NM_178457.1 K1363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr20:57767558 C>T maps to NM_178457.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr20:57829698 C>A maps to NM_178457.1 S1645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:57769436 C>A maps to NM_178457.1 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr20:57769481 C>A maps to NM_178457.1 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8279-01A-11D-2284-08 chr20:57766223 C>A maps to NM_178457.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr20:57766385 G>A maps to NM_178457.1 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8673-01A-11D-2393-08 chr20:57766623 C>T maps to NM_178457.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:57767444 C>T maps to NM_178457.1 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr20:57767781 C>T maps to NM_178457.1 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr20:57768488 C>A maps to NM_178457.1 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6836-01A-21D-1855-08 chr20:57768083 A>T maps to NM_178457.1 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:57769445 G>A maps to NM_178457.1 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr20:57769658 C>A maps to NM_178457.1 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr20:57828181 C>T maps to NM_178457.1 R1393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N1-01A-11D-A24P-08 chr20:57768950 A>T maps to NM_178457.1 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr20:57766529 C>T maps to NM_178457.1 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A55A-01A-11D-A25L-08 chr20:57769121 G>C maps to NM_178457.1 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z005-01A-01W-0746-08 chr19:57175468 G>A maps to NM_001005850.1 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-4112-01A-01D-1105-08 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:57176164 C>A maps to NM_001005850.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr19:57176383 T>A maps to NM_001005850.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7147-01A-11D-2036-08 chr19:57176524 C>T maps to NM_001005850.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7150-01A-21D-2036-08 chr19:57175426 G>A maps to NM_001005850.1 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7161-01A-11D-2036-08 chr19:57175426 G>A maps to NM_001005850.1 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6847-01A-11D-1945-08 chr19:57176149 C>T maps to NM_001005850.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:57175195 G>A maps to NM_001005850.1 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J2-8194-01A-11D-2238-08 chr19:57175630 G>T maps to NM_001005850.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5778-01A-01D-1625-08 chr19:52659498 G>A maps to NM_001102657.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr14:102792954 C>T maps to NM_018335.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z061-01A-01W-0747-08 chr14:102798179 G>A maps to NM_018335.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52570210 C>T maps to NM_001136499.1 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YQ-01A-11D-A25L-08 chr19:52568434 A>C maps to NM_001136499.1 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8205-01A-11D-2238-08 chr19:12187317 C>T maps to NM_001136501.1 H461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:12186444 T>C maps to NM_001136501.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7162-01A-21D-2063-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z041-01A-01W-0746-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-4123-01A-01D-1105-08 chr19:53855115 A>T maps to NM_138374.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-38-4631-01A-01D-1753-08 chr19:53855100 C>G maps to NM_138374.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6982-01A-11D-1945-08 chr19:53855271 C>T maps to NM_138374.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:53855529 G>C maps to NM_138374.1 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8092-01A-11D-2238-08 chr19:53854578 T>C maps to NM_138374.1 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8208-01A-11D-2238-08 chr19:53855451 A>G maps to NM_138374.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z053-01A-01W-0747-08 chr19:9868573 G>T maps to NM_001077624.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:9868261 T>C maps to NM_001077624.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:9869439 C>A maps to NM_001077624.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr19:21116874 G>T maps to NM_003429.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:21131980 A>T maps to NM_003429.4 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr3:32032112 A>G maps to NM_001137674.1 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr3:32031133 C>G maps to NM_001137674.1 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr3:32031983 T>A maps to NM_001137674.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3772-01A-01W-0928-08 chr3:32031134 A>G maps to NM_001137674.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr3:32031666 G>T maps to NM_001137674.1 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr7:149561357 C>T maps to NM_001099220.1 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6743-01A-11D-1855-08 chr7:149558927 C>T maps to NM_001099220.1 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr7:149558171 G>A maps to NM_001099220.1 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A48X-01A-11D-A24D-08 chr7:149559177 G>T maps to NM_001099220.1 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4677-01A-01D-1265-08 chr7:149545229 G>T maps to NM_001099220.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr7:149559329 C>T maps to NM_001099220.1 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4486-01A-01D-1265-08 chr19:12157505 G>A maps to NM_001080404.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8660-01A-11D-2393-08 chr19:12155311 C>A maps to NM_001080404.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr19:52887267 A>G maps to NM_001145434.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr19:52876488 G>T maps to NM_001145434.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr19:52887982 G>T maps to NM_001145434.1 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr19:20215046 G>T did not map to a codon.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:20230090 G>A maps to NM_007138.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:23542620 C>A maps to NM_003430.2 E1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr19:23543432 G>C maps to NM_003430.2 S783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-A46O-01A-11D-A24D-08 chr19:23543764 G>A maps to NM_003430.2 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-4679-01B-01D-1753-08 chr19:23543379 C>A maps to NM_003430.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7763-01A-11D-2167-08 chr19:23545332 G>A maps to NM_003430.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:23544934 A>T maps to NM_003430.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7714-01A-12D-2167-08 chr19:23543479 C>T maps to NM_003430.2 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7539-01A-11D-2063-08 chr7:64864224 G>T maps to NM_152626.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5049-01A-01D-1625-08 chr19:20027412 G>T maps to NM_031218.3 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr19:20027403 C>T maps to NM_031218.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr19:20044520 G>T maps to NM_031218.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7567-01A-11D-2063-08 chr19:20044840 T>C maps to NM_031218.3 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7947-01A-11D-2184-08 chr19:20026088 G>T maps to NM_031218.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z011-01A-01W-0746-08 chr19:22586296 C>T maps to NM_001098626.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:22574938 A>T maps to NM_001098626.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z042-01A-01W-0746-08 chr19:22574464 G>T maps to NM_001098626.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z062-01A-01W-0747-08 chr19:22586188 C>A maps to NM_001098626.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr19:22574548 G>C maps to NM_001098626.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-93-7347-01A-11D-2184-08 chr19:22585641 C>A maps to NM_001098626.1 G68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:22574631 T>A maps to NM_001098626.1 K469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr19:22586257 G>T maps to NM_001098626.1 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr19:22574650 G>T maps to NM_001098626.1 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4382-01A-01D-1931-08 chr19:22939969 T>A maps to ENST00000397104 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4402-01A-01D-1265-08 chr19:22941399 G>A maps to ENST00000397104 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z025-01A-01W-0746-08 chr19:22939801 T>A maps to ENST00000397104 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22939746 C>A maps to ENST00000397104 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr19:22940568 A>G maps to ENST00000397104 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr19:22941729 G>T maps to ENST00000397104 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr19:22939739 C>A did not map to a codon.
Sequencing variant TCGA-44-7670-01A-11D-2063-08 chr19:22939921 T>C maps to ENST00000397104 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7570-01A-11D-2036-08 chr19:22952126 C>A did not map to a codon.
Sequencing variant TCGA-55-8301-01A-11D-2284-08 chr19:22940781 A>G maps to ENST00000397104 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:22941657 G>A maps to ENST00000397104 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:22939927 G>T maps to ENST00000397104 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7974-01A-11D-2184-08 chr19:22941359 G>A maps to ENST00000397104 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8640-01A-11D-2393-08 chr19:22940809 G>T maps to ENST00000397104 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-80-5611-01A-01D-1625-08 chr19:22952000 C>T maps to ENST00000397104 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr19:22939488 G>T maps to ENST00000397104 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr19:22939347 C>T maps to ENST00000397104 E941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8033-01A-11D-2238-08 chr19:22942332 G>A maps to ENST00000397104 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:22939425 C>A maps to ENST00000397104 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr19:22940041 T>C maps to ENST00000397104 K763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr20:47888036 C>T maps to NM_021035.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr20:47886770 C>T maps to NM_021035.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7913-01B-11D-2238-08 chr20:47879978 T>C maps to NM_021035.2 E731E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr20:47886917 G>C maps to NM_021035.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7166-01A-12D-2063-08 chr20:47888275 C>A maps to NM_021035.2 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4417-01A-22D-1855-08 chr7:100865999 G>T maps to NM_006349.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr7:100865909 G>A maps to NM_006349.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4250-01A-01D-1105-08 chr19:5456194 G>T maps to NM_181710.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr19:5455750 C>G maps to NM_181710.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-A490-01A-11D-A24D-08 chr19:5456734 C>A maps to NM_181710.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7159-01A-11D-2036-08 chr19:5455571 C>T maps to NM_181710.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8056-01A-11D-2238-08 chr19:5456134 A>C maps to NM_181710.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-A4BC-01A-11D-A24D-08 chr19:5456383 C>T maps to NM_181710.3 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr19:5455879 C>A maps to NM_181710.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr11:60635066 C>G maps to NM_207341.2 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr11:60638430 T>G maps to NM_207341.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7659-01A-11D-2063-08 chr11:60642985 G>C did not map to a codon.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr11:60638463 C>T maps to NM_207341.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr16:21213477 G>A maps to NM_003460.1 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z057-01A-01W-0747-08 chr16:21220984 C>G maps to NM_003460.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4494-01A-01D-1265-08 chr16:21213574 G>A maps to NM_003460.1 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr16:21215359 G>C maps to NM_003460.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6831-01A-11D-1855-08 chr16:21214497 T>C maps to NM_003460.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8514-01A-11D-2393-08 chr7:76062964 G>C did not map to a codon.
Sequencing variant TCGA-05-4418-01A-01D-1265-08 chr1:238048737 G>T maps to NM_021186.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4432-01A-01D-1265-08 chr1:238053191 C>A maps to NM_021186.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z018-01A-01W-0746-08 chr1:238048569 G>T maps to NM_021186.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z021-01A-01W-0746-08 chr1:238053263 G>T maps to NM_021186.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr1:238048068 G>T maps to NM_021186.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-35-5375-01A-01D-1625-08 chr1:238048521 G>A maps to NM_021186.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr1:238051763 C>A maps to NM_021186.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr1:238050168 C>A did not map to a codon.
Sequencing variant TCGA-44-6778-01A-11D-1855-08 chr1:238045793 G>T maps to NM_021186.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7662-01A-11D-2063-08 chr1:238051726 C>A maps to NM_021186.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-4507-01A-01D-1265-08 chr1:238048821 C>G maps to NM_021186.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6767-01A-11D-1855-08 chr1:238048491 T>A maps to NM_021186.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5936-01A-11D-1625-08 chr1:238048575 G>T maps to NM_021186.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-5899-01A-11D-1625-08 chr1:238048072 G>A maps to NM_021186.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8203-01A-11D-2238-08 chr1:238048462 A>T did not map to a codon.
Sequencing variant TCGA-62-A46P-01A-11D-A24D-08 chr1:238053381 G>T maps to NM_021186.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4676-01A-01D-1753-08 chr1:238053779 A>T maps to NM_021186.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7039-01A-11D-1945-08 chr1:238049088 C>A maps to NM_021186.3 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VK-01A-11D-A25L-08 chr1:238048737 G>T maps to NM_021186.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8025-01A-11D-2238-08 chr1:238045784 G>T maps to NM_021186.3 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4SV-01A-11D-A24P-08 chr1:238053767 T>A maps to NM_021186.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TA-01A-21D-A24P-08 chr1:238051807 G>T maps to NM_021186.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z022-01A-01W-0746-08 chr7:50121487 C>A maps to NM_007009.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7576-01A-11D-2063-08 chr7:50070790 C>A maps to NM_007009.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8506-01A-11D-2393-08 chr7:50121397 C>T maps to NM_007009.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr7:50121454 C>A maps to NM_007009.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7978-01A-11D-2184-08 chr7:50057883 G>C maps to NM_007009.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-75-5122-01A-01D-1753-08 chr7:50070835 A>G maps to NM_007009.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-7554-01A-11D-2036-08 chr7:50023025 T>C maps to NM_007009.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031515 C>T maps to NM_199321.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-1592-01A-01D-0969-08 chr17:38031553 C>T maps to NM_199321.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N5-01A-11D-A24P-08 chr17:38033004 C>A maps to NM_199321.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YP-01A-11D-A25L-08 chr17:38032983 G>A maps to NM_199321.2 Q313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z000-01A-01W-0746-08 chr3:102187939 C>A maps to NM_175056.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z031-01A-01W-0746-08 chr3:102196309 C>T maps to NM_175056.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z055-01A-01W-0747-08 chr3:102175128 A>G maps to NM_175056.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr3:102176645 G>T maps to NM_175056.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-8255-01A-11D-2284-08 chr3:102187858 G>T maps to NM_175056.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4668-01A-01D-1265-08 chr3:102181146 T>A maps to NM_175056.1 L218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr1:71544195 C>T maps to NM_203350.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NJ-A4YF-01A-12D-A25L-08 chr1:71538210 C>A maps to NM_203350.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8398-01A-11D-2323-08 chr2:136026549 C>T maps to NM_032143.2 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr2:135982055 C>A maps to NM_032143.2 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7562-01A-11D-2238-08 chr23:15841213 G>T did not map to a codon.
Sequencing variant TCGA-97-7938-01A-11D-2167-08 chr23:15840939 G>T did not map to a codon.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:58551816 G>C did not map to a codon.
Sequencing variant TCGA-49-4487-01A-21D-1855-08 chr19:58551839 C>T maps to NM_182572.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5946-01A-11D-1753-08 chr19:58549467 C>A maps to NM_182572.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8399-01A-21D-2323-08 chr19:58565248 C>A maps to NM_182572.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-73-4666-01A-01D-1265-08 chr19:58549359 G>T maps to NM_182572.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7154-01A-11D-2036-08 chr19:58565064 C>T maps to NM_182572.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr16:3140342 C>T maps to NM_032805.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z028-01A-01W-0746-08 chr16:3140534 C>A maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr16:3142677 C>T maps to NM_032805.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:3139853 G>T maps to NM_032805.1 C472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr16:3142080 G>T maps to NM_032805.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr16:3139795 C>A maps to NM_032805.1 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TI-01A-21D-A24P-08 chr16:3142059 C>T maps to NM_032805.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z032-01A-01W-0746-08 chr19:58601463 G>A maps to NM_001145542.1 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8616-01A-11D-2393-08 chr19:58596174 C>T maps to NM_001145542.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7973-01A-11D-2184-08 chr19:58596564 G>A maps to NM_001145542.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr19:58596188 C>A maps to NM_001145542.1 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr19:58601748 C>A maps to NM_001145542.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:33956898 C>T maps to NM_145238.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:33956997 C>T maps to NM_145238.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:33957237 C>T maps to NM_145238.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6972-01A-11D-1945-08 chr1:33957288 C>T maps to NM_145238.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1679-01A-21D-2063-08 chr7:99654700 G>C maps to NM_145914.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-67-3771-01A-01D-1040-01 chr7:99662083 G>A maps to NM_145914.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6712-01A-11D-1855-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-6968-01A-11D-1945-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-7954-01A-11D-2184-08 chr19:58850394 G>A maps to NM_181846.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr19:58846459 C>T maps to NM_181846.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MN-A4N4-01A-12D-A24P-08 chr19:58850178 G>A maps to NM_181846.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4397-01A-01D-1265-08 chr19:58189693 C>T maps to NM_152677.2 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-A4EZ-01A-12D-A24P-08 chr19:58189555 C>A maps to NM_152677.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:58189837 C>T maps to NM_152677.2 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-5779-01A-01D-1625-08 chr19:58189889 G>T maps to NM_152677.2 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:58187633 G>T maps to NM_152677.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr19:58189660 T>A maps to NM_152677.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z060-01A-01W-0747-08 chr19:56736247 C>A maps to NM_024303.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8089-01A-11D-2238-08 chr19:56733209 C>A maps to NM_024303.1 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4424-01A-22D-1855-08 chr19:56701606 C>A maps to NM_001080456.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z017-01A-01W-0746-08 chr19:56701624 C>G maps to NM_001080456.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7907-01A-11D-2167-08 chr19:56704300 C>A maps to NM_001080456.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr19:56704271 G>A maps to NM_001080456.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-69-7979-01A-11D-2184-08 chr19:56703265 G>T maps to NM_001080456.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7148-01A-11D-2036-08 chr19:56704113 A>T maps to NM_001080456.2 L103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8358-01A-11D-2323-08 chr19:56701794 T>A maps to NM_001080456.2 K297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-99-8028-01A-11D-2238-08 chr19:56704258 C>A maps to NM_001080456.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4398-01A-01D-1265-08 chr2:187698690 G>A maps to NM_182521.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5425-01A-02D-1625-08 chr2:187703836 G>A maps to NM_182521.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-5644-01A-21D-2036-08 chr2:187692725 T>C maps to NM_182521.2 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-6145-01A-11D-1753-08 chr2:187712477 C>T maps to NM_182521.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr2:187694607 C>A did not map to a codon.
Sequencing variant TCGA-86-A4JF-01A-11D-A24P-08 chr2:187698687 C>T maps to NM_182521.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr20:44506099 C>T maps to NM_080752.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-17-Z043-01A-01W-0746-08 chr20:44506135 C>T maps to NM_080752.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-2656-01A-02D-0969-08 chr20:44505619 C>T maps to NM_080752.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-49-6745-01A-11D-1855-08 chr20:44506471 C>T maps to NM_080752.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-6590-01A-12D-1855-08 chr19:13939466 G>A maps to NM_023072.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7155-01A-11D-2036-08 chr19:13919734 G>A maps to NM_023072.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-8662-01A-11D-2393-08 chr19:13915655 G>T maps to NM_023072.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-A4VP-01A-21D-A25L-08 chr19:13941074 C>T maps to NM_023072.2 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7667-01A-31D-2063-08 chr1:45484448 G>T maps to NM_020883.1 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-62-8402-01A-11D-2323-08 chr1:45506178 G>A maps to NM_020883.1 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-91-6829-01A-21D-1855-08 chr1:45506069 T>A maps to NM_020883.1 K584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr6:116988238 C>G maps to NM_145062.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-6851-01A-11D-1945-08 chr6:116956995 C>T maps to NM_145062.2 *579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-A4M5-01A-11D-A24P-08 chr6:116977966 G>A maps to NM_145062.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr11:113608400 C>A maps to NM_004724.2 G637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4390-01A-02D-1753-08 chr15:66811349 G>T maps to NM_017975.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr15:66821248 G>A maps to NM_017975.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4427-01A-21D-1855-08 chr10:58119777 C>A did not map to a codon.
Sequencing variant TCGA-69-A59K-01A-11D-A25L-08 chr10:58118364 C>T maps to NM_032997.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-97-8179-01A-11D-2284-08 chr10:58118707 C>A maps to NM_032997.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-5715-01A-01D-1625-08 chr23:57935302 A>T did not map to a codon.
Sequencing variant TCGA-17-Z033-01A-01W-0746-08 chr23:57934638 A>T did not map to a codon.
Sequencing variant TCGA-44-A47G-01A-21D-A24D-08 chr23:57935350 T>A did not map to a codon.
Sequencing variant TCGA-49-4488-01A-01D-1753-08 chr23:57936548 G>T did not map to a codon.
Sequencing variant TCGA-67-6215-01A-11D-1753-08 chr23:57935081 G>T did not map to a codon.
Sequencing variant TCGA-69-7765-01A-11D-2167-08 chr23:57934460 C>A did not map to a codon.
Sequencing variant TCGA-73-4670-01A-01D-1265-08 chr23:57934537 C>A did not map to a codon.
Sequencing variant TCGA-75-6214-01A-41D-1945-08 chr23:57935509 G>T did not map to a codon.
Sequencing variant TCGA-78-7220-01A-11D-2036-08 chr23:57935120 T>C did not map to a codon.
Sequencing variant TCGA-95-A4VN-01A-11D-A25L-08 chr23:57935969 C>A did not map to a codon.
Sequencing variant TCGA-99-7458-01A-11D-2036-08 chr23:57936014 C>A did not map to a codon.
Sequencing variant TCGA-05-4396-01A-21D-1855-08 chr23:57620751 G>C did not map to a codon.
Sequencing variant TCGA-53-7626-01A-12D-2063-08 chr23:57620763 A>T did not map to a codon.
Sequencing variant TCGA-55-8302-01A-11D-2323-08 chr23:57619060 G>T did not map to a codon.
Sequencing variant TCGA-91-8499-01A-11D-2393-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-L9-A444-01A-21D-A24D-08 chr23:57620123 G>A did not map to a codon.
Sequencing variant TCGA-53-7624-01A-11D-2063-08 chr3:126180668 C>A maps to NM_025112.4 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:126180821 C>G maps to NM_025112.4 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-7994-01A-11D-2184-08 chr3:126185040 G>A maps to NM_025112.4 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-64-1676-01A-01D-0969-08 chr3:126180701 C>A maps to NM_025112.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MP-A4TD-01A-32D-A25L-08 chr3:126181063 C>A did not map to a codon.
Sequencing variant TCGA-05-4405-01A-21D-1855-08 chr7:143080396 G>C maps to NM_001010972.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-44-7660-01A-11D-2063-08 chr7:143085735 C>T maps to NM_001010972.1 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-05-4410-01A-21D-1855-08 chr17:4008082 C>A maps to NM_015113.3 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-50-5944-01A-11D-1753-08 chr17:3990762 C>T maps to NM_015113.3 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-55-8620-01A-11D-2393-08 chr17:3967956 G>A maps to NM_015113.3 A1472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-78-7152-01A-11D-2036-08 chr17:3935492 C>G maps to NM_015113.3 V2273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-86-8073-01A-11D-2238-08 chr17:3989092 C>G maps to NM_015113.3 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-95-7043-01A-11D-1945-08 chr17:3955430 C>A did not map to a codon.
Sequencing variant TCGA-55-A492-01A-11D-A24D-08 chr1:78097931 C>A maps to NM_015534.4 E370*. Only missense variants will be evaluated by CHASM.
